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You searched for subject:(CXCR4). Showing records 1 – 30 of 151 total matches.

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1. CAMPELO JUNIOR, Evônio de Barros. Coinfecção GBV-C e HIV em pacientes acompanhados no serviço de doenças infecciosas e parasitárias do HC-UFPE .

Degree: 2012, Universidade Federal de Pernambuco

 Desde 1967, momento do seu surgimento no mundo científico, o GB vírus C (GBV-C) permanece conhecido como vírus indolente, todavia não obstante,pesquisas têm reveladoadespeito da… (more)

Subjects/Keywords: HIV; GBV-C; CCR5; CXCR4

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

CAMPELO JUNIOR, E. d. B. (2012). Coinfecção GBV-C e HIV em pacientes acompanhados no serviço de doenças infecciosas e parasitárias do HC-UFPE . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/18505

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

CAMPELO JUNIOR, Evônio de Barros. “Coinfecção GBV-C e HIV em pacientes acompanhados no serviço de doenças infecciosas e parasitárias do HC-UFPE .” 2012. Thesis, Universidade Federal de Pernambuco. Accessed December 01, 2020. http://repositorio.ufpe.br/handle/123456789/18505.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

CAMPELO JUNIOR, Evônio de Barros. “Coinfecção GBV-C e HIV em pacientes acompanhados no serviço de doenças infecciosas e parasitárias do HC-UFPE .” 2012. Web. 01 Dec 2020.

Vancouver:

CAMPELO JUNIOR EdB. Coinfecção GBV-C e HIV em pacientes acompanhados no serviço de doenças infecciosas e parasitárias do HC-UFPE . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2012. [cited 2020 Dec 01]. Available from: http://repositorio.ufpe.br/handle/123456789/18505.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

CAMPELO JUNIOR EdB. Coinfecção GBV-C e HIV em pacientes acompanhados no serviço de doenças infecciosas e parasitárias do HC-UFPE . [Thesis]. Universidade Federal de Pernambuco; 2012. Available from: http://repositorio.ufpe.br/handle/123456789/18505

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Minnesota

2. Lepley, Michael Alan. Identification of arterial phenotype in endothelial cells derived from human pluripotent stem cells.

Degree: MS, Stem Cell Biology, 2013, University of Minnesota

 The use of human pluripotent stem cells (HPSC) to generate mature endothelial cells (EC) has been described previously, but is an inefficient process. We adopted… (more)

Subjects/Keywords: Arterial; CXCR4; Endothelial; PI3K

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APA (6th Edition):

Lepley, M. A. (2013). Identification of arterial phenotype in endothelial cells derived from human pluripotent stem cells. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162844

Chicago Manual of Style (16th Edition):

Lepley, Michael Alan. “Identification of arterial phenotype in endothelial cells derived from human pluripotent stem cells.” 2013. Masters Thesis, University of Minnesota. Accessed December 01, 2020. http://hdl.handle.net/11299/162844.

MLA Handbook (7th Edition):

Lepley, Michael Alan. “Identification of arterial phenotype in endothelial cells derived from human pluripotent stem cells.” 2013. Web. 01 Dec 2020.

Vancouver:

Lepley MA. Identification of arterial phenotype in endothelial cells derived from human pluripotent stem cells. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/11299/162844.

Council of Science Editors:

Lepley MA. Identification of arterial phenotype in endothelial cells derived from human pluripotent stem cells. [Masters Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/162844


Loyola University Chicago

3. Staren, Daniel M. Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin.

Degree: MS, Molecular Biology, 2012, Loyola University Chicago

  Ubiquitin has previously been identified as another natural agonist of CXC chemokine receptor 4 (CXCR4). In addition, recent evidence suggests that ubiquitin may activate… (more)

Subjects/Keywords: CXCR4; Ubiquitin; Molecular Biology

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APA (6th Edition):

Staren, D. M. (2012). Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin. (Thesis). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_theses/840

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Staren, Daniel M. “Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin.” 2012. Thesis, Loyola University Chicago. Accessed December 01, 2020. https://ecommons.luc.edu/luc_theses/840.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Staren, Daniel M. “Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin.” 2012. Web. 01 Dec 2020.

Vancouver:

Staren DM. Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin. [Internet] [Thesis]. Loyola University Chicago; 2012. [cited 2020 Dec 01]. Available from: https://ecommons.luc.edu/luc_theses/840.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Staren DM. Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin. [Thesis]. Loyola University Chicago; 2012. Available from: https://ecommons.luc.edu/luc_theses/840

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Georgia State University

4. Gaines, Theresa D. DESIGN, SYNTHESIS AND ANALYSIS OF SMALL MOLECULE HETEROCYCLIC AROMATIC-BASED CXCR4 MODULATORS.

Degree: PhD, Chemistry, 2017, Georgia State University

CXCR4 is a chemokine receptor that has been linked to several disease related pathways including: HIV-1 proliferation, autoimmune disorders, inflammatory disease and cancer metastasis.… (more)

Subjects/Keywords: chemokine; CXCR4; CXCL12; Inflammation; metastasis

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APA (6th Edition):

Gaines, T. D. (2017). DESIGN, SYNTHESIS AND ANALYSIS OF SMALL MOLECULE HETEROCYCLIC AROMATIC-BASED CXCR4 MODULATORS. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/134

Chicago Manual of Style (16th Edition):

Gaines, Theresa D. “DESIGN, SYNTHESIS AND ANALYSIS OF SMALL MOLECULE HETEROCYCLIC AROMATIC-BASED CXCR4 MODULATORS.” 2017. Doctoral Dissertation, Georgia State University. Accessed December 01, 2020. https://scholarworks.gsu.edu/chemistry_diss/134.

MLA Handbook (7th Edition):

Gaines, Theresa D. “DESIGN, SYNTHESIS AND ANALYSIS OF SMALL MOLECULE HETEROCYCLIC AROMATIC-BASED CXCR4 MODULATORS.” 2017. Web. 01 Dec 2020.

Vancouver:

Gaines TD. DESIGN, SYNTHESIS AND ANALYSIS OF SMALL MOLECULE HETEROCYCLIC AROMATIC-BASED CXCR4 MODULATORS. [Internet] [Doctoral dissertation]. Georgia State University; 2017. [cited 2020 Dec 01]. Available from: https://scholarworks.gsu.edu/chemistry_diss/134.

Council of Science Editors:

Gaines TD. DESIGN, SYNTHESIS AND ANALYSIS OF SMALL MOLECULE HETEROCYCLIC AROMATIC-BASED CXCR4 MODULATORS. [Doctoral Dissertation]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/chemistry_diss/134

5. Freitas, Christelle. Impact d’un gain de fonction de CXCR4 sur la différenciation des cellules souches et des progéniteurs hématopoïétiques : Impact of gain-of-function mutation in CXCR4 on hematopoietic stem and progenitor cells differentiation.

Degree: Docteur es, Immunologie, 2016, Université Paris-Saclay (ComUE)

Le Syndrome WHIM (SW) est un déficit immuno-hématologique rare qui se caractérise notamment par une profonde leucopénie circulante. Le SW résulte principalement de mutations hétérozygotes… (more)

Subjects/Keywords: Hématologie; Syndrome WHIM; Cxcr4; Hematology; WHIM Syndrome; Cxcr4

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APA (6th Edition):

Freitas, C. (2016). Impact d’un gain de fonction de CXCR4 sur la différenciation des cellules souches et des progéniteurs hématopoïétiques : Impact of gain-of-function mutation in CXCR4 on hematopoietic stem and progenitor cells differentiation. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS099

Chicago Manual of Style (16th Edition):

Freitas, Christelle. “Impact d’un gain de fonction de CXCR4 sur la différenciation des cellules souches et des progéniteurs hématopoïétiques : Impact of gain-of-function mutation in CXCR4 on hematopoietic stem and progenitor cells differentiation.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed December 01, 2020. http://www.theses.fr/2016SACLS099.

MLA Handbook (7th Edition):

Freitas, Christelle. “Impact d’un gain de fonction de CXCR4 sur la différenciation des cellules souches et des progéniteurs hématopoïétiques : Impact of gain-of-function mutation in CXCR4 on hematopoietic stem and progenitor cells differentiation.” 2016. Web. 01 Dec 2020.

Vancouver:

Freitas C. Impact d’un gain de fonction de CXCR4 sur la différenciation des cellules souches et des progéniteurs hématopoïétiques : Impact of gain-of-function mutation in CXCR4 on hematopoietic stem and progenitor cells differentiation. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2016SACLS099.

Council of Science Editors:

Freitas C. Impact d’un gain de fonction de CXCR4 sur la différenciation des cellules souches et des progéniteurs hématopoïétiques : Impact of gain-of-function mutation in CXCR4 on hematopoietic stem and progenitor cells differentiation. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS099


Dalhousie University

6. Tufts, Julia. ADENOSINE AS AN ENVIRONMENTAL STRESSOR AFFECTING HSP27 AND CXCR4 IN EPITHELIAL CELLS.

Degree: MS, Department of Biology, 2013, Dalhousie University

 Solid tumours are a hostile tissue environment in which the cells are exposed to many stresses including hypoxia. One consequence of hypoxic conditions is an… (more)

Subjects/Keywords: HSP27; Hypoxia; Breast cancer; Adenosine; CXCR4

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APA (6th Edition):

Tufts, J. (2013). ADENOSINE AS AN ENVIRONMENTAL STRESSOR AFFECTING HSP27 AND CXCR4 IN EPITHELIAL CELLS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/21408

Chicago Manual of Style (16th Edition):

Tufts, Julia. “ADENOSINE AS AN ENVIRONMENTAL STRESSOR AFFECTING HSP27 AND CXCR4 IN EPITHELIAL CELLS.” 2013. Masters Thesis, Dalhousie University. Accessed December 01, 2020. http://hdl.handle.net/10222/21408.

MLA Handbook (7th Edition):

Tufts, Julia. “ADENOSINE AS AN ENVIRONMENTAL STRESSOR AFFECTING HSP27 AND CXCR4 IN EPITHELIAL CELLS.” 2013. Web. 01 Dec 2020.

Vancouver:

Tufts J. ADENOSINE AS AN ENVIRONMENTAL STRESSOR AFFECTING HSP27 AND CXCR4 IN EPITHELIAL CELLS. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10222/21408.

Council of Science Editors:

Tufts J. ADENOSINE AS AN ENVIRONMENTAL STRESSOR AFFECTING HSP27 AND CXCR4 IN EPITHELIAL CELLS. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/21408


Temple University

7. Kim, Jae Kyun. CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse.

Degree: PhD, 2016, Temple University

Pharmacology

The role of chemokines as chemotactic cytokines and their functions in the immune system and related pathologies are well defined. Recently, strong evidence supporting… (more)

Subjects/Keywords: Pharmacology;

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APA (6th Edition):

Kim, J. K. (2016). CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,399036

Chicago Manual of Style (16th Edition):

Kim, Jae Kyun. “CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse.” 2016. Doctoral Dissertation, Temple University. Accessed December 01, 2020. http://digital.library.temple.edu/u?/p245801coll10,399036.

MLA Handbook (7th Edition):

Kim, Jae Kyun. “CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse.” 2016. Web. 01 Dec 2020.

Vancouver:

Kim JK. CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Dec 01]. Available from: http://digital.library.temple.edu/u?/p245801coll10,399036.

Council of Science Editors:

Kim JK. CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,399036


Boston University

8. Hunter, Zachary Richard. Whole genome sequencing reveals that recurrent MYD88 and CXCR4 mutations underlie the genomic landscape of Waldenström's macroglobulinemia.

Degree: PhD, Pathology & Laboratory Medicine, 2015, Boston University

 Waldenström's Macroglobulinemia (WM) is a rare, indolent, non-Hodgkin's lymphoma whose molecular pathology remains poorly understood. This disease is characterized by the accumulation of IgM-secreting lymphoplasmacytic… (more)

Subjects/Keywords: Genetics; CXCR4; Lymphoma; Lymphoplasmacytic; MYD88; Waldenstrom; WHIM

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APA (6th Edition):

Hunter, Z. R. (2015). Whole genome sequencing reveals that recurrent MYD88 and CXCR4 mutations underlie the genomic landscape of Waldenström's macroglobulinemia. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/15632

Chicago Manual of Style (16th Edition):

Hunter, Zachary Richard. “Whole genome sequencing reveals that recurrent MYD88 and CXCR4 mutations underlie the genomic landscape of Waldenström's macroglobulinemia.” 2015. Doctoral Dissertation, Boston University. Accessed December 01, 2020. http://hdl.handle.net/2144/15632.

MLA Handbook (7th Edition):

Hunter, Zachary Richard. “Whole genome sequencing reveals that recurrent MYD88 and CXCR4 mutations underlie the genomic landscape of Waldenström's macroglobulinemia.” 2015. Web. 01 Dec 2020.

Vancouver:

Hunter ZR. Whole genome sequencing reveals that recurrent MYD88 and CXCR4 mutations underlie the genomic landscape of Waldenström's macroglobulinemia. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2144/15632.

Council of Science Editors:

Hunter ZR. Whole genome sequencing reveals that recurrent MYD88 and CXCR4 mutations underlie the genomic landscape of Waldenström's macroglobulinemia. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/15632


Boston University

9. Mitchell, Brendon C. The chemokine receptor 4 (CXCR4) in primary cutaneous melanoma – correlation with established histopathologic prognosticators, BRAF status and expression of its ligand CXCL12.

Degree: 2014, Boston University

 Dysregulation of the chemokine receptor 4 (CXCR4) and its primary ligand CXCL12 (SDF-1, stromal cell-derived factor-1), has been implicated in the progression of melanoma and… (more)

Subjects/Keywords: Medicine; BRAF; CXCL12; CXCR4; Immunohistochemistry; Melanoma

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APA (6th Edition):

Mitchell, B. C. (2014). The chemokine receptor 4 (CXCR4) in primary cutaneous melanoma – correlation with established histopathologic prognosticators, BRAF status and expression of its ligand CXCL12. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/14324

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mitchell, Brendon C. “The chemokine receptor 4 (CXCR4) in primary cutaneous melanoma – correlation with established histopathologic prognosticators, BRAF status and expression of its ligand CXCL12.” 2014. Thesis, Boston University. Accessed December 01, 2020. http://hdl.handle.net/2144/14324.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mitchell, Brendon C. “The chemokine receptor 4 (CXCR4) in primary cutaneous melanoma – correlation with established histopathologic prognosticators, BRAF status and expression of its ligand CXCL12.” 2014. Web. 01 Dec 2020.

Vancouver:

Mitchell BC. The chemokine receptor 4 (CXCR4) in primary cutaneous melanoma – correlation with established histopathologic prognosticators, BRAF status and expression of its ligand CXCL12. [Internet] [Thesis]. Boston University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2144/14324.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mitchell BC. The chemokine receptor 4 (CXCR4) in primary cutaneous melanoma – correlation with established histopathologic prognosticators, BRAF status and expression of its ligand CXCL12. [Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14324

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat de Valencia

10. Ballester García, Sandra. Papel de los receptores angiogénicos del VEGF en la apoptosis y migración celular de la leucemia linfática crónica-B. Correlación con los receptores de quimiocinas CXCR4, CCR7 Y CD49d y las características clínicas de los pacientes .

Degree: 2015, Universitat de Valencia

 La leucemia linfática crónica B es un síndrome linfoproliferativo caracterizado por un balance entre la proliferación celular en los tejidos y la apoptosis espontánea que… (more)

Subjects/Keywords: leucemia linfática crónica B; vegf; cxcr4

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APA (6th Edition):

Ballester García, S. (2015). Papel de los receptores angiogénicos del VEGF en la apoptosis y migración celular de la leucemia linfática crónica-B. Correlación con los receptores de quimiocinas CXCR4, CCR7 Y CD49d y las características clínicas de los pacientes . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/50822

Chicago Manual of Style (16th Edition):

Ballester García, Sandra. “Papel de los receptores angiogénicos del VEGF en la apoptosis y migración celular de la leucemia linfática crónica-B. Correlación con los receptores de quimiocinas CXCR4, CCR7 Y CD49d y las características clínicas de los pacientes .” 2015. Doctoral Dissertation, Universitat de Valencia. Accessed December 01, 2020. http://hdl.handle.net/10550/50822.

MLA Handbook (7th Edition):

Ballester García, Sandra. “Papel de los receptores angiogénicos del VEGF en la apoptosis y migración celular de la leucemia linfática crónica-B. Correlación con los receptores de quimiocinas CXCR4, CCR7 Y CD49d y las características clínicas de los pacientes .” 2015. Web. 01 Dec 2020.

Vancouver:

Ballester García S. Papel de los receptores angiogénicos del VEGF en la apoptosis y migración celular de la leucemia linfática crónica-B. Correlación con los receptores de quimiocinas CXCR4, CCR7 Y CD49d y las características clínicas de los pacientes . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10550/50822.

Council of Science Editors:

Ballester García S. Papel de los receptores angiogénicos del VEGF en la apoptosis y migración celular de la leucemia linfática crónica-B. Correlación con los receptores de quimiocinas CXCR4, CCR7 Y CD49d y las características clínicas de los pacientes . [Doctoral Dissertation]. Universitat de Valencia; 2015. Available from: http://hdl.handle.net/10550/50822


Virginia Tech

11. Park, Myeongseon. Dissecting the impact of macrophage migration inhibitory factor (MIF) on host immune response.

Degree: PhD, Animal and Poultry Sciences, 2018, Virginia Tech

 Macrophage migration inhibitory factor (MIF) has been implicated in mediating both innate and adaptive immune responses in inflammatory and infectious diseases. The sequence and structure… (more)

Subjects/Keywords: MIF; chicken; Eimeria; CXCR4; CD74; CRISPR/Cas9

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APA (6th Edition):

Park, M. (2018). Dissecting the impact of macrophage migration inhibitory factor (MIF) on host immune response. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/97565

Chicago Manual of Style (16th Edition):

Park, Myeongseon. “Dissecting the impact of macrophage migration inhibitory factor (MIF) on host immune response.” 2018. Doctoral Dissertation, Virginia Tech. Accessed December 01, 2020. http://hdl.handle.net/10919/97565.

MLA Handbook (7th Edition):

Park, Myeongseon. “Dissecting the impact of macrophage migration inhibitory factor (MIF) on host immune response.” 2018. Web. 01 Dec 2020.

Vancouver:

Park M. Dissecting the impact of macrophage migration inhibitory factor (MIF) on host immune response. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10919/97565.

Council of Science Editors:

Park M. Dissecting the impact of macrophage migration inhibitory factor (MIF) on host immune response. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/97565


University of Louisville

12. Meier, Jason Bradley, 1980-. Structure-based design of inhibitors of CXCR4.

Degree: PhD, 2011, University of Louisville

 Metastasis is a complex process requiring directed migration of metastatic cells to favorable microenvironments. Increased CXCR4 expression has been implicated in more invasive, aggressive and… (more)

Subjects/Keywords: CXCR4; metastasis; GPCR; intracellular; QSAR; molecular dynamics

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APA (6th Edition):

Meier, Jason Bradley, 1. (2011). Structure-based design of inhibitors of CXCR4. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/962 ; https://ir.library.louisville.edu/etd/962

Chicago Manual of Style (16th Edition):

Meier, Jason Bradley, 1980-. “Structure-based design of inhibitors of CXCR4.” 2011. Doctoral Dissertation, University of Louisville. Accessed December 01, 2020. 10.18297/etd/962 ; https://ir.library.louisville.edu/etd/962.

MLA Handbook (7th Edition):

Meier, Jason Bradley, 1980-. “Structure-based design of inhibitors of CXCR4.” 2011. Web. 01 Dec 2020.

Vancouver:

Meier, Jason Bradley 1. Structure-based design of inhibitors of CXCR4. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2020 Dec 01]. Available from: 10.18297/etd/962 ; https://ir.library.louisville.edu/etd/962.

Council of Science Editors:

Meier, Jason Bradley 1. Structure-based design of inhibitors of CXCR4. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/962 ; https://ir.library.louisville.edu/etd/962


Georgia State University

13. Garcia, Francisco Javier, Jr. Synthesis & Evaluation Of Thiophene Derivatives As CXCR4 Antagonists.

Degree: MS, Chemistry, 2017, Georgia State University

  There is a lack of good CXCR4 inhibitors that treat cancer cell metastasis and autoimmune diseases without serious drawbacks. AMD3100 and WZ811 are the… (more)

Subjects/Keywords: CXCR4; Chemokine; Cancer metastasis; Pharmacophore; and AMD3100

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APA (6th Edition):

Garcia, Francisco Javier, J. (2017). Synthesis & Evaluation Of Thiophene Derivatives As CXCR4 Antagonists. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/100

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Garcia, Francisco Javier, Jr. “Synthesis & Evaluation Of Thiophene Derivatives As CXCR4 Antagonists.” 2017. Thesis, Georgia State University. Accessed December 01, 2020. https://scholarworks.gsu.edu/chemistry_theses/100.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Garcia, Francisco Javier, Jr. “Synthesis & Evaluation Of Thiophene Derivatives As CXCR4 Antagonists.” 2017. Web. 01 Dec 2020.

Vancouver:

Garcia, Francisco Javier J. Synthesis & Evaluation Of Thiophene Derivatives As CXCR4 Antagonists. [Internet] [Thesis]. Georgia State University; 2017. [cited 2020 Dec 01]. Available from: https://scholarworks.gsu.edu/chemistry_theses/100.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Garcia, Francisco Javier J. Synthesis & Evaluation Of Thiophene Derivatives As CXCR4 Antagonists. [Thesis]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/chemistry_theses/100

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Johannes Gutenberg Universität Mainz

14. Pante, Saskia Veronika. Die Rolle von Chemokinrezeptor CXCR4 und Connective Tissue Growth Factor innerhalb der Tumor-Stroma-Interaktion in der akuten myeloischen Leukämie.

Degree: 2014, Johannes Gutenberg Universität Mainz

 Die akute myeloische Leukämie (AML) ist eine heterogene Erkrankung der hämatopoetischen Vorläuferzelle, die durch unkontrollierte Vermehrung und ein reduziertes Differenzierungsverhalten gekennzeichnet ist. Aufgrund von Therapieresistenzen… (more)

Subjects/Keywords: Leukämie; Therapieresistenz; Stroma; CXCR4; CTGF; leukemia; resistance to therapy; stroma; CXCR4; CTGF; Life sciences

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APA (6th Edition):

Pante, S. V. (2014). Die Rolle von Chemokinrezeptor CXCR4 und Connective Tissue Growth Factor innerhalb der Tumor-Stroma-Interaktion in der akuten myeloischen Leukämie. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3758/

Chicago Manual of Style (16th Edition):

Pante, Saskia Veronika. “Die Rolle von Chemokinrezeptor CXCR4 und Connective Tissue Growth Factor innerhalb der Tumor-Stroma-Interaktion in der akuten myeloischen Leukämie.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed December 01, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2014/3758/.

MLA Handbook (7th Edition):

Pante, Saskia Veronika. “Die Rolle von Chemokinrezeptor CXCR4 und Connective Tissue Growth Factor innerhalb der Tumor-Stroma-Interaktion in der akuten myeloischen Leukämie.” 2014. Web. 01 Dec 2020.

Vancouver:

Pante SV. Die Rolle von Chemokinrezeptor CXCR4 und Connective Tissue Growth Factor innerhalb der Tumor-Stroma-Interaktion in der akuten myeloischen Leukämie. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2020 Dec 01]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3758/.

Council of Science Editors:

Pante SV. Die Rolle von Chemokinrezeptor CXCR4 und Connective Tissue Growth Factor innerhalb der Tumor-Stroma-Interaktion in der akuten myeloischen Leukämie. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3758/

15. Martin, Pauline. Modélisation et caractérisation de cellules souches tumorales et métastasiques et approches thérapeutiques : Modeling and characterization of tumorigenic and metastatic cancer stem cells, and therapeutic approaches.

Degree: Docteur es, Interactions cellulaires et moléculaires, 2014, Nice

Les cellules souches cancéreuses (CSC) sont les cellules responsables du pouvoir tumoral et/ou métastasique, et résistent à la plus part des molécules anticancéreuses. L’expression de… (more)

Subjects/Keywords: Cellules souches cancéreuses; Oct4; CXCR4; Lopinavir; Cancer stem cells; Oct4; CXCR4; Lopinavir

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APA (6th Edition):

Martin, P. (2014). Modélisation et caractérisation de cellules souches tumorales et métastasiques et approches thérapeutiques : Modeling and characterization of tumorigenic and metastatic cancer stem cells, and therapeutic approaches. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2014NICE4101

Chicago Manual of Style (16th Edition):

Martin, Pauline. “Modélisation et caractérisation de cellules souches tumorales et métastasiques et approches thérapeutiques : Modeling and characterization of tumorigenic and metastatic cancer stem cells, and therapeutic approaches.” 2014. Doctoral Dissertation, Nice. Accessed December 01, 2020. http://www.theses.fr/2014NICE4101.

MLA Handbook (7th Edition):

Martin, Pauline. “Modélisation et caractérisation de cellules souches tumorales et métastasiques et approches thérapeutiques : Modeling and characterization of tumorigenic and metastatic cancer stem cells, and therapeutic approaches.” 2014. Web. 01 Dec 2020.

Vancouver:

Martin P. Modélisation et caractérisation de cellules souches tumorales et métastasiques et approches thérapeutiques : Modeling and characterization of tumorigenic and metastatic cancer stem cells, and therapeutic approaches. [Internet] [Doctoral dissertation]. Nice; 2014. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2014NICE4101.

Council of Science Editors:

Martin P. Modélisation et caractérisation de cellules souches tumorales et métastasiques et approches thérapeutiques : Modeling and characterization of tumorigenic and metastatic cancer stem cells, and therapeutic approaches. [Doctoral Dissertation]. Nice; 2014. Available from: http://www.theses.fr/2014NICE4101


Universidade Estadual de Campinas

16. Melo, Rita de Cássia Carvalho, 1988-. Investigação funcional de CXCR7 na hematopoese normal e leucêmica: CXCR7 functional investigation in normal and leukemic hematopoiesis.

Degree: 2016, Universidade Estadual de Campinas

 Abstract: The interaction of CXCL12 chemokine to CXCR4 has been shown to be essential in the regulation of normal and leukemic hematopoiesis. Recently, another receptor… (more)

Subjects/Keywords: Receptores CXCR4; Camundongos; Movimento celular; Leucemia; Hematopoese; Receptores, CXCR4; Mice; Cell movement; Leukemia; Hematopoiesis

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APA (6th Edition):

Melo, Rita de Cássia Carvalho, 1. (2016). Investigação funcional de CXCR7 na hematopoese normal e leucêmica: CXCR7 functional investigation in normal and leukemic hematopoiesis. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/313057

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Melo, Rita de Cássia Carvalho, 1988-. “Investigação funcional de CXCR7 na hematopoese normal e leucêmica: CXCR7 functional investigation in normal and leukemic hematopoiesis.” 2016. Thesis, Universidade Estadual de Campinas. Accessed December 01, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/313057.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Melo, Rita de Cássia Carvalho, 1988-. “Investigação funcional de CXCR7 na hematopoese normal e leucêmica: CXCR7 functional investigation in normal and leukemic hematopoiesis.” 2016. Web. 01 Dec 2020.

Vancouver:

Melo, Rita de Cássia Carvalho 1. Investigação funcional de CXCR7 na hematopoese normal e leucêmica: CXCR7 functional investigation in normal and leukemic hematopoiesis. [Internet] [Thesis]. Universidade Estadual de Campinas; 2016. [cited 2020 Dec 01]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/313057.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Melo, Rita de Cássia Carvalho 1. Investigação funcional de CXCR7 na hematopoese normal e leucêmica: CXCR7 functional investigation in normal and leukemic hematopoiesis. [Thesis]. Universidade Estadual de Campinas; 2016. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/313057

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Montpellier II

17. Duquenne, Charline. Modulation de l’activité des corécepteurs CCR5 et CXCR4 du VIH 1 comme stratégie thérapeutique : étude des deux isoformes de CXCR4 et interaction de CCR5 avec le récepteur S1P1 : Modulation of CCR5 and CXCR4 HIV-1 coreceptor activities as a therapeutic strategy : studying the two CXCR4 isoforms and the interaction of CCR5 with S1P1.

Degree: Docteur es, Biologie Santé, 2013, Université Montpellier II

CCR5 et CXCR4 sont les corécepteurs d'entrée du VIH utilisés par le virus in vivo en plus du récepteur principal CD4 pour infecter les cellules.… (more)

Subjects/Keywords: S1p1; Vih; Ccr5; Cxcr4; Rcpg; Fty720; S1p1; Hiv; Ccr5; Cxcr4; Gpcr; Fty720

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APA (6th Edition):

Duquenne, C. (2013). Modulation de l’activité des corécepteurs CCR5 et CXCR4 du VIH 1 comme stratégie thérapeutique : étude des deux isoformes de CXCR4 et interaction de CCR5 avec le récepteur S1P1 : Modulation of CCR5 and CXCR4 HIV-1 coreceptor activities as a therapeutic strategy : studying the two CXCR4 isoforms and the interaction of CCR5 with S1P1. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2013MON20188

Chicago Manual of Style (16th Edition):

Duquenne, Charline. “Modulation de l’activité des corécepteurs CCR5 et CXCR4 du VIH 1 comme stratégie thérapeutique : étude des deux isoformes de CXCR4 et interaction de CCR5 avec le récepteur S1P1 : Modulation of CCR5 and CXCR4 HIV-1 coreceptor activities as a therapeutic strategy : studying the two CXCR4 isoforms and the interaction of CCR5 with S1P1.” 2013. Doctoral Dissertation, Université Montpellier II. Accessed December 01, 2020. http://www.theses.fr/2013MON20188.

MLA Handbook (7th Edition):

Duquenne, Charline. “Modulation de l’activité des corécepteurs CCR5 et CXCR4 du VIH 1 comme stratégie thérapeutique : étude des deux isoformes de CXCR4 et interaction de CCR5 avec le récepteur S1P1 : Modulation of CCR5 and CXCR4 HIV-1 coreceptor activities as a therapeutic strategy : studying the two CXCR4 isoforms and the interaction of CCR5 with S1P1.” 2013. Web. 01 Dec 2020.

Vancouver:

Duquenne C. Modulation de l’activité des corécepteurs CCR5 et CXCR4 du VIH 1 comme stratégie thérapeutique : étude des deux isoformes de CXCR4 et interaction de CCR5 avec le récepteur S1P1 : Modulation of CCR5 and CXCR4 HIV-1 coreceptor activities as a therapeutic strategy : studying the two CXCR4 isoforms and the interaction of CCR5 with S1P1. [Internet] [Doctoral dissertation]. Université Montpellier II; 2013. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2013MON20188.

Council of Science Editors:

Duquenne C. Modulation de l’activité des corécepteurs CCR5 et CXCR4 du VIH 1 comme stratégie thérapeutique : étude des deux isoformes de CXCR4 et interaction de CCR5 avec le récepteur S1P1 : Modulation of CCR5 and CXCR4 HIV-1 coreceptor activities as a therapeutic strategy : studying the two CXCR4 isoforms and the interaction of CCR5 with S1P1. [Doctoral Dissertation]. Université Montpellier II; 2013. Available from: http://www.theses.fr/2013MON20188


Université Montpellier II

18. Armando, Sylvain. Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leur effecteurs. : Quaternary arrangements of the CXCR4-CCR2 homo- and hetero-oligomers and of their complexes with their signaling effectors.

Degree: Docteur es, Neurosciences, 2010, Université Montpellier II

Les récepteurs couplés aux protéines G (RCPG) sont la famille de récepteurs membranaires la plus représentée chez les vertébrés, et la plus grande cible thérapeutique… (more)

Subjects/Keywords: Cxcr4; Tétramère; Bret; Asymétrie; Protéines G; Arrestines; Cxcr4; Tetramer; Bret; Asymetry; G protein; Arrestin

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APA (6th Edition):

Armando, S. (2010). Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leur effecteurs. : Quaternary arrangements of the CXCR4-CCR2 homo- and hetero-oligomers and of their complexes with their signaling effectors. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2010MON20208

Chicago Manual of Style (16th Edition):

Armando, Sylvain. “Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leur effecteurs. : Quaternary arrangements of the CXCR4-CCR2 homo- and hetero-oligomers and of their complexes with their signaling effectors.” 2010. Doctoral Dissertation, Université Montpellier II. Accessed December 01, 2020. http://www.theses.fr/2010MON20208.

MLA Handbook (7th Edition):

Armando, Sylvain. “Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leur effecteurs. : Quaternary arrangements of the CXCR4-CCR2 homo- and hetero-oligomers and of their complexes with their signaling effectors.” 2010. Web. 01 Dec 2020.

Vancouver:

Armando S. Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leur effecteurs. : Quaternary arrangements of the CXCR4-CCR2 homo- and hetero-oligomers and of their complexes with their signaling effectors. [Internet] [Doctoral dissertation]. Université Montpellier II; 2010. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2010MON20208.

Council of Science Editors:

Armando S. Structure quaternaire des récepteurs de chimiokines CXCR4 et CCR2 et interaction avec leur effecteurs. : Quaternary arrangements of the CXCR4-CCR2 homo- and hetero-oligomers and of their complexes with their signaling effectors. [Doctoral Dissertation]. Université Montpellier II; 2010. Available from: http://www.theses.fr/2010MON20208

19. Heuninck, Joyce. Analysis of CXCR4 and ACKR3 oligomerisation : Etude de l’oligomérisation des récepteurs aux chimiokines CXCR4 et ACKR3.

Degree: Docteur es, Biologie Santé, 2019, Montpellier

 Mon travail de thèse s’est focalisé sur l’étude des récepteurs CXCR4 et ACKR3, deux récepteurs aux chimiokines. Ceux-ci jouent des rôles majeurs dans différentes fonctions… (more)

Subjects/Keywords: Gpcr; Oligomérisation; Cancer; Pharmacologie; Cxcr4; Ackr3; Gpcr; Oligomerisation; Cancer; Pharmacology; Cxcr4; Ackr3

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APA (6th Edition):

Heuninck, J. (2019). Analysis of CXCR4 and ACKR3 oligomerisation : Etude de l’oligomérisation des récepteurs aux chimiokines CXCR4 et ACKR3. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2019MONTT018

Chicago Manual of Style (16th Edition):

Heuninck, Joyce. “Analysis of CXCR4 and ACKR3 oligomerisation : Etude de l’oligomérisation des récepteurs aux chimiokines CXCR4 et ACKR3.” 2019. Doctoral Dissertation, Montpellier. Accessed December 01, 2020. http://www.theses.fr/2019MONTT018.

MLA Handbook (7th Edition):

Heuninck, Joyce. “Analysis of CXCR4 and ACKR3 oligomerisation : Etude de l’oligomérisation des récepteurs aux chimiokines CXCR4 et ACKR3.” 2019. Web. 01 Dec 2020.

Vancouver:

Heuninck J. Analysis of CXCR4 and ACKR3 oligomerisation : Etude de l’oligomérisation des récepteurs aux chimiokines CXCR4 et ACKR3. [Internet] [Doctoral dissertation]. Montpellier; 2019. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2019MONTT018.

Council of Science Editors:

Heuninck J. Analysis of CXCR4 and ACKR3 oligomerisation : Etude de l’oligomérisation des récepteurs aux chimiokines CXCR4 et ACKR3. [Doctoral Dissertation]. Montpellier; 2019. Available from: http://www.theses.fr/2019MONTT018


Université Paris-Sud – Paris XI

20. Biajoux, Vincent. Impact d’un gain de fonction de Cxcr4 sur le développement et la compartimentalisation périphérique des lymphocytes : Impact of a gain-of-Cxcr4-function in lymphocyte development and peripheral trafficking.

Degree: Docteur es, Immunologie, 2013, Université Paris-Sud – Paris XI

Le syndrome WHIM (SW) est un déficit immuno-hématologique rare causé principalement par des mutations autosomales dominantes du gène CXCR4 qui entrainent une troncation du domaine… (more)

Subjects/Keywords: Chimiokine; CXCL12; CXCR4; Lymphocyte; Signalisation; Syndrome WHIM; Chemokine; CXCL12; CXCR4; Lymphocyte; Cell signaling; WHIM Syndrome

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APA (6th Edition):

Biajoux, V. (2013). Impact d’un gain de fonction de Cxcr4 sur le développement et la compartimentalisation périphérique des lymphocytes : Impact of a gain-of-Cxcr4-function in lymphocyte development and peripheral trafficking. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA114825

Chicago Manual of Style (16th Edition):

Biajoux, Vincent. “Impact d’un gain de fonction de Cxcr4 sur le développement et la compartimentalisation périphérique des lymphocytes : Impact of a gain-of-Cxcr4-function in lymphocyte development and peripheral trafficking.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 01, 2020. http://www.theses.fr/2013PA114825.

MLA Handbook (7th Edition):

Biajoux, Vincent. “Impact d’un gain de fonction de Cxcr4 sur le développement et la compartimentalisation périphérique des lymphocytes : Impact of a gain-of-Cxcr4-function in lymphocyte development and peripheral trafficking.” 2013. Web. 01 Dec 2020.

Vancouver:

Biajoux V. Impact d’un gain de fonction de Cxcr4 sur le développement et la compartimentalisation périphérique des lymphocytes : Impact of a gain-of-Cxcr4-function in lymphocyte development and peripheral trafficking. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2013PA114825.

Council of Science Editors:

Biajoux V. Impact d’un gain de fonction de Cxcr4 sur le développement et la compartimentalisation périphérique des lymphocytes : Impact of a gain-of-Cxcr4-function in lymphocyte development and peripheral trafficking. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA114825


Université Paris-Sud – Paris XI

21. Meuris, Floriane. L’axe de signalisation CXCL12/CXCR4 : un nouveau facteur de l’hôte impliqué dans la carcinogenèse induite par les papillomavirus humains : The CXCL12/CXCR4 signaling pathway : a new host factor involved in human papillomavirus-induced carcinogenesis.

Degree: Docteur es, Immunologie, 2015, Université Paris-Sud – Paris XI

Les papillomavirus humains (HPV), dont on dénombre plus de 300 types différents, infectent spécifiquement les épithéliums. Ces infections sont communes et généralement asymptomatiques. Cependant, lorsqu’elles… (more)

Subjects/Keywords: Papillomavirus humains; CXCL12/CXCR4; Syndrome WHIM; Carcinogenèse; Human papillomavirus; CXCL12/CXCR4; WHIM syndrome; Carcinogenesis

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APA (6th Edition):

Meuris, F. (2015). L’axe de signalisation CXCL12/CXCR4 : un nouveau facteur de l’hôte impliqué dans la carcinogenèse induite par les papillomavirus humains : The CXCL12/CXCR4 signaling pathway : a new host factor involved in human papillomavirus-induced carcinogenesis. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA114833

Chicago Manual of Style (16th Edition):

Meuris, Floriane. “L’axe de signalisation CXCL12/CXCR4 : un nouveau facteur de l’hôte impliqué dans la carcinogenèse induite par les papillomavirus humains : The CXCL12/CXCR4 signaling pathway : a new host factor involved in human papillomavirus-induced carcinogenesis.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 01, 2020. http://www.theses.fr/2015PA114833.

MLA Handbook (7th Edition):

Meuris, Floriane. “L’axe de signalisation CXCL12/CXCR4 : un nouveau facteur de l’hôte impliqué dans la carcinogenèse induite par les papillomavirus humains : The CXCL12/CXCR4 signaling pathway : a new host factor involved in human papillomavirus-induced carcinogenesis.” 2015. Web. 01 Dec 2020.

Vancouver:

Meuris F. L’axe de signalisation CXCL12/CXCR4 : un nouveau facteur de l’hôte impliqué dans la carcinogenèse induite par les papillomavirus humains : The CXCL12/CXCR4 signaling pathway : a new host factor involved in human papillomavirus-induced carcinogenesis. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2015PA114833.

Council of Science Editors:

Meuris F. L’axe de signalisation CXCL12/CXCR4 : un nouveau facteur de l’hôte impliqué dans la carcinogenèse induite par les papillomavirus humains : The CXCL12/CXCR4 signaling pathway : a new host factor involved in human papillomavirus-induced carcinogenesis. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA114833

22. Desnoyer, Aude. Etude de l'impact clinique et immunologique d'un traitement par lénalidomide dans la maladie de Kaposi liée au VIH : Clinical and immunological impact of lenalidomide in patients with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy.

Degree: Docteur es, Immunologie, 2015, Université Paris-Saclay (ComUE)

L'objectif de cette thèse menée dans le cadre de l'essai clinique ANRS 154 Lenakap a été d'étudier l'impact clinique et immunologique d'un traitement par lénalidomide… (more)

Subjects/Keywords: Maladie de Kaposi; Lénalidomide; Vih; Cxcl12; Cxcr4; Cxcr7; Kaposi's sarcoma; Lenalidomide; Hiv; Cxcl12; Cxcr4; Cxcr7

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APA (6th Edition):

Desnoyer, A. (2015). Etude de l'impact clinique et immunologique d'un traitement par lénalidomide dans la maladie de Kaposi liée au VIH : Clinical and immunological impact of lenalidomide in patients with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2015SACLS017

Chicago Manual of Style (16th Edition):

Desnoyer, Aude. “Etude de l'impact clinique et immunologique d'un traitement par lénalidomide dans la maladie de Kaposi liée au VIH : Clinical and immunological impact of lenalidomide in patients with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy.” 2015. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed December 01, 2020. http://www.theses.fr/2015SACLS017.

MLA Handbook (7th Edition):

Desnoyer, Aude. “Etude de l'impact clinique et immunologique d'un traitement par lénalidomide dans la maladie de Kaposi liée au VIH : Clinical and immunological impact of lenalidomide in patients with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy.” 2015. Web. 01 Dec 2020.

Vancouver:

Desnoyer A. Etude de l'impact clinique et immunologique d'un traitement par lénalidomide dans la maladie de Kaposi liée au VIH : Clinical and immunological impact of lenalidomide in patients with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2015. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2015SACLS017.

Council of Science Editors:

Desnoyer A. Etude de l'impact clinique et immunologique d'un traitement par lénalidomide dans la maladie de Kaposi liée au VIH : Clinical and immunological impact of lenalidomide in patients with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2015. Available from: http://www.theses.fr/2015SACLS017

23. MarkÃnia KÃlia Santos Alves. Identifying of molecular alterations associated to expression of CD133, CXCR4, CD44 and OLIG2 and CDKN2A methylation in promoter in astrocytic tumors.

Degree: PhD, 2014, Universidade Federal do Ceará

 Tumores sÃo populaÃÃes celulares heterogÃneas hierarquicamente organizadas, cujas cÃlulas-tronco possuem importÃncia relevante desde que sÃo cÃlulas com a capacidade de se renovarem e de gerarem… (more)

Subjects/Keywords: CANCEROLOGIA; Astrocitomas; MetilaÃÃo; p16; CÃlulas-tronco; CD133, CXCR4; CD44; OLIG2; Astrocytoma; Methylation; p16; Stem-cell; CD133, CXCR4; CD44; OLIG2; Tumores

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APA (6th Edition):

Alves, M. K. S. (2014). Identifying of molecular alterations associated to expression of CD133, CXCR4, CD44 and OLIG2 and CDKN2A methylation in promoter in astrocytic tumors. (Doctoral Dissertation). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14421 ;

Chicago Manual of Style (16th Edition):

Alves, MarkÃnia KÃlia Santos. “Identifying of molecular alterations associated to expression of CD133, CXCR4, CD44 and OLIG2 and CDKN2A methylation in promoter in astrocytic tumors.” 2014. Doctoral Dissertation, Universidade Federal do Ceará. Accessed December 01, 2020. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14421 ;.

MLA Handbook (7th Edition):

Alves, MarkÃnia KÃlia Santos. “Identifying of molecular alterations associated to expression of CD133, CXCR4, CD44 and OLIG2 and CDKN2A methylation in promoter in astrocytic tumors.” 2014. Web. 01 Dec 2020.

Vancouver:

Alves MKS. Identifying of molecular alterations associated to expression of CD133, CXCR4, CD44 and OLIG2 and CDKN2A methylation in promoter in astrocytic tumors. [Internet] [Doctoral dissertation]. Universidade Federal do Ceará 2014. [cited 2020 Dec 01]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14421 ;.

Council of Science Editors:

Alves MKS. Identifying of molecular alterations associated to expression of CD133, CXCR4, CD44 and OLIG2 and CDKN2A methylation in promoter in astrocytic tumors. [Doctoral Dissertation]. Universidade Federal do Ceará 2014. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14421 ;

24. Vincenzi, Marian. Interactions protéines-molécules biotechnologiques originales : une approche intégrée de RMN et de modélisation moléculaire : Targeting protein interactions with biotechnological original molecules : a NMR and molecular modelling integrated approach.

Degree: Docteur es, Chimie organique, 2016, Bordeaux; Università degli studi di Napoli Federico II

Ce travail de thèse PhD concerne l'application d'une approche intégrée pour obtenir une meilleure compréhension des mécanismes d'action de Akt et CXCR4, surexprimées dans différents… (more)

Subjects/Keywords: Akt; Pyrrolo[1,2-a]quinoxaline; Allostérie; CXCR4; CXCL12; CPC; Amphiphiles; Akt; Pyrrolo[1,2-a]quinoxaline; Allostery; CXCR4; CXCL12; CPC; Amphiphiles

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APA (6th Edition):

Vincenzi, M. (2016). Interactions protéines-molécules biotechnologiques originales : une approche intégrée de RMN et de modélisation moléculaire : Targeting protein interactions with biotechnological original molecules : a NMR and molecular modelling integrated approach. (Doctoral Dissertation). Bordeaux; Università degli studi di Napoli Federico II. Retrieved from http://www.theses.fr/2016BORD0042

Chicago Manual of Style (16th Edition):

Vincenzi, Marian. “Interactions protéines-molécules biotechnologiques originales : une approche intégrée de RMN et de modélisation moléculaire : Targeting protein interactions with biotechnological original molecules : a NMR and molecular modelling integrated approach.” 2016. Doctoral Dissertation, Bordeaux; Università degli studi di Napoli Federico II. Accessed December 01, 2020. http://www.theses.fr/2016BORD0042.

MLA Handbook (7th Edition):

Vincenzi, Marian. “Interactions protéines-molécules biotechnologiques originales : une approche intégrée de RMN et de modélisation moléculaire : Targeting protein interactions with biotechnological original molecules : a NMR and molecular modelling integrated approach.” 2016. Web. 01 Dec 2020.

Vancouver:

Vincenzi M. Interactions protéines-molécules biotechnologiques originales : une approche intégrée de RMN et de modélisation moléculaire : Targeting protein interactions with biotechnological original molecules : a NMR and molecular modelling integrated approach. [Internet] [Doctoral dissertation]. Bordeaux; Università degli studi di Napoli Federico II; 2016. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2016BORD0042.

Council of Science Editors:

Vincenzi M. Interactions protéines-molécules biotechnologiques originales : une approche intégrée de RMN et de modélisation moléculaire : Targeting protein interactions with biotechnological original molecules : a NMR and molecular modelling integrated approach. [Doctoral Dissertation]. Bordeaux; Università degli studi di Napoli Federico II; 2016. Available from: http://www.theses.fr/2016BORD0042

25. Daubeuf, Francois. Neutraligands de la chimiokine CXCL12 dans l'asthme : Neutraligands of the chemokine CXCL12 in asthma.

Degree: Docteur es, Pharmacologie, 2013, Université de Strasbourg

La liaison de CXCL12 à ses récepteurs CXCR4 et CXCR7 peut-être bloquée par un neutraligand de CXCL12, la chalcone 4, qui présente une activité anti-inflammatoire… (more)

Subjects/Keywords: Neutraligand; Chimiokine; Cxcl12; Asthme; Souris; Inflammation; Cxcr4; Eosinophile; Neutraligand; Chemokine; Cxcl12; Asthma; Mice; Inflammation; Cxcr4; Eosinophil; 572.8; 615.7

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APA (6th Edition):

Daubeuf, F. (2013). Neutraligands de la chimiokine CXCL12 dans l'asthme : Neutraligands of the chemokine CXCL12 in asthma. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAJ112

Chicago Manual of Style (16th Edition):

Daubeuf, Francois. “Neutraligands de la chimiokine CXCL12 dans l'asthme : Neutraligands of the chemokine CXCL12 in asthma.” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed December 01, 2020. http://www.theses.fr/2013STRAJ112.

MLA Handbook (7th Edition):

Daubeuf, Francois. “Neutraligands de la chimiokine CXCL12 dans l'asthme : Neutraligands of the chemokine CXCL12 in asthma.” 2013. Web. 01 Dec 2020.

Vancouver:

Daubeuf F. Neutraligands de la chimiokine CXCL12 dans l'asthme : Neutraligands of the chemokine CXCL12 in asthma. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2013STRAJ112.

Council of Science Editors:

Daubeuf F. Neutraligands de la chimiokine CXCL12 dans l'asthme : Neutraligands of the chemokine CXCL12 in asthma. [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAJ112

26. Smith, Nikaïa. Étude moléculaire du TNF-Related Apoptosis Induced Ligand (TRAIL) et de l’activation du Toll-Like Receptor 7 (TLR7) dans les cellules dendritiques plasmacytoïdes lors de la réponse antivirale : Molecular study of the TNF-Related Apoptosis Induced Ligand (TRAIL) and of Toll-Like Receptor 7 (TLR7) activation in plasmacytoid dendritic cells during viral infections.

Degree: Docteur es, Immunologie, 2015, Sorbonne Paris Cité

Les pDC représentent la première ligne de défense de l’organisme contre les pathogènes et établissent le lien essentiel entre l’immunité innée et adaptative. Les pDC… (more)

Subjects/Keywords: Cellules dendritiques plasmacytoïdes; Interferon de type I; Amines; CXCR4; SiRNA; Plasmacytoid dendritic cells; Type I interferon; Amines; CXCR4; SiRNA; 571.96

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APA (6th Edition):

Smith, N. (2015). Étude moléculaire du TNF-Related Apoptosis Induced Ligand (TRAIL) et de l’activation du Toll-Like Receptor 7 (TLR7) dans les cellules dendritiques plasmacytoïdes lors de la réponse antivirale : Molecular study of the TNF-Related Apoptosis Induced Ligand (TRAIL) and of Toll-Like Receptor 7 (TLR7) activation in plasmacytoid dendritic cells during viral infections. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2015USPCB145

Chicago Manual of Style (16th Edition):

Smith, Nikaïa. “Étude moléculaire du TNF-Related Apoptosis Induced Ligand (TRAIL) et de l’activation du Toll-Like Receptor 7 (TLR7) dans les cellules dendritiques plasmacytoïdes lors de la réponse antivirale : Molecular study of the TNF-Related Apoptosis Induced Ligand (TRAIL) and of Toll-Like Receptor 7 (TLR7) activation in plasmacytoid dendritic cells during viral infections.” 2015. Doctoral Dissertation, Sorbonne Paris Cité. Accessed December 01, 2020. http://www.theses.fr/2015USPCB145.

MLA Handbook (7th Edition):

Smith, Nikaïa. “Étude moléculaire du TNF-Related Apoptosis Induced Ligand (TRAIL) et de l’activation du Toll-Like Receptor 7 (TLR7) dans les cellules dendritiques plasmacytoïdes lors de la réponse antivirale : Molecular study of the TNF-Related Apoptosis Induced Ligand (TRAIL) and of Toll-Like Receptor 7 (TLR7) activation in plasmacytoid dendritic cells during viral infections.” 2015. Web. 01 Dec 2020.

Vancouver:

Smith N. Étude moléculaire du TNF-Related Apoptosis Induced Ligand (TRAIL) et de l’activation du Toll-Like Receptor 7 (TLR7) dans les cellules dendritiques plasmacytoïdes lors de la réponse antivirale : Molecular study of the TNF-Related Apoptosis Induced Ligand (TRAIL) and of Toll-Like Receptor 7 (TLR7) activation in plasmacytoid dendritic cells during viral infections. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2015. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2015USPCB145.

Council of Science Editors:

Smith N. Étude moléculaire du TNF-Related Apoptosis Induced Ligand (TRAIL) et de l’activation du Toll-Like Receptor 7 (TLR7) dans les cellules dendritiques plasmacytoïdes lors de la réponse antivirale : Molecular study of the TNF-Related Apoptosis Induced Ligand (TRAIL) and of Toll-Like Receptor 7 (TLR7) activation in plasmacytoid dendritic cells during viral infections. [Doctoral Dissertation]. Sorbonne Paris Cité; 2015. Available from: http://www.theses.fr/2015USPCB145

27. Benbrika, Radhia. Etude des mécanismes impliqués dans le processus métastatique dans le cancer colique humain : implication de l'axe CXCL12/CXCR4/CXCR7 : Study of the mechanisms involved in the metastatic process in human colic cancer : implication of the CXCL12 / CXCR4 / CXCR7 axis.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Université de Strasbourg

Malgré les diagnostics précoces et les avancées thérapeutiques, le taux de mortalité chez les patients diagnostiqués d’un CCR au stade métastatique reste très élevé. L’objectif… (more)

Subjects/Keywords: CXCL12; Épigénétique; CXCR4; CXCR7; Métastases; CCR; CRISPR-Cas9; CXCL12; Epigenetic; CXCR4; CXCR7; Metastasis; CRC; CRISPR-Cas9; 572.8; 616.99

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APA (6th Edition):

Benbrika, R. (2018). Etude des mécanismes impliqués dans le processus métastatique dans le cancer colique humain : implication de l'axe CXCL12/CXCR4/CXCR7 : Study of the mechanisms involved in the metastatic process in human colic cancer : implication of the CXCL12 / CXCR4 / CXCR7 axis. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAJ125

Chicago Manual of Style (16th Edition):

Benbrika, Radhia. “Etude des mécanismes impliqués dans le processus métastatique dans le cancer colique humain : implication de l'axe CXCL12/CXCR4/CXCR7 : Study of the mechanisms involved in the metastatic process in human colic cancer : implication of the CXCL12 / CXCR4 / CXCR7 axis.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed December 01, 2020. http://www.theses.fr/2018STRAJ125.

MLA Handbook (7th Edition):

Benbrika, Radhia. “Etude des mécanismes impliqués dans le processus métastatique dans le cancer colique humain : implication de l'axe CXCL12/CXCR4/CXCR7 : Study of the mechanisms involved in the metastatic process in human colic cancer : implication of the CXCL12 / CXCR4 / CXCR7 axis.” 2018. Web. 01 Dec 2020.

Vancouver:

Benbrika R. Etude des mécanismes impliqués dans le processus métastatique dans le cancer colique humain : implication de l'axe CXCL12/CXCR4/CXCR7 : Study of the mechanisms involved in the metastatic process in human colic cancer : implication of the CXCL12 / CXCR4 / CXCR7 axis. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2018STRAJ125.

Council of Science Editors:

Benbrika R. Etude des mécanismes impliqués dans le processus métastatique dans le cancer colique humain : implication de l'axe CXCL12/CXCR4/CXCR7 : Study of the mechanisms involved in the metastatic process in human colic cancer : implication of the CXCL12 / CXCR4 / CXCR7 axis. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAJ125


Université Paris-Sud – Paris XI

28. Bignon, Alexandre. Dérégulation des récepteurs de chimiokine CCR1 et CXCR4 dans le Lupus Erythémateux Disséminé et la Lymphopénie T CD4+ Idiopathique : Dysfunctions of the chemokine receptors CCR1 et CXCR4 in Systemic Lupus Erythematosus (SLE) and Idiopathic CD4+ T-cell Lymphopenia (ICL).

Degree: Docteur es, Immunologie, 2014, Université Paris-Sud – Paris XI

L’objectif de ma thèse a été d’étudier l’expression et l’activité de deux récepteurs de chimiokine dans deux désordres immunitaires, CCR1 dans le modèle murin NZB/W… (more)

Subjects/Keywords: Chimiokines; CCR1; CXCR4; Lupus Erythémateux Disséminé; Lymphopénie T CD4+ Idiopathique; Chemokines; CCR1; CXCR4; Systemic Lupus Erythematosus; Idiopathic CD4+ T-cell lymphopenia

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APA (6th Edition):

Bignon, A. (2014). Dérégulation des récepteurs de chimiokine CCR1 et CXCR4 dans le Lupus Erythémateux Disséminé et la Lymphopénie T CD4+ Idiopathique : Dysfunctions of the chemokine receptors CCR1 et CXCR4 in Systemic Lupus Erythematosus (SLE) and Idiopathic CD4+ T-cell Lymphopenia (ICL). (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114818

Chicago Manual of Style (16th Edition):

Bignon, Alexandre. “Dérégulation des récepteurs de chimiokine CCR1 et CXCR4 dans le Lupus Erythémateux Disséminé et la Lymphopénie T CD4+ Idiopathique : Dysfunctions of the chemokine receptors CCR1 et CXCR4 in Systemic Lupus Erythematosus (SLE) and Idiopathic CD4+ T-cell Lymphopenia (ICL).” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 01, 2020. http://www.theses.fr/2014PA114818.

MLA Handbook (7th Edition):

Bignon, Alexandre. “Dérégulation des récepteurs de chimiokine CCR1 et CXCR4 dans le Lupus Erythémateux Disséminé et la Lymphopénie T CD4+ Idiopathique : Dysfunctions of the chemokine receptors CCR1 et CXCR4 in Systemic Lupus Erythematosus (SLE) and Idiopathic CD4+ T-cell Lymphopenia (ICL).” 2014. Web. 01 Dec 2020.

Vancouver:

Bignon A. Dérégulation des récepteurs de chimiokine CCR1 et CXCR4 dans le Lupus Erythémateux Disséminé et la Lymphopénie T CD4+ Idiopathique : Dysfunctions of the chemokine receptors CCR1 et CXCR4 in Systemic Lupus Erythematosus (SLE) and Idiopathic CD4+ T-cell Lymphopenia (ICL). [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2014PA114818.

Council of Science Editors:

Bignon A. Dérégulation des récepteurs de chimiokine CCR1 et CXCR4 dans le Lupus Erythémateux Disséminé et la Lymphopénie T CD4+ Idiopathique : Dysfunctions of the chemokine receptors CCR1 et CXCR4 in Systemic Lupus Erythematosus (SLE) and Idiopathic CD4+ T-cell Lymphopenia (ICL). [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114818

29. Nguyen, Julie. Rôle de la désensibilisation de CXCR4 dans l'homéostasie médullaire chez la souris : Role of Cxcr4 desensitization in the maintenance of bone marrow homeostasis in mice.

Degree: Docteur es, Immunologie, 2018, Université Paris-Saclay (ComUE)

Le couple CXCL12/CXCR4 joue un rôle essentiel dans le maintien de l’homéostasie des cellules souches et progéniteurs hématopoïétiques (CSPHs) et constitue un axe clé par… (more)

Subjects/Keywords: Cxcl12/cxcr4; Syndrome WHIM; Hématopoïèse; Cellules souches mésenchymateuses; Cxcl12/cxcr4; WHIM Syndrome; Hematopoiesis; Mesenchymal stem cells

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APA (6th Edition):

Nguyen, J. (2018). Rôle de la désensibilisation de CXCR4 dans l'homéostasie médullaire chez la souris : Role of Cxcr4 desensitization in the maintenance of bone marrow homeostasis in mice. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS485

Chicago Manual of Style (16th Edition):

Nguyen, Julie. “Rôle de la désensibilisation de CXCR4 dans l'homéostasie médullaire chez la souris : Role of Cxcr4 desensitization in the maintenance of bone marrow homeostasis in mice.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed December 01, 2020. http://www.theses.fr/2018SACLS485.

MLA Handbook (7th Edition):

Nguyen, Julie. “Rôle de la désensibilisation de CXCR4 dans l'homéostasie médullaire chez la souris : Role of Cxcr4 desensitization in the maintenance of bone marrow homeostasis in mice.” 2018. Web. 01 Dec 2020.

Vancouver:

Nguyen J. Rôle de la désensibilisation de CXCR4 dans l'homéostasie médullaire chez la souris : Role of Cxcr4 desensitization in the maintenance of bone marrow homeostasis in mice. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2018SACLS485.

Council of Science Editors:

Nguyen J. Rôle de la désensibilisation de CXCR4 dans l'homéostasie médullaire chez la souris : Role of Cxcr4 desensitization in the maintenance of bone marrow homeostasis in mice. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS485

30. Gallego, Carmen. Interactions hôte-virus : la chimiokine CXCL12 et ses récepteurs CXCR4 et ACKR3 dans le cycle de vie du papillomavirus humain et la carcinogènese associée : Host-virus interactions : the CXCL12 chemokine and receptors CXCR4 and ACKR3 in Human Papillomavirus life cycle and -induced carcinogenesis.

Degree: Docteur es, Immunologie, 2019, Université Paris-Saclay (ComUE)

Membres épithéliotropes de notre virome, les papillomavirus humains (HPV) causent majoritairement des infections asymptomatiques ou bénignes, contrôlées par les mécanismes de défense de l'hôte à… (more)

Subjects/Keywords: Papillomavirus humain; Cxcl12; Cxcr4; Ackr3; Immunologie de la peau; Cancer; Human papillomavirus; Cxcl12; Cxcr4; Ackr3; Skin immunity; Cancer

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gallego, C. (2019). Interactions hôte-virus : la chimiokine CXCL12 et ses récepteurs CXCR4 et ACKR3 dans le cycle de vie du papillomavirus humain et la carcinogènese associée : Host-virus interactions : the CXCL12 chemokine and receptors CXCR4 and ACKR3 in Human Papillomavirus life cycle and -induced carcinogenesis. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS337

Chicago Manual of Style (16th Edition):

Gallego, Carmen. “Interactions hôte-virus : la chimiokine CXCL12 et ses récepteurs CXCR4 et ACKR3 dans le cycle de vie du papillomavirus humain et la carcinogènese associée : Host-virus interactions : the CXCL12 chemokine and receptors CXCR4 and ACKR3 in Human Papillomavirus life cycle and -induced carcinogenesis.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed December 01, 2020. http://www.theses.fr/2019SACLS337.

MLA Handbook (7th Edition):

Gallego, Carmen. “Interactions hôte-virus : la chimiokine CXCL12 et ses récepteurs CXCR4 et ACKR3 dans le cycle de vie du papillomavirus humain et la carcinogènese associée : Host-virus interactions : the CXCL12 chemokine and receptors CXCR4 and ACKR3 in Human Papillomavirus life cycle and -induced carcinogenesis.” 2019. Web. 01 Dec 2020.

Vancouver:

Gallego C. Interactions hôte-virus : la chimiokine CXCL12 et ses récepteurs CXCR4 et ACKR3 dans le cycle de vie du papillomavirus humain et la carcinogènese associée : Host-virus interactions : the CXCL12 chemokine and receptors CXCR4 and ACKR3 in Human Papillomavirus life cycle and -induced carcinogenesis. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2019SACLS337.

Council of Science Editors:

Gallego C. Interactions hôte-virus : la chimiokine CXCL12 et ses récepteurs CXCR4 et ACKR3 dans le cycle de vie du papillomavirus humain et la carcinogènese associée : Host-virus interactions : the CXCL12 chemokine and receptors CXCR4 and ACKR3 in Human Papillomavirus life cycle and -induced carcinogenesis. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS337

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