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You searched for subject:(Lymphotoxin b ta receptor). Showing records 1 – 30 of 19823 total matches.

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1. NG JUN XIANG. ROLE OF LYMPHOTOXIN B RECEPTOR SIGNALING IN LYMPH NODE LYMPHANGIOGENESIS INDUCED BY IMMUNIZATION.

Degree: 2013, National University of Singapore

Subjects/Keywords: Lymphotoxin B Receptor; Lymphangiogenesis; Lymph Node; Matrix Metalloproteinase-13

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APA (6th Edition):

XIANG, N. J. (2013). ROLE OF LYMPHOTOXIN B RECEPTOR SIGNALING IN LYMPH NODE LYMPHANGIOGENESIS INDUCED BY IMMUNIZATION. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/38816

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):

XIANG, NG JUN. “ROLE OF LYMPHOTOXIN B RECEPTOR SIGNALING IN LYMPH NODE LYMPHANGIOGENESIS INDUCED BY IMMUNIZATION.” 2013. Thesis, National University of Singapore. Accessed April 13, 2021. http://scholarbank.nus.edu.sg/handle/10635/38816.

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

MLA Handbook (7th Edition):

XIANG, NG JUN. “ROLE OF LYMPHOTOXIN B RECEPTOR SIGNALING IN LYMPH NODE LYMPHANGIOGENESIS INDUCED BY IMMUNIZATION.” 2013. Web. 13 Apr 2021.

Vancouver:

XIANG NJ. ROLE OF LYMPHOTOXIN B RECEPTOR SIGNALING IN LYMPH NODE LYMPHANGIOGENESIS INDUCED BY IMMUNIZATION. [Internet] [Thesis]. National University of Singapore; 2013. [cited 2021 Apr 13]. Available from: http://scholarbank.nus.edu.sg/handle/10635/38816.

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

Council of Science Editors:

XIANG NJ. ROLE OF LYMPHOTOXIN B RECEPTOR SIGNALING IN LYMPH NODE LYMPHANGIOGENESIS INDUCED BY IMMUNIZATION. [Thesis]. National University of Singapore; 2013. Available from: http://scholarbank.nus.edu.sg/handle/10635/38816

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

2. Otsmane, Belkacem. Dualité fonctionnelle de LIGHT : Implication dans la Mort du Motoneurone et dans la Régénération Axonale : Functional duality of LIGHT : From axon regeneration to death signalling.

Degree: Docteur es, Neurosciences, 2012, Aix Marseille Université

LIGHT, un membre de la famille du TNF, déclenche la mort des motoneurones et contribue à la progression de la dégénérescence des motoneurones chez les… (more)

Subjects/Keywords: Light; Lymphotoxine béta récepteur; Régénération axonale; Sclérose latérale amyotrophique; Motoneurone; Compartimentalisation; Light; Lymphotoxin béta receptor; Axon regeneration; Amyotrophic lateral sclerosis; Motoneuron; Compartimentalisation

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APA (6th Edition):

Otsmane, B. (2012). Dualité fonctionnelle de LIGHT : Implication dans la Mort du Motoneurone et dans la Régénération Axonale : Functional duality of LIGHT : From axon regeneration to death signalling. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2012AIXM4015

Chicago Manual of Style (16th Edition):

Otsmane, Belkacem. “Dualité fonctionnelle de LIGHT : Implication dans la Mort du Motoneurone et dans la Régénération Axonale : Functional duality of LIGHT : From axon regeneration to death signalling.” 2012. Doctoral Dissertation, Aix Marseille Université. Accessed April 13, 2021. http://www.theses.fr/2012AIXM4015.

MLA Handbook (7th Edition):

Otsmane, Belkacem. “Dualité fonctionnelle de LIGHT : Implication dans la Mort du Motoneurone et dans la Régénération Axonale : Functional duality of LIGHT : From axon regeneration to death signalling.” 2012. Web. 13 Apr 2021.

Vancouver:

Otsmane B. Dualité fonctionnelle de LIGHT : Implication dans la Mort du Motoneurone et dans la Régénération Axonale : Functional duality of LIGHT : From axon regeneration to death signalling. [Internet] [Doctoral dissertation]. Aix Marseille Université 2012. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2012AIXM4015.

Council of Science Editors:

Otsmane B. Dualité fonctionnelle de LIGHT : Implication dans la Mort du Motoneurone et dans la Régénération Axonale : Functional duality of LIGHT : From axon regeneration to death signalling. [Doctoral Dissertation]. Aix Marseille Université 2012. Available from: http://www.theses.fr/2012AIXM4015


Vanderbilt University

3. Nyhoff, Lindsay Elizabeth. Bruton's typrosine kinase and autoreactive B lymphocytes: Roles in development, survival, and disease.

Degree: PhD, Microbiology and Immunology, 2017, Vanderbilt University

 Bruton’s tyrosine kinase (BTK) is a tec-family kinase present in B lymphocytes and innate immune cells. BTK is an important regulator of B cell autoreactivity.… (more)

Subjects/Keywords: B cell receptor; K/BxN; B-1a; B-1b

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APA (6th Edition):

Nyhoff, L. E. (2017). Bruton's typrosine kinase and autoreactive B lymphocytes: Roles in development, survival, and disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11076

Chicago Manual of Style (16th Edition):

Nyhoff, Lindsay Elizabeth. “Bruton's typrosine kinase and autoreactive B lymphocytes: Roles in development, survival, and disease.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed April 13, 2021. http://hdl.handle.net/1803/11076.

MLA Handbook (7th Edition):

Nyhoff, Lindsay Elizabeth. “Bruton's typrosine kinase and autoreactive B lymphocytes: Roles in development, survival, and disease.” 2017. Web. 13 Apr 2021.

Vancouver:

Nyhoff LE. Bruton's typrosine kinase and autoreactive B lymphocytes: Roles in development, survival, and disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1803/11076.

Council of Science Editors:

Nyhoff LE. Bruton's typrosine kinase and autoreactive B lymphocytes: Roles in development, survival, and disease. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/11076

4. Tanaka, Tetsuya; Sho, Masayuki; Takayama, Tomoyoshi; Wakatsuki, Kohei; Matsumoto, Sohei; Migita, Kazuhiro; Ito, Masahiro; Hamada, Kaoru. Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. : 食道扁平上皮癌におきてエンドセリンB受容体の高発現は腫瘍の血管新生と予後に関与する.

Degree: 博士(医学), 2014, Nara Medical University / 奈良県立医科大学

BACKGROUND:The endothelin axis has been shown to have a pivotal role in several human malignancies. The aim of this study was to clarify the clinical… (more)

Subjects/Keywords: endothelin B receptor; oesophageal cancer; angiogenesis

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APA (6th Edition):

Tanaka, Tetsuya; Sho, Masayuki; Takayama, Tomoyoshi; Wakatsuki, Kohei; Matsumoto, Sohei; Migita, Kazuhiro; Ito, Masahiro; Hamada, K. (2014). Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. : 食道扁平上皮癌におきてエンドセリンB受容体の高発現は腫瘍の血管新生と予後に関与する. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/2720

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):

Tanaka, Tetsuya; Sho, Masayuki; Takayama, Tomoyoshi; Wakatsuki, Kohei; Matsumoto, Sohei; Migita, Kazuhiro; Ito, Masahiro; Hamada, Kaoru. “Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. : 食道扁平上皮癌におきてエンドセリンB受容体の高発現は腫瘍の血管新生と予後に関与する.” 2014. Thesis, Nara Medical University / 奈良県立医科大学. Accessed April 13, 2021. http://hdl.handle.net/10564/2720.

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

MLA Handbook (7th Edition):

Tanaka, Tetsuya; Sho, Masayuki; Takayama, Tomoyoshi; Wakatsuki, Kohei; Matsumoto, Sohei; Migita, Kazuhiro; Ito, Masahiro; Hamada, Kaoru. “Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. : 食道扁平上皮癌におきてエンドセリンB受容体の高発現は腫瘍の血管新生と予後に関与する.” 2014. Web. 13 Apr 2021.

Vancouver:

Tanaka, Tetsuya; Sho, Masayuki; Takayama, Tomoyoshi; Wakatsuki, Kohei; Matsumoto, Sohei; Migita, Kazuhiro; Ito, Masahiro; Hamada K. Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. : 食道扁平上皮癌におきてエンドセリンB受容体の高発現は腫瘍の血管新生と予後に関与する. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10564/2720.

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

Council of Science Editors:

Tanaka, Tetsuya; Sho, Masayuki; Takayama, Tomoyoshi; Wakatsuki, Kohei; Matsumoto, Sohei; Migita, Kazuhiro; Ito, Masahiro; Hamada K. Endothelin B receptor expression correlates with tumour angiogenesis and prognosis in oesophageal squamous cell carcinoma. : 食道扁平上皮癌におきてエンドセリンB受容体の高発現は腫瘍の血管新生と予後に関与する. [Thesis]. Nara Medical University / 奈良県立医科大学; 2014. Available from: http://hdl.handle.net/10564/2720

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


University of Wollongong

5. Pupovac, Aleta. P2X7 receptor-induced CD23 shedding from B cells.

Degree: Doctor of Philosophy, 2014, University of Wollongong

  The P2X7 receptor is a ligand-gated cation channel, which is expressed on a variety of cell types, including human B cells. P2X7 activation induces… (more)

Subjects/Keywords: Purinergic signalling; lgE receptor; B cells

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APA (6th Edition):

Pupovac, A. (2014). P2X7 receptor-induced CD23 shedding from B cells. (Doctoral Dissertation). University of Wollongong. Retrieved from ; https://ro.uow.edu.au/theses/4349

Chicago Manual of Style (16th Edition):

Pupovac, Aleta. “P2X7 receptor-induced CD23 shedding from B cells.” 2014. Doctoral Dissertation, University of Wollongong. Accessed April 13, 2021. ; https://ro.uow.edu.au/theses/4349.

MLA Handbook (7th Edition):

Pupovac, Aleta. “P2X7 receptor-induced CD23 shedding from B cells.” 2014. Web. 13 Apr 2021.

Vancouver:

Pupovac A. P2X7 receptor-induced CD23 shedding from B cells. [Internet] [Doctoral dissertation]. University of Wollongong; 2014. [cited 2021 Apr 13]. Available from: ; https://ro.uow.edu.au/theses/4349.

Council of Science Editors:

Pupovac A. P2X7 receptor-induced CD23 shedding from B cells. [Doctoral Dissertation]. University of Wollongong; 2014. Available from: ; https://ro.uow.edu.au/theses/4349


Australian National University

6. de Guzman, Sarah Yvonne. Analysis of membrane exchange between lymphocytes .

Degree: 2016, Australian National University

 Membrane transfer is the cell-to-cell contact dependent exchange of plasma membrane and surface molecules between cells. It has been described for a wide range of… (more)

Subjects/Keywords: Trogocytosis; B lymphocytes; antigen receptor sharing

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APA (6th Edition):

de Guzman, S. Y. (2016). Analysis of membrane exchange between lymphocytes . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/116891

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):

de Guzman, Sarah Yvonne. “Analysis of membrane exchange between lymphocytes .” 2016. Thesis, Australian National University. Accessed April 13, 2021. http://hdl.handle.net/1885/116891.

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

MLA Handbook (7th Edition):

de Guzman, Sarah Yvonne. “Analysis of membrane exchange between lymphocytes .” 2016. Web. 13 Apr 2021.

Vancouver:

de Guzman SY. Analysis of membrane exchange between lymphocytes . [Internet] [Thesis]. Australian National University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1885/116891.

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

Council of Science Editors:

de Guzman SY. Analysis of membrane exchange between lymphocytes . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/116891

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


University of Louisville

7. Dascani, Paul Lorenzo. CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus.

Degree: PhD, 2018, University of Louisville

  Loss of function mutation in CD11b has been associated with incidence of systemic lupus erythematosus (SLE), a disease driven by B cell production of… (more)

Subjects/Keywords: B cell; systemic lupus erythematosus; CD11b; B cell receptor; Immunity

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APA (6th Edition):

Dascani, P. L. (2018). CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076

Chicago Manual of Style (16th Edition):

Dascani, Paul Lorenzo. “CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus.” 2018. Doctoral Dissertation, University of Louisville. Accessed April 13, 2021. 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076.

MLA Handbook (7th Edition):

Dascani, Paul Lorenzo. “CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus.” 2018. Web. 13 Apr 2021.

Vancouver:

Dascani PL. CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus. [Internet] [Doctoral dissertation]. University of Louisville; 2018. [cited 2021 Apr 13]. Available from: 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076.

Council of Science Editors:

Dascani PL. CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus. [Doctoral Dissertation]. University of Louisville; 2018. Available from: 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076

8. Taise Natali Landgraf. Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1.

Degree: 2012, University of São Paulo

Alguns fatores de virulência em bactérias de microbiota normal, tais como sideróforos moléculas captadoras de ferro e determinadas fímbrias, possibilitam que esses microorganismos causem infecção… (more)

Subjects/Keywords: Ativação policlonal; Células B; MyD88; Receptor de IL-1; Receptor de sideróforo; B cells; IL-1 receptor; MyD88; Polyclonal activation; Siderophore receptor

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APA (6th Edition):

Landgraf, T. N. (2012). Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/

Chicago Manual of Style (16th Edition):

Landgraf, Taise Natali. “Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1.” 2012. Masters Thesis, University of São Paulo. Accessed April 13, 2021. http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/.

MLA Handbook (7th Edition):

Landgraf, Taise Natali. “Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1.” 2012. Web. 13 Apr 2021.

Vancouver:

Landgraf TN. Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2021 Apr 13]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/.

Council of Science Editors:

Landgraf TN. Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/

9. Alysson Zanatta. Expressão proteíca do gene HOXA10 e dos receptores de estrogênio e progesterona no epitélio, estroma e tecido muscular liso perilesional de endometriose e do reto-sigmoide.

Degree: 2013, University of São Paulo

 INTRODUÇÃO: Apesar de a endometriose profunda (EPF) ser a forma da doença de maior repercussão clínica, os estudos sobre a doença costumam ser baseados em… (more)

Subjects/Keywords: Endometriose de retosigmoide; Endometriose profunda; Gene HOXA10; Receptor de estrogênio alfa; Receptor de estrogênio beta; Receptor de progesterona; Receptor de progesterona B; Deep endometriosis; Estrogen receptor-alfa; Estrogen receptor-beta; HOXA gene; Progesterone receptor-B; Progesterone receptor; Rectosigmoid endometriosis

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APA (6th Edition):

Zanatta, A. (2013). Expressão proteíca do gene HOXA10 e dos receptores de estrogênio e progesterona no epitélio, estroma e tecido muscular liso perilesional de endometriose e do reto-sigmoide. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5139/tde-06112013-085759/

Chicago Manual of Style (16th Edition):

Zanatta, Alysson. “Expressão proteíca do gene HOXA10 e dos receptores de estrogênio e progesterona no epitélio, estroma e tecido muscular liso perilesional de endometriose e do reto-sigmoide.” 2013. Doctoral Dissertation, University of São Paulo. Accessed April 13, 2021. http://www.teses.usp.br/teses/disponiveis/5/5139/tde-06112013-085759/.

MLA Handbook (7th Edition):

Zanatta, Alysson. “Expressão proteíca do gene HOXA10 e dos receptores de estrogênio e progesterona no epitélio, estroma e tecido muscular liso perilesional de endometriose e do reto-sigmoide.” 2013. Web. 13 Apr 2021.

Vancouver:

Zanatta A. Expressão proteíca do gene HOXA10 e dos receptores de estrogênio e progesterona no epitélio, estroma e tecido muscular liso perilesional de endometriose e do reto-sigmoide. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2021 Apr 13]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5139/tde-06112013-085759/.

Council of Science Editors:

Zanatta A. Expressão proteíca do gene HOXA10 e dos receptores de estrogênio e progesterona no epitélio, estroma e tecido muscular liso perilesional de endometriose e do reto-sigmoide. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/5/5139/tde-06112013-085759/


University of California – San Francisco

10. Viet, Chi Tonglien. Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain.

Degree: Nursing, 2011, University of California – San Francisco

 Cancer pain creates a poor quality of life for cancer patients. Chroniccancer pain is a major public health problem in which little progress has been… (more)

Subjects/Keywords: Oncology; cancer pain; demethylating drug; endothelin B receptor; methylation; mu-opioid receptor; oral cancer

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APA (6th Edition):

Viet, C. T. (2011). Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0w61j9tp

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):

Viet, Chi Tonglien. “Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain.” 2011. Thesis, University of California – San Francisco. Accessed April 13, 2021. http://www.escholarship.org/uc/item/0w61j9tp.

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

MLA Handbook (7th Edition):

Viet, Chi Tonglien. “Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain.” 2011. Web. 13 Apr 2021.

Vancouver:

Viet CT. Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/0w61j9tp.

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

Council of Science Editors:

Viet CT. Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/0w61j9tp

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


University of Washington

11. Tao, Wucheng. GABA-B receptors regulate extrasynaptic GABA-A receptors.

Degree: PhD, 2015, University of Washington

 Classically, GABAB receptors regulate neurotransmission primarily through presynaptic mechanisms that inhibit neurotransmitter release, and thus inhibit GABAA receptor function. Many studies have shown that postsynaptic… (more)

Subjects/Keywords: extrasynaptic GABA-A receptor; GABA-B receptor; PKA; PKC; Physiology; physiology and biophysics

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APA (6th Edition):

Tao, W. (2015). GABA-B receptors regulate extrasynaptic GABA-A receptors. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/27563

Chicago Manual of Style (16th Edition):

Tao, Wucheng. “GABA-B receptors regulate extrasynaptic GABA-A receptors.” 2015. Doctoral Dissertation, University of Washington. Accessed April 13, 2021. http://hdl.handle.net/1773/27563.

MLA Handbook (7th Edition):

Tao, Wucheng. “GABA-B receptors regulate extrasynaptic GABA-A receptors.” 2015. Web. 13 Apr 2021.

Vancouver:

Tao W. GABA-B receptors regulate extrasynaptic GABA-A receptors. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1773/27563.

Council of Science Editors:

Tao W. GABA-B receptors regulate extrasynaptic GABA-A receptors. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/27563


Cornell University

12. Apoorva, Fnu. ENGINEERED TECHNOLOGIES TO STUDY THE ROLE OF MECHANICAL SIGNALS IN HUMAN LYMPHOMA GROWTH AND THERAPEUTIC RESPONSE.

Degree: PhD, Mechanical Engineering, 2018, Cornell University

 Diffuse Large B cell lymphoma (DLBCL) is the most common lymphoma representing ~30% of all B cell Non-Hodgkin lymphomas. DLBCL is a heterogeneous disease associated… (more)

Subjects/Keywords: micr-bioreactor; microenvironment; Organoid; Mechanical engineering; B cell receptor; Diffuse Large B Cell Lymphoma; Integrins

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APA (6th Edition):

Apoorva, F. (2018). ENGINEERED TECHNOLOGIES TO STUDY THE ROLE OF MECHANICAL SIGNALS IN HUMAN LYMPHOMA GROWTH AND THERAPEUTIC RESPONSE. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59334

Chicago Manual of Style (16th Edition):

Apoorva, Fnu. “ENGINEERED TECHNOLOGIES TO STUDY THE ROLE OF MECHANICAL SIGNALS IN HUMAN LYMPHOMA GROWTH AND THERAPEUTIC RESPONSE.” 2018. Doctoral Dissertation, Cornell University. Accessed April 13, 2021. http://hdl.handle.net/1813/59334.

MLA Handbook (7th Edition):

Apoorva, Fnu. “ENGINEERED TECHNOLOGIES TO STUDY THE ROLE OF MECHANICAL SIGNALS IN HUMAN LYMPHOMA GROWTH AND THERAPEUTIC RESPONSE.” 2018. Web. 13 Apr 2021.

Vancouver:

Apoorva F. ENGINEERED TECHNOLOGIES TO STUDY THE ROLE OF MECHANICAL SIGNALS IN HUMAN LYMPHOMA GROWTH AND THERAPEUTIC RESPONSE. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1813/59334.

Council of Science Editors:

Apoorva F. ENGINEERED TECHNOLOGIES TO STUDY THE ROLE OF MECHANICAL SIGNALS IN HUMAN LYMPHOMA GROWTH AND THERAPEUTIC RESPONSE. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59334

13. G. Varano. THE ROLE OF THE B CELL ANTIGEN RECEPTOR IN A MOUSE MODEL OF NON-HODGKIN LYMPHOMA.

Degree: 2013, Università degli Studi di Milano

 The B cell antigen receptor (BCR) plays a central role both in early B-cell development and in mature B cells, where it controls survival and… (more)

Subjects/Keywords: Lymphoma; B-Cell-Receptor; B lymphocytes; c-MYC; Settore MED/04 - Patologia Generale

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APA (6th Edition):

Varano, G. (2013). THE ROLE OF THE B CELL ANTIGEN RECEPTOR IN A MOUSE MODEL OF NON-HODGKIN LYMPHOMA. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/219066

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):

Varano, G.. “THE ROLE OF THE B CELL ANTIGEN RECEPTOR IN A MOUSE MODEL OF NON-HODGKIN LYMPHOMA.” 2013. Thesis, Università degli Studi di Milano. Accessed April 13, 2021. http://hdl.handle.net/2434/219066.

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

MLA Handbook (7th Edition):

Varano, G.. “THE ROLE OF THE B CELL ANTIGEN RECEPTOR IN A MOUSE MODEL OF NON-HODGKIN LYMPHOMA.” 2013. Web. 13 Apr 2021.

Vancouver:

Varano G. THE ROLE OF THE B CELL ANTIGEN RECEPTOR IN A MOUSE MODEL OF NON-HODGKIN LYMPHOMA. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2434/219066.

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

Council of Science Editors:

Varano G. THE ROLE OF THE B CELL ANTIGEN RECEPTOR IN A MOUSE MODEL OF NON-HODGKIN LYMPHOMA. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/219066

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


University of California – San Francisco

14. Wheeler, Matthew Lewis. Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism.

Degree: Biomedical Sciences, 2013, University of California – San Francisco

 Recognition of cognate antigen by the B cell antigen receptor (BCR) is one of the primary events that ultimately facilitate the production of pathogen-specific antibodies… (more)

Subjects/Keywords: Immunology; antibody response; B cell receptor; B lymphocyte; diacylglycerol; reactive oxygen species; signal transduction

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APA (6th Edition):

Wheeler, M. L. (2013). Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3657t2n7

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):

Wheeler, Matthew Lewis. “Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism.” 2013. Thesis, University of California – San Francisco. Accessed April 13, 2021. http://www.escholarship.org/uc/item/3657t2n7.

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

MLA Handbook (7th Edition):

Wheeler, Matthew Lewis. “Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism.” 2013. Web. 13 Apr 2021.

Vancouver:

Wheeler ML. Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/3657t2n7.

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

Council of Science Editors:

Wheeler ML. Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/3657t2n7

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


University of Western Ontario

15. Turkistany, Shereen. The Role of PU.1 and Spi-B in B Cell Acute Lymphoblastic Leukemia.

Degree: 2013, University of Western Ontario

 ETV6-RUNX1 is the most common chromosomal alteration in pediatric B cell acute lymphoblastic leukemia. ETV6-RUNX1 represses RUNX1 target genes. However, little is known about the… (more)

Subjects/Keywords: B cell acute lymphoblastic leukemia; ETV6-RUNX1 B-ALL; PU.1. SPIB; B cell receptor signaling (BCR).; Medical Immunology

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APA (6th Edition):

Turkistany, S. (2013). The Role of PU.1 and Spi-B in B Cell Acute Lymphoblastic Leukemia. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1225

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):

Turkistany, Shereen. “The Role of PU.1 and Spi-B in B Cell Acute Lymphoblastic Leukemia.” 2013. Thesis, University of Western Ontario. Accessed April 13, 2021. https://ir.lib.uwo.ca/etd/1225.

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

MLA Handbook (7th Edition):

Turkistany, Shereen. “The Role of PU.1 and Spi-B in B Cell Acute Lymphoblastic Leukemia.” 2013. Web. 13 Apr 2021.

Vancouver:

Turkistany S. The Role of PU.1 and Spi-B in B Cell Acute Lymphoblastic Leukemia. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2021 Apr 13]. Available from: https://ir.lib.uwo.ca/etd/1225.

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

Council of Science Editors:

Turkistany S. The Role of PU.1 and Spi-B in B Cell Acute Lymphoblastic Leukemia. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1225

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

16. Singh, Dinesh Kumar. Control of B Cell receptor mediated signaling; -.

Degree: Genetic Engineering and Biotechanology, 2005, Jawaharlal Nehru University

non

Bibliography p.90-128

Advisors/Committee Members: Rao, V S Kanury.

Subjects/Keywords: B-Cell, signaling; receptor

Page 1

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APA (6th Edition):

Singh, D. K. (2005). Control of B Cell receptor mediated signaling; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/28769

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):

Singh, Dinesh Kumar. “Control of B Cell receptor mediated signaling; -.” 2005. Thesis, Jawaharlal Nehru University. Accessed April 13, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/28769.

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

MLA Handbook (7th Edition):

Singh, Dinesh Kumar. “Control of B Cell receptor mediated signaling; -.” 2005. Web. 13 Apr 2021.

Vancouver:

Singh DK. Control of B Cell receptor mediated signaling; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2005. [cited 2021 Apr 13]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28769.

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

Council of Science Editors:

Singh DK. Control of B Cell receptor mediated signaling; -. [Thesis]. Jawaharlal Nehru University; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28769

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


UCLA

17. Castaneda, Julie Theresa. Linking Cannabinoid Receptor Type II (CB2) Biology to Function.

Degree: Molecular Toxicology, 2016, UCLA

 Cannabinoids, the primary bioactive components in marijuana, bind and signal through endogenous cannabinoid receptors. mRNA encoding for the cannabinoid receptor type II (CB2) predominates in… (more)

Subjects/Keywords: Toxicology; Immunology; Biology; activation; B cells; cannabinoid; Marijuana; receptor; trafficking

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APA (6th Edition):

Castaneda, J. T. (2016). Linking Cannabinoid Receptor Type II (CB2) Biology to Function. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4jv306dg

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):

Castaneda, Julie Theresa. “Linking Cannabinoid Receptor Type II (CB2) Biology to Function.” 2016. Thesis, UCLA. Accessed April 13, 2021. http://www.escholarship.org/uc/item/4jv306dg.

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

MLA Handbook (7th Edition):

Castaneda, Julie Theresa. “Linking Cannabinoid Receptor Type II (CB2) Biology to Function.” 2016. Web. 13 Apr 2021.

Vancouver:

Castaneda JT. Linking Cannabinoid Receptor Type II (CB2) Biology to Function. [Internet] [Thesis]. UCLA; 2016. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/4jv306dg.

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

Council of Science Editors:

Castaneda JT. Linking Cannabinoid Receptor Type II (CB2) Biology to Function. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/4jv306dg

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


University of Manitoba

18. Dielschneider, Rebecca. Targeting Susceptible Signaling Pathways in Chronic Lymphocytic Leukemia.

Degree: Immunology, 2014, University of Manitoba

 Chronic lymphocytic leukemia (CLL) is a cancer of B cells and is the most common leukemia in North America. Current therapies are fraught with challenges,… (more)

Subjects/Keywords: Leukemia; Cancer; ZAP-70; Lysosome; B Cell Receptor

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APA (6th Edition):

Dielschneider, R. (2014). Targeting Susceptible Signaling Pathways in Chronic Lymphocytic Leukemia. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31681

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):

Dielschneider, Rebecca. “Targeting Susceptible Signaling Pathways in Chronic Lymphocytic Leukemia.” 2014. Thesis, University of Manitoba. Accessed April 13, 2021. http://hdl.handle.net/1993/31681.

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

MLA Handbook (7th Edition):

Dielschneider, Rebecca. “Targeting Susceptible Signaling Pathways in Chronic Lymphocytic Leukemia.” 2014. Web. 13 Apr 2021.

Vancouver:

Dielschneider R. Targeting Susceptible Signaling Pathways in Chronic Lymphocytic Leukemia. [Internet] [Thesis]. University of Manitoba; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1993/31681.

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

Council of Science Editors:

Dielschneider R. Targeting Susceptible Signaling Pathways in Chronic Lymphocytic Leukemia. [Thesis]. University of Manitoba; 2014. Available from: http://hdl.handle.net/1993/31681

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


University of Edinburgh

19. Festuccia, Nicola. Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development.

Degree: PhD, 2013, University of Edinburgh

 Embryonic stem (ES) cell pluripotency is sustained by a network of transcription factors centred on Oct4, Sox2 and Nanog. Whilst Oct4 and Sox2 expression is… (more)

Subjects/Keywords: 572; transcriptional profiling; embryonic stem; Nanog; Estrogen-related receptor b; Esrrb

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APA (6th Edition):

Festuccia, N. (2013). Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/12232

Chicago Manual of Style (16th Edition):

Festuccia, Nicola. “Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed April 13, 2021. http://hdl.handle.net/1842/12232.

MLA Handbook (7th Edition):

Festuccia, Nicola. “Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development.” 2013. Web. 13 Apr 2021.

Vancouver:

Festuccia N. Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1842/12232.

Council of Science Editors:

Festuccia N. Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/12232


University of Illinois – Urbana-Champaign

20. Low, Jianrong. Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies.

Degree: PhD, 0318, 2013, University of Illinois – Urbana-Champaign

 T cells play a vital role in the adaptive immune response against viral infections. Virus-specific T cells recognize infected cells through a heterodimeric surface receptor(more)

Subjects/Keywords: T cell receptor; Protein engineering; yeast display; hepatitis B virus

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APA (6th Edition):

Low, J. (2013). Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42491

Chicago Manual of Style (16th Edition):

Low, Jianrong. “Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 13, 2021. http://hdl.handle.net/2142/42491.

MLA Handbook (7th Edition):

Low, Jianrong. “Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies.” 2013. Web. 13 Apr 2021.

Vancouver:

Low J. Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2142/42491.

Council of Science Editors:

Low J. Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42491


University of Iowa

21. Buchta, Claire Marie. Mechanisms of TLR signaling and cooperation in B lymphocytes.

Degree: PhD, Immunology, 2014, University of Iowa

B lymphocytes play important roles in antibody production, cytokine production, and antigen presentation to T cells. Ligation of Toll-like receptors (TLRs) on B cells… (more)

Subjects/Keywords: B lymphocyte; Toll-like receptor; TRAF5; Immunology of Infectious Disease

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APA (6th Edition):

Buchta, C. M. (2014). Mechanisms of TLR signaling and cooperation in B lymphocytes. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4584

Chicago Manual of Style (16th Edition):

Buchta, Claire Marie. “Mechanisms of TLR signaling and cooperation in B lymphocytes.” 2014. Doctoral Dissertation, University of Iowa. Accessed April 13, 2021. https://ir.uiowa.edu/etd/4584.

MLA Handbook (7th Edition):

Buchta, Claire Marie. “Mechanisms of TLR signaling and cooperation in B lymphocytes.” 2014. Web. 13 Apr 2021.

Vancouver:

Buchta CM. Mechanisms of TLR signaling and cooperation in B lymphocytes. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2021 Apr 13]. Available from: https://ir.uiowa.edu/etd/4584.

Council of Science Editors:

Buchta CM. Mechanisms of TLR signaling and cooperation in B lymphocytes. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4584


University of Texas – Austin

22. Hoi, Kam Hon. Global survey of the immunoglobulin repertoire using next generation sequencing technology.

Degree: PhD, Biomedical Engineering, 2014, University of Texas – Austin

 Specific and sensitive recognition of foreign agents is a critical attribute of the overall effective immune system required for maintaining host protection against challenge from… (more)

Subjects/Keywords: B cell receptor; Antibody repertoire; Next generation sequencing; Bioinformatics

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APA (6th Edition):

Hoi, K. H. (2014). Global survey of the immunoglobulin repertoire using next generation sequencing technology. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28322

Chicago Manual of Style (16th Edition):

Hoi, Kam Hon. “Global survey of the immunoglobulin repertoire using next generation sequencing technology.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed April 13, 2021. http://hdl.handle.net/2152/28322.

MLA Handbook (7th Edition):

Hoi, Kam Hon. “Global survey of the immunoglobulin repertoire using next generation sequencing technology.” 2014. Web. 13 Apr 2021.

Vancouver:

Hoi KH. Global survey of the immunoglobulin repertoire using next generation sequencing technology. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2152/28322.

Council of Science Editors:

Hoi KH. Global survey of the immunoglobulin repertoire using next generation sequencing technology. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/28322

23. Antonio Augusto Araujo Pinto da Silva. Estudo experimental do sistema Ta-Ge e da região rica em Ta do ternário Ta-Ge-B.

Degree: 2011, University of São Paulo

Os motores a jato são componentes importantes e complexos de engenharia cuja eficiência e desempenho estão diretamente ligados à temperatura de operação na câmara de… (more)

Subjects/Keywords: Diagrama de Fases; Sistema Ta-Ge; Sistema Ta-Ge-B; Phase Diagram; Ta-Ge System; Ta-Ge-B System

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APA (6th Edition):

Silva, A. A. A. P. d. (2011). Estudo experimental do sistema Ta-Ge e da região rica em Ta do ternário Ta-Ge-B. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/97/97134/tde-26092012-144523/

Chicago Manual of Style (16th Edition):

Silva, Antonio Augusto Araujo Pinto da. “Estudo experimental do sistema Ta-Ge e da região rica em Ta do ternário Ta-Ge-B.” 2011. Masters Thesis, University of São Paulo. Accessed April 13, 2021. http://www.teses.usp.br/teses/disponiveis/97/97134/tde-26092012-144523/.

MLA Handbook (7th Edition):

Silva, Antonio Augusto Araujo Pinto da. “Estudo experimental do sistema Ta-Ge e da região rica em Ta do ternário Ta-Ge-B.” 2011. Web. 13 Apr 2021.

Vancouver:

Silva AAAPd. Estudo experimental do sistema Ta-Ge e da região rica em Ta do ternário Ta-Ge-B. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2021 Apr 13]. Available from: http://www.teses.usp.br/teses/disponiveis/97/97134/tde-26092012-144523/.

Council of Science Editors:

Silva AAAPd. Estudo experimental do sistema Ta-Ge e da região rica em Ta do ternário Ta-Ge-B. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/97/97134/tde-26092012-144523/

24. Papageorgiou, Aristea. Αιματολογική μελέτη συστηματικών αυτοάνοσων νοσημάτων: μοριακή μελέτη της λεμφωματογένεσης σε σύνδρομο sjogren.

Degree: 2015, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Sjogren’s syndrome (SS) is characterized by the highest risk among all autoimmune diseases for malignant transformation and lymphoma development. BAFF has been implicated in the… (more)

Subjects/Keywords: Σύνδρομο Sjogren; NON-HODGKIN'S ΛΕΜΦΩΜΑ; Πρόγνωση επιβίωσης; B-cell activating factor receptor; Sjogren syndorme; B - non Hodgkin's lymphomas; Survival; B-cell activating factor receptor

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APA (6th Edition):

Papageorgiou, A. (2015). Αιματολογική μελέτη συστηματικών αυτοάνοσων νοσημάτων: μοριακή μελέτη της λεμφωματογένεσης σε σύνδρομο sjogren. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/35722

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):

Papageorgiou, Aristea. “Αιματολογική μελέτη συστηματικών αυτοάνοσων νοσημάτων: μοριακή μελέτη της λεμφωματογένεσης σε σύνδρομο sjogren.” 2015. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 13, 2021. http://hdl.handle.net/10442/hedi/35722.

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

MLA Handbook (7th Edition):

Papageorgiou, Aristea. “Αιματολογική μελέτη συστηματικών αυτοάνοσων νοσημάτων: μοριακή μελέτη της λεμφωματογένεσης σε σύνδρομο sjogren.” 2015. Web. 13 Apr 2021.

Vancouver:

Papageorgiou A. Αιματολογική μελέτη συστηματικών αυτοάνοσων νοσημάτων: μοριακή μελέτη της λεμφωματογένεσης σε σύνδρομο sjogren. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10442/hedi/35722.

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

Council of Science Editors:

Papageorgiou A. Αιματολογική μελέτη συστηματικών αυτοάνοσων νοσημάτων: μοριακή μελέτη της λεμφωματογένεσης σε σύνδρομο sjogren. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. Available from: http://hdl.handle.net/10442/hedi/35722

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

25. Immediato-Daien, Claire. Analyse des lymphocytes B dans la polyarthrite rhumatoïde : phénotypage, étude des B régulateurs et des lymphocytes B comme biomarqueurs de réponse aux biomédicaments. : Study of B cells in rheumatoid arthritis : phenotyping, regulatory B cell analysis and B cells as predictive biomarker of response to biodrugs.

Degree: Docteur es, Biologie Cellulaire, 2014, Université Montpellier I

 Le lymphocyte B (LB) joue un rôle important dans la polyarthrite rhumatoïde (PR), en produisant des auto-anticorps qui ont un rôle pathogène, en activant les… (more)

Subjects/Keywords: Polyarthrite rhumatoïde; Lymphocytes B; B régulateurs; Anti-TNF; Inhibiteur du récepteur de l'IL-6; Rheumatoid arthritis; B cells; Regulatory B cells; TNF inhibitors; Anti-IL-6 receptor

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APA (6th Edition):

Immediato-Daien, C. (2014). Analyse des lymphocytes B dans la polyarthrite rhumatoïde : phénotypage, étude des B régulateurs et des lymphocytes B comme biomarqueurs de réponse aux biomédicaments. : Study of B cells in rheumatoid arthritis : phenotyping, regulatory B cell analysis and B cells as predictive biomarker of response to biodrugs. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2014MON1T001

Chicago Manual of Style (16th Edition):

Immediato-Daien, Claire. “Analyse des lymphocytes B dans la polyarthrite rhumatoïde : phénotypage, étude des B régulateurs et des lymphocytes B comme biomarqueurs de réponse aux biomédicaments. : Study of B cells in rheumatoid arthritis : phenotyping, regulatory B cell analysis and B cells as predictive biomarker of response to biodrugs.” 2014. Doctoral Dissertation, Université Montpellier I. Accessed April 13, 2021. http://www.theses.fr/2014MON1T001.

MLA Handbook (7th Edition):

Immediato-Daien, Claire. “Analyse des lymphocytes B dans la polyarthrite rhumatoïde : phénotypage, étude des B régulateurs et des lymphocytes B comme biomarqueurs de réponse aux biomédicaments. : Study of B cells in rheumatoid arthritis : phenotyping, regulatory B cell analysis and B cells as predictive biomarker of response to biodrugs.” 2014. Web. 13 Apr 2021.

Vancouver:

Immediato-Daien C. Analyse des lymphocytes B dans la polyarthrite rhumatoïde : phénotypage, étude des B régulateurs et des lymphocytes B comme biomarqueurs de réponse aux biomédicaments. : Study of B cells in rheumatoid arthritis : phenotyping, regulatory B cell analysis and B cells as predictive biomarker of response to biodrugs. [Internet] [Doctoral dissertation]. Université Montpellier I; 2014. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2014MON1T001.

Council of Science Editors:

Immediato-Daien C. Analyse des lymphocytes B dans la polyarthrite rhumatoïde : phénotypage, étude des B régulateurs et des lymphocytes B comme biomarqueurs de réponse aux biomédicaments. : Study of B cells in rheumatoid arthritis : phenotyping, regulatory B cell analysis and B cells as predictive biomarker of response to biodrugs. [Doctoral Dissertation]. Université Montpellier I; 2014. Available from: http://www.theses.fr/2014MON1T001


University of Toronto

26. Davani, Dariush. Positive and Negative Selection of Developing Antigen Specific B Cells in a Gut Associated Lymphoid Organ, the Bursa of Fabricius.

Degree: 2013, University of Toronto

Abstract Surface immunoglobulin (sIg) expression is a critical checkpoint in the early stages of B cell development. However it remains controversial as to whether sIg… (more)

Subjects/Keywords: B cell development; GALTB lmphopoiesis; Comparetive immunology; Avian B lymphopoiesis; B cell Positive and Negative selection; BCR; BCR fusion; B cell receptor ligation; Bursa of Fabricious; VLR; Antigen; 0982

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

APA (6th Edition):

Davani, D. (2013). Positive and Negative Selection of Developing Antigen Specific B Cells in a Gut Associated Lymphoid Organ, the Bursa of Fabricius. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68888

Chicago Manual of Style (16th Edition):

Davani, Dariush. “Positive and Negative Selection of Developing Antigen Specific B Cells in a Gut Associated Lymphoid Organ, the Bursa of Fabricius.” 2013. Doctoral Dissertation, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/68888.

MLA Handbook (7th Edition):

Davani, Dariush. “Positive and Negative Selection of Developing Antigen Specific B Cells in a Gut Associated Lymphoid Organ, the Bursa of Fabricius.” 2013. Web. 13 Apr 2021.

Vancouver:

Davani D. Positive and Negative Selection of Developing Antigen Specific B Cells in a Gut Associated Lymphoid Organ, the Bursa of Fabricius. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/68888.

Council of Science Editors:

Davani D. Positive and Negative Selection of Developing Antigen Specific B Cells in a Gut Associated Lymphoid Organ, the Bursa of Fabricius. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/68888


University of Illinois – Chicago

27. Lu, Yunlong. Novel Treatment for ER+ Treatment Resistant Breast Cancer.

Degree: 2019, University of Illinois – Chicago

 Estrogen receptors (ERs) are nuclear hormone receptors and regulate many target genes associated with cell survival, growth and development. ERs act as transcription factors and… (more)

Subjects/Keywords: Breast cancer; ER+; basic-amino selective estrogen receptor degraders (B-SERDs); Selective mixed-function estrogen receptor degraders (SMERDs)

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APA (6th Edition):

Lu, Y. (2019). Novel Treatment for ER+ Treatment Resistant Breast Cancer. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/23690

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):

Lu, Yunlong. “Novel Treatment for ER+ Treatment Resistant Breast Cancer.” 2019. Thesis, University of Illinois – Chicago. Accessed April 13, 2021. http://hdl.handle.net/10027/23690.

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

MLA Handbook (7th Edition):

Lu, Yunlong. “Novel Treatment for ER+ Treatment Resistant Breast Cancer.” 2019. Web. 13 Apr 2021.

Vancouver:

Lu Y. Novel Treatment for ER+ Treatment Resistant Breast Cancer. [Internet] [Thesis]. University of Illinois – Chicago; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10027/23690.

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

Council of Science Editors:

Lu Y. Novel Treatment for ER+ Treatment Resistant Breast Cancer. [Thesis]. University of Illinois – Chicago; 2019. Available from: http://hdl.handle.net/10027/23690

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


University of Washington

28. Olson, Branden. Statistical Methods for Adaptive Immune Receptor Repertoire Analysis and Comparison.

Degree: PhD, 2021, University of Washington

B and T cell receptors, also known as adaptive immune receptors, perform key roles in adaptive immunity. These proteins identify and deal with foreign invaders… (more)

Subjects/Keywords: B cell receptor; Computational biology; Optimal transport; Statistical immunology; Statistical methods; T cell receptor; Statistics; Immunology; Bioinformatics; Statistics

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APA (6th Edition):

Olson, B. (2021). Statistical Methods for Adaptive Immune Receptor Repertoire Analysis and Comparison. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/46895

Chicago Manual of Style (16th Edition):

Olson, Branden. “Statistical Methods for Adaptive Immune Receptor Repertoire Analysis and Comparison.” 2021. Doctoral Dissertation, University of Washington. Accessed April 13, 2021. http://hdl.handle.net/1773/46895.

MLA Handbook (7th Edition):

Olson, Branden. “Statistical Methods for Adaptive Immune Receptor Repertoire Analysis and Comparison.” 2021. Web. 13 Apr 2021.

Vancouver:

Olson B. Statistical Methods for Adaptive Immune Receptor Repertoire Analysis and Comparison. [Internet] [Doctoral dissertation]. University of Washington; 2021. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1773/46895.

Council of Science Editors:

Olson B. Statistical Methods for Adaptive Immune Receptor Repertoire Analysis and Comparison. [Doctoral Dissertation]. University of Washington; 2021. Available from: http://hdl.handle.net/1773/46895


Freie Universität Berlin

29. Sieger, Nadine. CD22 ligation inhibits downstream B-cell receptor signaling and Ca2+ flux upon activation.

Degree: 2012, Freie Universität Berlin

 Background: CD22 is a surface molecule exclusively expressed on B lymphocytes involved in adhesion and B-cell receptor (BCR) signaling. By recruiting a tyrosine-phosphatase to its… (more)

Subjects/Keywords: CD22; Epratuzumab; B-cell receptor signaling; B-cell targets; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Sieger, N. (2012). CD22 ligation inhibits downstream B-cell receptor signaling and Ca2+ flux upon activation. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-9421

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):

Sieger, Nadine. “CD22 ligation inhibits downstream B-cell receptor signaling and Ca2+ flux upon activation.” 2012. Thesis, Freie Universität Berlin. Accessed April 13, 2021. http://dx.doi.org/10.17169/refubium-9421.

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

MLA Handbook (7th Edition):

Sieger, Nadine. “CD22 ligation inhibits downstream B-cell receptor signaling and Ca2+ flux upon activation.” 2012. Web. 13 Apr 2021.

Vancouver:

Sieger N. CD22 ligation inhibits downstream B-cell receptor signaling and Ca2+ flux upon activation. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2021 Apr 13]. Available from: http://dx.doi.org/10.17169/refubium-9421.

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

Council of Science Editors:

Sieger N. CD22 ligation inhibits downstream B-cell receptor signaling and Ca2+ flux upon activation. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-9421

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

30. Takegami, Norihiko. RANK/RANKL/OPG system in the intervertebral disc.

Degree: 博士(医学), 2018, Mie University / 三重大学

Background: The receptor activator of NF-κB ligand (RANKL), a member of the TNF ligand superfamily, is known to regulate bone metabolism. The expression of each… (more)

Subjects/Keywords: Receptor activator of nuclear factor kappa B; Receptor activator of nuclear factor kappa B ligand; Osteoprotegerin; Intervertebral disc; Cartilaginous endplate; Proinflammatory cytokine

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

APA (6th Edition):

Takegami, N. (2018). RANK/RANKL/OPG system in the intervertebral disc. (Thesis). Mie University / 三重大学. Retrieved from http://hdl.handle.net/10076/00017511

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):

Takegami, Norihiko. “RANK/RANKL/OPG system in the intervertebral disc.” 2018. Thesis, Mie University / 三重大学. Accessed April 13, 2021. http://hdl.handle.net/10076/00017511.

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

MLA Handbook (7th Edition):

Takegami, Norihiko. “RANK/RANKL/OPG system in the intervertebral disc.” 2018. Web. 13 Apr 2021.

Vancouver:

Takegami N. RANK/RANKL/OPG system in the intervertebral disc. [Internet] [Thesis]. Mie University / 三重大学; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10076/00017511.

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

Council of Science Editors:

Takegami N. RANK/RANKL/OPG system in the intervertebral disc. [Thesis]. Mie University / 三重大学; 2018. Available from: http://hdl.handle.net/10076/00017511

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

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