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You searched for subject:(Neurokinin 1 Receptor NK1r ). Showing records 1 – 30 of 23943 total matches.

[1] [2] [3] [4] [5] … [799]

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University of Illinois – Chicago

1. Gregory R. Blass (7971221). Extreme Resistance to Hypercapnia-Induced Pulmonary Edema of the African Naked Mole-Rat.

Degree: 2014, University of Illinois – Chicago

 The African naked-mole rat lives chronically in a hypercapnia due to many individuals living together in small enclosed burrows. At extreme hypercapnia, pulmonary edema is… (more)

Subjects/Keywords: Uncategorized; substance P; hypercapnia; pulmonary edema; c-fiber; acidosis; hemokinin-1; naked mole-rat; Tachykinin 1 Gene (tac1); Neurokinin 1 Receptor (NK1r); Transient Receptor Potential Vanilloid 1 Channel (TrpV1); Acid-sensing Ion Channel (ASIC3); isoflurane; anesthetic; respiration; pulmonary inflammation; lavage

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APA (6th Edition):

(7971221), G. R. B. (2014). Extreme Resistance to Hypercapnia-Induced Pulmonary Edema of the African Naked Mole-Rat. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18916

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):

(7971221), Gregory R. Blass. “Extreme Resistance to Hypercapnia-Induced Pulmonary Edema of the African Naked Mole-Rat.” 2014. Thesis, University of Illinois – Chicago. Accessed May 09, 2021. http://hdl.handle.net/10027/18916.

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

MLA Handbook (7th Edition):

(7971221), Gregory R. Blass. “Extreme Resistance to Hypercapnia-Induced Pulmonary Edema of the African Naked Mole-Rat.” 2014. Web. 09 May 2021.

Vancouver:

(7971221) GRB. Extreme Resistance to Hypercapnia-Induced Pulmonary Edema of the African Naked Mole-Rat. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10027/18916.

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

Council of Science Editors:

(7971221) GRB. Extreme Resistance to Hypercapnia-Induced Pulmonary Edema of the African Naked Mole-Rat. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18916

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


Monash University

2. GARCIA, PAULINA DANIELA RAMIREZ. pH-responsive nanoparticles for endosomal targeting.

Degree: Pharmacy and Pharmaceutical Sciences, 2019, Monash University

 It has been recently demonstrated that Neurokinin 1 receptor (NK1R) endosomal signalling participates in pain transmission and it has therefore been proposed that endosomal NK1R(more)

Subjects/Keywords: Cell Biology; Neuroscience; Pharmacology; Nanomaterials; Nanomedicine; Pain; Nanoparticles; Nanomedicine; Pharmacology; GPCRs; Neurokinin 1 Receptor; Analgesia; Endosomal signalling; Drug delivery

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APA (6th Edition):

GARCIA, P. D. R. (2019). pH-responsive nanoparticles for endosomal targeting. (Thesis). Monash University. Retrieved from http://hdl.handle.net/10.26180/5dd3520a722e3

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, PAULINA DANIELA RAMIREZ. “pH-responsive nanoparticles for endosomal targeting.” 2019. Thesis, Monash University. Accessed May 09, 2021. http://hdl.handle.net/10.26180/5dd3520a722e3.

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

MLA Handbook (7th Edition):

GARCIA, PAULINA DANIELA RAMIREZ. “pH-responsive nanoparticles for endosomal targeting.” 2019. Web. 09 May 2021.

Vancouver:

GARCIA PDR. pH-responsive nanoparticles for endosomal targeting. [Internet] [Thesis]. Monash University; 2019. [cited 2021 May 09]. Available from: http://hdl.handle.net/10.26180/5dd3520a722e3.

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

Council of Science Editors:

GARCIA PDR. pH-responsive nanoparticles for endosomal targeting. [Thesis]. Monash University; 2019. Available from: http://hdl.handle.net/10.26180/5dd3520a722e3

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


Universiteit Utrecht

3. Kleij, Hanneke Paulina Maria van der. Mast cell-nerve interactions in asthma.

Degree: 2002, Universiteit Utrecht

 Asthma is characterized by a chronic inflammatory reaction in the airways. Roughly, asthma can be subdivided into atopic asthma involving elevated levels of serum IgE… (more)

Subjects/Keywords: Farmacie; asthma; mast cell; neurokinin 1 receptor; substance P; sensory nerve

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APA (6th Edition):

Kleij, H. P. M. v. d. (2002). Mast cell-nerve interactions in asthma. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/333

Chicago Manual of Style (16th Edition):

Kleij, Hanneke Paulina Maria van der. “Mast cell-nerve interactions in asthma.” 2002. Doctoral Dissertation, Universiteit Utrecht. Accessed May 09, 2021. http://dspace.library.uu.nl:8080/handle/1874/333.

MLA Handbook (7th Edition):

Kleij, Hanneke Paulina Maria van der. “Mast cell-nerve interactions in asthma.” 2002. Web. 09 May 2021.

Vancouver:

Kleij HPMvd. Mast cell-nerve interactions in asthma. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2002. [cited 2021 May 09]. Available from: http://dspace.library.uu.nl:8080/handle/1874/333.

Council of Science Editors:

Kleij HPMvd. Mast cell-nerve interactions in asthma. [Doctoral Dissertation]. Universiteit Utrecht; 2002. Available from: http://dspace.library.uu.nl:8080/handle/1874/333


Freie Universität Berlin

4. Lux, Christian Nicolas. The role of substance P in the peripheral opioid analgesia.

Degree: 2010, Freie Universität Berlin

 Introduction: Opioids are very potent analgesics. Their main effect is mediated by binding to opioid receptors located in brain and spinal cord. But even on… (more)

Subjects/Keywords: leukocytes; opioid peptides; pain; peripheral nervous system; rats; neurokinin-1 receptor antagonist; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

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APA (6th Edition):

Lux, C. N. (2010). The role of substance P in the peripheral opioid analgesia. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10421

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):

Lux, Christian Nicolas. “The role of substance P in the peripheral opioid analgesia.” 2010. Thesis, Freie Universität Berlin. Accessed May 09, 2021. https://refubium.fu-berlin.de/handle/fub188/10421.

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

MLA Handbook (7th Edition):

Lux, Christian Nicolas. “The role of substance P in the peripheral opioid analgesia.” 2010. Web. 09 May 2021.

Vancouver:

Lux CN. The role of substance P in the peripheral opioid analgesia. [Internet] [Thesis]. Freie Universität Berlin; 2010. [cited 2021 May 09]. Available from: https://refubium.fu-berlin.de/handle/fub188/10421.

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

Council of Science Editors:

Lux CN. The role of substance P in the peripheral opioid analgesia. [Thesis]. Freie Universität Berlin; 2010. Available from: https://refubium.fu-berlin.de/handle/fub188/10421

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

5. KOH YUNG HUA. Regulation of substance P and Neurokinin-1 receptor expression in a mouse model of acute pancreatitis.

Degree: 2012, National University of Singapore

Subjects/Keywords: acute pancreatitis; caerulein; substance P; neurokinin-1 receptor; neutral endopeptidase; mouse

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APA (6th Edition):

HUA, K. Y. (2012). Regulation of substance P and Neurokinin-1 receptor expression in a mouse model of acute pancreatitis. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/34500

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):

HUA, KOH YUNG. “Regulation of substance P and Neurokinin-1 receptor expression in a mouse model of acute pancreatitis.” 2012. Thesis, National University of Singapore. Accessed May 09, 2021. http://scholarbank.nus.edu.sg/handle/10635/34500.

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

MLA Handbook (7th Edition):

HUA, KOH YUNG. “Regulation of substance P and Neurokinin-1 receptor expression in a mouse model of acute pancreatitis.” 2012. Web. 09 May 2021.

Vancouver:

HUA KY. Regulation of substance P and Neurokinin-1 receptor expression in a mouse model of acute pancreatitis. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2021 May 09]. Available from: http://scholarbank.nus.edu.sg/handle/10635/34500.

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

Council of Science Editors:

HUA KY. Regulation of substance P and Neurokinin-1 receptor expression in a mouse model of acute pancreatitis. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/34500

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

6. Kleij, Hanneke Paulina Maria van der. Mast cell-nerve interactions in asthma.

Degree: 2002, University Utrecht

 Asthma is characterized by a chronic inflammatory reaction in the airways. Roughly, asthma can be subdivided into atopic asthma involving elevated levels of serum IgE… (more)

Subjects/Keywords: asthma; mast cell; neurokinin 1 receptor; substance P; sensory nerve

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

APA (6th Edition):

Kleij, H. P. M. v. d. (2002). Mast cell-nerve interactions in asthma. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/333 ; URN:NBN:NL:UI:10-1874-333 ; 1874/333 ; URN:NBN:NL:UI:10-1874-333 ; https://dspace.library.uu.nl/handle/1874/333

Chicago Manual of Style (16th Edition):

Kleij, Hanneke Paulina Maria van der. “Mast cell-nerve interactions in asthma.” 2002. Doctoral Dissertation, University Utrecht. Accessed May 09, 2021. https://dspace.library.uu.nl/handle/1874/333 ; URN:NBN:NL:UI:10-1874-333 ; 1874/333 ; URN:NBN:NL:UI:10-1874-333 ; https://dspace.library.uu.nl/handle/1874/333.

MLA Handbook (7th Edition):

Kleij, Hanneke Paulina Maria van der. “Mast cell-nerve interactions in asthma.” 2002. Web. 09 May 2021.

Vancouver:

Kleij HPMvd. Mast cell-nerve interactions in asthma. [Internet] [Doctoral dissertation]. University Utrecht; 2002. [cited 2021 May 09]. Available from: https://dspace.library.uu.nl/handle/1874/333 ; URN:NBN:NL:UI:10-1874-333 ; 1874/333 ; URN:NBN:NL:UI:10-1874-333 ; https://dspace.library.uu.nl/handle/1874/333.

Council of Science Editors:

Kleij HPMvd. Mast cell-nerve interactions in asthma. [Doctoral Dissertation]. University Utrecht; 2002. Available from: https://dspace.library.uu.nl/handle/1874/333 ; URN:NBN:NL:UI:10-1874-333 ; 1874/333 ; URN:NBN:NL:UI:10-1874-333 ; https://dspace.library.uu.nl/handle/1874/333

7. Sylvie Brener. Expressão da substância P e de seu receptor Neuroquinina-1 em carcinomas espinocelulares de boca e sua implicação na atividade proliferativa tumoral.

Degree: 2009, University of São Paulo

 A substância P (SP) é um neuropeptídeo da família das taquicininas que regula numerosas funções biológicas por meio da ligação ao seu receptor altamente específico… (more)

Subjects/Keywords: Câncer de boca; Ki-67; Receptor neuroquinina-1; Substância P; Ki-67; Oral cancer; Receptor neurokinin-1; Substance P

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APA (6th Edition):

Brener, S. (2009). Expressão da substância P e de seu receptor Neuroquinina-1 em carcinomas espinocelulares de boca e sua implicação na atividade proliferativa tumoral. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/25/25136/tde-25032010-084600/

Chicago Manual of Style (16th Edition):

Brener, Sylvie. “Expressão da substância P e de seu receptor Neuroquinina-1 em carcinomas espinocelulares de boca e sua implicação na atividade proliferativa tumoral.” 2009. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/25/25136/tde-25032010-084600/.

MLA Handbook (7th Edition):

Brener, Sylvie. “Expressão da substância P e de seu receptor Neuroquinina-1 em carcinomas espinocelulares de boca e sua implicação na atividade proliferativa tumoral.” 2009. Web. 09 May 2021.

Vancouver:

Brener S. Expressão da substância P e de seu receptor Neuroquinina-1 em carcinomas espinocelulares de boca e sua implicação na atividade proliferativa tumoral. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/25/25136/tde-25032010-084600/.

Council of Science Editors:

Brener S. Expressão da substância P e de seu receptor Neuroquinina-1 em carcinomas espinocelulares de boca e sua implicação na atividade proliferativa tumoral. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/25/25136/tde-25032010-084600/

8. LIM SHI YING. INVESTIGATION OF CELL MEMBRANE DYNAMICS AND ORGANIZATION BY IMAGING FLUORESCENCE CORRELATION SPECTROSCOPY.

Degree: 2015, National University of Singapore

Subjects/Keywords: plasma membrane dynamics; plasma membrane organization; imaging FCS; fluorescence correlation spectroscopy; neurokinin-1 receptor; Substance P

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APA (6th Edition):

YING, L. S. (2015). INVESTIGATION OF CELL MEMBRANE DYNAMICS AND ORGANIZATION BY IMAGING FLUORESCENCE CORRELATION SPECTROSCOPY. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/121747

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):

YING, LIM SHI. “INVESTIGATION OF CELL MEMBRANE DYNAMICS AND ORGANIZATION BY IMAGING FLUORESCENCE CORRELATION SPECTROSCOPY.” 2015. Thesis, National University of Singapore. Accessed May 09, 2021. http://scholarbank.nus.edu.sg/handle/10635/121747.

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

MLA Handbook (7th Edition):

YING, LIM SHI. “INVESTIGATION OF CELL MEMBRANE DYNAMICS AND ORGANIZATION BY IMAGING FLUORESCENCE CORRELATION SPECTROSCOPY.” 2015. Web. 09 May 2021.

Vancouver:

YING LS. INVESTIGATION OF CELL MEMBRANE DYNAMICS AND ORGANIZATION BY IMAGING FLUORESCENCE CORRELATION SPECTROSCOPY. [Internet] [Thesis]. National University of Singapore; 2015. [cited 2021 May 09]. Available from: http://scholarbank.nus.edu.sg/handle/10635/121747.

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

Council of Science Editors:

YING LS. INVESTIGATION OF CELL MEMBRANE DYNAMICS AND ORGANIZATION BY IMAGING FLUORESCENCE CORRELATION SPECTROSCOPY. [Thesis]. National University of Singapore; 2015. Available from: http://scholarbank.nus.edu.sg/handle/10635/121747

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


Arizona State University

9. Williams, Stephanie Mitchell. Understanding the Role of Predictive, Diagnostic and Pathogenic Autoantibodies in Systemic Lupus Erythematosus and its Central Nervous System (CNS) Involvement.

Degree: PhD, Molecular and Cellular Biology, 2011, Arizona State University

 Systemic lupus erytematosus (SLE) is an autoimmune disease where the immune system is reactive to self antigens resulting in manifestations like glomerulonephritis and arthritis. The… (more)

Subjects/Keywords: Molecular Biology; Immunology; Neurosciences; Brain-Reactive Autoantibodies; CNS-Lupus; Diagnostic Autoantibodies; Neurokinin-1 Receptor; Pathogenic Autoantibodies; Predictive Autoantibodies

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APA (6th Edition):

Williams, S. M. (2011). Understanding the Role of Predictive, Diagnostic and Pathogenic Autoantibodies in Systemic Lupus Erythematosus and its Central Nervous System (CNS) Involvement. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/9359

Chicago Manual of Style (16th Edition):

Williams, Stephanie Mitchell. “Understanding the Role of Predictive, Diagnostic and Pathogenic Autoantibodies in Systemic Lupus Erythematosus and its Central Nervous System (CNS) Involvement.” 2011. Doctoral Dissertation, Arizona State University. Accessed May 09, 2021. http://repository.asu.edu/items/9359.

MLA Handbook (7th Edition):

Williams, Stephanie Mitchell. “Understanding the Role of Predictive, Diagnostic and Pathogenic Autoantibodies in Systemic Lupus Erythematosus and its Central Nervous System (CNS) Involvement.” 2011. Web. 09 May 2021.

Vancouver:

Williams SM. Understanding the Role of Predictive, Diagnostic and Pathogenic Autoantibodies in Systemic Lupus Erythematosus and its Central Nervous System (CNS) Involvement. [Internet] [Doctoral dissertation]. Arizona State University; 2011. [cited 2021 May 09]. Available from: http://repository.asu.edu/items/9359.

Council of Science Editors:

Williams SM. Understanding the Role of Predictive, Diagnostic and Pathogenic Autoantibodies in Systemic Lupus Erythematosus and its Central Nervous System (CNS) Involvement. [Doctoral Dissertation]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/9359


Universidade Estadual de Campinas

10. Saavedra, Flávia Medeiros, 1990-. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos.

Degree: Faculdade de Odontologia de Piracicaba; Programa de Pós-Graduação em Clínica Odontológica, 2017, Universidade Estadual de Campinas

Orientador: Alexandre Augusto Zaia

Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba

Made available in DSpace on 2018-09-01T19:27:45Z (GMT). No. of… (more)

Subjects/Keywords: Ligamento periodontal; Substância P; Receptores da neurocinina-1; Periodontal ligament; Substance P; Receptors, neurokinin-1

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APA (6th Edition):

Saavedra, Flávia Medeiros, 1. (2017). Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. (Masters Thesis). Universidade Estadual de Campinas. Retrieved from SAAVEDRA, Flávia Medeiros. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. 2017. 1 recurso online (71 p.). Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba, Piracicaba, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/331940>. Acesso em: 1 set. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/331940

Chicago Manual of Style (16th Edition):

Saavedra, Flávia Medeiros, 1990-. “Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos.” 2017. Masters Thesis, Universidade Estadual de Campinas. Accessed May 09, 2021. SAAVEDRA, Flávia Medeiros. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. 2017. 1 recurso online (71 p.). Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba, Piracicaba, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/331940>. Acesso em: 1 set. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/331940.

MLA Handbook (7th Edition):

Saavedra, Flávia Medeiros, 1990-. “Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos.” 2017. Web. 09 May 2021.

Vancouver:

Saavedra, Flávia Medeiros 1. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. [Internet] [Masters thesis]. Universidade Estadual de Campinas; 2017. [cited 2021 May 09]. Available from: SAAVEDRA, Flávia Medeiros. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. 2017. 1 recurso online (71 p.). Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba, Piracicaba, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/331940>. Acesso em: 1 set. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/331940.

Council of Science Editors:

Saavedra, Flávia Medeiros 1. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. [Masters Thesis]. Universidade Estadual de Campinas; 2017. Available from: SAAVEDRA, Flávia Medeiros. Avaliação da expressão de substância P, receptores Nk1 e citotoxicidade em cultura de fibroblastos após o contato com cimentos endodônticos. 2017. 1 recurso online (71 p.). Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba, Piracicaba, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/331940>. Acesso em: 1 set. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/331940

11. Pal, Kasturi. Role of C-Terminal Tails of G Protein Coupled Receptors on Beta-Arrestin 1/2 Dependent Signaling.

Degree: Cell, Molecular and Developmental Biology, 2013, University of California – Riverside

 Protease activated receptor 2 (PAR2) and Neurokinin 1 receptor (NK1R) are 7 transmembrane receptors (7TMRs), which signal by G alpha q leading to Ca2+ release… (more)

Subjects/Keywords: Pharmacology; Cellular biology; Molecular biology; Beta arrestin; Cofilin; G protein coupled receptors; Neurokinin 1 Receptor; Phosphorylation; Protease Activated Receptor 2

receptor 2 (PAR2) and Neurokinin 1 receptor (NK1R) are 7 transmembrane… …affinity than NK1R. We further show that initial Gαq signaling is necessary for β-arrestin 1/2… …recruitment to NK1R. PAR2 recruits β-arrestin 1/2 even when Gαq pathway is blocked. Assays with C… …Protease Activated Receptor 2 (PAR2) C-terminal Tail Direct β-arrestin 1/2 Recruitment… …and NK1R differ in β-arrestin 1/2 recruitment rates and binding affinities. 56 Fig 2.3… 

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APA (6th Edition):

Pal, K. (2013). Role of C-Terminal Tails of G Protein Coupled Receptors on Beta-Arrestin 1/2 Dependent Signaling. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/5h15c3k0

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):

Pal, Kasturi. “Role of C-Terminal Tails of G Protein Coupled Receptors on Beta-Arrestin 1/2 Dependent Signaling.” 2013. Thesis, University of California – Riverside. Accessed May 09, 2021. http://www.escholarship.org/uc/item/5h15c3k0.

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

MLA Handbook (7th Edition):

Pal, Kasturi. “Role of C-Terminal Tails of G Protein Coupled Receptors on Beta-Arrestin 1/2 Dependent Signaling.” 2013. Web. 09 May 2021.

Vancouver:

Pal K. Role of C-Terminal Tails of G Protein Coupled Receptors on Beta-Arrestin 1/2 Dependent Signaling. [Internet] [Thesis]. University of California – Riverside; 2013. [cited 2021 May 09]. Available from: http://www.escholarship.org/uc/item/5h15c3k0.

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

Council of Science Editors:

Pal K. Role of C-Terminal Tails of G Protein Coupled Receptors on Beta-Arrestin 1/2 Dependent Signaling. [Thesis]. University of California – Riverside; 2013. Available from: http://www.escholarship.org/uc/item/5h15c3k0

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


Monash University

12. Ramadasan, Priveena Nair. Role of Tachykinin-1 peptides in the regulation of habenular kisspeptin neurons in the zebrafish.

Degree: Medicine, Nursing and Health Sciences, 2017, Monash University

 Fear is a conserved emotion which serves as the root cause of psychiatric disorders such as phobias and depression. Hence understanding the neural pathway underlying… (more)

Subjects/Keywords: Neuroscience; Tachykinin-1; Substance P; Neurokinin-A; Kiss1; Sendide; Alarm substance; Fear

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

APA (6th Edition):

Ramadasan, P. N. (2017). Role of Tachykinin-1 peptides in the regulation of habenular kisspeptin neurons in the zebrafish. (Thesis). Monash University. Retrieved from https://doi.org/10.4225/03/58731818d11e0

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):

Ramadasan, Priveena Nair. “Role of Tachykinin-1 peptides in the regulation of habenular kisspeptin neurons in the zebrafish.” 2017. Thesis, Monash University. Accessed May 09, 2021. https://doi.org/10.4225/03/58731818d11e0.

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

MLA Handbook (7th Edition):

Ramadasan, Priveena Nair. “Role of Tachykinin-1 peptides in the regulation of habenular kisspeptin neurons in the zebrafish.” 2017. Web. 09 May 2021.

Vancouver:

Ramadasan PN. Role of Tachykinin-1 peptides in the regulation of habenular kisspeptin neurons in the zebrafish. [Internet] [Thesis]. Monash University; 2017. [cited 2021 May 09]. Available from: https://doi.org/10.4225/03/58731818d11e0.

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

Council of Science Editors:

Ramadasan PN. Role of Tachykinin-1 peptides in the regulation of habenular kisspeptin neurons in the zebrafish. [Thesis]. Monash University; 2017. Available from: https://doi.org/10.4225/03/58731818d11e0

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

13. Gu, Hongbo. Mass Spectrometry Analysis of Potential Biomarker Proteins.

Degree: PhD, Chemistry, 2012, Brown University

 Towards the full understanding the physiology of human Sigma-1 receptor (Sig-1R), we developed a novel ligand-based enrichment strategy and mass spectrometry analysis of the receptor.… (more)

Subjects/Keywords: Sigma-1 receptor

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APA (6th Edition):

Gu, H. (2012). Mass Spectrometry Analysis of Potential Biomarker Proteins. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297583/

Chicago Manual of Style (16th Edition):

Gu, Hongbo. “Mass Spectrometry Analysis of Potential Biomarker Proteins.” 2012. Doctoral Dissertation, Brown University. Accessed May 09, 2021. https://repository.library.brown.edu/studio/item/bdr:297583/.

MLA Handbook (7th Edition):

Gu, Hongbo. “Mass Spectrometry Analysis of Potential Biomarker Proteins.” 2012. Web. 09 May 2021.

Vancouver:

Gu H. Mass Spectrometry Analysis of Potential Biomarker Proteins. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2021 May 09]. Available from: https://repository.library.brown.edu/studio/item/bdr:297583/.

Council of Science Editors:

Gu H. Mass Spectrometry Analysis of Potential Biomarker Proteins. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297583/


Kyoto University / 京都大学

14. Misu, Ryosuke. Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems : 生殖内分泌系を制御する神経ペプチド受容体リガンドの創製研究.

Degree: 博士(薬科学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第18929号

薬科博第43号

Subjects/Keywords: gonadotropin-releasing hormone; GPR54; kisspeptin; neurokinin B; neurokinin-3 receptor; peptidomimetics

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APA (6th Edition):

Misu, R. (2015). Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems : 生殖内分泌系を制御する神経ペプチド受容体リガンドの創製研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/199501 ; http://dx.doi.org/10.14989/doctor.k18929

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):

Misu, Ryosuke. “Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems : 生殖内分泌系を制御する神経ペプチド受容体リガンドの創製研究.” 2015. Thesis, Kyoto University / 京都大学. Accessed May 09, 2021. http://hdl.handle.net/2433/199501 ; http://dx.doi.org/10.14989/doctor.k18929.

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

MLA Handbook (7th Edition):

Misu, Ryosuke. “Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems : 生殖内分泌系を制御する神経ペプチド受容体リガンドの創製研究.” 2015. Web. 09 May 2021.

Vancouver:

Misu R. Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems : 生殖内分泌系を制御する神経ペプチド受容体リガンドの創製研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/2433/199501 ; http://dx.doi.org/10.14989/doctor.k18929.

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

Council of Science Editors:

Misu R. Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems : 生殖内分泌系を制御する神経ペプチド受容体リガンドの創製研究. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/199501 ; http://dx.doi.org/10.14989/doctor.k18929

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


University of Arizona

15. Dacks, Penny Ann Frances. THE NEURONAL CIRCUITRY OF ESTROGENIC EFFECTS ON THERMOREGULATION .

Degree: 2010, University of Arizona

 Approximately 75% of menopausal women in the United States experience hot flushes but the etiology of this thermoregulatory disorder is unknown. The dominant theory is… (more)

Subjects/Keywords: estrogen; hot flush; neurokinin 3 receptor; neurokinin B; temperature; thermoregulation

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APA (6th Edition):

Dacks, P. A. F. (2010). THE NEURONAL CIRCUITRY OF ESTROGENIC EFFECTS ON THERMOREGULATION . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/195591

Chicago Manual of Style (16th Edition):

Dacks, Penny Ann Frances. “THE NEURONAL CIRCUITRY OF ESTROGENIC EFFECTS ON THERMOREGULATION .” 2010. Doctoral Dissertation, University of Arizona. Accessed May 09, 2021. http://hdl.handle.net/10150/195591.

MLA Handbook (7th Edition):

Dacks, Penny Ann Frances. “THE NEURONAL CIRCUITRY OF ESTROGENIC EFFECTS ON THERMOREGULATION .” 2010. Web. 09 May 2021.

Vancouver:

Dacks PAF. THE NEURONAL CIRCUITRY OF ESTROGENIC EFFECTS ON THERMOREGULATION . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2021 May 09]. Available from: http://hdl.handle.net/10150/195591.

Council of Science Editors:

Dacks PAF. THE NEURONAL CIRCUITRY OF ESTROGENIC EFFECTS ON THERMOREGULATION . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/195591


Jawaharlal Nehru University

16. Chandrashekar, Indu R. Structural characterization of Neurokinin 2 receptor selective peptide agonistsa molecular modeling and spectroscopic investigation; -.

Degree: Life Science, 2005, Jawaharlal Nehru University

None

Bibliography p.128-156

Advisors/Committee Members: Cowsik, M Sudha.

Subjects/Keywords: Modeling; Neurokinin-2; Peptide agonist; Receptor; Selective; Spectroscopic investigation

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APA (6th Edition):

Chandrashekar, I. R. (2005). Structural characterization of Neurokinin 2 receptor selective peptide agonistsa molecular modeling and spectroscopic investigation; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/16470

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):

Chandrashekar, Indu R. “Structural characterization of Neurokinin 2 receptor selective peptide agonistsa molecular modeling and spectroscopic investigation; -.” 2005. Thesis, Jawaharlal Nehru University. Accessed May 09, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/16470.

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

MLA Handbook (7th Edition):

Chandrashekar, Indu R. “Structural characterization of Neurokinin 2 receptor selective peptide agonistsa molecular modeling and spectroscopic investigation; -.” 2005. Web. 09 May 2021.

Vancouver:

Chandrashekar IR. Structural characterization of Neurokinin 2 receptor selective peptide agonistsa molecular modeling and spectroscopic investigation; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2005. [cited 2021 May 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16470.

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

Council of Science Editors:

Chandrashekar IR. Structural characterization of Neurokinin 2 receptor selective peptide agonistsa molecular modeling and spectroscopic investigation; -. [Thesis]. Jawaharlal Nehru University; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16470

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


Wayne State University

17. Jerome, Andrew. The Role Of Neurokinin Receptors And Satellite Glial Cells In Herpes Simplex Virus 1 Latency.

Degree: PhD, Anatomy and Cell Biology, 2018, Wayne State University

  The ability of herpes simplex virus 1 (HSV-1) to establish a lifelong infection in neurons of the trigeminal ganglion (TG) make it a constant… (more)

Subjects/Keywords: Herpes Simplex Virus; HSV Latency; Neurokinin Receptor; Satellite glial cells; Substance P; T Cells; Immunology and Infectious Disease; Neurosciences; Virology

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APA (6th Edition):

Jerome, A. (2018). The Role Of Neurokinin Receptors And Satellite Glial Cells In Herpes Simplex Virus 1 Latency. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/2032

Chicago Manual of Style (16th Edition):

Jerome, Andrew. “The Role Of Neurokinin Receptors And Satellite Glial Cells In Herpes Simplex Virus 1 Latency.” 2018. Doctoral Dissertation, Wayne State University. Accessed May 09, 2021. https://digitalcommons.wayne.edu/oa_dissertations/2032.

MLA Handbook (7th Edition):

Jerome, Andrew. “The Role Of Neurokinin Receptors And Satellite Glial Cells In Herpes Simplex Virus 1 Latency.” 2018. Web. 09 May 2021.

Vancouver:

Jerome A. The Role Of Neurokinin Receptors And Satellite Glial Cells In Herpes Simplex Virus 1 Latency. [Internet] [Doctoral dissertation]. Wayne State University; 2018. [cited 2021 May 09]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2032.

Council of Science Editors:

Jerome A. The Role Of Neurokinin Receptors And Satellite Glial Cells In Herpes Simplex Virus 1 Latency. [Doctoral Dissertation]. Wayne State University; 2018. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2032

18. LAU HON YEN. Role of neurogenic inflammation in the pathogenesis of acute pancreatitis and associated lung injury.

Degree: 2008, National University of Singapore

Subjects/Keywords: acute pancreatitis; neurogenic inflammation; neurokinin receptor; tachykinin; pancreas; lung

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APA (6th Edition):

YEN, L. H. (2008). Role of neurogenic inflammation in the pathogenesis of acute pancreatitis and associated lung injury. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/13002

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):

YEN, LAU HON. “Role of neurogenic inflammation in the pathogenesis of acute pancreatitis and associated lung injury.” 2008. Thesis, National University of Singapore. Accessed May 09, 2021. http://scholarbank.nus.edu.sg/handle/10635/13002.

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

MLA Handbook (7th Edition):

YEN, LAU HON. “Role of neurogenic inflammation in the pathogenesis of acute pancreatitis and associated lung injury.” 2008. Web. 09 May 2021.

Vancouver:

YEN LH. Role of neurogenic inflammation in the pathogenesis of acute pancreatitis and associated lung injury. [Internet] [Thesis]. National University of Singapore; 2008. [cited 2021 May 09]. Available from: http://scholarbank.nus.edu.sg/handle/10635/13002.

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

Council of Science Editors:

YEN LH. Role of neurogenic inflammation in the pathogenesis of acute pancreatitis and associated lung injury. [Thesis]. National University of Singapore; 2008. Available from: http://scholarbank.nus.edu.sg/handle/10635/13002

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

19. AKHIL KUMAR HEGDE RAMA. Role of Substance P in Sepsis.

Degree: 2009, National University of Singapore

Subjects/Keywords: sepsis; substance P; preprotachykinin-A; mice; microarray; neurokinin receptor

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APA (6th Edition):

RAMA, A. K. H. (2009). Role of Substance P in Sepsis. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16389

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):

RAMA, AKHIL KUMAR HEGDE. “Role of Substance P in Sepsis.” 2009. Thesis, National University of Singapore. Accessed May 09, 2021. http://scholarbank.nus.edu.sg/handle/10635/16389.

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

MLA Handbook (7th Edition):

RAMA, AKHIL KUMAR HEGDE. “Role of Substance P in Sepsis.” 2009. Web. 09 May 2021.

Vancouver:

RAMA AKH. Role of Substance P in Sepsis. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 May 09]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16389.

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

Council of Science Editors:

RAMA AKH. Role of Substance P in Sepsis. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/16389

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


Université de Montréal

20. Jizi, Khadije. Modulation par le récepteur neurokinine-1du mécanisme d’action des immunosuppresseurs chez les cellules T.

Degree: 2014, Université de Montréal

Subjects/Keywords: Cyclosporine A; Rapamycine; Tacrolimus; cellules Jurkat; Récepteur neurokinine-1; Endokinines; Cyclosporin A; Rapamycine; FK506; NFAT; Neurokinin-1 receptor; Endokinin; L-733,060; Health Sciences - Immunology / Sciences de la santé - Immunologie (UMI : 0982)

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APA (6th Edition):

Jizi, K. (2014). Modulation par le récepteur neurokinine-1du mécanisme d’action des immunosuppresseurs chez les cellules T. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/10906

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):

Jizi, Khadije. “Modulation par le récepteur neurokinine-1du mécanisme d’action des immunosuppresseurs chez les cellules T.” 2014. Thesis, Université de Montréal. Accessed May 09, 2021. http://hdl.handle.net/1866/10906.

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

MLA Handbook (7th Edition):

Jizi, Khadije. “Modulation par le récepteur neurokinine-1du mécanisme d’action des immunosuppresseurs chez les cellules T.” 2014. Web. 09 May 2021.

Vancouver:

Jizi K. Modulation par le récepteur neurokinine-1du mécanisme d’action des immunosuppresseurs chez les cellules T. [Internet] [Thesis]. Université de Montréal; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1866/10906.

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

Council of Science Editors:

Jizi K. Modulation par le récepteur neurokinine-1du mécanisme d’action des immunosuppresseurs chez les cellules T. [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/10906

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


Wake Forest University

21. Alzayadneh, Ebaa M. A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE.

Degree: 2014, Wake Forest University

 There is compelling evidence for a role of intracellular renin-angiotensin system (RAS) in cell signaling, function and cardiovascular pathologies. Diabetic nephropathy is a very common… (more)

Subjects/Keywords: Ang-(1-7)-Mas receptor

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APA (6th Edition):

Alzayadneh, E. M. (2014). A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/39401

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):

Alzayadneh, Ebaa M. “A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE.” 2014. Thesis, Wake Forest University. Accessed May 09, 2021. http://hdl.handle.net/10339/39401.

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

MLA Handbook (7th Edition):

Alzayadneh, Ebaa M. “A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE.” 2014. Web. 09 May 2021.

Vancouver:

Alzayadneh EM. A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE. [Internet] [Thesis]. Wake Forest University; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10339/39401.

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

Council of Science Editors:

Alzayadneh EM. A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE. [Thesis]. Wake Forest University; 2014. Available from: http://hdl.handle.net/10339/39401

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

22. Robinson, Ryan Everitt. RING finger protein PLR-1 blocks Wnt signaling by altering trafficking of Wnt receptors.

Degree: 2013, University of Nevada – Reno

 Secreted Wnt proteins control a wide range of essential developmental processes, including axon guidance and establishment of anteroposterior neuronal polarity. We identified a transmembrane RING… (more)

Subjects/Keywords: Frizzled; PLR-1; Wnt receptor

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APA (6th Edition):

Robinson, R. E. (2013). RING finger protein PLR-1 blocks Wnt signaling by altering trafficking of Wnt receptors. (Thesis). University of Nevada – Reno. Retrieved from http://hdl.handle.net/11714/3046

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):

Robinson, Ryan Everitt. “RING finger protein PLR-1 blocks Wnt signaling by altering trafficking of Wnt receptors.” 2013. Thesis, University of Nevada – Reno. Accessed May 09, 2021. http://hdl.handle.net/11714/3046.

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

MLA Handbook (7th Edition):

Robinson, Ryan Everitt. “RING finger protein PLR-1 blocks Wnt signaling by altering trafficking of Wnt receptors.” 2013. Web. 09 May 2021.

Vancouver:

Robinson RE. RING finger protein PLR-1 blocks Wnt signaling by altering trafficking of Wnt receptors. [Internet] [Thesis]. University of Nevada – Reno; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/11714/3046.

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

Council of Science Editors:

Robinson RE. RING finger protein PLR-1 blocks Wnt signaling by altering trafficking of Wnt receptors. [Thesis]. University of Nevada – Reno; 2013. Available from: http://hdl.handle.net/11714/3046

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

23. Cíntia Tusset. Pesquisa de mutações na neurocinina B e no seu receptor em pacientes com distúrbios puberais centrais idiopáticos.

Degree: 2012, University of São Paulo

 Mutações inativadoras nos genes TAC3 e TACR3, os quais codificam a neurocinina B (NKB) e o seu receptor NK3R, respectivamente, foram descritas em pacientes com… (more)

Subjects/Keywords: Hipogonadismo; Hormônio liberador de gonadotrofinas; Mutação; Neurocinina B; Puberdade precoce; Receptor da neurocinina B; Retardo constitucional do crescimento e desenvolvimento; Constitutional delay of growth and puberty; Gonadotropin- releasing hormone; Hypogonadism; Mutation; Neurokinin B; Neurokinin B receptor; Precocious puberty

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APA (6th Edition):

Tusset, C. (2012). Pesquisa de mutações na neurocinina B e no seu receptor em pacientes com distúrbios puberais centrais idiopáticos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-03092012-090655/

Chicago Manual of Style (16th Edition):

Tusset, Cíntia. “Pesquisa de mutações na neurocinina B e no seu receptor em pacientes com distúrbios puberais centrais idiopáticos.” 2012. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-03092012-090655/.

MLA Handbook (7th Edition):

Tusset, Cíntia. “Pesquisa de mutações na neurocinina B e no seu receptor em pacientes com distúrbios puberais centrais idiopáticos.” 2012. Web. 09 May 2021.

Vancouver:

Tusset C. Pesquisa de mutações na neurocinina B e no seu receptor em pacientes com distúrbios puberais centrais idiopáticos. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-03092012-090655/.

Council of Science Editors:

Tusset C. Pesquisa de mutações na neurocinina B e no seu receptor em pacientes com distúrbios puberais centrais idiopáticos. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-03092012-090655/

24. Misu, Ryosuke. Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems .

Degree: 2015, Kyoto University

Subjects/Keywords: gonadotropin-releasing hormone; GPR54; kisspeptin; neurokinin B; neurokinin-3 receptor; peptidomimetics

Page 1 Page 2 Page 3 Page 4

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APA (6th Edition):

Misu, R. (2015). Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/199501

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):

Misu, Ryosuke. “Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems .” 2015. Thesis, Kyoto University. Accessed May 09, 2021. http://hdl.handle.net/2433/199501.

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

MLA Handbook (7th Edition):

Misu, Ryosuke. “Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems .” 2015. Web. 09 May 2021.

Vancouver:

Misu R. Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems . [Internet] [Thesis]. Kyoto University; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/2433/199501.

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

Council of Science Editors:

Misu R. Development of Neuropeptide Receptor Ligands for the Control of Reproductive Systems . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/199501

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

25. Ellens, Elizabeth Rose. Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor.

Degree: 2014, North Dakota State University

 One of the oldest, extant, lineages of vertebrates, the sea lamprey, was used to clarify the evolutionary origin and divergence of the growth hormone receptor(more)

Subjects/Keywords: Evolution; Growth hormone receptor; Lamprey; Prolactin receptor; Somatolactin receptor; Type-1 cytokine receptor

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APA (6th Edition):

Ellens, E. R. (2014). Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor. (Thesis). North Dakota State University. Retrieved from http://hdl.handle.net/10365/26654

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):

Ellens, Elizabeth Rose. “Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor.” 2014. Thesis, North Dakota State University. Accessed May 09, 2021. http://hdl.handle.net/10365/26654.

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

MLA Handbook (7th Edition):

Ellens, Elizabeth Rose. “Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor.” 2014. Web. 09 May 2021.

Vancouver:

Ellens ER. Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor. [Internet] [Thesis]. North Dakota State University; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10365/26654.

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

Council of Science Editors:

Ellens ER. Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor. [Thesis]. North Dakota State University; 2014. Available from: http://hdl.handle.net/10365/26654

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

26. Yamamoto, Koki. Structure-activity Relationships for Development of Neurokinin-3 Receptor Antagonists with Reduced Environmental Impact .

Degree: 2019, Kyoto University

Subjects/Keywords: environmental impact; medicinal chemistry; structure-activity relationship; neurokinin-3 receptor; scaffold hopping; phodegradation

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

APA (6th Edition):

Yamamoto, K. (2019). Structure-activity Relationships for Development of Neurokinin-3 Receptor Antagonists with Reduced Environmental Impact . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242671

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):

Yamamoto, Koki. “Structure-activity Relationships for Development of Neurokinin-3 Receptor Antagonists with Reduced Environmental Impact .” 2019. Thesis, Kyoto University. Accessed May 09, 2021. http://hdl.handle.net/2433/242671.

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

MLA Handbook (7th Edition):

Yamamoto, Koki. “Structure-activity Relationships for Development of Neurokinin-3 Receptor Antagonists with Reduced Environmental Impact .” 2019. Web. 09 May 2021.

Vancouver:

Yamamoto K. Structure-activity Relationships for Development of Neurokinin-3 Receptor Antagonists with Reduced Environmental Impact . [Internet] [Thesis]. Kyoto University; 2019. [cited 2021 May 09]. Available from: http://hdl.handle.net/2433/242671.

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

Council of Science Editors:

Yamamoto K. Structure-activity Relationships for Development of Neurokinin-3 Receptor Antagonists with Reduced Environmental Impact . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242671

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


Universitat Rovira i Virgili

27. Saavedra García, Paula. FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells.

Degree: Departament de Medicina i Cirurgia, 2016, Universitat Rovira i Virgili

 Fatty acid-binding protein 4 (FABP4) is an adipose tissue-secreted adipokine that is involved in the regulation of energetic metabolism and inflammation. Increased levels of circulating… (more)

Subjects/Keywords: FABP4; Receptor de membrana; Citoqueratina 1; FABP4; Receptor de membrana; Citoqueratina 1; FABP4; Cell surface receptor; Cytokeratin 1; 577

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APA (6th Edition):

Saavedra García, P. (2016). FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/348560

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):

Saavedra García, Paula. “FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells.” 2016. Thesis, Universitat Rovira i Virgili. Accessed May 09, 2021. http://hdl.handle.net/10803/348560.

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

MLA Handbook (7th Edition):

Saavedra García, Paula. “FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells.” 2016. Web. 09 May 2021.

Vancouver:

Saavedra García P. FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells. [Internet] [Thesis]. Universitat Rovira i Virgili; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/10803/348560.

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

Council of Science Editors:

Saavedra García P. FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells. [Thesis]. Universitat Rovira i Virgili; 2016. Available from: http://hdl.handle.net/10803/348560

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


University of Gothenburg / Göteborgs Universitet

28. Svensson, Alexandra. Immune regulation of herpes simplex virus type 2 infection: Special emphasis on the transcription factor T-bet.

Degree: 2007, University of Gothenburg / Göteborgs Universitet

 Herpes simplex virus type 2 (HSV-2) is a sexually transmitted pathogen that infects the genital tract mucosa as well as local sensory neurons. It is… (more)

Subjects/Keywords: HSV-2; T-bet; Substance P; Neurokinin 1; IFN-alfa/beta signaling; Polymorphisms

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APA (6th Edition):

Svensson, A. (2007). Immune regulation of herpes simplex virus type 2 infection: Special emphasis on the transcription factor T-bet. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/852 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=15879125&dopt=Abstract ; http://dx.doi.org/doi:10.1016/j.jri.2006.09.002 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=16272337&dopt=Abstract

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):

Svensson, Alexandra. “Immune regulation of herpes simplex virus type 2 infection: Special emphasis on the transcription factor T-bet.” 2007. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed May 09, 2021. http://hdl.handle.net/2077/852 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=15879125&dopt=Abstract ; http://dx.doi.org/doi:10.1016/j.jri.2006.09.002 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=16272337&dopt=Abstract.

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

MLA Handbook (7th Edition):

Svensson, Alexandra. “Immune regulation of herpes simplex virus type 2 infection: Special emphasis on the transcription factor T-bet.” 2007. Web. 09 May 2021.

Vancouver:

Svensson A. Immune regulation of herpes simplex virus type 2 infection: Special emphasis on the transcription factor T-bet. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2007. [cited 2021 May 09]. Available from: http://hdl.handle.net/2077/852 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=15879125&dopt=Abstract ; http://dx.doi.org/doi:10.1016/j.jri.2006.09.002 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=16272337&dopt=Abstract.

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

Council of Science Editors:

Svensson A. Immune regulation of herpes simplex virus type 2 infection: Special emphasis on the transcription factor T-bet. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2007. Available from: http://hdl.handle.net/2077/852 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=15879125&dopt=Abstract ; http://dx.doi.org/doi:10.1016/j.jri.2006.09.002 ; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve&db=pubmed&list_uids=16272337&dopt=Abstract

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


University of Alberta

29. Li, Nicholas L. Regulation of the inhibitory receptor LIR-1 in human natural killer cells.

Degree: PhD, Department of Medical Microbiology and Immunology, 2013, University of Alberta

 Natural killer (NK) cells are innate immune lymphocytes that provide protection against virus infection and transformation. The cytolytic activity of NK cells is controlled by… (more)

Subjects/Keywords: Natural Killer Cells; LIR-1; Inhibitory Receptor

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

APA (6th Edition):

Li, N. L. (2013). Regulation of the inhibitory receptor LIR-1 in human natural killer cells. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/gt54kn99q

Chicago Manual of Style (16th Edition):

Li, Nicholas L. “Regulation of the inhibitory receptor LIR-1 in human natural killer cells.” 2013. Doctoral Dissertation, University of Alberta. Accessed May 09, 2021. https://era.library.ualberta.ca/files/gt54kn99q.

MLA Handbook (7th Edition):

Li, Nicholas L. “Regulation of the inhibitory receptor LIR-1 in human natural killer cells.” 2013. Web. 09 May 2021.

Vancouver:

Li NL. Regulation of the inhibitory receptor LIR-1 in human natural killer cells. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2021 May 09]. Available from: https://era.library.ualberta.ca/files/gt54kn99q.

Council of Science Editors:

Li NL. Regulation of the inhibitory receptor LIR-1 in human natural killer cells. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/gt54kn99q


University of Ottawa

30. Cherid, Hafsa. Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding .

Degree: 2014, University of Ottawa

 Impaired cell mediated immunity is the clinical hallmark of HIV infection yet the manner in which CD8 T-cells are disabled is not yet fully understood.… (more)

Subjects/Keywords: HIV-1 Tat; IL-7 receptor; CD127

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APA (6th Edition):

Cherid, H. (2014). Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/31556

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):

Cherid, Hafsa. “Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding .” 2014. Thesis, University of Ottawa. Accessed May 09, 2021. http://hdl.handle.net/10393/31556.

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

MLA Handbook (7th Edition):

Cherid, Hafsa. “Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding .” 2014. Web. 09 May 2021.

Vancouver:

Cherid H. Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding . [Internet] [Thesis]. University of Ottawa; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10393/31556.

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

Council of Science Editors:

Cherid H. Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding . [Thesis]. University of Ottawa; 2014. Available from: http://hdl.handle.net/10393/31556

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

[1] [2] [3] [4] [5] … [799]

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