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You searched for subject:(GPCR). Showing records 1 – 30 of 426 total matches.

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University of Georgia

1. Hammond, Dorothy Araba. Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs).

Degree: PhD, Bioinformatics, 2014, University of Georgia

 The functional differences that exist between alternatively spliced isoforms of genes can be substantial; it could be variations of the function of the “primary” full-length… (more)

Subjects/Keywords: GPCR

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

APA (6th Edition):

Hammond, D. A. (2014). Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs). (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/hammond_dorothy_a_201412_phd

Chicago Manual of Style (16th Edition):

Hammond, Dorothy Araba. “Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs).” 2014. Doctoral Dissertation, University of Georgia. Accessed August 14, 2020. http://purl.galileo.usg.edu/uga_etd/hammond_dorothy_a_201412_phd.

MLA Handbook (7th Edition):

Hammond, Dorothy Araba. “Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs).” 2014. Web. 14 Aug 2020.

Vancouver:

Hammond DA. Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs). [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2020 Aug 14]. Available from: http://purl.galileo.usg.edu/uga_etd/hammond_dorothy_a_201412_phd.

Council of Science Editors:

Hammond DA. Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs). [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/hammond_dorothy_a_201412_phd

2. 伊達山, 泉. Gタンパク質共役受容体の一次繊毛局在機構の解析 : Trafficking mechanism of ciliary G protein coupled receptors; G タンパクシツ キョウヤク ジュヨウタイ ノ イチジ センモウ キョクザイ キコウ ノ カイセキ.

Degree: 博士(バイオサイエンス), 2018, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: GPCR

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APA (6th Edition):

伊達山, . (2018). Gタンパク質共役受容体の一次繊毛局在機構の解析 : Trafficking mechanism of ciliary G protein coupled receptors; G タンパクシツ キョウヤク ジュヨウタイ ノ イチジ センモウ キョクザイ キコウ ノ カイセキ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/12337

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):

伊達山, 泉. “Gタンパク質共役受容体の一次繊毛局在機構の解析 : Trafficking mechanism of ciliary G protein coupled receptors; G タンパクシツ キョウヤク ジュヨウタイ ノ イチジ センモウ キョクザイ キコウ ノ カイセキ.” 2018. Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed August 14, 2020. http://hdl.handle.net/10061/12337.

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

MLA Handbook (7th Edition):

伊達山, 泉. “Gタンパク質共役受容体の一次繊毛局在機構の解析 : Trafficking mechanism of ciliary G protein coupled receptors; G タンパクシツ キョウヤク ジュヨウタイ ノ イチジ センモウ キョクザイ キコウ ノ カイセキ.” 2018. Web. 14 Aug 2020.

Vancouver:

伊達山 . Gタンパク質共役受容体の一次繊毛局在機構の解析 : Trafficking mechanism of ciliary G protein coupled receptors; G タンパクシツ キョウヤク ジュヨウタイ ノ イチジ センモウ キョクザイ キコウ ノ カイセキ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2018. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/10061/12337.

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

Council of Science Editors:

伊達山 . Gタンパク質共役受容体の一次繊毛局在機構の解析 : Trafficking mechanism of ciliary G protein coupled receptors; G タンパクシツ キョウヤク ジュヨウタイ ノ イチジ センモウ キョクザイ キコウ ノ カイセキ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2018. Available from: http://hdl.handle.net/10061/12337

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


Tulane University

3. McGraw, Claire. Cholesterol Dependent Signaling of the Adenosine A2a Receptor.

Degree: 2018, Tulane University

G-protein coupled receptors (GPCRs) represent the largest family of receptor proteins in the living world, having approximately 800 human genes predicted. GPCRs are therapeutically relevant,… (more)

Subjects/Keywords: GPCR; Cholesterol

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APA (6th Edition):

McGraw, C. (2018). Cholesterol Dependent Signaling of the Adenosine A2a Receptor. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:79080

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):

McGraw, Claire. “Cholesterol Dependent Signaling of the Adenosine A2a Receptor.” 2018. Thesis, Tulane University. Accessed August 14, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:79080.

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

MLA Handbook (7th Edition):

McGraw, Claire. “Cholesterol Dependent Signaling of the Adenosine A2a Receptor.” 2018. Web. 14 Aug 2020.

Vancouver:

McGraw C. Cholesterol Dependent Signaling of the Adenosine A2a Receptor. [Internet] [Thesis]. Tulane University; 2018. [cited 2020 Aug 14]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:79080.

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

Council of Science Editors:

McGraw C. Cholesterol Dependent Signaling of the Adenosine A2a Receptor. [Thesis]. Tulane University; 2018. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:79080

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


Queens University

4. Zara, Lian C. A G-protein coupled receptor is involved in the regulation of sleep and metabolism .

Degree: Biology, 2014, Queens University

 Sleep is an evolutionary conserved behaviour which in most species is essential for survival. However, the mechanisms involved in the genetic regulation of sleep remain… (more)

Subjects/Keywords: GPCR ; Genetics

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APA (6th Edition):

Zara, L. C. (2014). A G-protein coupled receptor is involved in the regulation of sleep and metabolism . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8645

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):

Zara, Lian C. “A G-protein coupled receptor is involved in the regulation of sleep and metabolism .” 2014. Thesis, Queens University. Accessed August 14, 2020. http://hdl.handle.net/1974/8645.

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

MLA Handbook (7th Edition):

Zara, Lian C. “A G-protein coupled receptor is involved in the regulation of sleep and metabolism .” 2014. Web. 14 Aug 2020.

Vancouver:

Zara LC. A G-protein coupled receptor is involved in the regulation of sleep and metabolism . [Internet] [Thesis]. Queens University; 2014. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/1974/8645.

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

Council of Science Editors:

Zara LC. A G-protein coupled receptor is involved in the regulation of sleep and metabolism . [Thesis]. Queens University; 2014. Available from: http://hdl.handle.net/1974/8645

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


University of Debrecen

5. Bajusz, Dávid. A P2Y12 receptor szerkezete és működése: in silico vizsgálatok .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2013, University of Debrecen

 A G-proteinhez kapcsolt receptorok (GPCR) alapvető fontosságú szerepet töltenek be a szervezet jelátviteli folyamatainak szabályozásában. A gyógyszerkutatás is felismerte jelentőségüket: a jelenlegi gyógyszerhatóanyagok kb. 40… (more)

Subjects/Keywords: molekulamodellezés; GPCR fehérje

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APA (6th Edition):

Bajusz, D. (2013). A P2Y12 receptor szerkezete és működése: in silico vizsgálatok . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/168146

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):

Bajusz, Dávid. “A P2Y12 receptor szerkezete és működése: in silico vizsgálatok .” 2013. Thesis, University of Debrecen. Accessed August 14, 2020. http://hdl.handle.net/2437/168146.

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

MLA Handbook (7th Edition):

Bajusz, Dávid. “A P2Y12 receptor szerkezete és működése: in silico vizsgálatok .” 2013. Web. 14 Aug 2020.

Vancouver:

Bajusz D. A P2Y12 receptor szerkezete és működése: in silico vizsgálatok . [Internet] [Thesis]. University of Debrecen; 2013. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/2437/168146.

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

Council of Science Editors:

Bajusz D. A P2Y12 receptor szerkezete és működése: in silico vizsgálatok . [Thesis]. University of Debrecen; 2013. Available from: http://hdl.handle.net/2437/168146

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


Tulane University

6. Jain, Abhinav Rabindra. G Protein-Coupled Receptor Expression and Signaling in Yeast: Design and Optimization of Host/Protein Platform for Therapeutic Development.

Degree: 2019, Tulane University

[email protected]

G protein-coupled receptors (GPCRs) constitute the largest family of human proteins with approximately around 800 genes and, are therapeutic targets for more than 35%… (more)

Subjects/Keywords: GPCR; Expression; Signaling

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APA (6th Edition):

Jain, A. R. (2019). G Protein-Coupled Receptor Expression and Signaling in Yeast: Design and Optimization of Host/Protein Platform for Therapeutic Development. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:108966

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):

Jain, Abhinav Rabindra. “G Protein-Coupled Receptor Expression and Signaling in Yeast: Design and Optimization of Host/Protein Platform for Therapeutic Development.” 2019. Thesis, Tulane University. Accessed August 14, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:108966.

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

MLA Handbook (7th Edition):

Jain, Abhinav Rabindra. “G Protein-Coupled Receptor Expression and Signaling in Yeast: Design and Optimization of Host/Protein Platform for Therapeutic Development.” 2019. Web. 14 Aug 2020.

Vancouver:

Jain AR. G Protein-Coupled Receptor Expression and Signaling in Yeast: Design and Optimization of Host/Protein Platform for Therapeutic Development. [Internet] [Thesis]. Tulane University; 2019. [cited 2020 Aug 14]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:108966.

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

Council of Science Editors:

Jain AR. G Protein-Coupled Receptor Expression and Signaling in Yeast: Design and Optimization of Host/Protein Platform for Therapeutic Development. [Thesis]. Tulane University; 2019. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:108966

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


Penn State University

7. Morse, Megan. Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling.

Degree: 2012, Penn State University

 Opioid receptors are G-protein coupled receptors (GPCRs) that are activated by opioid ligands. These ligands offer powerful medical benefits due to their analgesic properties, but… (more)

Subjects/Keywords: GPCR; Opioid; Receptor SIgnaling; DMR

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APA (6th Edition):

Morse, M. (2012). Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12691

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):

Morse, Megan. “Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling.” 2012. Thesis, Penn State University. Accessed August 14, 2020. https://submit-etda.libraries.psu.edu/catalog/12691.

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

MLA Handbook (7th Edition):

Morse, Megan. “Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling.” 2012. Web. 14 Aug 2020.

Vancouver:

Morse M. Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling. [Internet] [Thesis]. Penn State University; 2012. [cited 2020 Aug 14]. Available from: https://submit-etda.libraries.psu.edu/catalog/12691.

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

Council of Science Editors:

Morse M. Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/12691

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


University of Rochester

8. Yuan, Chujun. G protein βγ subunit mediated signaling specificity : implications for βγ subtypes and novel mechanisms of activation.

Degree: PhD, 2009, University of Rochester

 Activators of G protein signaling (AGS proteins) are a group of accessory proteins that can activate G protein signaling independent of a receptor. A new… (more)

Subjects/Keywords: AGS proteins; GPCR; G proteins

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APA (6th Edition):

Yuan, C. (2009). G protein βγ subunit mediated signaling specificity : implications for βγ subtypes and novel mechanisms of activation. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/6633

Chicago Manual of Style (16th Edition):

Yuan, Chujun. “G protein βγ subunit mediated signaling specificity : implications for βγ subtypes and novel mechanisms of activation.” 2009. Doctoral Dissertation, University of Rochester. Accessed August 14, 2020. http://hdl.handle.net/1802/6633.

MLA Handbook (7th Edition):

Yuan, Chujun. “G protein βγ subunit mediated signaling specificity : implications for βγ subtypes and novel mechanisms of activation.” 2009. Web. 14 Aug 2020.

Vancouver:

Yuan C. G protein βγ subunit mediated signaling specificity : implications for βγ subtypes and novel mechanisms of activation. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/1802/6633.

Council of Science Editors:

Yuan C. G protein βγ subunit mediated signaling specificity : implications for βγ subtypes and novel mechanisms of activation. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/6633

9. do Nascimento Júnior, Francisco. Classificação de Proteínas usando Máquinas de Aprendizagem e Descoberta de Padrões .

Degree: 2008, Universidade Federal de Pernambuco

 Máquinas de aprendizagem têm sido aplicadas em diferentes problemas em Bioinformática. Similarmente, algoritmos de descoberta de padrões também têm sido usados para descobrir motifs em… (more)

Subjects/Keywords: Classificação; Proteína; GPCR; SVM; Padrões

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APA (6th Edition):

do Nascimento Júnior, F. (2008). Classificação de Proteínas usando Máquinas de Aprendizagem e Descoberta de Padrões . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/1596

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):

do Nascimento Júnior, Francisco. “Classificação de Proteínas usando Máquinas de Aprendizagem e Descoberta de Padrões .” 2008. Thesis, Universidade Federal de Pernambuco. Accessed August 14, 2020. http://repositorio.ufpe.br/handle/123456789/1596.

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

MLA Handbook (7th Edition):

do Nascimento Júnior, Francisco. “Classificação de Proteínas usando Máquinas de Aprendizagem e Descoberta de Padrões .” 2008. Web. 14 Aug 2020.

Vancouver:

do Nascimento Júnior F. Classificação de Proteínas usando Máquinas de Aprendizagem e Descoberta de Padrões . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2008. [cited 2020 Aug 14]. Available from: http://repositorio.ufpe.br/handle/123456789/1596.

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

Council of Science Editors:

do Nascimento Júnior F. Classificação de Proteínas usando Máquinas de Aprendizagem e Descoberta de Padrões . [Thesis]. Universidade Federal de Pernambuco; 2008. Available from: http://repositorio.ufpe.br/handle/123456789/1596

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


University of California – San Francisco

10. Kelly, Lisa. EBI2 positions naïve and activated B cells.

Degree: Biomedical Sciences, 2011, University of California – San Francisco

 The immune system is organized to allow lymphocytes to survey for antigen and rapidly respond to an infection. B lymphocytes reside in B cell follicles… (more)

Subjects/Keywords: Immunology; B cells; chemokines; GPCR

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APA (6th Edition):

Kelly, L. (2011). EBI2 positions naïve and activated B cells. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0cf2v6js

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):

Kelly, Lisa. “EBI2 positions naïve and activated B cells.” 2011. Thesis, University of California – San Francisco. Accessed August 14, 2020. http://www.escholarship.org/uc/item/0cf2v6js.

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

MLA Handbook (7th Edition):

Kelly, Lisa. “EBI2 positions naïve and activated B cells.” 2011. Web. 14 Aug 2020.

Vancouver:

Kelly L. EBI2 positions naïve and activated B cells. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2020 Aug 14]. Available from: http://www.escholarship.org/uc/item/0cf2v6js.

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

Council of Science Editors:

Kelly L. EBI2 positions naïve and activated B cells. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/0cf2v6js

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


University of New South Wales

11. Campbell, Adrian. Identification of novel sites of interaction for α1 adrenoceptors.

Degree: Medical Sciences, 2015, University of New South Wales

 α1 adrenoceptors are three of the nine receptors that bind and respond to the hormones adrenaline and noradrenaline. α1 adrenoceptors mediate a number of physiological… (more)

Subjects/Keywords: Allosteric modulator; GPCR; Adrenoceptor

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APA (6th Edition):

Campbell, A. (2015). Identification of novel sites of interaction for α1 adrenoceptors. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Campbell, Adrian. “Identification of novel sites of interaction for α1 adrenoceptors.” 2015. Doctoral Dissertation, University of New South Wales. Accessed August 14, 2020. http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true.

MLA Handbook (7th Edition):

Campbell, Adrian. “Identification of novel sites of interaction for α1 adrenoceptors.” 2015. Web. 14 Aug 2020.

Vancouver:

Campbell A. Identification of novel sites of interaction for α1 adrenoceptors. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2020 Aug 14]. Available from: http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true.

Council of Science Editors:

Campbell A. Identification of novel sites of interaction for α1 adrenoceptors. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true

12. Pennock, Reagan L. Differential desensitization of pre- and postsynaptic mu opioid receptors regulating proopiomelanocortin neurons of the arcuate nucleus.

Degree: PhD, Biomedical Sciences, 2017, Colorado State University

 The mu opioid receptor (MOR) is the primary target of powerful opiate analgesics such as morphine and codeine. Repeated use of opiates, as may occur… (more)

Subjects/Keywords: electrophysiology; neurotransmission; diffusion; opioid; GPCR

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APA (6th Edition):

Pennock, R. L. (2017). Differential desensitization of pre- and postsynaptic mu opioid receptors regulating proopiomelanocortin neurons of the arcuate nucleus. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/181406

Chicago Manual of Style (16th Edition):

Pennock, Reagan L. “Differential desensitization of pre- and postsynaptic mu opioid receptors regulating proopiomelanocortin neurons of the arcuate nucleus.” 2017. Doctoral Dissertation, Colorado State University. Accessed August 14, 2020. http://hdl.handle.net/10217/181406.

MLA Handbook (7th Edition):

Pennock, Reagan L. “Differential desensitization of pre- and postsynaptic mu opioid receptors regulating proopiomelanocortin neurons of the arcuate nucleus.” 2017. Web. 14 Aug 2020.

Vancouver:

Pennock RL. Differential desensitization of pre- and postsynaptic mu opioid receptors regulating proopiomelanocortin neurons of the arcuate nucleus. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/10217/181406.

Council of Science Editors:

Pennock RL. Differential desensitization of pre- and postsynaptic mu opioid receptors regulating proopiomelanocortin neurons of the arcuate nucleus. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/181406


University of Rochester

13. Kan, Wei. M3 Muscarinic Receptor Interaction with Phospholipase C β3 Determines its Signaling Efficiency.

Degree: PhD, 2014, University of Rochester

 Phospholipase Cβ (PLCβ) enzymes are activated by G protein-coupled receptors (GPCRs), through receptor-catalyzed guanine nucleotide exchange on the Gαβγ heterotrimer containing Gq family G proteins.… (more)

Subjects/Keywords: Collision Coupling; GPCR; G Proteins; Phospholipase C; Scaffolding; PDZ; GPCR

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APA (6th Edition):

Kan, W. (2014). M3 Muscarinic Receptor Interaction with Phospholipase C β3 Determines its Signaling Efficiency. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28451

Chicago Manual of Style (16th Edition):

Kan, Wei. “M3 Muscarinic Receptor Interaction with Phospholipase C β3 Determines its Signaling Efficiency.” 2014. Doctoral Dissertation, University of Rochester. Accessed August 14, 2020. http://hdl.handle.net/1802/28451.

MLA Handbook (7th Edition):

Kan, Wei. “M3 Muscarinic Receptor Interaction with Phospholipase C β3 Determines its Signaling Efficiency.” 2014. Web. 14 Aug 2020.

Vancouver:

Kan W. M3 Muscarinic Receptor Interaction with Phospholipase C β3 Determines its Signaling Efficiency. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/1802/28451.

Council of Science Editors:

Kan W. M3 Muscarinic Receptor Interaction with Phospholipase C β3 Determines its Signaling Efficiency. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28451

14. Jha, Ankita. Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis : Contrôle quantitatif de l'organisation des GPcrs et de leur signalisation par endocytose pendant la morphogenèse epithéliale.

Degree: Docteur es, Biologie du developpement, 2017, Aix Marseille Université

Au cours de la gastrulation de l’embryon de Drosophile, l’activation apicale du cytosquelette d’acto-myosine orchestre la constriction apicale dans le mésoderme en invagination ainsi que… (more)

Subjects/Keywords: Gpcr; Quantitatif; Endocytose; Homo-Clusters; Gpcr; Quantitative; Endocytosis; Homo-Clusters; 571

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APA (6th Edition):

Jha, A. (2017). Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis : Contrôle quantitatif de l'organisation des GPcrs et de leur signalisation par endocytose pendant la morphogenèse epithéliale. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0393

Chicago Manual of Style (16th Edition):

Jha, Ankita. “Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis : Contrôle quantitatif de l'organisation des GPcrs et de leur signalisation par endocytose pendant la morphogenèse epithéliale.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed August 14, 2020. http://www.theses.fr/2017AIXM0393.

MLA Handbook (7th Edition):

Jha, Ankita. “Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis : Contrôle quantitatif de l'organisation des GPcrs et de leur signalisation par endocytose pendant la morphogenèse epithéliale.” 2017. Web. 14 Aug 2020.

Vancouver:

Jha A. Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis : Contrôle quantitatif de l'organisation des GPcrs et de leur signalisation par endocytose pendant la morphogenèse epithéliale. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2020 Aug 14]. Available from: http://www.theses.fr/2017AIXM0393.

Council of Science Editors:

Jha A. Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis : Contrôle quantitatif de l'organisation des GPcrs et de leur signalisation par endocytose pendant la morphogenèse epithéliale. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0393

15. Cutolo, Pasquale. Etude de l'interaction structurelle et fonctionnelle entre la chimiokine CXCL12 et ses récepteurs : CXCR4 et ACKR3/CXCR7 : Structural and functional study of the interaction between CXCL12 chemokine and its receptors : CXCR4 and ACKR3/CXCR7.

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

 L'axe formé par la chimiokine CXCL12 et son récepteur CXCR4 est conservé chez les vertébrés où il joue un rôle important dans l'embryogenèse et la… (more)

Subjects/Keywords: Chimiotaxie; Gpcr; Oligomerisation; Nanobodies; Modelisation; Chemotaxis; Gpcr; Oligomerization; Nanobodies; Modelization

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APA (6th Edition):

Cutolo, P. (2016). Etude de l'interaction structurelle et fonctionnelle entre la chimiokine CXCL12 et ses récepteurs : CXCR4 et ACKR3/CXCR7 : Structural and functional study of the interaction between CXCL12 chemokine and its receptors : CXCR4 and ACKR3/CXCR7. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS550

Chicago Manual of Style (16th Edition):

Cutolo, Pasquale. “Etude de l'interaction structurelle et fonctionnelle entre la chimiokine CXCL12 et ses récepteurs : CXCR4 et ACKR3/CXCR7 : Structural and functional study of the interaction between CXCL12 chemokine and its receptors : CXCR4 and ACKR3/CXCR7.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed August 14, 2020. http://www.theses.fr/2016SACLS550.

MLA Handbook (7th Edition):

Cutolo, Pasquale. “Etude de l'interaction structurelle et fonctionnelle entre la chimiokine CXCL12 et ses récepteurs : CXCR4 et ACKR3/CXCR7 : Structural and functional study of the interaction between CXCL12 chemokine and its receptors : CXCR4 and ACKR3/CXCR7.” 2016. Web. 14 Aug 2020.

Vancouver:

Cutolo P. Etude de l'interaction structurelle et fonctionnelle entre la chimiokine CXCL12 et ses récepteurs : CXCR4 et ACKR3/CXCR7 : Structural and functional study of the interaction between CXCL12 chemokine and its receptors : CXCR4 and ACKR3/CXCR7. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Aug 14]. Available from: http://www.theses.fr/2016SACLS550.

Council of Science Editors:

Cutolo P. Etude de l'interaction structurelle et fonctionnelle entre la chimiokine CXCL12 et ses récepteurs : CXCR4 et ACKR3/CXCR7 : Structural and functional study of the interaction between CXCL12 chemokine and its receptors : CXCR4 and ACKR3/CXCR7. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS550


University of Sydney

16. Alice, Brown. Allosteric Coupling in the Dimeric Calcium Sensing Receptor .

Degree: 2017, University of Sydney

 The Calcium Sensing Receptor (CaSR) is a Class C GPCR that supports systemic calcium homeostasis by sensing and responding to small fluctuations in serum calcium… (more)

Subjects/Keywords: Calcium-sensing receptor; GPCR; allosteric coupling

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APA (6th Edition):

Alice, B. (2017). Allosteric Coupling in the Dimeric Calcium Sensing Receptor . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17738

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):

Alice, Brown. “Allosteric Coupling in the Dimeric Calcium Sensing Receptor .” 2017. Thesis, University of Sydney. Accessed August 14, 2020. http://hdl.handle.net/2123/17738.

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

MLA Handbook (7th Edition):

Alice, Brown. “Allosteric Coupling in the Dimeric Calcium Sensing Receptor .” 2017. Web. 14 Aug 2020.

Vancouver:

Alice B. Allosteric Coupling in the Dimeric Calcium Sensing Receptor . [Internet] [Thesis]. University of Sydney; 2017. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/2123/17738.

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

Council of Science Editors:

Alice B. Allosteric Coupling in the Dimeric Calcium Sensing Receptor . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17738

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


Temple University

17. Woodall, Benjamin Philip. NOVEL ROLES FOR GRK2 IN METABOLIC HOMEOSTASIS AND SKELETAL MUSCLE PHYSIOLOGY.

Degree: PhD, 2016, Temple University

Biomedical Sciences

Over the past two decades, a vast body of research has demonstrated the importance of G protein-coupled receptor kinase 2 (GRK2) in the… (more)

Subjects/Keywords: Molecular biology;

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APA (6th Edition):

Woodall, B. P. (2016). NOVEL ROLES FOR GRK2 IN METABOLIC HOMEOSTASIS AND SKELETAL MUSCLE PHYSIOLOGY. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,391153

Chicago Manual of Style (16th Edition):

Woodall, Benjamin Philip. “NOVEL ROLES FOR GRK2 IN METABOLIC HOMEOSTASIS AND SKELETAL MUSCLE PHYSIOLOGY.” 2016. Doctoral Dissertation, Temple University. Accessed August 14, 2020. http://digital.library.temple.edu/u?/p245801coll10,391153.

MLA Handbook (7th Edition):

Woodall, Benjamin Philip. “NOVEL ROLES FOR GRK2 IN METABOLIC HOMEOSTASIS AND SKELETAL MUSCLE PHYSIOLOGY.” 2016. Web. 14 Aug 2020.

Vancouver:

Woodall BP. NOVEL ROLES FOR GRK2 IN METABOLIC HOMEOSTASIS AND SKELETAL MUSCLE PHYSIOLOGY. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Aug 14]. Available from: http://digital.library.temple.edu/u?/p245801coll10,391153.

Council of Science Editors:

Woodall BP. NOVEL ROLES FOR GRK2 IN METABOLIC HOMEOSTASIS AND SKELETAL MUSCLE PHYSIOLOGY. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,391153


University of Louisville

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

Degree: PhD, 2011, University of Louisville

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Meier, Jason Bradley, 1980-. “Structure-based design of inhibitors of CXCR4.” 2011. Doctoral Dissertation, University of Louisville. Accessed August 14, 2020. 10.18297/etd/962 ; https://ir.library.louisville.edu/etd/962.

MLA Handbook (7th Edition):

Meier, Jason Bradley, 1980-. “Structure-based design of inhibitors of CXCR4.” 2011. Web. 14 Aug 2020.

Vancouver:

Meier, Jason Bradley 1. Structure-based design of inhibitors of CXCR4. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2020 Aug 14]. Available from: 10.18297/etd/962 ; https://ir.library.louisville.edu/etd/962.

Council of Science Editors:

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


University of Louisville

19. Kumar, Pritesh Prakash, 1986-. Searching for novel ligands for the cannabinoid and related receptors.

Degree: MS, 2011, University of Louisville

 A cell-based, Homogenous Time Resolved Fluorescence (HTRF) method was optimized and used to test a library of 60 putative endocannabinoids for activity towards CB1 or… (more)

Subjects/Keywords: Cannabinoid; Diabetes; Screening; HTRF; GPR119; GPCR

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APA (6th Edition):

Kumar, Pritesh Prakash, 1. (2011). Searching for novel ligands for the cannabinoid and related receptors. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/780 ; https://ir.library.louisville.edu/etd/780

Chicago Manual of Style (16th Edition):

Kumar, Pritesh Prakash, 1986-. “Searching for novel ligands for the cannabinoid and related receptors.” 2011. Masters Thesis, University of Louisville. Accessed August 14, 2020. 10.18297/etd/780 ; https://ir.library.louisville.edu/etd/780.

MLA Handbook (7th Edition):

Kumar, Pritesh Prakash, 1986-. “Searching for novel ligands for the cannabinoid and related receptors.” 2011. Web. 14 Aug 2020.

Vancouver:

Kumar, Pritesh Prakash 1. Searching for novel ligands for the cannabinoid and related receptors. [Internet] [Masters thesis]. University of Louisville; 2011. [cited 2020 Aug 14]. Available from: 10.18297/etd/780 ; https://ir.library.louisville.edu/etd/780.

Council of Science Editors:

Kumar, Pritesh Prakash 1. Searching for novel ligands for the cannabinoid and related receptors. [Masters Thesis]. University of Louisville; 2011. Available from: 10.18297/etd/780 ; https://ir.library.louisville.edu/etd/780


McMaster University

20. Mahadeo, Crystal. INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR.

Degree: MSc, 2016, McMaster University

When released extracellularly, the purine nucleoside guanosine (Guo) can exert a wide range of physiological effects in vitro and in vivo. Guo can induce the… (more)

Subjects/Keywords: Guanosine; GPCR; G1 receptor; Binding Assay

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APA (6th Edition):

Mahadeo, C. (2016). INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/20626

Chicago Manual of Style (16th Edition):

Mahadeo, Crystal. “INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR.” 2016. Masters Thesis, McMaster University. Accessed August 14, 2020. http://hdl.handle.net/11375/20626.

MLA Handbook (7th Edition):

Mahadeo, Crystal. “INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR.” 2016. Web. 14 Aug 2020.

Vancouver:

Mahadeo C. INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR. [Internet] [Masters thesis]. McMaster University; 2016. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/11375/20626.

Council of Science Editors:

Mahadeo C. INVESTIGATING THE MECHANISM OF ACTION OF GUANOSINE BY THE G1 RECEPTOR. [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20626


Penn State University

21. Frey, Colleen Marie. A Novel Interaction between the A2a Adenosine Receptor and Ran Binding Protein 9 (RBP9) and the Role of RBP9 in GPCR Function .

Degree: 2010, Penn State University

 Several lines of evidence describe an involvement of the A2a adenosine receptor (A2aR), a seven transmembrane, G protein-coupled receptor (GPCR) in Parkinson’s disease (PD). Caffeine,… (more)

Subjects/Keywords: A2aR; GPCR; RBP9

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APA (6th Edition):

Frey, C. M. (2010). A Novel Interaction between the A2a Adenosine Receptor and Ran Binding Protein 9 (RBP9) and the Role of RBP9 in GPCR Function . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11338

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):

Frey, Colleen Marie. “A Novel Interaction between the A2a Adenosine Receptor and Ran Binding Protein 9 (RBP9) and the Role of RBP9 in GPCR Function .” 2010. Thesis, Penn State University. Accessed August 14, 2020. https://submit-etda.libraries.psu.edu/catalog/11338.

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

MLA Handbook (7th Edition):

Frey, Colleen Marie. “A Novel Interaction between the A2a Adenosine Receptor and Ran Binding Protein 9 (RBP9) and the Role of RBP9 in GPCR Function .” 2010. Web. 14 Aug 2020.

Vancouver:

Frey CM. A Novel Interaction between the A2a Adenosine Receptor and Ran Binding Protein 9 (RBP9) and the Role of RBP9 in GPCR Function . [Internet] [Thesis]. Penn State University; 2010. [cited 2020 Aug 14]. Available from: https://submit-etda.libraries.psu.edu/catalog/11338.

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

Council of Science Editors:

Frey CM. A Novel Interaction between the A2a Adenosine Receptor and Ran Binding Protein 9 (RBP9) and the Role of RBP9 in GPCR Function . [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/11338

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


Boston University

22. Berry, Justin David. Effects of rhodopsin phosphorylation on dark adaptation and the recovery of sensitivity.

Degree: PhD, Physiology, 2016, Boston University

 Vision requires the photoreceptors in the eye to rapidly respond to changes in light intensity. These processes are accomplished within rod photoreceptors by the visual… (more)

Subjects/Keywords: Physiology; GPCR; Dark adaptation; Phototransduction; Retina; Rhodopsin

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APA (6th Edition):

Berry, J. D. (2016). Effects of rhodopsin phosphorylation on dark adaptation and the recovery of sensitivity. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16720

Chicago Manual of Style (16th Edition):

Berry, Justin David. “Effects of rhodopsin phosphorylation on dark adaptation and the recovery of sensitivity.” 2016. Doctoral Dissertation, Boston University. Accessed August 14, 2020. http://hdl.handle.net/2144/16720.

MLA Handbook (7th Edition):

Berry, Justin David. “Effects of rhodopsin phosphorylation on dark adaptation and the recovery of sensitivity.” 2016. Web. 14 Aug 2020.

Vancouver:

Berry JD. Effects of rhodopsin phosphorylation on dark adaptation and the recovery of sensitivity. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/2144/16720.

Council of Science Editors:

Berry JD. Effects of rhodopsin phosphorylation on dark adaptation and the recovery of sensitivity. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/16720

23. G. Gelmini. CARATTERIZZAZIONE FUNZIONALE DEI MUTANTI DEL RECETTORE PER LA TIREOTROPINA (TSH).

Degree: 2013, Università degli Studi di Milano

 Context: Heterozygous mutations in the TSH receptor gene (TSHR) are associated with partial TSH resistance, characterized by isolated nonautoimmune hyperthyrotropinemia (NAHT). The prevalence and management… (more)

Subjects/Keywords: GPCR; TSH; MUTAZIONI; Settore MED/13 - Endocrinologia

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APA (6th Edition):

Gelmini, G. (2013). CARATTERIZZAZIONE FUNZIONALE DEI MUTANTI DEL RECETTORE PER LA TIREOTROPINA (TSH). (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/215882

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):

Gelmini, G.. “CARATTERIZZAZIONE FUNZIONALE DEI MUTANTI DEL RECETTORE PER LA TIREOTROPINA (TSH).” 2013. Thesis, Università degli Studi di Milano. Accessed August 14, 2020. http://hdl.handle.net/2434/215882.

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

MLA Handbook (7th Edition):

Gelmini, G.. “CARATTERIZZAZIONE FUNZIONALE DEI MUTANTI DEL RECETTORE PER LA TIREOTROPINA (TSH).” 2013. Web. 14 Aug 2020.

Vancouver:

Gelmini G. CARATTERIZZAZIONE FUNZIONALE DEI MUTANTI DEL RECETTORE PER LA TIREOTROPINA (TSH). [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/2434/215882.

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

Council of Science Editors:

Gelmini G. CARATTERIZZAZIONE FUNZIONALE DEI MUTANTI DEL RECETTORE PER LA TIREOTROPINA (TSH). [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/215882

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


Duke University

24. Henderson, Nicholas Trubiano. How Yeast Cells Find Their Mates .

Degree: 2019, Duke University

  Extracellular chemical gradients provide signals that guide a broad spectrum of different cellular processes. By accurately sensing and responding to chemical gradients, immune cells… (more)

Subjects/Keywords: Cellular biology; GPCR; Gradient Sensing; Polarity; Yeast

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APA (6th Edition):

Henderson, N. T. (2019). How Yeast Cells Find Their Mates . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/20094

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):

Henderson, Nicholas Trubiano. “How Yeast Cells Find Their Mates .” 2019. Thesis, Duke University. Accessed August 14, 2020. http://hdl.handle.net/10161/20094.

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

MLA Handbook (7th Edition):

Henderson, Nicholas Trubiano. “How Yeast Cells Find Their Mates .” 2019. Web. 14 Aug 2020.

Vancouver:

Henderson NT. How Yeast Cells Find Their Mates . [Internet] [Thesis]. Duke University; 2019. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/10161/20094.

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

Council of Science Editors:

Henderson NT. How Yeast Cells Find Their Mates . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/20094

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


University of Manchester

25. Lee, Lisa Li chun. Integrated Bioinformatic Approaches to the Prediction of Protein-Protein Interactions.

Degree: 2011, University of Manchester

 Protein-protein interactions (PPIs) play a fundamental role in many biologicalprocesses such as signal transduction from the extracelluar space to cytosol. Functionsof less characterized proteins can… (more)

Subjects/Keywords: PROTEIN-PROTEIN INTERACTION; MUTUAL INFORMATION; GPCR

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APA (6th Edition):

Lee, L. L. c. (2011). Integrated Bioinformatic Approaches to the Prediction of Protein-Protein Interactions. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:135915

Chicago Manual of Style (16th Edition):

Lee, Lisa Li chun. “Integrated Bioinformatic Approaches to the Prediction of Protein-Protein Interactions.” 2011. Doctoral Dissertation, University of Manchester. Accessed August 14, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:135915.

MLA Handbook (7th Edition):

Lee, Lisa Li chun. “Integrated Bioinformatic Approaches to the Prediction of Protein-Protein Interactions.” 2011. Web. 14 Aug 2020.

Vancouver:

Lee LLc. Integrated Bioinformatic Approaches to the Prediction of Protein-Protein Interactions. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Aug 14]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:135915.

Council of Science Editors:

Lee LLc. Integrated Bioinformatic Approaches to the Prediction of Protein-Protein Interactions. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:135915

26. Zhang, Boyang. Functional and Structural Insights into the First and Second Intracellular Domains for D1-Class Dopaminergic Receptors .

Degree: 2017, University of Ottawa

 Previous studies have shown that the subtype-specific pharmacological properties of D1-class receptors (D1R and D5R) can be attributed to their third intracellular domain and C-terminal… (more)

Subjects/Keywords: Dopamine; GPCR

…10 Figure 4. Molecular switches in GPCR activation… …13 Figure 5. Canonical life-cycle of GPCR… …Guanosine diphosphate GnRH: Gonadotropin-releasing hormone GPCR: G protein-coupled receptor GRK: G… …responses. 1.1 - GPCR Topography and Taxonomy All GPCR possess a common topology consisting of an… …G protein Cycle and Signalling Pathways At the heart of GPCR signalling is the G protein… 

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APA (6th Edition):

Zhang, B. (2017). Functional and Structural Insights into the First and Second Intracellular Domains for D1-Class Dopaminergic Receptors . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35932

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):

Zhang, Boyang. “Functional and Structural Insights into the First and Second Intracellular Domains for D1-Class Dopaminergic Receptors .” 2017. Thesis, University of Ottawa. Accessed August 14, 2020. http://hdl.handle.net/10393/35932.

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

MLA Handbook (7th Edition):

Zhang, Boyang. “Functional and Structural Insights into the First and Second Intracellular Domains for D1-Class Dopaminergic Receptors .” 2017. Web. 14 Aug 2020.

Vancouver:

Zhang B. Functional and Structural Insights into the First and Second Intracellular Domains for D1-Class Dopaminergic Receptors . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2020 Aug 14]. Available from: http://hdl.handle.net/10393/35932.

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

Council of Science Editors:

Zhang B. Functional and Structural Insights into the First and Second Intracellular Domains for D1-Class Dopaminergic Receptors . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/35932

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


Harvard University

27. Lahvic, Jamie L. Oxygenated Fatty Acids Enhance Hematopoiesis via the Receptor GPR132.

Degree: PhD, 2017, Harvard University

After their specification in early development, hematopoietic stem cells (HSCs) maintain the entire blood system throughout adulthood as well as upon transplantation. The processes of… (more)

Subjects/Keywords: Hematopoietic stem cell; fatty acid; GPCR; zebrafish

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APA (6th Edition):

Lahvic, J. L. (2017). Oxygenated Fatty Acids Enhance Hematopoiesis via the Receptor GPR132. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061504

Chicago Manual of Style (16th Edition):

Lahvic, Jamie L. “Oxygenated Fatty Acids Enhance Hematopoiesis via the Receptor GPR132.” 2017. Doctoral Dissertation, Harvard University. Accessed August 14, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061504.

MLA Handbook (7th Edition):

Lahvic, Jamie L. “Oxygenated Fatty Acids Enhance Hematopoiesis via the Receptor GPR132.” 2017. Web. 14 Aug 2020.

Vancouver:

Lahvic JL. Oxygenated Fatty Acids Enhance Hematopoiesis via the Receptor GPR132. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2020 Aug 14]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061504.

Council of Science Editors:

Lahvic JL. Oxygenated Fatty Acids Enhance Hematopoiesis via the Receptor GPR132. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061504


Iowa State University

28. Zamanian, Mostafa. Genomic and functional characterization of G protein-coupled receptors in the human pathogen Schistosoma mansoni and the model planarian Schmidtea mediterranea.

Degree: 2011, Iowa State University

 G protein-coupled receptors (GPCRs) constitute the largest known superfamily of integral membrane proteins, and represent a particularly lucrative set of chemotherapeutic targets. These seven transmembrane… (more)

Subjects/Keywords: Deorphanization; GPCR; Neuropeptide; Planaria; RNAi; Schistosomiasis

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APA (6th Edition):

Zamanian, M. (2011). Genomic and functional characterization of G protein-coupled receptors in the human pathogen Schistosoma mansoni and the model planarian Schmidtea mediterranea. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/12153

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):

Zamanian, Mostafa. “Genomic and functional characterization of G protein-coupled receptors in the human pathogen Schistosoma mansoni and the model planarian Schmidtea mediterranea.” 2011. Thesis, Iowa State University. Accessed August 14, 2020. https://lib.dr.iastate.edu/etd/12153.

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

MLA Handbook (7th Edition):

Zamanian, Mostafa. “Genomic and functional characterization of G protein-coupled receptors in the human pathogen Schistosoma mansoni and the model planarian Schmidtea mediterranea.” 2011. Web. 14 Aug 2020.

Vancouver:

Zamanian M. Genomic and functional characterization of G protein-coupled receptors in the human pathogen Schistosoma mansoni and the model planarian Schmidtea mediterranea. [Internet] [Thesis]. Iowa State University; 2011. [cited 2020 Aug 14]. Available from: https://lib.dr.iastate.edu/etd/12153.

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

Council of Science Editors:

Zamanian M. Genomic and functional characterization of G protein-coupled receptors in the human pathogen Schistosoma mansoni and the model planarian Schmidtea mediterranea. [Thesis]. Iowa State University; 2011. Available from: https://lib.dr.iastate.edu/etd/12153

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


University of California – San Francisco

29. Temkin, Paul. Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor.

Degree: Cell Biology, 2011, University of California – San Francisco

 This thesis addresses the endosomal sorting of the beta-2 adrenergic receptor (B2AR), a "typical" (family A) member of the large superfamily of seven-transmembrane signaling receptors,… (more)

Subjects/Keywords: Cellular biology; adrb2; B2AR; GPCR; Retromer; SNX27

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

APA (6th Edition):

Temkin, P. (2011). Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7zc0j3wd

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):

Temkin, Paul. “Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor.” 2011. Thesis, University of California – San Francisco. Accessed August 14, 2020. http://www.escholarship.org/uc/item/7zc0j3wd.

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

MLA Handbook (7th Edition):

Temkin, Paul. “Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor.” 2011. Web. 14 Aug 2020.

Vancouver:

Temkin P. Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2020 Aug 14]. Available from: http://www.escholarship.org/uc/item/7zc0j3wd.

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

Council of Science Editors:

Temkin P. Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/7zc0j3wd

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


University of California – San Francisco

30. Henry, Anastasia Gail. Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors.

Degree: Cell Biology, 2012, University of California – San Francisco

 This dissertation examines the role of ubiquitination in regulating the endocytic trafficking of opioid receptors, members of the large superfamily of seven-transmembrane receptors (7TMRs). The… (more)

Subjects/Keywords: Cellular biology; endocytosis; GPCR; signaling; ubiquitin

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

APA (6th Edition):

Henry, A. G. (2012). Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/5zj8675c

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):

Henry, Anastasia Gail. “Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors.” 2012. Thesis, University of California – San Francisco. Accessed August 14, 2020. http://www.escholarship.org/uc/item/5zj8675c.

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

MLA Handbook (7th Edition):

Henry, Anastasia Gail. “Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors.” 2012. Web. 14 Aug 2020.

Vancouver:

Henry AG. Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2020 Aug 14]. Available from: http://www.escholarship.org/uc/item/5zj8675c.

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

Council of Science Editors:

Henry AG. Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/5zj8675c

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

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