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You searched for subject:(ligand receptor interactions). Showing records 1 – 30 of 40 total matches.

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Texas A&M University

1. Jung, Hyunsook. SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES.

Degree: 2010, Texas A&M University

Ligand-receptor interactions are ubiquitous on cell membranes. Indeed, many important physiological functions primarily involve such interactions. These include cell signaling, pathogen binding, trafficking of lymphocytes,… (more)

Subjects/Keywords: supported lipid bilayer; ligand/receptor interactions

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APA (6th Edition):

Jung, H. (2010). SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499

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):

Jung, Hyunsook. “SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES.” 2010. Thesis, Texas A&M University. Accessed October 18, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499.

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

MLA Handbook (7th Edition):

Jung, Hyunsook. “SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES.” 2010. Web. 18 Oct 2019.

Vancouver:

Jung H. SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499.

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

Council of Science Editors:

Jung H. SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499

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


University of Kansas

2. Lee, Molly Marie. An Improved Synthesis of the Pacific Blue Fluorophore and Fluorescence-based Studies of Receptor-Ligand Interactions.

Degree: PhD, Medicinal Chemistry, 2016, University of Kansas

 Early-stage drug discovery and chemical biology projects often use fluorescence-based assays to obtain information about biological interactions and cellular processes. However, many of the best… (more)

Subjects/Keywords: Chemistry; Chemical biology; Fluorescence; FRET; Receptor-ligand interactions

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APA (6th Edition):

Lee, M. M. (2016). An Improved Synthesis of the Pacific Blue Fluorophore and Fluorescence-based Studies of Receptor-Ligand Interactions. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25773

Chicago Manual of Style (16th Edition):

Lee, Molly Marie. “An Improved Synthesis of the Pacific Blue Fluorophore and Fluorescence-based Studies of Receptor-Ligand Interactions.” 2016. Doctoral Dissertation, University of Kansas. Accessed October 18, 2019. http://hdl.handle.net/1808/25773.

MLA Handbook (7th Edition):

Lee, Molly Marie. “An Improved Synthesis of the Pacific Blue Fluorophore and Fluorescence-based Studies of Receptor-Ligand Interactions.” 2016. Web. 18 Oct 2019.

Vancouver:

Lee MM. An Improved Synthesis of the Pacific Blue Fluorophore and Fluorescence-based Studies of Receptor-Ligand Interactions. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1808/25773.

Council of Science Editors:

Lee MM. An Improved Synthesis of the Pacific Blue Fluorophore and Fluorescence-based Studies of Receptor-Ligand Interactions. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/25773


University of Ottawa

3. Sun, Jiayin. The Structural Basis for Lipid-Dependent Uncoupling of the Nicotinic Acetylcholine Receptor .

Degree: 2017, University of Ottawa

 In lipid membranes lacking activating lipids, the nicotinic acetylcholine receptor adopts an uncoupled conformation that binds ligand, but does not transition into an open conformation.… (more)

Subjects/Keywords: Structure; Lipid-protein interactions; Mechanism; Nicotinic acetylcholine receptor; Uncoupling; ELIC; Pentameric ligand-gated ion channels

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APA (6th Edition):

Sun, J. (2017). The Structural Basis for Lipid-Dependent Uncoupling of the Nicotinic Acetylcholine Receptor . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35642

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):

Sun, Jiayin. “The Structural Basis for Lipid-Dependent Uncoupling of the Nicotinic Acetylcholine Receptor .” 2017. Thesis, University of Ottawa. Accessed October 18, 2019. http://hdl.handle.net/10393/35642.

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

MLA Handbook (7th Edition):

Sun, Jiayin. “The Structural Basis for Lipid-Dependent Uncoupling of the Nicotinic Acetylcholine Receptor .” 2017. Web. 18 Oct 2019.

Vancouver:

Sun J. The Structural Basis for Lipid-Dependent Uncoupling of the Nicotinic Acetylcholine Receptor . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10393/35642.

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

Council of Science Editors:

Sun J. The Structural Basis for Lipid-Dependent Uncoupling of the Nicotinic Acetylcholine Receptor . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/35642

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


University of Cambridge

4. Sharma, Sumana. Genome-scale identification of cellular pathways required for cell surface recognition .

Degree: 2018, University of Cambridge

 A range of biochemically diverse molecules located in the plasma membrane— such as proteins, glycans, and lipids—mediate cellular recognition events, initiation of signalling pathways, and… (more)

Subjects/Keywords: CRISPR-Cas9; Low-affinity interaction; Cellular-signalling; Loss-of-function genetic screens; Glycoseaminoglycans; Receptor-ligand interactions; GABA receptor

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APA (6th Edition):

Sharma, S. (2018). Genome-scale identification of cellular pathways required for cell surface recognition . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/271825

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):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition .” 2018. Thesis, University of Cambridge. Accessed October 18, 2019. https://www.repository.cam.ac.uk/handle/1810/271825.

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

MLA Handbook (7th Edition):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition .” 2018. Web. 18 Oct 2019.

Vancouver:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/271825.

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

Council of Science Editors:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/271825

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


Indian Institute of Science

5. Majumdar, Ritankar. Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling.

Degree: 2012, Indian Institute of Science

 The glycoprotein hormones, Luteinizing Hormone (LH), human Chorionic Gonadotropin (hCG), Follicle Stimulating Hormone (FSH) and Thyroid Stimulating Hormone (TSH) are heterodimeric proteins with an identical… (more)

Subjects/Keywords: Glycoprotein Hormone Receptors; Glycoprotein Hormone Receptor Complexes - Modeling; Ligand Binding; Signal Transduction; Hormone Receptor Interactions; TSH Receptors; Thyrotropin Receptor; G-protein Coupled Receptors (GPCR); Biochemistry

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

APA (6th Edition):

Majumdar, R. (2012). Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2344

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):

Majumdar, Ritankar. “Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling.” 2012. Thesis, Indian Institute of Science. Accessed October 18, 2019. http://hdl.handle.net/2005/2344.

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

MLA Handbook (7th Edition):

Majumdar, Ritankar. “Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling.” 2012. Web. 18 Oct 2019.

Vancouver:

Majumdar R. Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling. [Internet] [Thesis]. Indian Institute of Science; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2005/2344.

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

Council of Science Editors:

Majumdar R. Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling. [Thesis]. Indian Institute of Science; 2012. Available from: http://hdl.handle.net/2005/2344

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


Indian Institute of Science

6. Majumdar, Ritankar. Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling.

Degree: 2012, Indian Institute of Science

 The glycoprotein hormones, Luteinizing Hormone (LH), human Chorionic Gonadotropin (hCG), Follicle Stimulating Hormone (FSH) and Thyroid Stimulating Hormone (TSH) are heterodimeric proteins with an identical… (more)

Subjects/Keywords: Glycoprotein Hormone Receptors; Glycoprotein Hormone Receptor Complexes - Modeling; Ligand Binding; Signal Transduction; Hormone Receptor Interactions; TSH Receptors; Thyrotropin Receptor; G-protein Coupled Receptors (GPCR); Biochemistry

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APA (6th Edition):

Majumdar, R. (2012). Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2344 ; http://etd.ncsi.iisc.ernet.in/abstracts/3015/G25337-Abs.pdf

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):

Majumdar, Ritankar. “Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling.” 2012. Thesis, Indian Institute of Science. Accessed October 18, 2019. http://etd.iisc.ernet.in/handle/2005/2344 ; http://etd.ncsi.iisc.ernet.in/abstracts/3015/G25337-Abs.pdf.

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

MLA Handbook (7th Edition):

Majumdar, Ritankar. “Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling.” 2012. Web. 18 Oct 2019.

Vancouver:

Majumdar R. Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling. [Internet] [Thesis]. Indian Institute of Science; 2012. [cited 2019 Oct 18]. Available from: http://etd.iisc.ernet.in/handle/2005/2344 ; http://etd.ncsi.iisc.ernet.in/abstracts/3015/G25337-Abs.pdf.

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

Council of Science Editors:

Majumdar R. Activation Of Glycoprotein Hormone Receptors : Role Of Different Receptor Domains In Hormone Binding And Signaling. [Thesis]. Indian Institute of Science; 2012. Available from: http://etd.iisc.ernet.in/handle/2005/2344 ; http://etd.ncsi.iisc.ernet.in/abstracts/3015/G25337-Abs.pdf

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


Dublin City University

7. Scheller, Agnieszka. Notch signaling pathway in human vascular smooth muscle cell differentiation.

Degree: School of Biotechnology, 2006, Dublin City University

 Notch receptor-ligand interactions are a highly conserved mechanism, originally described in developmental studies using Drosophilae, that regulate inter-cell communication and dictate, in part, vascular smooth… (more)

Subjects/Keywords: Biotechnology; Notch receptor-ligand interactions; vascular smooth muscle cell

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APA (6th Edition):

Scheller, A. (2006). Notch signaling pathway in human vascular smooth muscle cell differentiation. (Thesis). Dublin City University. Retrieved from http://doras.dcu.ie/16929/

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):

Scheller, Agnieszka. “Notch signaling pathway in human vascular smooth muscle cell differentiation.” 2006. Thesis, Dublin City University. Accessed October 18, 2019. http://doras.dcu.ie/16929/.

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

MLA Handbook (7th Edition):

Scheller, Agnieszka. “Notch signaling pathway in human vascular smooth muscle cell differentiation.” 2006. Web. 18 Oct 2019.

Vancouver:

Scheller A. Notch signaling pathway in human vascular smooth muscle cell differentiation. [Internet] [Thesis]. Dublin City University; 2006. [cited 2019 Oct 18]. Available from: http://doras.dcu.ie/16929/.

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

Council of Science Editors:

Scheller A. Notch signaling pathway in human vascular smooth muscle cell differentiation. [Thesis]. Dublin City University; 2006. Available from: http://doras.dcu.ie/16929/

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


University of Michigan

8. Dickendesher, Travis L. Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury.

Degree: PhD, Neuroscience, 2013, University of Michigan

 Depending on location and severity, injury to the adult mammalian central nervous system (CNS) typically results in neurological deficits ranging from mild motor impairment to… (more)

Subjects/Keywords: Mammalian Central Nervous System Repair; Axon Regeneration; Novel Ligand-Receptor Interactions; Spinal Cord Injury; Axon Degeneration; Excitotoxicity; Neurosciences; Health Sciences; Science

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APA (6th Edition):

Dickendesher, T. L. (2013). Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102322

Chicago Manual of Style (16th Edition):

Dickendesher, Travis L. “Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury.” 2013. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/102322.

MLA Handbook (7th Edition):

Dickendesher, Travis L. “Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury.” 2013. Web. 18 Oct 2019.

Vancouver:

Dickendesher TL. Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/102322.

Council of Science Editors:

Dickendesher TL. Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102322


Indian Institute of Science

9. Sharma, Ankur. Unfolding the Mechanism of Notch1 Receptor Activation : Implications in Cancer Stem Cell Targeting.

Degree: 2013, Indian Institute of Science

 Notch receptors and ligands are single-pass transmembrane proteins which play important roles in cell-cell communication. Notch in ‘harmony’ with other signaling pathways regulate the entire… (more)

Subjects/Keywords: Cancer Stem Cell Targeting; Notch Receptors; Notch Signaling; Notch Receptor Activation; Notch Receptor-Ligand Interactions; Human Notch1 Receptors; Breast Cancer Stem Cell Targeting; Chemotherapy Resistant Cancer Stem Cell Targeting; Notch1 Antibodies - Cancer Therapy; Notch1 Receptor Activation; Notch1 Signaling; Notch; Notch1 Ligand Binding Domain; Molecular Biology

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APA (6th Edition):

Sharma, A. (2013). Unfolding the Mechanism of Notch1 Receptor Activation : Implications in Cancer Stem Cell Targeting. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3472 ; http://etd.iisc.ernet.in/abstracts/4339/G25894-Abs.pdf

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):

Sharma, Ankur. “Unfolding the Mechanism of Notch1 Receptor Activation : Implications in Cancer Stem Cell Targeting.” 2013. Thesis, Indian Institute of Science. Accessed October 18, 2019. http://etd.iisc.ernet.in/2005/3472 ; http://etd.iisc.ernet.in/abstracts/4339/G25894-Abs.pdf.

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

MLA Handbook (7th Edition):

Sharma, Ankur. “Unfolding the Mechanism of Notch1 Receptor Activation : Implications in Cancer Stem Cell Targeting.” 2013. Web. 18 Oct 2019.

Vancouver:

Sharma A. Unfolding the Mechanism of Notch1 Receptor Activation : Implications in Cancer Stem Cell Targeting. [Internet] [Thesis]. Indian Institute of Science; 2013. [cited 2019 Oct 18]. Available from: http://etd.iisc.ernet.in/2005/3472 ; http://etd.iisc.ernet.in/abstracts/4339/G25894-Abs.pdf.

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

Council of Science Editors:

Sharma A. Unfolding the Mechanism of Notch1 Receptor Activation : Implications in Cancer Stem Cell Targeting. [Thesis]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ernet.in/2005/3472 ; http://etd.iisc.ernet.in/abstracts/4339/G25894-Abs.pdf

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


University of Michigan

10. Gagnon, Jessica K. Flexible Receptor Docking Method Development and Molecular Dynamics Studies Towards Targeting Dynamic Protein Surfaces.

Degree: PhD, Chemistry, 2015, University of Michigan

 Protein-protein interactions are integral for cellular function, playing a huge role in processes such as cell signaling and transcription regulation. Targeting these essential interactions with… (more)

Subjects/Keywords: flexible receptor docking development; CHARMM simulation package; computational biophysics; protein-ligand interactions; KIX domain of CREB binding protein; coarse-grained go-like models; Chemistry; Science

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

APA (6th Edition):

Gagnon, J. K. (2015). Flexible Receptor Docking Method Development and Molecular Dynamics Studies Towards Targeting Dynamic Protein Surfaces. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/116710

Chicago Manual of Style (16th Edition):

Gagnon, Jessica K. “Flexible Receptor Docking Method Development and Molecular Dynamics Studies Towards Targeting Dynamic Protein Surfaces.” 2015. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/116710.

MLA Handbook (7th Edition):

Gagnon, Jessica K. “Flexible Receptor Docking Method Development and Molecular Dynamics Studies Towards Targeting Dynamic Protein Surfaces.” 2015. Web. 18 Oct 2019.

Vancouver:

Gagnon JK. Flexible Receptor Docking Method Development and Molecular Dynamics Studies Towards Targeting Dynamic Protein Surfaces. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/116710.

Council of Science Editors:

Gagnon JK. Flexible Receptor Docking Method Development and Molecular Dynamics Studies Towards Targeting Dynamic Protein Surfaces. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/116710


ETH Zürich

11. Bisson, William Henry. Novel ligands for the neuronal nAChR: Synthesis, in vitro characterizations and binding models.

Degree: 2003, ETH Zürich

Subjects/Keywords: CHOLINERGE REZEPTOREN (NEUROLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); CHOLINERGIC RECEPTORS (NEUROLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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

APA (6th Edition):

Bisson, W. H. (2003). Novel ligands for the neuronal nAChR: Synthesis, in vitro characterizations and binding models. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/147763

Chicago Manual of Style (16th Edition):

Bisson, William Henry. “Novel ligands for the neuronal nAChR: Synthesis, in vitro characterizations and binding models.” 2003. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/147763.

MLA Handbook (7th Edition):

Bisson, William Henry. “Novel ligands for the neuronal nAChR: Synthesis, in vitro characterizations and binding models.” 2003. Web. 18 Oct 2019.

Vancouver:

Bisson WH. Novel ligands for the neuronal nAChR: Synthesis, in vitro characterizations and binding models. [Internet] [Doctoral dissertation]. ETH Zürich; 2003. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/147763.

Council of Science Editors:

Bisson WH. Novel ligands for the neuronal nAChR: Synthesis, in vitro characterizations and binding models. [Doctoral Dissertation]. ETH Zürich; 2003. Available from: http://hdl.handle.net/20.500.11850/147763


ETH Zürich

12. Prinz, Katja Bianca. In vitro Charakterisierung eines potentiellen PET-Liganden für den nAChR: Diplomarbeit.

Degree: 2000, ETH Zürich

Subjects/Keywords: CHOLINERGE REZEPTOREN (NEUROLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); CHOLINERGIC RECEPTORS (NEUROLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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

APA (6th Edition):

Prinz, K. B. (2000). In vitro Charakterisierung eines potentiellen PET-Liganden für den nAChR: Diplomarbeit. (Thesis). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145556

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):

Prinz, Katja Bianca. “In vitro Charakterisierung eines potentiellen PET-Liganden für den nAChR: Diplomarbeit.” 2000. Thesis, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/145556.

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

MLA Handbook (7th Edition):

Prinz, Katja Bianca. “In vitro Charakterisierung eines potentiellen PET-Liganden für den nAChR: Diplomarbeit.” 2000. Web. 18 Oct 2019.

Vancouver:

Prinz KB. In vitro Charakterisierung eines potentiellen PET-Liganden für den nAChR: Diplomarbeit. [Internet] [Thesis]. ETH Zürich; 2000. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/145556.

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

Council of Science Editors:

Prinz KB. In vitro Charakterisierung eines potentiellen PET-Liganden für den nAChR: Diplomarbeit. [Thesis]. ETH Zürich; 2000. Available from: http://hdl.handle.net/20.500.11850/145556

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


ETH Zürich

13. Schibig, Anita. Bindungsstudie am α₇-Rezeptor des nicotinischen Acetylcholin-Rezeptors mittels kompetitiver Verdrängungsanalyse.

Degree: 2002, ETH Zürich

Subjects/Keywords: REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); CHOLINERGE REZEPTOREN (NEUROLOGIE); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); CHOLINERGIC RECEPTORS (NEUROLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Schibig, A. (2002). Bindungsstudie am α₇-Rezeptor des nicotinischen Acetylcholin-Rezeptors mittels kompetitiver Verdrängungsanalyse. (Thesis). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/146896

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):

Schibig, Anita. “Bindungsstudie am α₇-Rezeptor des nicotinischen Acetylcholin-Rezeptors mittels kompetitiver Verdrängungsanalyse.” 2002. Thesis, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/146896.

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

MLA Handbook (7th Edition):

Schibig, Anita. “Bindungsstudie am α₇-Rezeptor des nicotinischen Acetylcholin-Rezeptors mittels kompetitiver Verdrängungsanalyse.” 2002. Web. 18 Oct 2019.

Vancouver:

Schibig A. Bindungsstudie am α₇-Rezeptor des nicotinischen Acetylcholin-Rezeptors mittels kompetitiver Verdrängungsanalyse. [Internet] [Thesis]. ETH Zürich; 2002. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/146896.

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

Council of Science Editors:

Schibig A. Bindungsstudie am α₇-Rezeptor des nicotinischen Acetylcholin-Rezeptors mittels kompetitiver Verdrängungsanalyse. [Thesis]. ETH Zürich; 2002. Available from: http://hdl.handle.net/20.500.11850/146896

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


ETH Zürich

14. Moser, Daniela Katrin. Radiosynthese und Tierexperimente mit einem neuen nikotinischen Acetylcholin-Rezeptor-Liganden.

Degree: 2003, ETH Zürich

Subjects/Keywords: REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); CHOLINERGE REZEPTOREN (NEUROLOGIE); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); CHOLINERGIC RECEPTORS (NEUROLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Moser, D. K. (2003). Radiosynthese und Tierexperimente mit einem neuen nikotinischen Acetylcholin-Rezeptor-Liganden. (Thesis). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/147639

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):

Moser, Daniela Katrin. “Radiosynthese und Tierexperimente mit einem neuen nikotinischen Acetylcholin-Rezeptor-Liganden.” 2003. Thesis, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/147639.

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

MLA Handbook (7th Edition):

Moser, Daniela Katrin. “Radiosynthese und Tierexperimente mit einem neuen nikotinischen Acetylcholin-Rezeptor-Liganden.” 2003. Web. 18 Oct 2019.

Vancouver:

Moser DK. Radiosynthese und Tierexperimente mit einem neuen nikotinischen Acetylcholin-Rezeptor-Liganden. [Internet] [Thesis]. ETH Zürich; 2003. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/147639.

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

Council of Science Editors:

Moser DK. Radiosynthese und Tierexperimente mit einem neuen nikotinischen Acetylcholin-Rezeptor-Liganden. [Thesis]. ETH Zürich; 2003. Available from: http://hdl.handle.net/20.500.11850/147639

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

15. HWANG LING CHIN. Development of a fluorescence correlation spectroscopy method for the study of biomolecular interactions.

Degree: 2007, National University of Singapore

Subjects/Keywords: Fluorescence cross-correlation spectroscopy; receptor-ligand binding; streptavidin-biotin; molecular interactions; dual-color; quantum dots

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APA (6th Edition):

CHIN, H. L. (2007). Development of a fluorescence correlation spectroscopy method for the study of biomolecular interactions. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16179

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):

CHIN, HWANG LING. “Development of a fluorescence correlation spectroscopy method for the study of biomolecular interactions.” 2007. Thesis, National University of Singapore. Accessed October 18, 2019. http://scholarbank.nus.edu.sg/handle/10635/16179.

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

MLA Handbook (7th Edition):

CHIN, HWANG LING. “Development of a fluorescence correlation spectroscopy method for the study of biomolecular interactions.” 2007. Web. 18 Oct 2019.

Vancouver:

CHIN HL. Development of a fluorescence correlation spectroscopy method for the study of biomolecular interactions. [Internet] [Thesis]. National University of Singapore; 2007. [cited 2019 Oct 18]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16179.

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

Council of Science Editors:

CHIN HL. Development of a fluorescence correlation spectroscopy method for the study of biomolecular interactions. [Thesis]. National University of Singapore; 2007. Available from: http://scholarbank.nus.edu.sg/handle/10635/16179

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


University of Illinois – Urbana-Champaign

16. Flood, Timothy. Advances in high-throughput screening: better compounds, novel targets, enhanced sensors.

Degree: PhD, 0335, 2013, University of Illinois – Urbana-Champaign

 High throughput screening (HTS) is the dominant force in modern drug discovery. Through the evaluation of large structure collections, novel drug leads can be rapidly… (more)

Subjects/Keywords: high-throughput screening (HTS); drug discovery; natural products; chemical diversity; screening collections; chemoinformatics; cheminformatics; Tanimoto similarity; molecular properties; RNA; RNA binding; myotonic dystrophy; type 1 myotonic dystrophy (DM1); MBNL1; biomolecular interactions; biosensors; protein-ligand interactions; estrogen receptor; estradiol; external cavity laser; photonic crystal; X-linked inhibitor of apoptosis protein (XIAP); SM-164

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APA (6th Edition):

Flood, T. (2013). Advances in high-throughput screening: better compounds, novel targets, enhanced sensors. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/44780

Chicago Manual of Style (16th Edition):

Flood, Timothy. “Advances in high-throughput screening: better compounds, novel targets, enhanced sensors.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 18, 2019. http://hdl.handle.net/2142/44780.

MLA Handbook (7th Edition):

Flood, Timothy. “Advances in high-throughput screening: better compounds, novel targets, enhanced sensors.” 2013. Web. 18 Oct 2019.

Vancouver:

Flood T. Advances in high-throughput screening: better compounds, novel targets, enhanced sensors. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2142/44780.

Council of Science Editors:

Flood T. Advances in high-throughput screening: better compounds, novel targets, enhanced sensors. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/44780


EPFL

17. Piguet, Joachim. Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics.

Degree: 2010, EPFL

 Membrane protein dynamics is of great importance for living organisms. The precise localization of proteins composing a synapse on the membrane facing a nerve terminus… (more)

Subjects/Keywords: fluorescence; microscopy; plasma membrane; membrane proteins; membrane proteins diffusion; single-molecule imaging; single-molecule tracking; pentameric ligand-gated ion channels; nicotinic acetylcholine receptor; serotonin receptor; synapse; neuromuscular junction; post-synaptic scaffold; rapsyn; myopathies; fluorescent proteins; Förster resonance energy transfer; FRET imaging; protein-protein interactions; protein trafficking; photo-activatable proteins; fluorescence; microscopie; membrane plasmique; protéines membranaires; diffusion de protéines membranaires; imagerie de molécules individuelles; suivi de molécules individuelles; canaux pentamèriques déclanchés par un ligand; récepteur nicotinique de l'acétylcholine; récepteur de la sérotonine; synapse; jonction neuromusculaire; structures post-synaptiques; rapsyn; myopathies; protéines fluorescentes; transfert d'énergie par résonance de Förster; imagerie de FRET; interactions protéine-protéine; acheminement de protéines; protéines photo activables

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APA (6th Edition):

Piguet, J. (2010). Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/151503

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):

Piguet, Joachim. “Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics.” 2010. Thesis, EPFL. Accessed October 18, 2019. http://infoscience.epfl.ch/record/151503.

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

MLA Handbook (7th Edition):

Piguet, Joachim. “Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics.” 2010. Web. 18 Oct 2019.

Vancouver:

Piguet J. Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics. [Internet] [Thesis]. EPFL; 2010. [cited 2019 Oct 18]. Available from: http://infoscience.epfl.ch/record/151503.

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

Council of Science Editors:

Piguet J. Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics. [Thesis]. EPFL; 2010. Available from: http://infoscience.epfl.ch/record/151503

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


ETH Zürich

18. Wirz, Christa. Pharmakologie von Liganden für den neuronalen nicotinischen Acetylcholin-Rezeptor: Reinigung, Methylierungen, Affinitätsbestimmungen.

Degree: 2001, ETH Zürich

Subjects/Keywords: ACETYLCHOLIN (NEUROLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); REZEPTOREN (NEUROLOGIE); METHYLIERUNG + DEMETHYLIERUNG (BIOCHEMIE); ACETYLCHOLINE (NEUROLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); RECEPTORS (NEUROLOGY); METHYLATION + DEMETHYLATION (BIOCHEMISTRY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Wirz, C. (2001). Pharmakologie von Liganden für den neuronalen nicotinischen Acetylcholin-Rezeptor: Reinigung, Methylierungen, Affinitätsbestimmungen. (Thesis). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145542

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):

Wirz, Christa. “Pharmakologie von Liganden für den neuronalen nicotinischen Acetylcholin-Rezeptor: Reinigung, Methylierungen, Affinitätsbestimmungen.” 2001. Thesis, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/145542.

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

MLA Handbook (7th Edition):

Wirz, Christa. “Pharmakologie von Liganden für den neuronalen nicotinischen Acetylcholin-Rezeptor: Reinigung, Methylierungen, Affinitätsbestimmungen.” 2001. Web. 18 Oct 2019.

Vancouver:

Wirz C. Pharmakologie von Liganden für den neuronalen nicotinischen Acetylcholin-Rezeptor: Reinigung, Methylierungen, Affinitätsbestimmungen. [Internet] [Thesis]. ETH Zürich; 2001. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/145542.

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

Council of Science Editors:

Wirz C. Pharmakologie von Liganden für den neuronalen nicotinischen Acetylcholin-Rezeptor: Reinigung, Methylierungen, Affinitätsbestimmungen. [Thesis]. ETH Zürich; 2001. Available from: http://hdl.handle.net/20.500.11850/145542

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


ETH Zürich

19. Kessler, Lea Janine. In vitro Charakterisierung eines potentiellen PET-Liganden für den NMDA-Rezeptor: Diplomarbeit.

Degree: 2000, ETH Zürich

Subjects/Keywords: N-METHYL-D-ASPARTATREZEPTOREN, NMDA-REZEPTOREN (NEUROLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); N-METHYL-D-ASPARTATE RECEPTORS, NMDA RECEPTORS (NEUROLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Kessler, L. J. (2000). In vitro Charakterisierung eines potentiellen PET-Liganden für den NMDA-Rezeptor: Diplomarbeit. (Thesis). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145559

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):

Kessler, Lea Janine. “In vitro Charakterisierung eines potentiellen PET-Liganden für den NMDA-Rezeptor: Diplomarbeit.” 2000. Thesis, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/145559.

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

MLA Handbook (7th Edition):

Kessler, Lea Janine. “In vitro Charakterisierung eines potentiellen PET-Liganden für den NMDA-Rezeptor: Diplomarbeit.” 2000. Web. 18 Oct 2019.

Vancouver:

Kessler LJ. In vitro Charakterisierung eines potentiellen PET-Liganden für den NMDA-Rezeptor: Diplomarbeit. [Internet] [Thesis]. ETH Zürich; 2000. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/145559.

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

Council of Science Editors:

Kessler LJ. In vitro Charakterisierung eines potentiellen PET-Liganden für den NMDA-Rezeptor: Diplomarbeit. [Thesis]. ETH Zürich; 2000. Available from: http://hdl.handle.net/20.500.11850/145559

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


ETH Zürich

20. Koller, Daniela. Short N-terminal regions of the calcitonin-like receptor define ligand specificity.

Degree: 2004, ETH Zürich

Subjects/Keywords: CALCITONIN (HORMONE); G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); CALCITONIN (HORMONES); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Koller, D. (2004). Short N-terminal regions of the calcitonin-like receptor define ligand specificity. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/148072

Chicago Manual of Style (16th Edition):

Koller, Daniela. “Short N-terminal regions of the calcitonin-like receptor define ligand specificity.” 2004. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/148072.

MLA Handbook (7th Edition):

Koller, Daniela. “Short N-terminal regions of the calcitonin-like receptor define ligand specificity.” 2004. Web. 18 Oct 2019.

Vancouver:

Koller D. Short N-terminal regions of the calcitonin-like receptor define ligand specificity. [Internet] [Doctoral dissertation]. ETH Zürich; 2004. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/148072.

Council of Science Editors:

Koller D. Short N-terminal regions of the calcitonin-like receptor define ligand specificity. [Doctoral Dissertation]. ETH Zürich; 2004. Available from: http://hdl.handle.net/20.500.11850/148072


ETH Zürich

21. Salonen, Laura Maria. Molecular recognition at the active site of factor Xa.

Degree: 2011, ETH Zürich

Subjects/Keywords: REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); ENZYMINHIBITOREN (BIOCHEMIE); FEINSTRUKTUR VON KRISTALLEN; PEPTIDHYDROLASEN, PROTEASEN (ENZYME); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); ENZYME INHIBITORS (BIOCHEMISTRY); FINE STRUCTURE OF CRYSTALS; PEPTIDE HYDROLASES, PROTEASES (ENZYMES); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Salonen, L. M. (2011). Molecular recognition at the active site of factor Xa. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/153128

Chicago Manual of Style (16th Edition):

Salonen, Laura Maria. “Molecular recognition at the active site of factor Xa.” 2011. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/153128.

MLA Handbook (7th Edition):

Salonen, Laura Maria. “Molecular recognition at the active site of factor Xa.” 2011. Web. 18 Oct 2019.

Vancouver:

Salonen LM. Molecular recognition at the active site of factor Xa. [Internet] [Doctoral dissertation]. ETH Zürich; 2011. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/153128.

Council of Science Editors:

Salonen LM. Molecular recognition at the active site of factor Xa. [Doctoral Dissertation]. ETH Zürich; 2011. Available from: http://hdl.handle.net/20.500.11850/153128


ETH Zürich

22. Stoltz, Moritz. Interactions of the alternative splicing factor RBFOX with non-coding RNAs.

Degree: 2015, ETH Zürich

Subjects/Keywords: RNA-BINDENDE PROTEINE; NICHTCODIERENDE RIBONUKLEINSÄUREN; REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); RNA BINDING PROTEINS; NON-CODING RIBONUCLEIC ACIDS; RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Stoltz, M. (2015). Interactions of the alternative splicing factor RBFOX with non-coding RNAs. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155196

Chicago Manual of Style (16th Edition):

Stoltz, Moritz. “Interactions of the alternative splicing factor RBFOX with non-coding RNAs.” 2015. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/155196.

MLA Handbook (7th Edition):

Stoltz, Moritz. “Interactions of the alternative splicing factor RBFOX with non-coding RNAs.” 2015. Web. 18 Oct 2019.

Vancouver:

Stoltz M. Interactions of the alternative splicing factor RBFOX with non-coding RNAs. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/155196.

Council of Science Editors:

Stoltz M. Interactions of the alternative splicing factor RBFOX with non-coding RNAs. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155196


ETH Zürich

23. Kessler, Lea Janine. Development of novel ligands for PET imaging of the metabotropic glutamate receptor subtype 5 (mGluR5).

Degree: 2004, ETH Zürich

Subjects/Keywords: POSITRONENEMISSIONSTOMOGRAPHIE (MEDIZINISCHE DIAGNOSTIK); METABOTROPE GLUTAMATREZEPTOREN (NEUROLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); POSITRON EMISSION TOMOGRAPHY (MEDICAL DIAGNOSTICS); METABOTROPIC GLUTAMATE RECEPTORS (NEUROLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Kessler, L. J. (2004). Development of novel ligands for PET imaging of the metabotropic glutamate receptor subtype 5 (mGluR5). (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/148318

Chicago Manual of Style (16th Edition):

Kessler, Lea Janine. “Development of novel ligands for PET imaging of the metabotropic glutamate receptor subtype 5 (mGluR5).” 2004. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/148318.

MLA Handbook (7th Edition):

Kessler, Lea Janine. “Development of novel ligands for PET imaging of the metabotropic glutamate receptor subtype 5 (mGluR5).” 2004. Web. 18 Oct 2019.

Vancouver:

Kessler LJ. Development of novel ligands for PET imaging of the metabotropic glutamate receptor subtype 5 (mGluR5). [Internet] [Doctoral dissertation]. ETH Zürich; 2004. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/148318.

Council of Science Editors:

Kessler LJ. Development of novel ligands for PET imaging of the metabotropic glutamate receptor subtype 5 (mGluR5). [Doctoral Dissertation]. ETH Zürich; 2004. Available from: http://hdl.handle.net/20.500.11850/148318

24. Bedi, Shimpi. Identification of Novel Ligands and Structural Requirements for Heterodimerization of the Liver X Receptor Alpha.

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

 LXRs, LXRa (NR1H3) and LXRß (NR1H2), are ligand-activated transcription factors that are members of the nuclear receptor superfamily. Oxysterols and nonsteroidal synthetic compounds bind directly… (more)

Subjects/Keywords: Biochemistry; Biomedical Research; Cellular Biology; Molecular Biology; Liver X Receptor; Peroxisome Proliferator-Activated Receptor; nuclear receptor; transcription factor; oxysterols; fatty acids; molecular docking; protein interface; ligand binding; binding affinities; protein-protein interactions; SREBP-1c; ApoA1

…activity, a strong dimerization interface, and a ligand binding pocket. 5 LIVER X RECEPTOR… …of ligand, the NRs repress transcription via direct interactions with transcriptional co… …x28;23). Allosteric interactions between subunits allow the receptor to function as… …positioned centrally and the ligand-LBP interactions involve residues from helices 3, 5 and 7… …Hydrophobic interactions and hydrogen bonds between the ligand and key residues in the LBP determine… 

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APA (6th Edition):

Bedi, S. (2017). Identification of Novel Ligands and Structural Requirements for Heterodimerization of the Liver X Receptor Alpha. (Doctoral Dissertation). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1495630797912988

Chicago Manual of Style (16th Edition):

Bedi, Shimpi. “Identification of Novel Ligands and Structural Requirements for Heterodimerization of the Liver X Receptor Alpha.” 2017. Doctoral Dissertation, Wright State University. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1495630797912988.

MLA Handbook (7th Edition):

Bedi, Shimpi. “Identification of Novel Ligands and Structural Requirements for Heterodimerization of the Liver X Receptor Alpha.” 2017. Web. 18 Oct 2019.

Vancouver:

Bedi S. Identification of Novel Ligands and Structural Requirements for Heterodimerization of the Liver X Receptor Alpha. [Internet] [Doctoral dissertation]. Wright State University; 2017. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1495630797912988.

Council of Science Editors:

Bedi S. Identification of Novel Ligands and Structural Requirements for Heterodimerization of the Liver X Receptor Alpha. [Doctoral Dissertation]. Wright State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1495630797912988


Vrije Universiteit Amsterdam

25. Kooistra, A.J. In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function .

Degree: 2015, Vrije Universiteit Amsterdam

Subjects/Keywords: GPCRs; virtual screening; membrane proteins; transmembrane proteins; computer-aided drug design; chemogenomics; functional selectivity; histamine receptor; adrenoceptor; antihistamine; site-directed mutagenesis; structure-affinity relationship; protein-ligand interactions; GPCR crystal structures

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APA (6th Edition):

Kooistra, A. J. (2015). In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/52308

Chicago Manual of Style (16th Edition):

Kooistra, A J. “In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function .” 2015. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 18, 2019. http://hdl.handle.net/1871/52308.

MLA Handbook (7th Edition):

Kooistra, A J. “In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function .” 2015. Web. 18 Oct 2019.

Vancouver:

Kooistra AJ. In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1871/52308.

Council of Science Editors:

Kooistra AJ. In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2015. Available from: http://hdl.handle.net/1871/52308


Universitat Pompeu Fabra

26. López Muñoz, Laura. Homology modeling and structural analysis of the antipsychotic drugs receptorome.

Degree: Departament de Ciències Experimentals i de la Salut, 2010, Universitat Pompeu Fabra

 Tradicionalmente se asumía que los fármacos terapéuticamente efectivos actuaban interaccionando con un único receptor. Actualmente está ampliamente reconocido que el efecto farmacológico de la mayoría… (more)

Subjects/Keywords: Receptores acoplados a proteína G (GPCR); Receptor 5-HT2A; Receptor D3; Receptor D2; Ligando; Clozapina; Derivados Benzofuranonas; Risperidona; Olanzapina; esquizofrenia; Derivados Benzofuranonas Derivados Benzolactámico; estudios de relación cuantitativa estructura- acti; Análisis de Componentes Principales (PCA); métodos de regresión; campos de interacción Molecular (MIF); Perfil Multireceptorial; modelado por homología; Docking; sitio de unión; interacciones moleculares; selectividad; afinidad de unión; Diana; Meta-Diana; efectos secundarios; fármaco antipsicótico típico; fármaco antipsicótico atípico; agonista; antagonista; membrana; receptoroma; rhodopsina; estructura de rayos X; descriptores moleculares; farmacología; análisis multivariante; procedimiento integrado; diseño de fármacos asistido por ordenador; Computer-aided drug design; Integrated approach; Multivariate analysis; Pharmacology; Molecular descriptors; X-ray structure; Rhodopsin; Receptorome; Membrane; Antagonist; Agonist; Atypical antipsychotic drug; Typical antipsychotic drug; Side effects; Off-target; Target; Selectivity; Binding affinity; Molecular interactions; Binding site; Homology modeling; Docking; Multireceptor profile; Molecular interaction Field (MIF); Partial Least Squares (PLS); Principal Component Analysis (PCA); 3D Quantitave Structural-Activity-Relationship (3D; Schizophrenia; Benzolactam Derivatives; Benzofuranone Derivatives; Risperidone; Olanzapine; Clozapine; Ligand; Adrenergic receptors; Muscarinic receptors; Histamine receptors; Serotonin receptors; Dopamine receptors; beta2-Adrenergic receptor; D2 receptor; D3 receptor; 5-HT2A receptor; G protein-coupled receptors (GPCR); 57

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

APA (6th Edition):

López Muñoz, L. (2010). Homology modeling and structural analysis of the antipsychotic drugs receptorome. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7228

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):

López Muñoz, Laura. “Homology modeling and structural analysis of the antipsychotic drugs receptorome.” 2010. Thesis, Universitat Pompeu Fabra. Accessed October 18, 2019. http://hdl.handle.net/10803/7228.

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

MLA Handbook (7th Edition):

López Muñoz, Laura. “Homology modeling and structural analysis of the antipsychotic drugs receptorome.” 2010. Web. 18 Oct 2019.

Vancouver:

López Muñoz L. Homology modeling and structural analysis of the antipsychotic drugs receptorome. [Internet] [Thesis]. Universitat Pompeu Fabra; 2010. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10803/7228.

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

Council of Science Editors:

López Muñoz L. Homology modeling and structural analysis of the antipsychotic drugs receptorome. [Thesis]. Universitat Pompeu Fabra; 2010. Available from: http://hdl.handle.net/10803/7228

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


ETH Zürich

27. Cabrele, Chiara. The Neuropeptide Y family: molecular characterization of the multi-ligand/multi-receptor system.

Degree: 1999, ETH Zürich

Subjects/Keywords: NEUROPEPTID-Y-FAMILIE (PEPTIDE); G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); NEUROREZEPTOREN (NEUROLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); AGONISTEN + ANTAGONISTEN (PHARMAKOLOGIE); NEUROPEPTIDE Y FAMILY (PEPTIDES); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); NEURORECEPTORS (NEUROLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); AGONISTS + ANTAGONISTS (PHARMACOLOGY); info:eu-repo/classification/ddc/610; info:eu-repo/classification/ddc/570; Medical sciences, medicine; Life sciences

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

APA (6th Edition):

Cabrele, C. (1999). The Neuropeptide Y family: molecular characterization of the multi-ligand/multi-receptor system. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/144384

Chicago Manual of Style (16th Edition):

Cabrele, Chiara. “The Neuropeptide Y family: molecular characterization of the multi-ligand/multi-receptor system.” 1999. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/144384.

MLA Handbook (7th Edition):

Cabrele, Chiara. “The Neuropeptide Y family: molecular characterization of the multi-ligand/multi-receptor system.” 1999. Web. 18 Oct 2019.

Vancouver:

Cabrele C. The Neuropeptide Y family: molecular characterization of the multi-ligand/multi-receptor system. [Internet] [Doctoral dissertation]. ETH Zürich; 1999. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/144384.

Council of Science Editors:

Cabrele C. The Neuropeptide Y family: molecular characterization of the multi-ligand/multi-receptor system. [Doctoral Dissertation]. ETH Zürich; 1999. Available from: http://hdl.handle.net/20.500.11850/144384


ETH Zürich

28. Gujer, Remo. Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors.

Degree: 2001, ETH Zürich

Subjects/Keywords: CALCITONINGEN-BEZOGENES PEPTID (BIOCHEMIE); G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); GLYKOSYLIERUNGSREAKTIONEN + GLYKOSYLIERUNG (BIOCHEMIE); CALCITONIN GENE-RELATED PEPTIDE (BIOCHEMISTRY); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); GLYCOSYLATION REACTIONS + GLYCOSYLATION (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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

APA (6th Edition):

Gujer, R. (2001). Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145067

Chicago Manual of Style (16th Edition):

Gujer, Remo. “Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors.” 2001. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/145067.

MLA Handbook (7th Edition):

Gujer, Remo. “Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors.” 2001. Web. 18 Oct 2019.

Vancouver:

Gujer R. Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors. [Internet] [Doctoral dissertation]. ETH Zürich; 2001. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/145067.

Council of Science Editors:

Gujer R. Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors. [Doctoral Dissertation]. ETH Zürich; 2001. Available from: http://hdl.handle.net/20.500.11850/145067


ETH Zürich

29. Müller-Steiner, Sarah. Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors.

Degree: 2003, ETH Zürich

Subjects/Keywords: G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); CALCITONINGEN-BEZOGENES PEPTID (BIOCHEMIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); CALCITONIN GENE-RELATED PEPTIDE (BIOCHEMISTRY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/610; Life sciences; Medical sciences, medicine

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

APA (6th Edition):

Müller-Steiner, S. (2003). Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/147770

Chicago Manual of Style (16th Edition):

Müller-Steiner, Sarah. “Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors.” 2003. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/147770.

MLA Handbook (7th Edition):

Müller-Steiner, Sarah. “Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors.” 2003. Web. 18 Oct 2019.

Vancouver:

Müller-Steiner S. Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors. [Internet] [Doctoral dissertation]. ETH Zürich; 2003. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/147770.

Council of Science Editors:

Müller-Steiner S. Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors. [Doctoral Dissertation]. ETH Zürich; 2003. Available from: http://hdl.handle.net/20.500.11850/147770


ETH Zürich

30. Honer, Michael. ³HCGP 61594: the first photoaffinity ligand for a structural analysis and dif ferentiation of the glycine antagonist site of NMDA receptor subtypes.

Degree: 1999, ETH Zürich

Subjects/Keywords: N-METHYL-D-ASPARTATREZEPTOREN, NMDA-REZEPTOREN (NEUROLOGIE); PHOTOAFFINITÄTSMARKIERUNG (BIOLOGIE); BINDUNGSSTELLEN VON REZEPTOREN (MOLEKULARBIOLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); GLYZINREZEPTOREN (NEUROLOGIE); N-METHYL-D-ASPARTATE RECEPTORS, NMDA RECEPTORS (NEUROLOGY); PHOTOAFFINITY LABELLING (BIOLOGY); BINDING SITES OF RECEPTORS (MOLECULAR BIOLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); GLYCINE RECEPTORS (NEUROLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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

APA (6th Edition):

Honer, M. (1999). ³HCGP 61594: the first photoaffinity ligand for a structural analysis and dif ferentiation of the glycine antagonist site of NMDA receptor subtypes. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/144055

Chicago Manual of Style (16th Edition):

Honer, Michael. “³HCGP 61594: the first photoaffinity ligand for a structural analysis and dif ferentiation of the glycine antagonist site of NMDA receptor subtypes.” 1999. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/144055.

MLA Handbook (7th Edition):

Honer, Michael. “³HCGP 61594: the first photoaffinity ligand for a structural analysis and dif ferentiation of the glycine antagonist site of NMDA receptor subtypes.” 1999. Web. 18 Oct 2019.

Vancouver:

Honer M. ³HCGP 61594: the first photoaffinity ligand for a structural analysis and dif ferentiation of the glycine antagonist site of NMDA receptor subtypes. [Internet] [Doctoral dissertation]. ETH Zürich; 1999. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/144055.

Council of Science Editors:

Honer M. ³HCGP 61594: the first photoaffinity ligand for a structural analysis and dif ferentiation of the glycine antagonist site of NMDA receptor subtypes. [Doctoral Dissertation]. ETH Zürich; 1999. Available from: http://hdl.handle.net/20.500.11850/144055

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