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You searched for subject:(Constitutive androstane receptor CAR ). Showing records 1 – 30 of 9156 total matches.

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1. Sberna, Anne-Laure. Etude du rôle du récepteur nucléaire CAR, Constitutive Androstane Receptor, dans le métabolisme des lipides et la susceptibilité à l'athérosclérose : Role of the nuclear receptor CAR, constitutive androstane receptor, in lipoprotein metabolism and atherosclerosis.

Degree: Docteur es, Sciences de l'alimentation, 2011, Université de Bourgogne

 Le récepteur CAR, Constitutive Androstane Receptor, appartient à la-famille NR1 des récepteurs nucléaires. Initialement décrit comme un récepteur orphelin, CAR est en fait activé par… (more)

Subjects/Keywords: CAR (Constitutive Androstane Receptor); (3,3’,5,5’-Tétrachloro-1,4-bis(pyridyloxy)benzene); VLDL récepteur; Triglycérides; Acides biliaires; Athérosclérose; CAR (Constitutive Androstane Receptor); TCPOBOP (3,3',5,5'-Tetrachloro-1,4-bis(pyridyloxy)benzene); VLDL receptor; Triglycerides; Bile acids; Atherosclerosis; 572.4; 612.3; 616.1

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

APA (6th Edition):

Sberna, A. (2011). Etude du rôle du récepteur nucléaire CAR, Constitutive Androstane Receptor, dans le métabolisme des lipides et la susceptibilité à l'athérosclérose : Role of the nuclear receptor CAR, constitutive androstane receptor, in lipoprotein metabolism and atherosclerosis. (Doctoral Dissertation). Université de Bourgogne. Retrieved from http://www.theses.fr/2011DIJOS094

Chicago Manual of Style (16th Edition):

Sberna, Anne-Laure. “Etude du rôle du récepteur nucléaire CAR, Constitutive Androstane Receptor, dans le métabolisme des lipides et la susceptibilité à l'athérosclérose : Role of the nuclear receptor CAR, constitutive androstane receptor, in lipoprotein metabolism and atherosclerosis.” 2011. Doctoral Dissertation, Université de Bourgogne. Accessed January 25, 2021. http://www.theses.fr/2011DIJOS094.

MLA Handbook (7th Edition):

Sberna, Anne-Laure. “Etude du rôle du récepteur nucléaire CAR, Constitutive Androstane Receptor, dans le métabolisme des lipides et la susceptibilité à l'athérosclérose : Role of the nuclear receptor CAR, constitutive androstane receptor, in lipoprotein metabolism and atherosclerosis.” 2011. Web. 25 Jan 2021.

Vancouver:

Sberna A. Etude du rôle du récepteur nucléaire CAR, Constitutive Androstane Receptor, dans le métabolisme des lipides et la susceptibilité à l'athérosclérose : Role of the nuclear receptor CAR, constitutive androstane receptor, in lipoprotein metabolism and atherosclerosis. [Internet] [Doctoral dissertation]. Université de Bourgogne; 2011. [cited 2021 Jan 25]. Available from: http://www.theses.fr/2011DIJOS094.

Council of Science Editors:

Sberna A. Etude du rôle du récepteur nucléaire CAR, Constitutive Androstane Receptor, dans le métabolisme des lipides et la susceptibilité à l'athérosclérose : Role of the nuclear receptor CAR, constitutive androstane receptor, in lipoprotein metabolism and atherosclerosis. [Doctoral Dissertation]. Université de Bourgogne; 2011. Available from: http://www.theses.fr/2011DIJOS094

2. Barretto, Sharon Ann. Etude des interactions bidirectionnelles entre le microbiote intestinal et les récepteurs aux xénobiotiques CAR et PXR : Insights into the bidirectional interactions between the gut microbiota and the xenobiotic receptors CAR and PXR.

Degree: Docteur es, Maladies métaboliques et cardiovasculaires, 2019, Université Toulouse III – Paul Sabatier

Le pregnane X receptor (PXR, NR1I2) et le récepteur constitutif aux androstanes (CAR, NR1I3) sont deux récepteurs nucléaires hépatiques et intestinaux qui régulent la transcription… (more)

Subjects/Keywords: Antibiotiques; Xénobiotiques; Microbiote intestinal; Constitutive androstane receptor; Pregnane X receptor; Antibiotics; Xenobiotics; Gut microbiota; Constitutive androstane receptor; Pregnane X receptor

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APA (6th Edition):

Barretto, S. A. (2019). Etude des interactions bidirectionnelles entre le microbiote intestinal et les récepteurs aux xénobiotiques CAR et PXR : Insights into the bidirectional interactions between the gut microbiota and the xenobiotic receptors CAR and PXR. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2019TOU30233

Chicago Manual of Style (16th Edition):

Barretto, Sharon Ann. “Etude des interactions bidirectionnelles entre le microbiote intestinal et les récepteurs aux xénobiotiques CAR et PXR : Insights into the bidirectional interactions between the gut microbiota and the xenobiotic receptors CAR and PXR.” 2019. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed January 25, 2021. http://www.theses.fr/2019TOU30233.

MLA Handbook (7th Edition):

Barretto, Sharon Ann. “Etude des interactions bidirectionnelles entre le microbiote intestinal et les récepteurs aux xénobiotiques CAR et PXR : Insights into the bidirectional interactions between the gut microbiota and the xenobiotic receptors CAR and PXR.” 2019. Web. 25 Jan 2021.

Vancouver:

Barretto SA. Etude des interactions bidirectionnelles entre le microbiote intestinal et les récepteurs aux xénobiotiques CAR et PXR : Insights into the bidirectional interactions between the gut microbiota and the xenobiotic receptors CAR and PXR. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2019. [cited 2021 Jan 25]. Available from: http://www.theses.fr/2019TOU30233.

Council of Science Editors:

Barretto SA. Etude des interactions bidirectionnelles entre le microbiote intestinal et les récepteurs aux xénobiotiques CAR et PXR : Insights into the bidirectional interactions between the gut microbiota and the xenobiotic receptors CAR and PXR. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2019. Available from: http://www.theses.fr/2019TOU30233

3. Xu, Chenshu. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.

Degree: PhD, Pharmacology & Toxicology, 2011, University of Kansas

 Liver-enriched nuclear receptor (NR) proteins regulate the expression and activity of several pivotal hepatic biochemical pathways including the uptake, metabolism and excretion of cholesterol, bile… (more)

Subjects/Keywords: Pharmacology; Toxicology; Carboxylesterase; Constitutive androstane receptor; Inflammation; Pregnane x receptor; Sumoylation

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APA (6th Edition):

Xu, C. (2011). REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9708

Chicago Manual of Style (16th Edition):

Xu, Chenshu. “REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.” 2011. Doctoral Dissertation, University of Kansas. Accessed January 25, 2021. http://hdl.handle.net/1808/9708.

MLA Handbook (7th Edition):

Xu, Chenshu. “REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.” 2011. Web. 25 Jan 2021.

Vancouver:

Xu C. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1808/9708.

Council of Science Editors:

Xu C. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9708

4. Breuker, Cyril. Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte.

Degree: Docteur es, Sciences du médicament, 2010, Université Montpellier I

CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X Receptor, NR1I2) sont deux récepteurs nucléaires dédiés à la reconna issance et à l'élimination de molécules… (more)

Subjects/Keywords: Récepteur nucléaire; Pregnane X Receptor; Constitutive Androstane Receptor; Métabolisme des médicaments; Perturbateur métabolique; Nuclear receptor; Pregnane X Receptor; Constitutive Androstane Receptor; Drugs metabolism; Metabolic disruptive

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APA (6th Edition):

Breuker, C. (2010). Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2010MON13522

Chicago Manual of Style (16th Edition):

Breuker, Cyril. “Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte.” 2010. Doctoral Dissertation, Université Montpellier I. Accessed January 25, 2021. http://www.theses.fr/2010MON13522.

MLA Handbook (7th Edition):

Breuker, Cyril. “Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte.” 2010. Web. 25 Jan 2021.

Vancouver:

Breuker C. Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte. [Internet] [Doctoral dissertation]. Université Montpellier I; 2010. [cited 2021 Jan 25]. Available from: http://www.theses.fr/2010MON13522.

Council of Science Editors:

Breuker C. Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte. [Doctoral Dissertation]. Université Montpellier I; 2010. Available from: http://www.theses.fr/2010MON13522

5. Leguelinel, Géraldine. Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer.

Degree: Docteur es, Biologie Santé, 2011, Université Montpellier I

Le cancer colorectal est marqué par une importante mortalité dans les stades avancés du fait du fort taux de récidives tumorales après chimiothérapie. La prédiction… (more)

Subjects/Keywords: Xénorécepteurs; Métabolisme intratumoral; Cancer colorectal; Chimiosensibilité; Constitutive Androstane Receptor; Pregnane X Receptor; Xenoreceptors; Intratumoral metabolism; Colorectal cancer; Chemosensibility; Constitutive Androstane Receptor; Pregnane X Receptor

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APA (6th Edition):

Leguelinel, G. (2011). Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2011MON13512

Chicago Manual of Style (16th Edition):

Leguelinel, Géraldine. “Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer.” 2011. Doctoral Dissertation, Université Montpellier I. Accessed January 25, 2021. http://www.theses.fr/2011MON13512.

MLA Handbook (7th Edition):

Leguelinel, Géraldine. “Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer.” 2011. Web. 25 Jan 2021.

Vancouver:

Leguelinel G. Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer. [Internet] [Doctoral dissertation]. Université Montpellier I; 2011. [cited 2021 Jan 25]. Available from: http://www.theses.fr/2011MON13512.

Council of Science Editors:

Leguelinel G. Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer. [Doctoral Dissertation]. Université Montpellier I; 2011. Available from: http://www.theses.fr/2011MON13512

6. Touloupi, Katerina. Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital.

Degree: 2015, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

The magnitude of the genes belonging to the ALDH superfamily in organism’s welfare andespecially their protection against xenobiotics, as well as the accumulating evidence that… (more)

Subjects/Keywords: Αλδεϋδικές αφυδρογονάσες 1Α1 και 1Α7; Πυρηνικοί υποδοχείς; Ιδιοσυστατικός υποδοχέας ανδροστενών; Υποδοχέας πρεγνανίου; φαινοβαρβιτάλη; Καρβονιτρίλιο της πρεγνενολόνης; Μετρήσεις γονιδίου αναφοράς; Δοκιμασίες ανοσοκαθίζησης χρωματίνης; Aldehyde dehydrogenases (ALDHs) 1A1 and 1A7; Nuclear receptors; Constitutive androstane receptor (CAR);

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APA (6th Edition):

Touloupi, K. (2015). Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/43024

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):

Touloupi, Katerina. “Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital.” 2015. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed January 25, 2021. http://hdl.handle.net/10442/hedi/43024.

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

MLA Handbook (7th Edition):

Touloupi, Katerina. “Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital.” 2015. Web. 25 Jan 2021.

Vancouver:

Touloupi K. Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2015. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10442/hedi/43024.

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

Council of Science Editors:

Touloupi K. Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2015. Available from: http://hdl.handle.net/10442/hedi/43024

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

7. Roques, Beatrice. Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat.

Degree: Docteur es, Pathologie, Toxicologie, Génétique et Nutrition, 2012, Toulouse, INSA

Le fipronil, insecticide largement utilisé, est un perturbateur thyroïdien chez le rat modulant le catabolisme hépatique des hormones thyroïdiennes. Ses effets chez le mouton, considéré… (more)

Subjects/Keywords: Perturbateur endocrinien; Fipronil; Fipronil sulfone; Fonction thyroïdienne; Métabolisme hépatique; Rat; Souris transgéniques; Hépatocytes; Constitutive Androstane Receptor; Pregnane X Receptor; Endocrine disruptor; Fipronil; Fipronil sulfone; Thyroid function; Hepatic metabolism; Rat; Transgenic mice; Hepatocytes; Constitutive Androstane Receptor; Pregnane X Receptor; 613

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APA (6th Edition):

Roques, B. (2012). Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat. (Doctoral Dissertation). Toulouse, INSA. Retrieved from http://www.theses.fr/2012ISAT0029

Chicago Manual of Style (16th Edition):

Roques, Beatrice. “Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat.” 2012. Doctoral Dissertation, Toulouse, INSA. Accessed January 25, 2021. http://www.theses.fr/2012ISAT0029.

MLA Handbook (7th Edition):

Roques, Beatrice. “Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat.” 2012. Web. 25 Jan 2021.

Vancouver:

Roques B. Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat. [Internet] [Doctoral dissertation]. Toulouse, INSA; 2012. [cited 2021 Jan 25]. Available from: http://www.theses.fr/2012ISAT0029.

Council of Science Editors:

Roques B. Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat. [Doctoral Dissertation]. Toulouse, INSA; 2012. Available from: http://www.theses.fr/2012ISAT0029


University of Arizona

8. Beilke, Lisa D. Mechanisms of Hepatoprotection in a Murine Model of Bile Acid-Induced Intrahepatic Cholestasis .

Degree: 2008, University of Arizona

 There are many causes of cholestasis, which results when the flow of bile acids is slowed or stopped. Bile acids are hydrophobic molecules synthesized from… (more)

Subjects/Keywords: Cholestasis; bile acid; biosynthesis; apoptosis; constitutive androstane receptor

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APA (6th Edition):

Beilke, L. D. (2008). Mechanisms of Hepatoprotection in a Murine Model of Bile Acid-Induced Intrahepatic Cholestasis . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/194264

Chicago Manual of Style (16th Edition):

Beilke, Lisa D. “Mechanisms of Hepatoprotection in a Murine Model of Bile Acid-Induced Intrahepatic Cholestasis .” 2008. Doctoral Dissertation, University of Arizona. Accessed January 25, 2021. http://hdl.handle.net/10150/194264.

MLA Handbook (7th Edition):

Beilke, Lisa D. “Mechanisms of Hepatoprotection in a Murine Model of Bile Acid-Induced Intrahepatic Cholestasis .” 2008. Web. 25 Jan 2021.

Vancouver:

Beilke LD. Mechanisms of Hepatoprotection in a Murine Model of Bile Acid-Induced Intrahepatic Cholestasis . [Internet] [Doctoral dissertation]. University of Arizona; 2008. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10150/194264.

Council of Science Editors:

Beilke LD. Mechanisms of Hepatoprotection in a Murine Model of Bile Acid-Induced Intrahepatic Cholestasis . [Doctoral Dissertation]. University of Arizona; 2008. Available from: http://hdl.handle.net/10150/194264


Penn State University

9. Zamule, Stephanie M. ROLE OF THE CONSTITUTIVE ANDROSTANE RECEPTOR IN THE DERIVATION OF HEPATIC-LIKE CELLS FROM HUMAN EMBRYONIC STEM CELLS.

Degree: 2010, Penn State University

 The liver performs an array of functions vital to life including detoxification, production of serum proteins, maintenance of cholesterol homeostasis, production and clearance of bile… (more)

Subjects/Keywords: embryonic stem cells; constitutive androstane receptor; liver; differentiation; nuclear receptor; development; lentivirus

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APA (6th Edition):

Zamule, S. M. (2010). ROLE OF THE CONSTITUTIVE ANDROSTANE RECEPTOR IN THE DERIVATION OF HEPATIC-LIKE CELLS FROM HUMAN EMBRYONIC STEM CELLS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10496

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):

Zamule, Stephanie M. “ROLE OF THE CONSTITUTIVE ANDROSTANE RECEPTOR IN THE DERIVATION OF HEPATIC-LIKE CELLS FROM HUMAN EMBRYONIC STEM CELLS.” 2010. Thesis, Penn State University. Accessed January 25, 2021. https://submit-etda.libraries.psu.edu/catalog/10496.

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

MLA Handbook (7th Edition):

Zamule, Stephanie M. “ROLE OF THE CONSTITUTIVE ANDROSTANE RECEPTOR IN THE DERIVATION OF HEPATIC-LIKE CELLS FROM HUMAN EMBRYONIC STEM CELLS.” 2010. Web. 25 Jan 2021.

Vancouver:

Zamule SM. ROLE OF THE CONSTITUTIVE ANDROSTANE RECEPTOR IN THE DERIVATION OF HEPATIC-LIKE CELLS FROM HUMAN EMBRYONIC STEM CELLS. [Internet] [Thesis]. Penn State University; 2010. [cited 2021 Jan 25]. Available from: https://submit-etda.libraries.psu.edu/catalog/10496.

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

Council of Science Editors:

Zamule SM. ROLE OF THE CONSTITUTIVE ANDROSTANE RECEPTOR IN THE DERIVATION OF HEPATIC-LIKE CELLS FROM HUMAN EMBRYONIC STEM CELLS. [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/10496

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


North Carolina State University

10. Jackson, Jonathan Patrick. The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases.

Degree: PhD, Toxicology, 2007, North Carolina State University

 The CYP2C subfamily of cytochrome P450 monoxygenases (P450) is responsible for the metabolism of approximately 20% of therapeutic drugs. Recently, phenytoin has been reported to… (more)

Subjects/Keywords: Cyp2c37; Cyp2c29; Nuclear Receptors; Pregnane X Receptor; Constitutive Androstane Receptor; Phenytoin; Phenobarbital; Drug Induction

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APA (6th Edition):

Jackson, J. P. (2007). The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4828

Chicago Manual of Style (16th Edition):

Jackson, Jonathan Patrick. “The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases.” 2007. Doctoral Dissertation, North Carolina State University. Accessed January 25, 2021. http://www.lib.ncsu.edu/resolver/1840.16/4828.

MLA Handbook (7th Edition):

Jackson, Jonathan Patrick. “The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases.” 2007. Web. 25 Jan 2021.

Vancouver:

Jackson JP. The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases. [Internet] [Doctoral dissertation]. North Carolina State University; 2007. [cited 2021 Jan 25]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4828.

Council of Science Editors:

Jackson JP. The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases. [Doctoral Dissertation]. North Carolina State University; 2007. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4828


University of Kansas

11. Pacyniak, Erik Kristofer. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Polybrominated diphenyl ethers (PBDEs) were introduced in the late 1970's as additive flame retardants incorporated into textiles, electronics, plastics and furniture. Although 2,2',3,3',4,4',5,5',6,6'-decabromodiphenyl ether (BDE209)… (more)

Subjects/Keywords: Toxicology; Constitutive androstane receptor; Nuclear receptors; Organic anion transporting polypeptide; Polybrominated diphenyl ethers; Pregnane x receptor

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APA (6th Edition):

Pacyniak, E. K. (2010). Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7717

Chicago Manual of Style (16th Edition):

Pacyniak, Erik Kristofer. “Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.” 2010. Doctoral Dissertation, University of Kansas. Accessed January 25, 2021. http://hdl.handle.net/1808/7717.

MLA Handbook (7th Edition):

Pacyniak, Erik Kristofer. “Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.” 2010. Web. 25 Jan 2021.

Vancouver:

Pacyniak EK. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1808/7717.

Council of Science Editors:

Pacyniak EK. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7717


University of Queensland

12. Hu, Hao. Transcriptional regulation of human stress responsive cytochrome P450 2A6 (CYP2A6) by p53.

Degree: School of Medicine, 2016, University of Queensland

Subjects/Keywords: Cytochrome P450 2A6 (CYP2A6); Bilirubin (BR); Haem oxygenase1 (HMOX1); Benzo[α]pyrene (BaP); Nuclear factor erythroid 2-like 2 (Nrf-2); Tumour suppressor p53; Constitutive androstane receptor (CAR); CEBP α; Octamer-1 (Oct-1); Hepatocyte nuclear factor-4α (HNF-4α); 060107 Enzymes; 060111 Signal Transduction; 060199 Biochemistry and Cell Biology not elsewhere classified

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APA (6th Edition):

Hu, H. (2016). Transcriptional regulation of human stress responsive cytochrome P450 2A6 (CYP2A6) by p53. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:405743

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):

Hu, Hao. “Transcriptional regulation of human stress responsive cytochrome P450 2A6 (CYP2A6) by p53.” 2016. Thesis, University of Queensland. Accessed January 25, 2021. http://espace.library.uq.edu.au/view/UQ:405743.

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

MLA Handbook (7th Edition):

Hu, Hao. “Transcriptional regulation of human stress responsive cytochrome P450 2A6 (CYP2A6) by p53.” 2016. Web. 25 Jan 2021.

Vancouver:

Hu H. Transcriptional regulation of human stress responsive cytochrome P450 2A6 (CYP2A6) by p53. [Internet] [Thesis]. University of Queensland; 2016. [cited 2021 Jan 25]. Available from: http://espace.library.uq.edu.au/view/UQ:405743.

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

Council of Science Editors:

Hu H. Transcriptional regulation of human stress responsive cytochrome P450 2A6 (CYP2A6) by p53. [Thesis]. University of Queensland; 2016. Available from: http://espace.library.uq.edu.au/view/UQ:405743

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


Penn State University

13. De Keyser, Joshua Gordon. ALTERNATIVE SPLICING OF THE HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR GENE CREATES RECEPTORS WITH UNIQUE FUNCTION AND LIGAND SPECIFICITY .

Degree: 2009, Penn State University

 The human constitutive androstane receptor (CAR) regulates the expression of genes involved in xenobiotic metabolism in the liver. The CAR gene utilizes multiple alternative splicing… (more)

Subjects/Keywords: phthalates; alternative splicing; constitutive androstane receptor; drug and xenobiotic metabolism; meclizine; nuclear receptors; gene induction

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APA (6th Edition):

De Keyser, J. G. (2009). ALTERNATIVE SPLICING OF THE HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR GENE CREATES RECEPTORS WITH UNIQUE FUNCTION AND LIGAND SPECIFICITY . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/9350

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

Chicago Manual of Style (16th Edition):

De Keyser, Joshua Gordon. “ALTERNATIVE SPLICING OF THE HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR GENE CREATES RECEPTORS WITH UNIQUE FUNCTION AND LIGAND SPECIFICITY .” 2009. Thesis, Penn State University. Accessed January 25, 2021. https://submit-etda.libraries.psu.edu/catalog/9350.

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

MLA Handbook (7th Edition):

De Keyser, Joshua Gordon. “ALTERNATIVE SPLICING OF THE HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR GENE CREATES RECEPTORS WITH UNIQUE FUNCTION AND LIGAND SPECIFICITY .” 2009. Web. 25 Jan 2021.

Vancouver:

De Keyser JG. ALTERNATIVE SPLICING OF THE HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR GENE CREATES RECEPTORS WITH UNIQUE FUNCTION AND LIGAND SPECIFICITY . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Jan 25]. Available from: https://submit-etda.libraries.psu.edu/catalog/9350.

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

Council of Science Editors:

De Keyser JG. ALTERNATIVE SPLICING OF THE HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR GENE CREATES RECEPTORS WITH UNIQUE FUNCTION AND LIGAND SPECIFICITY . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/9350

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


University of Melbourne

14. Davenport, Alexander. Investigating the functional biology of chimeric antigen receptor T cells.

Degree: 2017, University of Melbourne

 Despite the success of autologous chimeric antigen receptor (CAR) T cells to treat patients with refractory B cell acute lymphoblastic leukaemia, (ALL) and lymphoma, there… (more)

Subjects/Keywords: immunology; cancer immunology; immunotherapy; cancer; CAR; chimeric antigen receptor; T cell; CAR T cell

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APA (6th Edition):

Davenport, A. (2017). Investigating the functional biology of chimeric antigen receptor T cells. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/137338

Chicago Manual of Style (16th Edition):

Davenport, Alexander. “Investigating the functional biology of chimeric antigen receptor T cells.” 2017. Doctoral Dissertation, University of Melbourne. Accessed January 25, 2021. http://hdl.handle.net/11343/137338.

MLA Handbook (7th Edition):

Davenport, Alexander. “Investigating the functional biology of chimeric antigen receptor T cells.” 2017. Web. 25 Jan 2021.

Vancouver:

Davenport A. Investigating the functional biology of chimeric antigen receptor T cells. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/11343/137338.

Council of Science Editors:

Davenport A. Investigating the functional biology of chimeric antigen receptor T cells. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/137338

15. Fukumasu, Heidge. Sobre os efeitos quimiopreventivos e antitumorais do guaraná, Paullinia cupana Mart var. sorbilis, em modelos experimentais in vivo e in vitro.

Degree: PhD, Patologia Experimental e Comparada, 2008, University of São Paulo

O câncer é a segunda maior causa de morte no Brasil, atrás apenas de doenças cardíacas. Por isto, é evidente que grandes recursos sejam direcionados… (more)

Subjects/Keywords: Biotransformação de xenobióticos; Cancer; Câncer; Cancer Chemoprevention; CAR receptor; Conexina43; Connexin43; guarana; Guaraná; Quimioprevenção do câncer; Receptor CAR; Xenobiotic metabolism

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APA (6th Edition):

Fukumasu, H. (2008). Sobre os efeitos quimiopreventivos e antitumorais do guaraná, Paullinia cupana Mart var. sorbilis, em modelos experimentais in vivo e in vitro. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10133/tde-30042009-162117/ ;

Chicago Manual of Style (16th Edition):

Fukumasu, Heidge. “Sobre os efeitos quimiopreventivos e antitumorais do guaraná, Paullinia cupana Mart var. sorbilis, em modelos experimentais in vivo e in vitro.” 2008. Doctoral Dissertation, University of São Paulo. Accessed January 25, 2021. http://www.teses.usp.br/teses/disponiveis/10/10133/tde-30042009-162117/ ;.

MLA Handbook (7th Edition):

Fukumasu, Heidge. “Sobre os efeitos quimiopreventivos e antitumorais do guaraná, Paullinia cupana Mart var. sorbilis, em modelos experimentais in vivo e in vitro.” 2008. Web. 25 Jan 2021.

Vancouver:

Fukumasu H. Sobre os efeitos quimiopreventivos e antitumorais do guaraná, Paullinia cupana Mart var. sorbilis, em modelos experimentais in vivo e in vitro. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2021 Jan 25]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10133/tde-30042009-162117/ ;.

Council of Science Editors:

Fukumasu H. Sobre os efeitos quimiopreventivos e antitumorais do guaraná, Paullinia cupana Mart var. sorbilis, em modelos experimentais in vivo e in vitro. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/10/10133/tde-30042009-162117/ ;


McMaster University

16. Hammill, Joanne. PRE-CLINICAL DEVELOPMENT OF SYNTHETIC RECEPTOR-ENGINEERED T LYMPHOCYTES FOR THE TREATMENT OF CANCER: NOVEL RECEPTORS AND UNDERSTANDING TOXICITY.

Degree: PhD, 2018, McMaster University

Advances in our understanding of the molecular events leading to cancer have facilitated the development of next-generation targeted therapies. Among the most promising new approaches… (more)

Subjects/Keywords: Immunology; Immuno-oncology; Chimeric antigen receptor; CAR-T cells

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APA (6th Edition):

Hammill, J. (2018). PRE-CLINICAL DEVELOPMENT OF SYNTHETIC RECEPTOR-ENGINEERED T LYMPHOCYTES FOR THE TREATMENT OF CANCER: NOVEL RECEPTORS AND UNDERSTANDING TOXICITY. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22904

Chicago Manual of Style (16th Edition):

Hammill, Joanne. “PRE-CLINICAL DEVELOPMENT OF SYNTHETIC RECEPTOR-ENGINEERED T LYMPHOCYTES FOR THE TREATMENT OF CANCER: NOVEL RECEPTORS AND UNDERSTANDING TOXICITY.” 2018. Doctoral Dissertation, McMaster University. Accessed January 25, 2021. http://hdl.handle.net/11375/22904.

MLA Handbook (7th Edition):

Hammill, Joanne. “PRE-CLINICAL DEVELOPMENT OF SYNTHETIC RECEPTOR-ENGINEERED T LYMPHOCYTES FOR THE TREATMENT OF CANCER: NOVEL RECEPTORS AND UNDERSTANDING TOXICITY.” 2018. Web. 25 Jan 2021.

Vancouver:

Hammill J. PRE-CLINICAL DEVELOPMENT OF SYNTHETIC RECEPTOR-ENGINEERED T LYMPHOCYTES FOR THE TREATMENT OF CANCER: NOVEL RECEPTORS AND UNDERSTANDING TOXICITY. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/11375/22904.

Council of Science Editors:

Hammill J. PRE-CLINICAL DEVELOPMENT OF SYNTHETIC RECEPTOR-ENGINEERED T LYMPHOCYTES FOR THE TREATMENT OF CANCER: NOVEL RECEPTORS AND UNDERSTANDING TOXICITY. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/22904


University of Melbourne

17. Mills, Jane Kathleen. Combining TIL and CAR for adoptive cell therapy in metastatic melanoma.

Degree: 2019, University of Melbourne

 Background Metastatic melanoma is a highly lethal disease, and until recently patients had limited therapeutic options. Knowledge and understanding of the role the immune system… (more)

Subjects/Keywords: melanoma; metastatic; adoptive cell therapy; ACT; chimeric antigen receptor; CAR; immunotherapy

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APA (6th Edition):

Mills, J. K. (2019). Combining TIL and CAR for adoptive cell therapy in metastatic melanoma. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/228933

Chicago Manual of Style (16th Edition):

Mills, Jane Kathleen. “Combining TIL and CAR for adoptive cell therapy in metastatic melanoma.” 2019. Masters Thesis, University of Melbourne. Accessed January 25, 2021. http://hdl.handle.net/11343/228933.

MLA Handbook (7th Edition):

Mills, Jane Kathleen. “Combining TIL and CAR for adoptive cell therapy in metastatic melanoma.” 2019. Web. 25 Jan 2021.

Vancouver:

Mills JK. Combining TIL and CAR for adoptive cell therapy in metastatic melanoma. [Internet] [Masters thesis]. University of Melbourne; 2019. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/11343/228933.

Council of Science Editors:

Mills JK. Combining TIL and CAR for adoptive cell therapy in metastatic melanoma. [Masters Thesis]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/228933


Wright State University

18. Kolawole, Abimbola Olayinka. The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1.

Degree: PhD, Biomedical Sciences PhD, 2011, Wright State University

 A major factor in virus entry into cells is localization and abundance of the primary receptor. The Coxsackievirus and adenovirus receptor (CAR) is the primary… (more)

Subjects/Keywords: Biomedical Research; coxsackievirus and adenovirus receptor; CAR; MAGI-1; adenovirus; epithelia

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APA (6th Edition):

Kolawole, A. O. (2011). The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1. (Doctoral Dissertation). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325

Chicago Manual of Style (16th Edition):

Kolawole, Abimbola Olayinka. “The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1.” 2011. Doctoral Dissertation, Wright State University. Accessed January 25, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325.

MLA Handbook (7th Edition):

Kolawole, Abimbola Olayinka. “The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1.” 2011. Web. 25 Jan 2021.

Vancouver:

Kolawole AO. The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1. [Internet] [Doctoral dissertation]. Wright State University; 2011. [cited 2021 Jan 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325.

Council of Science Editors:

Kolawole AO. The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1. [Doctoral Dissertation]. Wright State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325


University of Georgia

19. Meehan, Thomas Paul. In vivo consequences of the expression of constitutively active luteinizing hormone receptors.

Degree: 2014, University of Georgia

 Luteinizing hormone (LH) is critical for reproduction in mammals. Its activity is delineated through the signaling of a member of the G-protein coupled receptor superfamily,… (more)

Subjects/Keywords: Luteinizing hormone; Chorionic gonadotropin; Luteinizing hormone receptor; Precocious puberty; Constitutive activity; Transgenic mice; Tetracycline-regulated

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APA (6th Edition):

Meehan, T. P. (2014). In vivo consequences of the expression of constitutively active luteinizing hormone receptors. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/21115

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):

Meehan, Thomas Paul. “In vivo consequences of the expression of constitutively active luteinizing hormone receptors.” 2014. Thesis, University of Georgia. Accessed January 25, 2021. http://hdl.handle.net/10724/21115.

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

MLA Handbook (7th Edition):

Meehan, Thomas Paul. “In vivo consequences of the expression of constitutively active luteinizing hormone receptors.” 2014. Web. 25 Jan 2021.

Vancouver:

Meehan TP. In vivo consequences of the expression of constitutively active luteinizing hormone receptors. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/10724/21115.

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

Council of Science Editors:

Meehan TP. In vivo consequences of the expression of constitutively active luteinizing hormone receptors. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/21115

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


University of Pennsylvania

20. Klichinsky, Michael. Human Chimeric Antigen Receptor Macrophages For Cancer Immunotherapy.

Degree: 2018, University of Pennsylvania

 Despite recent landmark advances in chimeric antigen receptor (CAR) T cell immunotherapy for the treatment of human cancer, metastatic solid tumors remain an intractable challenge.… (more)

Subjects/Keywords: car macrophage; chimeric antigen receptor; chimeric antigen receptor macrophage; macrophage; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology; Pharmacology

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APA (6th Edition):

Klichinsky, M. (2018). Human Chimeric Antigen Receptor Macrophages For Cancer Immunotherapy. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3137

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):

Klichinsky, Michael. “Human Chimeric Antigen Receptor Macrophages For Cancer Immunotherapy.” 2018. Thesis, University of Pennsylvania. Accessed January 25, 2021. https://repository.upenn.edu/edissertations/3137.

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

MLA Handbook (7th Edition):

Klichinsky, Michael. “Human Chimeric Antigen Receptor Macrophages For Cancer Immunotherapy.” 2018. Web. 25 Jan 2021.

Vancouver:

Klichinsky M. Human Chimeric Antigen Receptor Macrophages For Cancer Immunotherapy. [Internet] [Thesis]. University of Pennsylvania; 2018. [cited 2021 Jan 25]. Available from: https://repository.upenn.edu/edissertations/3137.

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

Council of Science Editors:

Klichinsky M. Human Chimeric Antigen Receptor Macrophages For Cancer Immunotherapy. [Thesis]. University of Pennsylvania; 2018. Available from: https://repository.upenn.edu/edissertations/3137

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


University of Manchester

21. Campion, Katherine. Characterisation of calcium-sensing receptor extracellular pH sensitivity and intracellular signal integration.

Degree: PhD, 2013, University of Manchester

 Parathyroid hormone (PTH) secretion maintains free-ionised extracellular calcium (Ca2+o) homeostasis under the control of the calcium-sensing receptor (CaR). In humans and dogs, blood acidosis and… (more)

Subjects/Keywords: 612.4; Calcium sensing-receptor; GCPR; calcium homeostasis; cAMP; pH; proton; intracellular signalling; CaSR; CaR

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APA (6th Edition):

Campion, K. (2013). Characterisation of calcium-sensing receptor extracellular pH sensitivity and intracellular signal integration. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-calciumsensing-receptor-extracellular-ph-sensitivity-and-intracellular-signal-integration(e11adf01-4748-42ed-8679-f8b990d79dea).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632201

Chicago Manual of Style (16th Edition):

Campion, Katherine. “Characterisation of calcium-sensing receptor extracellular pH sensitivity and intracellular signal integration.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 25, 2021. https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-calciumsensing-receptor-extracellular-ph-sensitivity-and-intracellular-signal-integration(e11adf01-4748-42ed-8679-f8b990d79dea).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632201.

MLA Handbook (7th Edition):

Campion, Katherine. “Characterisation of calcium-sensing receptor extracellular pH sensitivity and intracellular signal integration.” 2013. Web. 25 Jan 2021.

Vancouver:

Campion K. Characterisation of calcium-sensing receptor extracellular pH sensitivity and intracellular signal integration. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Jan 25]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-calciumsensing-receptor-extracellular-ph-sensitivity-and-intracellular-signal-integration(e11adf01-4748-42ed-8679-f8b990d79dea).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632201.

Council of Science Editors:

Campion K. Characterisation of calcium-sensing receptor extracellular pH sensitivity and intracellular signal integration. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-calciumsensing-receptor-extracellular-ph-sensitivity-and-intracellular-signal-integration(e11adf01-4748-42ed-8679-f8b990d79dea).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632201


Wright State University

22. Brockman, Trisha Lynn. Binding and entry mechanisms of adenovirus in polarized epithelial cells.

Degree: MS, Biological Sciences, 2014, Wright State University

 Adenovirus’s primary receptor, the Coxsackievirus and adenovirus receptor (CAR), has two transmembrane isoforms with differential localization within polarized epithelial cells (CAREx7 (basolateral), CAREx8 (apical)). I… (more)

Subjects/Keywords: Biochemistry; Biology; Cellular Biology; Adenovirus; CAR; Coxsackievirus and adenovirus receptor; Src-family kinases; Half-life

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APA (6th Edition):

Brockman, T. L. (2014). Binding and entry mechanisms of adenovirus in polarized epithelial cells. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1410214584

Chicago Manual of Style (16th Edition):

Brockman, Trisha Lynn. “Binding and entry mechanisms of adenovirus in polarized epithelial cells.” 2014. Masters Thesis, Wright State University. Accessed January 25, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=wright1410214584.

MLA Handbook (7th Edition):

Brockman, Trisha Lynn. “Binding and entry mechanisms of adenovirus in polarized epithelial cells.” 2014. Web. 25 Jan 2021.

Vancouver:

Brockman TL. Binding and entry mechanisms of adenovirus in polarized epithelial cells. [Internet] [Masters thesis]. Wright State University; 2014. [cited 2021 Jan 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1410214584.

Council of Science Editors:

Brockman TL. Binding and entry mechanisms of adenovirus in polarized epithelial cells. [Masters Thesis]. Wright State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1410214584


University of Edinburgh

23. O'Neill, Nathanael. Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells.

Degree: PhD, 2020, University of Edinburgh

 GABAA receptors (GABAARs) are the principal inhibitory neurotransmitter receptors in the adult mammalian central nervous system. GABAARs mediate two forms of inhibition: fast, phasic conductance;… (more)

Subjects/Keywords: GABAergic; GABAA Receptor; GABA; Interneuron; hippocampus; electrophysiology; patch-clamp; LTP; benzodiazepine; spontaneous activity; constitutive activity; epilepsy

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APA (6th Edition):

O'Neill, N. (2020). Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/37176

Chicago Manual of Style (16th Edition):

O'Neill, Nathanael. “Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells.” 2020. Doctoral Dissertation, University of Edinburgh. Accessed January 25, 2021. http://hdl.handle.net/1842/37176.

MLA Handbook (7th Edition):

O'Neill, Nathanael. “Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells.” 2020. Web. 25 Jan 2021.

Vancouver:

O'Neill N. Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2020. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1842/37176.

Council of Science Editors:

O'Neill N. Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells. [Doctoral Dissertation]. University of Edinburgh; 2020. Available from: http://hdl.handle.net/1842/37176


University of Edinburgh

24. O'Neill, Nathanael. Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells.

Degree: PhD, 2020, University of Edinburgh

 GABAA receptors (GABAARs) are the principal inhibitory neurotransmitter receptors in the adult mammalian central nervous system. GABAARs mediate two forms of inhibition: fast, phasic conductance;… (more)

Subjects/Keywords: GABAergic; GABAA Receptor; GABA; Interneuron; hippocampus; electrophysiology; patch-clamp; LTP; benzodiazepine; spontaneous activity; constitutive activity; epilepsy

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APA (6th Edition):

O'Neill, N. (2020). Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from https://doi.org/10.7488/era/477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810231

Chicago Manual of Style (16th Edition):

O'Neill, Nathanael. “Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells.” 2020. Doctoral Dissertation, University of Edinburgh. Accessed January 25, 2021. https://doi.org/10.7488/era/477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810231.

MLA Handbook (7th Edition):

O'Neill, Nathanael. “Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells.” 2020. Web. 25 Jan 2021.

Vancouver:

O'Neill N. Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2020. [cited 2021 Jan 25]. Available from: https://doi.org/10.7488/era/477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810231.

Council of Science Editors:

O'Neill N. Functional characterisation of spontaneously active GABAA receptors in rat dentate gyrus granule cells. [Doctoral Dissertation]. University of Edinburgh; 2020. Available from: https://doi.org/10.7488/era/477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810231

25. Li, Qilan. Constitutive receptor activation and pharmacological modeling: the adenosine A2b receptor as a prototype.

Degree: 2008, Leiden/Amsterdam Center for Drug Research, LACDR, Faculty of Science, Leiden University

 In this thesis a combined approach is described to investigate the constitutive activity of G protein protein-coupled receptors (GPCRs) using human adenosine A2B receptors and… (more)

Subjects/Keywords: Constitutive receptor activation; Pharmacological modeling; Adenosine A2B receptor; Inverse agonist; Allosteric modulation; Constitutive receptor activation; Pharmacological modeling; Adenosine A2B receptor; Inverse agonist; Allosteric modulation

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APA (6th Edition):

Li, Q. (2008). Constitutive receptor activation and pharmacological modeling: the adenosine A2b receptor as a prototype. (Doctoral Dissertation). Leiden/Amsterdam Center for Drug Research, LACDR, Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/13396

Chicago Manual of Style (16th Edition):

Li, Qilan. “Constitutive receptor activation and pharmacological modeling: the adenosine A2b receptor as a prototype.” 2008. Doctoral Dissertation, Leiden/Amsterdam Center for Drug Research, LACDR, Faculty of Science, Leiden University. Accessed January 25, 2021. http://hdl.handle.net/1887/13396.

MLA Handbook (7th Edition):

Li, Qilan. “Constitutive receptor activation and pharmacological modeling: the adenosine A2b receptor as a prototype.” 2008. Web. 25 Jan 2021.

Vancouver:

Li Q. Constitutive receptor activation and pharmacological modeling: the adenosine A2b receptor as a prototype. [Internet] [Doctoral dissertation]. Leiden/Amsterdam Center for Drug Research, LACDR, Faculty of Science, Leiden University; 2008. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1887/13396.

Council of Science Editors:

Li Q. Constitutive receptor activation and pharmacological modeling: the adenosine A2b receptor as a prototype. [Doctoral Dissertation]. Leiden/Amsterdam Center for Drug Research, LACDR, Faculty of Science, Leiden University; 2008. Available from: http://hdl.handle.net/1887/13396


UCLA

26. Lorenzini, Michael Hideo. Engineering Robust T-Cell Response Against Immunosuppressive Tumors.

Degree: Bioengineering, 2016, UCLA

 With the establishment of clinically effective adoptive T-cell therapy for metastatic cancer, efforts are growing to advance T-cell therapy for new indications, especially solid tumors.… (more)

Subjects/Keywords: Immunology; Biomedical engineering; Molecular biology; Adoptive cell therapy; Cancer immunosuppression; Cancer immunotherapy; CAR-T cells; Chimeric antigen receptor; TGF beta

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APA (6th Edition):

Lorenzini, M. H. (2016). Engineering Robust T-Cell Response Against Immunosuppressive Tumors. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/26h6c920

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):

Lorenzini, Michael Hideo. “Engineering Robust T-Cell Response Against Immunosuppressive Tumors.” 2016. Thesis, UCLA. Accessed January 25, 2021. http://www.escholarship.org/uc/item/26h6c920.

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

MLA Handbook (7th Edition):

Lorenzini, Michael Hideo. “Engineering Robust T-Cell Response Against Immunosuppressive Tumors.” 2016. Web. 25 Jan 2021.

Vancouver:

Lorenzini MH. Engineering Robust T-Cell Response Against Immunosuppressive Tumors. [Internet] [Thesis]. UCLA; 2016. [cited 2021 Jan 25]. Available from: http://www.escholarship.org/uc/item/26h6c920.

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

Council of Science Editors:

Lorenzini MH. Engineering Robust T-Cell Response Against Immunosuppressive Tumors. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/26h6c920

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


University of California – San Diego

27. Allen, Molly Elizabeth. Using Light to Improve CAR T Cell Immunotherapy Development and Applications.

Degree: Bioengineering, 2019, University of California – San Diego

 Cancer is the second-leading cause of death worldwide. Over the past two decades, chimeric antigen receptor (CAR) T cell therapy has emerged as a promising… (more)

Subjects/Keywords: Bioengineering; Molecular biology; Biomedical engineering; Biosensor; Chimeric Antigen Receptor (CAR); Immunotherapy; Optogenetics; Synthetic Biology; T cell

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APA (6th Edition):

Allen, M. E. (2019). Using Light to Improve CAR T Cell Immunotherapy Development and Applications. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/8bk4w5hc

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):

Allen, Molly Elizabeth. “Using Light to Improve CAR T Cell Immunotherapy Development and Applications.” 2019. Thesis, University of California – San Diego. Accessed January 25, 2021. http://www.escholarship.org/uc/item/8bk4w5hc.

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

MLA Handbook (7th Edition):

Allen, Molly Elizabeth. “Using Light to Improve CAR T Cell Immunotherapy Development and Applications.” 2019. Web. 25 Jan 2021.

Vancouver:

Allen ME. Using Light to Improve CAR T Cell Immunotherapy Development and Applications. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2021 Jan 25]. Available from: http://www.escholarship.org/uc/item/8bk4w5hc.

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

Council of Science Editors:

Allen ME. Using Light to Improve CAR T Cell Immunotherapy Development and Applications. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/8bk4w5hc

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


University of Pennsylvania

28. Lo, Albert. Finding Common Ground to Treat Primary and Metastatic Cancer: The Potential of Targeting Tumor Stroma.

Degree: 2016, University of Pennsylvania

 Primary carcinomas and metastases are complex organ-like structures composed of malignant parenchymal epithelial tissues and a desmoplastic stroma formed by accumulation of hematopoietic cells, mesenchymal… (more)

Subjects/Keywords: Cancer-associated fibroblasts (CAFs); Chimeric antigen receptor (CAR) T cells; Fibroblast activation protein (FAP); Tumor microenvironment; Oncology

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APA (6th Edition):

Lo, A. (2016). Finding Common Ground to Treat Primary and Metastatic Cancer: The Potential of Targeting Tumor Stroma. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1862

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):

Lo, Albert. “Finding Common Ground to Treat Primary and Metastatic Cancer: The Potential of Targeting Tumor Stroma.” 2016. Thesis, University of Pennsylvania. Accessed January 25, 2021. https://repository.upenn.edu/edissertations/1862.

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

MLA Handbook (7th Edition):

Lo, Albert. “Finding Common Ground to Treat Primary and Metastatic Cancer: The Potential of Targeting Tumor Stroma.” 2016. Web. 25 Jan 2021.

Vancouver:

Lo A. Finding Common Ground to Treat Primary and Metastatic Cancer: The Potential of Targeting Tumor Stroma. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2021 Jan 25]. Available from: https://repository.upenn.edu/edissertations/1862.

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

Council of Science Editors:

Lo A. Finding Common Ground to Treat Primary and Metastatic Cancer: The Potential of Targeting Tumor Stroma. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/1862

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

29. Peeters, Miriam Cornelia. Activation of G protein-coupled receptors: the role of extracellular loops in adenosine receptors.

Degree: 2011, Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University

 The research described in this thesis has provided new insights in the activation mechanism of class A GPCRs and in particular of adenosine receptors. By… (more)

Subjects/Keywords: Adenosine receptors; Constitutive activity; Extracellular loops; G protein-coupled receptor; Mutagenesis; Receptor activation and inactivation; S. cerevisiae; Adenosine receptors; Constitutive activity; Extracellular loops; G protein-coupled receptor; Mutagenesis; Receptor activation and inactivation; S. cerevisiae

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APA (6th Edition):

Peeters, M. C. (2011). Activation of G protein-coupled receptors: the role of extracellular loops in adenosine receptors. (Doctoral Dissertation). Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University. Retrieved from http://hdl.handle.net/1887/18092

Chicago Manual of Style (16th Edition):

Peeters, Miriam Cornelia. “Activation of G protein-coupled receptors: the role of extracellular loops in adenosine receptors.” 2011. Doctoral Dissertation, Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University. Accessed January 25, 2021. http://hdl.handle.net/1887/18092.

MLA Handbook (7th Edition):

Peeters, Miriam Cornelia. “Activation of G protein-coupled receptors: the role of extracellular loops in adenosine receptors.” 2011. Web. 25 Jan 2021.

Vancouver:

Peeters MC. Activation of G protein-coupled receptors: the role of extracellular loops in adenosine receptors. [Internet] [Doctoral dissertation]. Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University; 2011. [cited 2021 Jan 25]. Available from: http://hdl.handle.net/1887/18092.

Council of Science Editors:

Peeters MC. Activation of G protein-coupled receptors: the role of extracellular loops in adenosine receptors. [Doctoral Dissertation]. Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University; 2011. Available from: http://hdl.handle.net/1887/18092


Texas Medical Center

30. Crossland, Denise L. CD56-SPECIFIC T CELLS: USING GENETICALLY ENGINEERED T CELLS TO REDIRECT SPECIFICITY TO A T CELL EXPRESSED ANTIGEN.

Degree: PhD, 2014, Texas Medical Center

  The CD56 antigen is expressed on several deadly malignancies currently lacking long-term efficacious therapies. Chimeric antigen receptor (CAR) based immunotherapies have shown both safety… (more)

Subjects/Keywords: Chimeric Antigen Receptor; CAR; Neural Cell Adhesion Molecule; NCAM; CD56; Fratricide; Autolysis; T cell immunotherapy; self-targeting; CD56CAR; Cancer Biology; Medicine and Health Sciences

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APA (6th Edition):

Crossland, D. L. (2014). CD56-SPECIFIC T CELLS: USING GENETICALLY ENGINEERED T CELLS TO REDIRECT SPECIFICITY TO A T CELL EXPRESSED ANTIGEN. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/493

Chicago Manual of Style (16th Edition):

Crossland, Denise L. “CD56-SPECIFIC T CELLS: USING GENETICALLY ENGINEERED T CELLS TO REDIRECT SPECIFICITY TO A T CELL EXPRESSED ANTIGEN.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed January 25, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/493.

MLA Handbook (7th Edition):

Crossland, Denise L. “CD56-SPECIFIC T CELLS: USING GENETICALLY ENGINEERED T CELLS TO REDIRECT SPECIFICITY TO A T CELL EXPRESSED ANTIGEN.” 2014. Web. 25 Jan 2021.

Vancouver:

Crossland DL. CD56-SPECIFIC T CELLS: USING GENETICALLY ENGINEERED T CELLS TO REDIRECT SPECIFICITY TO A T CELL EXPRESSED ANTIGEN. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2021 Jan 25]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/493.

Council of Science Editors:

Crossland DL. CD56-SPECIFIC T CELLS: USING GENETICALLY ENGINEERED T CELLS TO REDIRECT SPECIFICITY TO A T CELL EXPRESSED ANTIGEN. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/493

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