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Showing results (121-130 of 131) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
A hybrid implementation-effectiveness randomized trial of CYP2D6-guided postoperative pain managementCameron D Thomas, Hari K Parvataneni, Chancellor F Gray, et al.
Human Molecular Genetics|October 29, 2004
A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262LFabrizio de Mattia, Paul J M Savelkoul, Daniel G Bichet, et al.
Diabetologia|April 7, 2017
SUCNR1-mediated chemotaxis of macrophages aggravates obesity-induced inflammation and diabetesJanna A van Diepen, Joris H Robben, Guido J Hooiveld, et al.
American Journal of Physiology. Renal Physiology|May 31, 2018
MicroRNA-132 controls water homeostasis through regulating MECP2-mediated vasopressin synthesisRoel Bijkerk, Christiane Trimpert, Coen van Solingen, et al.
The Journal of Clinical Endocrinology and Metabolism|October 15, 2010
Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous familyEva Morava, Jirko Kühnisch, Jefte M Drijvers, et al.
Frontiers in Endocrinology|March 29, 2021
Succinate Mediates Tumorigenic Effects <i>via</i> Succinate Receptor 1: Potential for New Targeted Treatment Strategies in Succinate Dehydrogenase Deficient ParagangliomasDieter M Matlac, Katerina Hadrava Vanova, Nicole Bechmann, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2002
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidusNannette Marr, Daniel G Bichet, Susan Hoefs, et al.
Human Molecular Genetics|April 2, 2009
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathwaySimon T Cliffe, Jamie M Kramer, Khalid Hussain, et al.
Science (New York, N.Y.)|September 27, 2014
mTOR- and HIF-1α-mediated aerobic glycolysis as metabolic basis for trained immunityShih-Chin Cheng, Jessica Quintin, Robert A Cramer, et al.
Current Biology : CB|November 3, 2020
How the COVID-19 pandemic highlights the necessity of animal researchLisa Genzel, Roger Adan, Anton Berns, et al.
Pageof 14

Showing results (121-130 of 131) with videos related to

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Pageof 14
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
A hybrid implementation-effectiveness randomized trial of CYP2D6-guided postoperative pain managementCameron D Thomas, Hari K Parvataneni, Chancellor F Gray, et al.
Human Molecular Genetics|October 29, 2004
A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262LFabrizio de Mattia, Paul J M Savelkoul, Daniel G Bichet, et al.
Diabetologia|April 7, 2017
SUCNR1-mediated chemotaxis of macrophages aggravates obesity-induced inflammation and diabetesJanna A van Diepen, Joris H Robben, Guido J Hooiveld, et al.
American Journal of Physiology. Renal Physiology|May 31, 2018
MicroRNA-132 controls water homeostasis through regulating MECP2-mediated vasopressin synthesisRoel Bijkerk, Christiane Trimpert, Coen van Solingen, et al.
The Journal of Clinical Endocrinology and Metabolism|October 15, 2010
Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous familyEva Morava, Jirko Kühnisch, Jefte M Drijvers, et al.
Frontiers in Endocrinology|March 29, 2021
Succinate Mediates Tumorigenic Effects <i>via</i> Succinate Receptor 1: Potential for New Targeted Treatment Strategies in Succinate Dehydrogenase Deficient ParagangliomasDieter M Matlac, Katerina Hadrava Vanova, Nicole Bechmann, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2002
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidusNannette Marr, Daniel G Bichet, Susan Hoefs, et al.
Human Molecular Genetics|April 2, 2009
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathwaySimon T Cliffe, Jamie M Kramer, Khalid Hussain, et al.
Science (New York, N.Y.)|September 27, 2014
mTOR- and HIF-1α-mediated aerobic glycolysis as metabolic basis for trained immunityShih-Chin Cheng, Jessica Quintin, Robert A Cramer, et al.
Current Biology : CB|November 3, 2020
How the COVID-19 pandemic highlights the necessity of animal researchLisa Genzel, Roger Adan, Anton Berns, et al.
Pageof 14