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Wuttke

Showing results (771-780 of 814) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 1, 2015
Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression ConsortiumMatthias Wuttke, Craig S Wong, Elke Wühl, et al.
BMC Cancer|August 19, 2021
MONARCC: a randomised phase II study of panitumumab monotherapy and panitumumab plus 5-fluorouracil as first-line therapy for RAS and BRAF wildtype metastatic colorectal cancer: a study by the Australasian Gastrointestinal Trials Group (AGITG)Ho Wai Derrick Siu, Niall Tebbutt, Lorraine Chantrill, et al.
Journal of Neurophysiology|February 27, 2025
Comprehensive analysis of human dendritic spine morphology and densityKerstin D Schünemann, Roxanne M Hattingh, Matthijs B Verhoog, et al.
Trials|March 19, 2026
Protocol of a dyadic, app-supported collaborative care intervention trial for informal caregivers of people living with dementia-the multi-center living@home studyEva Gläser, Fabian Kleinke, Milena Armanowski, et al.
Elife|May 8, 2020
Spen links RNA-mediated endogenous retrovirus silencing and X chromosome inactivationAva C Carter, Jin Xu, Meagan Y Nakamoto, et al.
Nature Genetics|January 22, 2020
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humansPascal Schlosser, Yong Li, Peggy Sekula, et al.
Nature Communications|July 17, 2021
Discovery and prioritization of variants and genes for kidney function in >1.2 million individualsKira J Stanzick, Yong Li, Pascal Schlosser, et al.
Immunity|March 31, 2021
Single-cell chromatin accessibility landscape identifies tissue repair program in human regulatory T cellsMichael Delacher, Malte Simon, Lieke Sanderink, et al.
Nature Genetics|January 2, 2025
Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traitsNora Scherer, Daniel Fässler, Oleg Borisov, et al.
The Journal of Clinical Investigation|May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leakYvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Pageof 82

Showing results (771-780 of 814) with videos related to

Sort By:
Pageof 82
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 1, 2015
Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression ConsortiumMatthias Wuttke, Craig S Wong, Elke Wühl, et al.
BMC Cancer|August 19, 2021
MONARCC: a randomised phase II study of panitumumab monotherapy and panitumumab plus 5-fluorouracil as first-line therapy for RAS and BRAF wildtype metastatic colorectal cancer: a study by the Australasian Gastrointestinal Trials Group (AGITG)Ho Wai Derrick Siu, Niall Tebbutt, Lorraine Chantrill, et al.
Journal of Neurophysiology|February 27, 2025
Comprehensive analysis of human dendritic spine morphology and densityKerstin D Schünemann, Roxanne M Hattingh, Matthijs B Verhoog, et al.
Trials|March 19, 2026
Protocol of a dyadic, app-supported collaborative care intervention trial for informal caregivers of people living with dementia-the multi-center living@home studyEva Gläser, Fabian Kleinke, Milena Armanowski, et al.
Elife|May 8, 2020
Spen links RNA-mediated endogenous retrovirus silencing and X chromosome inactivationAva C Carter, Jin Xu, Meagan Y Nakamoto, et al.
Nature Genetics|January 22, 2020
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humansPascal Schlosser, Yong Li, Peggy Sekula, et al.
Nature Communications|July 17, 2021
Discovery and prioritization of variants and genes for kidney function in >1.2 million individualsKira J Stanzick, Yong Li, Pascal Schlosser, et al.
Immunity|March 31, 2021
Single-cell chromatin accessibility landscape identifies tissue repair program in human regulatory T cellsMichael Delacher, Malte Simon, Lieke Sanderink, et al.
Nature Genetics|January 2, 2025
Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traitsNora Scherer, Daniel Fässler, Oleg Borisov, et al.
The Journal of Clinical Investigation|May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leakYvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Pageof 82