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Peter Mundel

Showing results (81-90 of 88) with videos related to

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Diabetes|October 17, 2009
Nephrin is expressed on the surface of insulin vesicles and facilitates glucose-stimulated insulin releaseAlessia Fornoni, Jongmin Jeon, Javier Varona Santos, et al.
Nature Medicine|December 18, 2007
Modification of kidney barrier function by the urokinase receptorChangli Wei, Clemens C Möller, Mehmet M Altintas, et al.
Nature Genetics|June 1, 2005
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal functionJochen Reiser, Krishna R Polu, Clemens C Möller, et al.
The New England Journal of Medicine|November 12, 2013
Abatacept in B7-1-positive proteinuric kidney diseaseChih-Chuan Yu, Alessia Fornoni, Astrid Weins, et al.
Science Advances|July 20, 2022
Transplanted organoids empower human preclinical assessment of drug candidate for the clinicAmy D Westerling-Bui, Eva Maria Fast, Thomas W Soare, et al.
Nature Genetics|July 3, 2007
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyBhaswati Pandit, Anna Sarkozy, Len A Pennacchio, et al.
The Journal of Clinical Investigation|October 12, 2011
FGF23 induces left ventricular hypertrophyChristian Faul, Ansel P Amaral, Behzad Oskouei, et al.
The Journal of Clinical Investigation|May 5, 2011
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F Heeringa, Gil Chernin, Moumita Chaki, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Diabetes|October 17, 2009
Nephrin is expressed on the surface of insulin vesicles and facilitates glucose-stimulated insulin releaseAlessia Fornoni, Jongmin Jeon, Javier Varona Santos, et al.
Nature Medicine|December 18, 2007
Modification of kidney barrier function by the urokinase receptorChangli Wei, Clemens C Möller, Mehmet M Altintas, et al.
Nature Genetics|June 1, 2005
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal functionJochen Reiser, Krishna R Polu, Clemens C Möller, et al.
The New England Journal of Medicine|November 12, 2013
Abatacept in B7-1-positive proteinuric kidney diseaseChih-Chuan Yu, Alessia Fornoni, Astrid Weins, et al.
Science Advances|July 20, 2022
Transplanted organoids empower human preclinical assessment of drug candidate for the clinicAmy D Westerling-Bui, Eva Maria Fast, Thomas W Soare, et al.
Nature Genetics|July 3, 2007
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathyBhaswati Pandit, Anna Sarkozy, Len A Pennacchio, et al.
The Journal of Clinical Investigation|October 12, 2011
FGF23 induces left ventricular hypertrophyChristian Faul, Ansel P Amaral, Behzad Oskouei, et al.
The Journal of Clinical Investigation|May 5, 2011
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F Heeringa, Gil Chernin, Moumita Chaki, et al.
Pageof 9