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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Adrian S Woolf

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022

Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.

Nature Communications|November 24, 2018

Molecular insights into genome-wide association studies of chronic kidney disease-defining traitsXiaoguang Xu, James M Eales, Artur Akbarov, et al.

Journal of the American Society of Nephrology : JASN|April 25, 2009

HNF1B mutations associate with hypomagnesemia and renal magnesium wastingShazia Adalat, Adrian S Woolf, Karen A Johnstone, et al.

The Journal of Clinical Investigation|September 13, 2019

Loss-of-function variants in myocardin cause congenital megabladder in humans and miceArjan C Houweling, Glenda M Beaman, Alex V Postma, et al.

Cell Reports|June 19, 2026

Osr1-expressing mesoderm contributes to lymphatic vessel assembly and complexity in the mammalian kidneyDaniyal J Jafree, Lauren G Russell, Athanasia Stathopoulou, et al.

Nature Genetics|September 27, 2016

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neuronsXavier Caubit, Paolo Gubellini, Joris Andrieux, et al.

Kidney International|June 18, 2004

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneitySongshan Jiang, Jordan Gitlin, Fang-Ming Deng, et al.

American Journal of Human Genetics|March 16, 2007

Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral refluxWeining Lu, Albertien M van Eerde, Xueping Fan, et al.

American Journal of Human Genetics|January 15, 2013

LRIG2 mutations cause urofacial syndromeHelen M Stuart, Neil A Roberts, Berk Burgu, et al.

European Heart Journal|November 18, 2020

Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidneyXiao Jiang, James M Eales, David Scannali, et al.

Pageof 18

Search research articles

Showing results (151-160 of 173) with videos related to

Sort By:

Pageof 18

Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022

Nature Communications|November 24, 2018

Molecular insights into genome-wide association studies of chronic kidney disease-defining traitsXiaoguang Xu, James M Eales, Artur Akbarov, et al.

Journal of the American Society of Nephrology : JASN|April 25, 2009

HNF1B mutations associate with hypomagnesemia and renal magnesium wastingShazia Adalat, Adrian S Woolf, Karen A Johnstone, et al.

The Journal of Clinical Investigation|September 13, 2019

Loss-of-function variants in myocardin cause congenital megabladder in humans and miceArjan C Houweling, Glenda M Beaman, Alex V Postma, et al.

Cell Reports|June 19, 2026

Osr1-expressing mesoderm contributes to lymphatic vessel assembly and complexity in the mammalian kidneyDaniyal J Jafree, Lauren G Russell, Athanasia Stathopoulou, et al.

Nature Genetics|September 27, 2016

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neuronsXavier Caubit, Paolo Gubellini, Joris Andrieux, et al.

Kidney International|June 18, 2004

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneitySongshan Jiang, Jordan Gitlin, Fang-Ming Deng, et al.