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Adrian S Woolf

Showing results (81-90 of 173) with videos related to

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Journal of the American Society of Nephrology : JASN|July 26, 2002
Immunolocalization of cystinosin, the protein defective in cystinosisMushfequr R Haq, Vasiliki Kalatzis, Marie-Claire Gubler, et al.
Journal of the American Society of Nephrology : JASN|September 20, 2001
Hepatocyte nuclear factor-1beta: a new kindred with renal cysts and diabetes and gene expression in normal human developmentMaria Kolatsi-Joannou, Coralie Bingham, Sian Ellard, et al.
Journal of Cell Science|January 27, 2011
Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1Carla A M Lopes, Suzanna L Prosser, Leila Romio, et al.
Human Molecular Genetics|April 3, 2014
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in XenopusNeil A Roberts, Adrian S Woolf, Helen M Stuart, et al.
Scientific Reports|August 14, 2023
Predicting congenital renal tract malformation genes using machine learningMitra Kabir, Helen M Stuart, Filipa M Lopes, et al.
Nephron|August 7, 2020
Aberrant Differentiation of Human Pluripotent Stem Cell-Derived Kidney Precursor Cells inside Mouse Vascularized BioreactorsParisa Ranjzad, Jessica Jinks, Amir P Salahi, et al.
Plos One|November 22, 2013
Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomasGuangping Tai, Parisa Ranjzad, Fiona Marriage, et al.
Journal of Nephrology|June 5, 2024
A targeted gene panel illuminates pathogenesis in young people with unexplained kidney failureFelicity Beal, Natalie Forrester, Elizabeth Watson, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Human Molecular Genetics|October 31, 2008
Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome geneMaria I Ferrante, Leila Romio, Silvia Castro, et al.
Pageof 18

Showing results (81-90 of 173) with videos related to

Sort By:
Pageof 18
Journal of the American Society of Nephrology : JASN|July 26, 2002
Immunolocalization of cystinosin, the protein defective in cystinosisMushfequr R Haq, Vasiliki Kalatzis, Marie-Claire Gubler, et al.
Journal of the American Society of Nephrology : JASN|September 20, 2001
Hepatocyte nuclear factor-1beta: a new kindred with renal cysts and diabetes and gene expression in normal human developmentMaria Kolatsi-Joannou, Coralie Bingham, Sian Ellard, et al.
Journal of Cell Science|January 27, 2011
Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1Carla A M Lopes, Suzanna L Prosser, Leila Romio, et al.
Human Molecular Genetics|April 3, 2014
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in XenopusNeil A Roberts, Adrian S Woolf, Helen M Stuart, et al.
Scientific Reports|August 14, 2023
Predicting congenital renal tract malformation genes using machine learningMitra Kabir, Helen M Stuart, Filipa M Lopes, et al.
Nephron|August 7, 2020
Aberrant Differentiation of Human Pluripotent Stem Cell-Derived Kidney Precursor Cells inside Mouse Vascularized BioreactorsParisa Ranjzad, Jessica Jinks, Amir P Salahi, et al.
Plos One|November 22, 2013
Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomasGuangping Tai, Parisa Ranjzad, Fiona Marriage, et al.
Journal of Nephrology|June 5, 2024
A targeted gene panel illuminates pathogenesis in young people with unexplained kidney failureFelicity Beal, Natalie Forrester, Elizabeth Watson, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Human Molecular Genetics|October 31, 2008
Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome geneMaria I Ferrante, Leila Romio, Silvia Castro, et al.
Pageof 18