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Adrian S Woolf

Showing results (111-120 of 173) with videos related to

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Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
Cell Death & Disease|December 18, 2024
Tumor- and host-derived heparanase-2 (Hpa2) attenuates tumorigenicity: role of Hpa2 in macrophage polarization and BRD7 nuclear localizationSoaad Soboh, Avital Vorontsova, Malik Farhoud, et al.
Elife|July 11, 2024
Human <i>HPSE2</i> gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndromeFilipa M Lopes, Celine Grenier, Benjamin W Jarvis, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
A paradoxical teratogenic mechanism for retinoic acidLeo M Y Lee, Chun-Yin Leung, Walfred W C Tang, et al.
Kidney International|November 21, 2025
Molecular pathways of kidney development and their applications to clinical researchFriederike Ehrhart, Helge Martens, Norman D Rosenblum, et al.
Kidney International Reports|October 26, 2020
Early B-cell Factor 3-Related Genetic Disease Can Mimic Urofacial SyndromeJ Robert Harkness, Glenda M Beaman, Keng W Teik, et al.
Journal of the American Society of Nephrology : JASN|June 4, 2015
Vascular Endothelial Growth Factor C for Polycystic Kidney DiseasesJennifer L Huang, Adrian S Woolf, Maria Kolatsi-Joannou, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 26, 2006
Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindredLarissa Kerecuk, Anaar Sajoo, Lesley McGregor, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 3, 2006
Mutation analyses of Uroplakin II in children with renal tract malformationsDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Lancet (London, England)|May 20, 2015
Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndromeJamie M Ellingford, Panagiotis I Sergouniotis, Rachel Lennon, et al.
Pageof 18

Showing results (111-120 of 173) with videos related to

Sort By:
Pageof 18
Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
Cell Death & Disease|December 18, 2024
Tumor- and host-derived heparanase-2 (Hpa2) attenuates tumorigenicity: role of Hpa2 in macrophage polarization and BRD7 nuclear localizationSoaad Soboh, Avital Vorontsova, Malik Farhoud, et al.
Elife|July 11, 2024
Human <i>HPSE2</i> gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndromeFilipa M Lopes, Celine Grenier, Benjamin W Jarvis, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
A paradoxical teratogenic mechanism for retinoic acidLeo M Y Lee, Chun-Yin Leung, Walfred W C Tang, et al.
Kidney International|November 21, 2025
Molecular pathways of kidney development and their applications to clinical researchFriederike Ehrhart, Helge Martens, Norman D Rosenblum, et al.
Kidney International Reports|October 26, 2020
Early B-cell Factor 3-Related Genetic Disease Can Mimic Urofacial SyndromeJ Robert Harkness, Glenda M Beaman, Keng W Teik, et al.
Journal of the American Society of Nephrology : JASN|June 4, 2015
Vascular Endothelial Growth Factor C for Polycystic Kidney DiseasesJennifer L Huang, Adrian S Woolf, Maria Kolatsi-Joannou, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 26, 2006
Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindredLarissa Kerecuk, Anaar Sajoo, Lesley McGregor, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 3, 2006
Mutation analyses of Uroplakin II in children with renal tract malformationsDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Lancet (London, England)|May 20, 2015
Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndromeJamie M Ellingford, Panagiotis I Sergouniotis, Rachel Lennon, et al.
Pageof 18