Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Adrian S Woolf

Showing results (121-130 of 173) with videos related to

Pageof 18
Sort By:
Journal of the American Society of Nephrology : JASN|December 5, 2009
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxHeather J Cordell, Rebecca Darlay, Pimphen Charoen, et al.
Human Molecular Genetics|December 17, 2021
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defectsIrene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, et al.
The American Journal of Pathology|December 7, 2006
Galectin-3 associates with the primary cilium and modulates cyst growth in congenital polycystic kidney diseaseMiliyun G Chiu, Tanya M Johnson, Adrian S Woolf, et al.
European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.
Kidney International Reports|July 13, 2023
Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder DiseaseCeline Grenier, Filipa M Lopes, Anna M Cueto-González, et al.
Clinical Genetics|August 24, 2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder diseaseGlenda M Beaman, Gabriella Galatà, Keng W Teik, et al.
Journal of the American Society of Nephrology : JASN|May 13, 2005
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failureDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Journal of Pediatric Urology|May 4, 2007
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformationsDagan Jenkins, Maria Bitner-Glindzicz, Louise Thomasson, et al.
Stem Cell Reports|May 24, 2024
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformationsIoannis Bantounas, Kirsty M Rooney, Filipa M Lopes, et al.
Kidney International|March 29, 2002
Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutationsCoralie Bingham, Sian Ellard, Trevor R P Cole, et al.
Pageof 18

Showing results (121-130 of 173) with videos related to

Sort By:
Pageof 18
Journal of the American Society of Nephrology : JASN|December 5, 2009
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxHeather J Cordell, Rebecca Darlay, Pimphen Charoen, et al.
Human Molecular Genetics|December 17, 2021
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defectsIrene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, et al.
The American Journal of Pathology|December 7, 2006
Galectin-3 associates with the primary cilium and modulates cyst growth in congenital polycystic kidney diseaseMiliyun G Chiu, Tanya M Johnson, Adrian S Woolf, et al.
European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.
Kidney International Reports|July 13, 2023
Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder DiseaseCeline Grenier, Filipa M Lopes, Anna M Cueto-González, et al.
Clinical Genetics|August 24, 2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder diseaseGlenda M Beaman, Gabriella Galatà, Keng W Teik, et al.
Journal of the American Society of Nephrology : JASN|May 13, 2005
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failureDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
Journal of Pediatric Urology|May 4, 2007
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformationsDagan Jenkins, Maria Bitner-Glindzicz, Louise Thomasson, et al.
Stem Cell Reports|May 24, 2024
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformationsIoannis Bantounas, Kirsty M Rooney, Filipa M Lopes, et al.
Kidney International|March 29, 2002
Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutationsCoralie Bingham, Sian Ellard, Trevor R P Cole, et al.
Pageof 18