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Generation of Functioning Nephrons by Implanting Human Pluripotent Stem Cell-Derived Kidney Progenitors

Stem cell reports, 2018-03, Vol.10 (3), p.766-779

2018

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Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics

Kidney international, 2019-03, Vol.95 (3), p.624-635

2019

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Vascular growth factors play critical roles in kidney glomeruli

Clinical science (1979), 2015-12, Vol.129 (12), p.1225-1236

2015

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Molecular insights into genome-wide association studies of chronic kidney disease-defining traits

Nature communications, 2018-11, Vol.9 (1), p.4800-12, Article 4800

2018

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The term CAKUT has outlived its usefulness: the case for the prosecution

Pediatric nephrology (Berlin, West), 2022-11, Vol.37 (11), p.2785-2791

Woolf, Adrian S.

2022

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Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1

Journal of cell science, 2011-02, Vol.124 (4), p.600-612

2011

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Predicting congenital renal tract malformation genes using machine learning

Scientific reports, 2023-08, Vol.13 (1), p.13204-13204, Article 13204

2023

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Growing a new human kidney

Kidney international, 2019-10, Vol.96 (4), p.871-882

Woolf, Adrian S.

2019

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Making human collecting ducts and modeling disease in the laboratory

Kidney international, 2021-08, Vol.100 (2), p.263-265

Woolf, Adrian S.

2021

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Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterning

Kidney international, 2016-12, Vol.90 (6), p.1274-1284

2016

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Monocyte-derived peritoneal macrophages protect C57BL/6 mice against surgery-induced adhesions

Frontiers in immunology, 2022-10, Vol.13, p.1000491

2022

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Building human renal tracts

Journal of pediatric surgery, 2022-02, Vol.57 (2), p.172-177

Woolf, Adrian S.

2022

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The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation

Human molecular genetics, 2010-12, Vol.19 (23), p.4663-4676

2010

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paradoxical teratogenic mechanism for retinoic acid

Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (34), p.13668-13673

2012

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Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome

eLife, 2024-07, Vol.13

2024

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Vascular Endothelial Growth Factor C for Polycystic Kidney Diseases

Journal of the American Society of Nephrology, 2016-01, Vol.27 (1), p.69-77

2016

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Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomas

PloS one, 2013-11, Vol.8 (11), p.e81167-e81167

2013

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Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder

Scientific reports, 2021-07, Vol.11 (1), p.15529-15529, Article 15529

2021

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Genetic Background is a Key Determinant of Glomerular Extracellular Matrix Composition and Organization

Journal of the American Society of Nephrology, 2015-12, Vol.26 (12), p.3021-3034

2015

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Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene

Human molecular genetics, 2009-01, Vol.18 (2), p.289-303

2009

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Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome

American journal of human genetics, 2011-11, Vol.89 (5), p.668-674

2011

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Podocyte-specific expression of angiopoietin-2 causes proteinuria and apoptosis of glomerular endothelia

Journal of the American Society of Nephrology, 2007-08, Vol.18 (8), p.2320-2329

2007

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HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood

Kidney international reports, 2019-09, Vol.4 (9), p.1304-1311

2019

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Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome

The Lancet (British edition), 2015-05, Vol.385 (9980), p.1916-1916

2015

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Generation of Functioning Nephrons by Implanting Human Pluripotent Stem Cell-Derived Kidney Progenitors

Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics

Vascular growth factors play critical roles in kidney glomeruli

Molecular insights into genome-wide association studies of chronic kidney disease-defining traits

The term CAKUT has outlived its usefulness: the case for the prosecution

Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1

Predicting congenital renal tract malformation genes using machine learning

Growing a new human kidney

Making human collecting ducts and modeling disease in the laboratory

Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterning

Monocyte-derived peritoneal macrophages protect C57BL/6 mice against surgery-induced adhesions

Building human renal tracts

The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation

paradoxical teratogenic mechanism for retinoic acid

Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome

Vascular Endothelial Growth Factor C for Polycystic Kidney Diseases

Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomas

Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder

Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease

Genetic Background is a Key Determinant of Glomerular Extracellular Matrix Composition and Organization

Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene

Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome

Podocyte-specific expression of angiopoietin-2 causes proteinuria and apoptosis of glomerular endothelia

HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood

Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome

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