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List of works by Adrian S. Woolf

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Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux

scientific article
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

scientific article
Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease

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

scientific article published on January 25, 2011
HNF1B mutations associate with hypomagnesemia and renal magnesium wasting

scientific article
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4

scientific journal article
Medical versus surgical treatment in children with severe bilateral vesicoureteric reflux and bilateral nephropathy: a randomised trial

scientific article
Protein restriction in pregnancy is associated with increased apoptosis of mesenchymal cells at the start of rat metanephrogenesis.

scientific article published in April 2002
Podocyte-specific expression of angiopoietin-2 causes proteinuria and apoptosis of glomerular endothelia

scientific article published on 11 July 2007
Primary vesicoureteric reflux as a predictor of renal damage in children hospitalized with urinary tract infection: a systematic review and meta-analysis

scientific article
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs

scientific article (publication date: May 2005)
Evolving concepts in human renal dysplasia

scientific article published on April 2004
De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney Failure

scientific article published on 11 May 2005
Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract

scientific article published on 24 January 2009
The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation

scientific journal article
A paradoxical teratogenic mechanism for retinoic acid.

scientific article
Targeted glomerular angiopoietin-1 therapy for early diabetic kidney disease.

scientific article published on 5 September 2013
Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations

scientific article
Taxol inhibits progression of congenital polycystic kidney disease

scientific article published in Nature
A molecular and genetic view of human renal and urinary tract malformations.

scientific article
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.

scientific article
Mutations in HPSE2 cause urofacial syndrome

scientific article
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development

scientific article published in April 1995
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome

scientific article published on November 2011
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux

scientific article
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

scientific article
Oral-facial-digital syndrome type 1 is another dominant polycystic kidney disease: clinical, radiological and histopathological features of a new kindred.

scientific article
Angiopoietin-1 therapy enhances fibrosis and inflammation following folic acid-induced acute renal injury.

scientific article published on 14 May 2008
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity

scientific article
Immunohistochemical analysis of Sonic hedgehog signalling in normal human urinary tract development

scientific article
LRIG2 mutations cause urofacial syndrome

scientific article
Angiopoietin correlates with glomerular capillary loss in anti-glomerular basement membrane glomerulonephritis

scientific article published in June 2002
Fras1, a basement membrane-associated protein mutated in Fraser syndrome, mediates both the initiation of the mammalian kidney and the integrity of renal glomeruli

scientific article published on 11 September 2008
Generation of Functioning Nephrons by Implanting Human Pluripotent Stem Cell-Derived Kidney Progenitors

scientific article published on 7 February 2018
Measures of kidney function by minimally invasive techniques correlate with histological glomerular damage in SCID mice with adriamycin-induced nephropathy

scientific article
Corticosteroid-induced kidney dysmorphogenesis is associated with deregulated expression of known cystogenic molecules, as well as Indian hedgehog

scientific article published on 9 December 2009
Albuminuria is associated with too few glomeruli and too much testosterone

scientific article published on 27 February 2013
Circulating angiopoietin-2 is a marker for early cardiovascular disease in children on chronic dialysis

scientific article
Angiopoietin growth factors and Tie receptor tyrosine kinases in renal vascular development.

scientific article
Effects of oxygen on vascular patterning in Tie1/LacZ metanephric kidneys in vitro

scientific article published in June 1998
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease

scientific article
Proteinuria, hypertension and chronic renal failure in X-linked Kallmann's syndrome, a defined genetic cause of solitary functioning kidney

scientific article published in August 1998
Cell biology of ureter development.

scientific article
The P2X7 ATP receptor modulates renal cyst development in vitro

scientific article
Microarray interrogation of human metanephric mesenchymal cells highlights potentially important molecules in vivo.

scientific article published on 19 September 2006
Development of embryonic stem cells in recombinant kidneys

scientific article published on October 2012
Uroplakins: new molecular players in the biology of urinary tract malformations.

scientific article published on 20 December 2006
Vascular Endothelial Growth Factor C for Polycystic Kidney Diseases

scientific article
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

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

scientific article published on 02 September 2016

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