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The American Journal of Pathology|April 28, 2005
Implication of Wt1 in the pathogenesis of nephrogenic failure in a mouse model of retinoic acid-induced caudal regression syndromeHerman K W Tse, Maran B W Leung, Adrian S Woolf, et al.Plos One|February 15, 2013
Circulating angiopoietin-2 is a marker for early cardiovascular disease in children on chronic dialysisRukshana C Shroff, Karen L Price, Maria Kolatsi-Joannou, et al.Journal of the American Society of Nephrology : JASN|February 22, 2003
OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cellsLeila Romio, Victoria Wright, Karen Price, et al.Journal of the National Cancer Institute|August 16, 2001
Epoetin treatment of anemia associated with cancer therapy: a systematic review and meta-analysis of controlled clinical trialsJ Seidenfeld, M Piper, C Flamm, et al.Journal of Pediatric Urology|May 1, 2022
Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophy-epispadias complexGlenda M Beaman, Adrian S Woolf, Filipa M Lopes, et al.Kidney International|September 7, 2016
Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterningHortensja Ł Brzóska, Angela M d'Esposito, Maria Kolatsi-Joannou, et al.Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of ABL1 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.American Journal of Human Genetics|November 22, 2000
Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney diseaseC Bingham, M P Bulman, S Ellard, et al.Elife|July 11, 2024
Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndromeFilipa M Lopes, Celine Grenier, Benjamin W Jarvis, et al.Pageof 31