Published in Cell on August 10, 2001
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Finding signals that regulate alternative splicing in the post-genomic era. Genome Biol (2002) 4.73
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Alternatively spliced isoforms of WT1 control podocyte-specific gene expression. Kidney Int (2015) 0.91
The molecular and cellular basis of gonadal sex reversal in mice and humans. Wiley Interdiscip Rev Dev Biol (2012) 0.91
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The Wilms' tumor suppressor WT1 is associated with melanoma proliferation. Pflugers Arch (2007) 0.88
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Wilms' tumor protein Wt1 is an activator of the anti-Müllerian hormone receptor gene Amhr2. Mol Cell Biol (2007) 0.87
Colocalization of WT1 and cell proliferation reveals conserved mechanisms in temperature-dependent sex determination. Genesis (2003) 0.87
Germ cells are not required to establish the female pathway in mouse fetal gonads. PLoS One (2012) 0.87
A mammal-specific exon of WT1 is not required for development or fertility. Mol Cell Biol (2002) 0.87
Inducible nephrin transgene expression in podocytes rescues nephrin-deficient mice from perinatal death. Am J Pathol (2009) 0.86
The predominant WT1 isoform (+KTS) encodes a DNA-binding protein targeting the planar cell polarity gene Scribble in renal podocytes. Mol Cancer Res (2010) 0.86
WT1 marker is not sufficient for distinguishing between melanoma and melanocytic nevi. J Cutan Pathol (2009) 0.85
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Wt1 in the kidney--a tale in mouse models. Pediatr Nephrol (2013) 0.83
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Regulation of male sex determination: genital ridge formation and Sry activation in mice. Cell Mol Life Sci (2014) 0.83
FOXL2 transcriptionally represses Sf1 expression by antagonizing WT1 during ovarian development in mice. FASEB J (2014) 0.82
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Transcriptional regulation of podocyte disease. Transl Res (2007) 0.80
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Mice lacking the 68-amino-acid, mammal-specific N-terminal extension of WT1 develop normally and are fertile. Mol Cell Biol (2003) 0.79
Alternative splicing at GYNNGY 5' splice sites: more noise, less regulation. Nucleic Acids Res (2014) 0.78
Transgenic expression of Map3k4 rescues T-associated sex reversal (Tas) in mice. Hum Mol Genet (2014) 0.78
WT1 expression in the human fetus during development. Eur J Histochem (2015) 0.78
AHR regulates WT1 genetic programming during murine nephrogenesis. Mol Med (2011) 0.77
It's a bit over, is that ok? The subtle surplus from tandem alternative splicing. RNA Biol (2015) 0.77
New clues to the puzzle of mammalian sex determination. Genome Biol (2001) 0.77
A mutant Ahr allele protects the embryonic kidney from hydrocarbon-induced deficits in fetal programming. Environ Health Perspect (2011) 0.77
A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation. PLoS One (2012) 0.77
Ex vivo cultures combined with vivo-morpholino induced gene knockdown provide a system to assess the role of WT1 and GATA4 during gonad differentiation. PLoS One (2017) 0.75
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Hermaphrodism and sex reversal associated with the dominant hemimelia mutation in XY mice. Proc Jpn Acad Ser B Phys Biol Sci (2009) 0.75
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Organ specific regenerative markers in peri-organ adipose: kidney. Lipids Health Dis (2011) 0.75
Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome. Indian J Med Res (2016) 0.75
Dysregulation of WTI (-KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation. Sci Rep (2017) 0.75
NPHS2 mutations account for only 15% of nephrotic syndrome cases. BMC Med Genet (2015) 0.75
Transcription factor Wilms' tumor 1 regulates developmental RNAs through 3' UTR interaction. Genes Dev (2017) 0.75
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In mammalian foetal testes, SOX9 regulates expression of its target genes by binding to genomic regions with conserved signatures. Nucleic Acids Res (2017) 0.75
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NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet (2000) 7.98
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YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis. Development (1999) 2.71
X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males. J Am Soc Nephrol (2000) 2.71
Sox9 induces testis development in XX transgenic mice. Nat Genet (2001) 2.43
Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat Genet (1997) 2.38
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6. Hum Mol Genet (2001) 2.38
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