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The Wilms tumor gene, Wt1, is required for Sox9 expression and maintenance of tubular architecture in the developing testis

Autor: Gao, Fei, Maiti, S., Alam, N., Zhang, Zuochun, Deng, J.M., Behringer, R.R., Lécureuil, Charlotte, Guillou, Florian Jean Louis, Huff, V.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2006, 103 (32), pp.11987-11992

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::713198680d4c77c128a8dff511ef0ce5
https://hal.inrae.fr/hal-02657626

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences

Autor: Huff, V, Jaffe, N, Saunders, G F, Strong, L C, Villalba, F, Ruteshouser, E C

The WT1 gene is known to play a role in at least some cases of Wilms tumor (WT). The first exon of the gene is highly GC rich and contains many short tandem di- and trinucleotide repeats, interrupted direct repeats, and CCTG (CAGG) motifs that have b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1ea44f7e6b0fa9085c8494f40912e1d6
https://europepmc.org/articles/PMC1801329/

Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT

Autor: Huff, V, Miwa, H, Haber, D A, Call, K M, Housman, D, Strong, L C, Saunders, G F

The inactivation of two alleles at a locus on the short arm of chromosome 11 (band 11p13) has been suggested to be critical steps in the development of Wilms tumor (WT), a childhood kidney tumor. Two similar candidate WT cDNA clones (WT33 and LK15) h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0736810b0224b9f323955f9815df4cdc
https://europepmc.org/articles/PMC1683037/

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