Detalhe da pesquisa
1.
Wt1 directs the lineage specification of sertoli and granulosa cells by repressing Sf1 expression.
Development;
144(1): 44-53, 2017 01 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27888191
2.
Reprogramming of Sertoli cells to fetal-like Leydig cells by Wt1 ablation.
Proc Natl Acad Sci U S A;
112(13): 4003-8, 2015 Mar 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25775596
3.
Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour.
J Med Genet;
53(6): 385-8, 2016 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26566882
4.
Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation.
Hum Mol Genet;
23(2): 333-41, 2014 Jan 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24009315
5.
Rare variant detection using family-based sequencing analysis.
Proc Natl Acad Sci U S A;
110(10): 3985-90, 2013 Mar 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23426633
6.
The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans.
PLoS Genet;
9(8): e1003645, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23935527
7.
Wilms tumor genetics: a new, UnX-pected twist to the story.
Cancer Cell;
11(2): 105-7, 2007 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17292822
8.
Left-sided cryptorchidism in mice with Wilms' tumour 1 gene deletion in gubernaculum testis.
J Pathol;
230(1): 39-47, 2013 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23288785
9.
Ubiquitin specific protease 18 (Usp18) is a WT1 transcriptional target.
Exp Cell Res;
319(5): 612-22, 2013 Mar 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23291318
10.
Hallmark discoveries in the biology of Wilms tumour.
Nat Rev Urol;
21(3): 158-180, 2024 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37848532
11.
Children's Oncology Group's 2013 blueprint for research: renal tumors.
Pediatr Blood Cancer;
60(6): 994-1000, 2013 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23255438
12.
Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study.
J Pathol;
228(1): 119-30, 2012 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22374738
13.
The Genetic and Epigenetic Features of Bilateral Wilms Tumor Predisposition: A Report from the Children's Oncology Group AREN18B5-Q Study.
Res Sq;
2023 Mar 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36993649
14.
Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q.
Nat Commun;
14(1): 8006, 2023 Dec 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38110397
15.
Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 study.
Cell Rep Med;
3(6): 100644, 2022 06 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35617957
16.
Long-term outcomes for infants with very low risk Wilms tumor treated with surgery alone in National Wilms Tumor Study-5.
Ann Surg;
251(3): 555-8, 2010 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20142733
17.
Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome.
Pediatr Blood Cancer;
53(7): 1349-51, 2009 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19653292
18.
Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors.
Genes Chromosomes Cancer;
47(6): 461-70, 2008 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18311776
19.
Wilm's tumor 1 promotes memory flexibility.
Nat Commun;
10(1): 3756, 2019 08 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31434897
20.
Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group.
Pediatr Blood Cancer;
50(2): 236-41, 2008 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17539021