Detalhe da pesquisa
1.
Bromodomain 4 inhibition leads to MYCN downregulation in Wilms tumor.
Pediatr Blood Cancer
; 69(2): e29401, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34693628
2.
WT1-Mutant Wilms Tumor Progression Is Associated With Diverting Clonal Mutations of CTNNB1.
J Pediatr Hematol Oncol
; 43(2): e180-e183, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31876779
3.
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.
J Pathol
; 243(2): 242-254, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28727142
4.
Reduction of the tumorigenic potential of human retinoblastoma cell lines by TFF1 overexpression involves p53/caspase signaling and miR-18a regulation.
Int J Cancer
; 141(3): 549-560, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28481041
5.
Classification of a frameshift/extended and a stop mutation in WT1 as gain-of-function mutations that activate cell cycle genes and promote Wilms tumour cell proliferation.
Hum Mol Genet
; 23(15): 3958-74, 2014 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24619359
6.
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.
Carcinogenesis
; 35(2): 315-23, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24127187
7.
A pooled analysis of the outcome of prospective colonoscopic surveillance for familial colorectal cancer.
Int J Cancer
; 134(4): 939-47, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23901040
8.
Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families.
Int J Cancer
; 135(1): 69-77, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24493211
9.
Evaluation of chromosome 11p imbalances in aniridia and Wilms tumor patients.
Am J Med Genet A
; 161A(5): 958-64, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23494989
10.
A novel inverted 17p13.3 microduplication disrupting PAFAH1B1 (LIS1) in a girl with syndromic lissencephaly.
Am J Med Genet A
; 161A(6): 1453-8, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23633430
11.
Genetics of pediatric renal tumors.
Pediatr Nephrol
; 28(1): 13-23, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22461142
12.
Gene expression studies of WT1 mutant Wilms tumor cell lines in the frame work of published kidney development data reveals their early kidney stem cell origin.
PLoS One
; 18(1): e0270380, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36689432
13.
Pathological assessment of mismatch repair gene variants in Lynch syndrome: past, present, and future.
Hum Mutat
; 33(12): 1617-25, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22833534
14.
Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm.
Hum Mol Genet
; 19(9): 1651-68, 2010 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20106868
15.
Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome.
J Med Genet
; 48(8): 513-9, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21712435
16.
Frequent long-range epigenetic silencing of protocadherin gene clusters on chromosome 5q31 in Wilms' tumor.
PLoS Genet
; 5(11): e1000745, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19956686
17.
WT1-dependent sulfatase expression maintains the normal glomerular filtration barrier.
J Am Soc Nephrol
; 22(7): 1286-96, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21719793
18.
Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations.
Cancers (Basel)
; 13(1)2020 Dec 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33379206
19.
Response to: Design of a core classification process for DNA mismatch repair variations of a priori unknown functional significance.
Hum Mutat
; 34(6): 923-4, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23554108
20.
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
Eur J Hum Genet
; 16(5): 587-92, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18301448