Detalhe da pesquisa
1.
Asymmetric Pericentrosomal CD133 Endosomes Induce the Unequal Autophagic Activity During Cytokinesis in CD133-Positive Human Neuroblastoma Cells.
Stem Cells
; 40(4): 371-384, 2022 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35284915
2.
Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney.
Genes Chromosomes Cancer
; 60(8): 546-558, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33896058
3.
Blastemal predominant type Wilms tumor in Japan: Japan Children's Cancer Group.
Pediatr Int
; 61(4): 351-357, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30786111
4.
Outcome of renal tumors registered in Japan Wilms Tumor Study-2 (JWiTS-2): A report from the Japan Children's Cancer Group (JCCG).
Pediatr Blood Cancer
; 65(7): e27056, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29630767
5.
BRCA1 alterations with additional defects in DNA damage response genes may confer chemoresistance to BRCA-like breast cancers treated with neoadjuvant chemotherapy.
Genes Chromosomes Cancer
; 56(5): 405-420, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28124401
6.
Clinical prognostic value of DNA methylation in hepatoblastoma: Four novel tumor suppressor candidates.
Cancer Sci
; 107(6): 812-9, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26991471
7.
Anaplastic histology Wilms' tumors registered to the Japan Wilms' Tumor Study Group are less aggressive than that in the National Wilms' Tumor Study 5.
Pediatr Surg Int
; 32(9): 851-5, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27473009
8.
Evidence of asymmetric cell division and centrosome inheritance in human neuroblastoma cells.
Proc Natl Acad Sci U S A
; 109(44): 18048-53, 2012 Oct 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-23064640
9.
Management of pediatric renal tumor: Past and future trials of the Japan Wilms Tumor Study Group.
Pediatr Int
; 57(5): 828-31, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26267611
10.
Bilateral Wilms tumors treated according to the Japan Wilms Tumor Study Group protocol.
Pediatr Blood Cancer
; 61(7): 1184-9, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24623612
11.
Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor.
Pediatr Blood Cancer
; 66(1): e27442, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30221469
12.
AMP kinase-related kinase NUAK2 affects tumor growth, migration, and clinical outcome of human melanoma.
Proc Natl Acad Sci U S A
; 108(16): 6597-602, 2011 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21460252
13.
Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.
Genes Chromosomes Cancer
; 52(3): 274-86, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23225212
14.
Alterations of the genes involved in the PI3K and estrogen-receptor pathways influence outcome in human epidermal growth factor receptor 2-positive and hormone receptor-positive breast cancer patients treated with trastuzumab-containing neoadjuvant chemotherapy.
BMC Cancer
; 13: 241, 2013 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-23679233
15.
RASSF1A methylation indicates a poor prognosis in hepatoblastoma patients.
Pediatr Surg Int
; 29(11): 1147-52, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23989600
16.
Molecular Regulation of Autophagy and Asymmetric Cell Division by Cancer Stem Cell Marker CD133.
Cells
; 12(5)2023 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36899954
17.
Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children.
Cancer Sci
; 103(6): 1129-35, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22409817
18.
Methylation of the RASSF1A promoter is predictive of poor outcome among patients with Wilms tumor.
Pediatr Blood Cancer
; 59(3): 499-505, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22457227
19.
Association of germline or somatic TP53 missense mutation with oncogene amplification in tumors developed in patients with Li-Fraumeni or Li-Fraumeni-like syndrome.
Genes Chromosomes Cancer
; 50(7): 535-45, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21484931
20.
Genome-wide analysis of allelic imbalances reveals 4q deletions as a poor prognostic factor and MDM4 amplification at 1q32.1 in hepatoblastoma.
Genes Chromosomes Cancer
; 49(7): 596-609, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20461752