Detalhe da pesquisa
1.
HMGB1 released by mesothelial cells drives the development of asbestos-induced mesothelioma.
Proc Natl Acad Sci U S A
; 120(39): e2307999120, 2023 09 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37729199
2.
Heterozygous germline BLM mutations increase susceptibility to asbestos and mesothelioma.
Proc Natl Acad Sci U S A
; 117(52): 33466-33473, 2020 12 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33318203
3.
Risk prediction for metastasis of clear cell renal cell carcinoma using digital multiplex ligation-dependent probe amplification.
Cancer Sci
; 113(1): 297-307, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34687579
4.
Short somatic alterations at the site of copy number variation in breast cancer.
Cancer Sci
; 112(1): 444-453, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32860329
5.
High-density array-CGH with targeted NGS unmask multiple noncontiguous minute deletions on chromosome 3p21 in mesothelioma.
Proc Natl Acad Sci U S A
; 113(47): 13432-13437, 2016 11 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27834213
6.
Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700s.
PLoS Genet
; 11(12): e1005633, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26683624
7.
Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders.
BMC Med Genet
; 18(1): 37, 2017 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28347285
8.
Somatic alteration and depleted nuclear expression of BAP1 in human esophageal squamous cell carcinoma.
Cancer Sci
; 106(9): 1118-29, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26081045
9.
Frequent genomic rearrangements of BRCA1 associated protein-1 (BAP1) gene in Japanese malignant mesothelioma-characterization of deletions at exon level.
J Hum Genet
; 60(10): 647-9, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26246155
10.
Frequent inactivation of the BAP1 gene in epithelioid-type malignant mesothelioma.
Cancer Sci
; 103(5): 868-74, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22321046
11.
Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.
Hum Genet
; 131(1): 121-30, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21735174
12.
Medical and Surgical Care of Patients With Mesothelioma and Their Relatives Carrying Germline BAP1 Mutations.
J Thorac Oncol
; 17(7): 873-889, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35462085
13.
Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis.
Biochem Biophys Res Commun
; 402(2): 438-42, 2010 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20955688
14.
The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population: the Takahata study.
J Hum Genet
; 55(12): 791-5, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20844548
15.
Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: identification of a 7.2-kb microdeletion using oligonucleotide tiling microarray.
Am J Med Genet A
; 152A(1): 133-40, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20034086
16.
HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.
Pediatr Nephrol
; 25(6): 1073-9, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20155289
17.
Mesothelioma developing in carriers of inherited genetic mutations.
Transl Lung Cancer Res
; 9(Suppl 1): S67-S76, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32206572
18.
Genetic polymorphisms of paraoxonase-1 are associated with chronic kidney disease in Japanese women.
Kidney Int
; 76(2): 183-9, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19357718
19.
A functional polymorphism of the TNF-alpha gene that is associated with type 2 DM.
Biochem Biophys Res Commun
; 369(3): 943-7, 2008 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-18328809
20.
Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM.
Biochem Biophys Res Commun
; 374(3): 576-80, 2008 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-18656447