Detalhe da pesquisa
1.
Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma.
Proc Natl Acad Sci U S A
; 110(33): 13481-6, 2013 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-23901115
2.
Mutational and functional analysis of the tumor-suppressor PTPRD in human melanoma.
Hum Mutat
; 35(11): 1301-10, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25113440
3.
Organization for rare diseases India (ORDI) - addressing the challenges and opportunities for the Indian rare diseases' community.
Genet Res (Camb)
; 96: e009, 2014 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25579084
4.
Translational utility of next-generation sequencing.
Genomics
; 102(3): 137-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23631825
5.
Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma.
BMC Genomics
; 13: 505, 2012 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-23006843
6.
Analysis of the disintegrin-metalloproteinases family reveals ADAM29 and ADAM7 are often mutated in melanoma.
Hum Mutat
; 32(6): E2148-75, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21618342
7.
Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers.
Proc Natl Acad Sci U S A
; 105(42): 16224-9, 2008 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-18852474
8.
Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Sci Rep
; 9(1): 4523, 2019 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30850615
9.
RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Sci Rep
; 8(1): 653, 2018 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29330521
10.
MultiDimensional ClinOmics for Precision Therapy of Children and Adolescent Young Adults with Relapsed and Refractory Cancer: A Report from the Center for Cancer Research.
Clin Cancer Res
; 22(15): 3810-20, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26994145
11.
Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes.
Front Genet
; 6: 215, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26136771
12.
Recurrent inactivating RASA2 mutations in melanoma.
Nat Genet
; 47(12): 1408-10, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26502337
13.
Somatic mutations in MAP3K5 attenuate its proapoptotic function in melanoma through increased binding to thioredoxin.
J Invest Dermatol
; 134(2): 452-460, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24008424
14.
Mining exomic sequencing data to identify mutated antigens recognized by adoptively transferred tumor-reactive T cells.
Nat Med
; 19(6): 747-52, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23644516
15.
Delving into somatic variation in sporadic melanoma.
Pigment Cell Melanoma Res
; 25(2): 155-70, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22260482
16.
Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
Nat Genet
; 43(5): 442-6, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21499247
17.
Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma.
Nat Genet
; 43(11): 1119-26, 2011 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-21946352
18.
Novel somatic mutations in heterotrimeric G proteins in melanoma.
Cancer Biol Ther
; 10(1): 33-7, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20424519
19.
Mutational and functional analysis reveals ADAMTS18 metalloproteinase as a novel driver in melanoma.
Mol Cancer Res
; 8(11): 1513-25, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21047771
20.
Analysis of the tyrosine kinome in melanoma reveals recurrent mutations in ERBB4.
Nat Genet
; 41(10): 1127-32, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19718025