Detalhe da pesquisa
1.
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy.
Haematologica;
106(11): 3004-3007, 2021 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34233450
2.
A programmable method for massively parallel targeted sequencing.
Nucleic Acids Res;
42(10): e88, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24782526
3.
A cross-sample statistical model for SNP detection in short-read sequencing data.
Nucleic Acids Res;
40(1): e5, 2012 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22064853
4.
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
Nucleic Acids Res;
40(1): e2, 2012 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22013163
5.
The Human OligoGenome Resource: a database of oligonucleotide capture probes for resequencing target regions across the human genome.
Nucleic Acids Res;
40(Database issue): D1137-43, 2012 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22102592
6.
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.
Blood Adv;
7(20): 6092-6107, 2023 10 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37406166
7.
Targeted sequencing library preparation by genomic DNA circularization.
BMC Biotechnol;
11: 122, 2011 Dec 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22168766
8.
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.
Blood Adv;
4(6): 1131-1144, 2020 03 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32208489
9.
The liver pharmacological and xenobiotic gene response repertoire.
Mol Syst Biol;
4: 175, 2008.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18364709
10.
Development of a large-scale chemogenomics database to improve drug candidate selection and to understand mechanisms of chemical toxicity and action.
J Biotechnol;
119(3): 219-44, 2005 Sep 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16005536
11.
Metastatic tumor evolution and organoid modeling implicate TGFBR2 as a cancer driver in diffuse gastric cancer.
Genome Biol;
15(8): 428, 2014 Aug 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25315765
12.
Identification of Insertion Deletion Mutations from Deep Targeted Resequencing.
J Data Mining Genomics Proteomics;
4(3)2013 Jul 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24511426
13.
Efficient targeted resequencing of human germline and cancer genomes by oligonucleotide-selective sequencing.
Nat Biotechnol;
29(11): 1024-7, 2011 Oct 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22020387
14.
A flexible approach for highly multiplexed candidate gene targeted resequencing.
PLoS One;
6(6): e21088, 2011.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21738606
15.
Performance comparison of whole-genome sequencing platforms.
Nat Biotechnol;
30(1): 78-82, 2011 Dec 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22178993
16.
A gene expression signature that predicts the future onset of drug-induced renal tubular toxicity.
Toxicol Pathol;
33(6): 675-83, 2005.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16239200
17.
Classification of a large microarray data set: algorithm comparison and analysis of drug signatures.
Genome Res;
15(5): 724-36, 2005 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15867433
18.
Molecular basis for fungal selectivity of novel antimitotic compounds.
Antimicrob Agents Chemother;
47(7): 2273-82, 2003 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12821479