Detalhe da pesquisa
1.
A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.
Genetics
; 173(1): 297-307, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16489219
2.
Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms.
PLoS One
; 10(8): e0135755, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26291700
3.
Endoplasmic reticulum resident protein 44 (ERp44) deficiency in mice and zebrafish leads to cardiac developmental and functional defects.
J Am Heart Assoc
; 3(5): e001018, 2014 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25332179
4.
Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.
Hum Mol Genet
; 12(10): 1131-43, 2003 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12719377
5.
Mutation, SNP, and isoform analysis of fibroblast growth factor receptor 3 (FGFR3) in 150 newly diagnosed multiple myeloma patients.
Blood
; 102(2): 772-3, 2003 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12835230