Detalhe da pesquisa
1.
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.
BMC Med Genet
; 12: 54, 2011 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21496248
2.
Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysis.
Ophthalmology
; 118(6): 1130-6, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21269699
3.
ZZ domain of dystrophin and utrophin: topology and mapping of a beta-dystroglycan interaction site.
Biochem J
; 401(3): 667-77, 2007 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17009962
4.
Pathological pattern of Mdx mice diaphragm correlates with gradual expression of the short utrophin isoform Up71.
Biochim Biophys Acta
; 1762(3): 362-72, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16457992
5.
alpha7B integrin changes in mdx mouse muscles after L-arginine administration.
FEBS Lett
; 579(5): 1079-84, 2005 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-15710394
6.
Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families.
Eur J Hum Genet
; 19(12): 1256-63, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21792230