Detalhe da pesquisa
1.
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.
J Biol Chem
; 287(34): 28975-85, 2012 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22700964
2.
Investigation of SUMO pathway genes in the etiology of nonsyndromic cleft lip with or without cleft palate.
Birth Defects Res A Clin Mol Teratol
; 94(6): 459-63, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22492558
3.
A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation.
Hum Mutat
; 30(1): 61-8, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18615734
4.
The glycinergic system in human startle disease: a genetic screening approach.
Front Mol Neurosci
; 3: 8, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20407582
5.
Defective glycinergic synaptic transmission in zebrafish motility mutants.
Front Mol Neurosci
; 2: 26, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-20161699
6.
A critical role for glycine transporters in hyperexcitability disorders.
Front Mol Neurosci
; 1: 1, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18946534
7.
Highly effective SNP-based association mapping and management of recessive defects in livestock.
Nat Genet
; 40(4): 449-54, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18344998
8.
Endogenous neurogenesis in the human brain following cerebral infarction.
Regen Med
; 2(1): 69-74, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17465777