Detalhe da pesquisa
1.
Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders.
Psychol Med
; 43(6): 1207-17, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22225676
2.
TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies.
Mol Psychiatry
; 16(6): 647-63, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20368705
3.
Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways.
Mol Psychiatry
; 15(7): 702-11, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19139748
4.
More CLEC16A gene variants associated with multiple sclerosis.
Acta Neurol Scand
; 123(6): 400-6, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20849399
5.
The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders.
J Neural Transm (Vienna)
; 116(6): 649-57, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18607529
6.
IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.
Genes Immun
; 9(3): 259-63, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18354419
7.
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy.
Biochem Biophys Res Commun
; 377(2): 379-383, 2008 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-18851951
8.
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene.
J Neuroimmunol
; 279: 46-9, 2015 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25670000
9.
Sequence fossils, triplet expansion, and reconstruction of earliest codons.
Gene
; 205(1-2): 1-6, 1997 Dec 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-9461374
10.
Compositional mapping of the human dystrophin-encoding gene.
Gene
; 122(2): 329-35, 1992 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-1487147
11.
Conservation of a putative AP1 binding site and complete homology to a fetal brain EST in a region upstream of the core muscle promoter in the human dystrophin gene.
Gene
; 200(1-2): 173-6, 1997 Oct 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-9373152
12.
Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism.
Mol Psychiatry
; 13(9): 831-2, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18711446
13.
Interphase cell flow cytometry as a means of monitoring genomic size in normal and neoplastoid cell cultures.
Cancer Genet Cytogenet
; 24(2): 191-204, 1987 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-3791174
14.
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy.
J Neurol
; 241(5): 331-4, 1994 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-8006687
15.
Campomelic dysplasia without sex reversal in a Turkish patient is due to mutation Ala119Val within the SOX9 gene.
Clin Dysmorphol
; 10(3): 197-201, 2001 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-11446414
16.
Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation.
J Med Genet
; 41(3): e26, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-14985397
17.
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans.
Horm Metab Res
; 39(11): 840-4, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17992642
18.
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.
J Neural Transm (Vienna)
; 114(4): 513-21, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17093889
19.
Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy.
Genomics
; 4(4): 592-6, 1989 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-2568331
20.
Noninteger pitch and nuclease sensitivity of chromatin DNA.
Biochemistry
; 18(3): 454-6, 1979 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-420792