Detalhe da pesquisa
1.
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophy.
Brain
; 145(12): 4202-4209, 2022 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35953447
2.
Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression.
Hum Mutat
; 34(8): 1160-71, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23649844
3.
Enhanced differentiation of the mouse oli-neu oligodendroglial cell line using optimized culture conditions.
BMC Res Notes
; 16(1): 161, 2023 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37542275
4.
scMAPA: Identification of cell-type-specific alternative polyadenylation in complex tissues.
Gigascience
; 112022 04 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35488860
5.
Glycogen synthase kinase 3beta as a likely target for the action of lithium on circadian clocks.
Chronobiol Int
; 21(1): 43-55, 2004 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15129823
6.
Autosomal dominant leukodystrophy caused by lamin B1 duplications a clinical and molecular case study of altered nuclear function and disease.
Methods Cell Biol
; 98: 337-57, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20816241
7.
Chance in our strands?
J Genet
; 83(2): 117-9, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15536252
8.
Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus.
Am J Med Genet B Neuropsychiatr Genet
; 133B(1): 124-6, 2005 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-15457499