Detalhe da pesquisa
1.
Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome.
Nature
; 592(7855): 596-600, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33762729
2.
The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology.
Hum Mol Genet
; 29(13): 2109-2123, 2020 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32186706
3.
Properties of VIP+ synapses in the suprachiasmatic nucleus highlight their role in circadian rhythm.
J Neurophysiol
; 115(6): 2701-4, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26581865
4.
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1.
Am J Hum Genet
; 93(3): 506-14, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24011988
5.
Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice.
Elife
; 102021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33494858
6.
A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans.
Laryngoscope
; 124(3): E95-103, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23946138
7.
Genetic mapping and exome sequencing identify variants associated with five novel diseases.
PLoS One
; 7(1): e28936, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22279524