Detalhe da pesquisa
1.
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain.
Mol Cell
; 81(22): 4663-4676.e8, 2021 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34637754
2.
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
Am J Hum Genet
; 110(6): 963-978, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37196654
3.
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain.
Mol Cell
; 81(22): 4757, 2021 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34798045
4.
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
J Med Genet
; 60(12): 1224-1234, 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37586838
5.
Clinical Manifestations in a Girl with NAA10-Related Syndrome and Genotype-Phenotype Correlation in Females.
Genes (Basel)
; 12(6)2021 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34200686
6.
Human cytomegalovirus DNA polymerase catalytic subunit pUL54 possesses independently acting nuclear localization and ppUL44 binding motifs.
Traffic
; 7(10): 1322-32, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16911590