Detalhe da pesquisa
1.
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.
Hum Mol Genet
; 32(9): 1497-1510, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36579832
2.
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.
Hum Genet
; 140(8): 1183-1200, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34076780
3.
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.
Hum Mol Genet
; 27(7): 1212-1227, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29365100
4.
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
Am J Hum Genet
; 99(2): 253-74, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27453576
5.
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.
Hum Mol Genet
; 2018 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29947777
6.
Functional characterization of TBR1 variants in neurodevelopmental disorder.
Sci Rep
; 8(1): 14279, 2018 09 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30250039
7.
The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers.
Sci Rep
; 6: 20911, 2016 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26867680
8.
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
J Neurodev Disord
; 8: 44, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27933109
9.
Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.
J Vis Exp
; (87)2014 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24893771
10.
De novo TBR1 mutations in sporadic autism disrupt protein functions.
Nat Commun
; 5: 4954, 2014 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25232744
11.
A conserved surface on the ligand binding domain of nuclear receptors for allosteric control.
Mol Cell Endocrinol
; 348(2): 394-402, 2012 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-21878368
12.
The oncoprotein BCL11A binds to orphan nuclear receptor TLX and potentiates its transrepressive function.
PLoS One
; 7(6): e37963, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22675500