Detalhe da pesquisa
1.
PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS.
EMBO Rep
; 25(3): 1256-1281, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38429579
2.
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.
Hum Mol Genet
; 32(15): 2485-2501, 2023 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37171606
3.
Generation of a mouse model of the neurodevelopmental disorder with dysmorphic facies and distal limb anomalies syndrome.
Hum Mol Genet
; 31(20): 3405-3421, 2022 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35604347
4.
Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson-Forssman-Lehmann Syndrome.
Hum Mol Genet
; 30(7): 575-594, 2021 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33772537
5.
ATRX affects the repair of telomeric DSBs by promoting cohesion and a DAXX-dependent activity.
PLoS Biol
; 18(1): e3000594, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31895940
6.
Correction to: C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum.
J Neuroinflammation
; 17(1): 32, 2020 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31973732
7.
C3aR signaling and gliosis in response to neurodevelopmental damage in the cerebellum.
J Neuroinflammation
; 16(1): 135, 2019 Jul 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31272467
8.
The role of ISWI chromatin remodeling complexes in brain development and neurodevelopmental disorders.
Mol Cell Neurosci
; 87: 55-64, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29249292
9.
Retinal interneuron survival requires non-cell-autonomous Atrx activity.
Hum Mol Genet
; 25(21): 4787-4803, 2016 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28173139
10.
Genome-wide characterisation of Foxa1 binding sites reveals several mechanisms for regulating neuronal differentiation in midbrain dopamine cells.
Development
; 142(7): 1315-24, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25804738
11.
A Notch-Gli2 axis sustains Hedgehog responsiveness of neural progenitors and Müller glia.
Dev Biol
; 411(1): 85-100, 2016 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26795056
12.
Hedgehog regulates Norrie disease protein to drive neural progenitor self-renewal.
Hum Mol Genet
; 22(5): 1005-16, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23201751
13.
Conditional c-MYC activation in catecholaminergic cells drives distinct neuroendocrine tumors: neuroblastoma vs somatostatinoma.
bioRxiv
; 2024 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38559042
14.
The imitation switch ATPase Snf2l is required for superovulation and regulates Fgl2 in differentiating mouse granulosa cells.
Biol Reprod
; 88(6): 142, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23616592
15.
VGF is required for recovery after focal stroke.
Exp Neurol
; 362: 114326, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36682400
16.
Novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of Hoxa cluster genes and promotion of neuronal lineage.
Neurooncol Adv
; 5(1): vdad003, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36845293
17.
PHF6 interacts with the nucleosome remodeling and deacetylation (NuRD) complex.
J Proteome Res
; 11(8): 4326-37, 2012 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22720776
18.
Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
Hum Mol Genet
; 18(5): 966-77, 2009 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19088125
19.
Impaired SNF2L Chromatin Remodeling Prolongs Accessibility at Promoters Enriched for Fos/Jun Binding Sites and Delays Granule Neuron Differentiation.
Front Mol Neurosci
; 14: 680280, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34295220
20.
Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse Retina.
Neuroscience
; 452: 169-180, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33197500