Detalhe da pesquisa
1.
Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency.
PLoS Genet
; 19(10): e1010952, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37782669
2.
Stabilization of ß-catenin promotes melanocyte specification at the expense of the Schwann cell lineage.
Development
; 149(2)2022 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34878101
3.
Zebrafish smarcc1a mutants reveal requirements for BAF chromatin remodeling complexes in distinguishing the atrioventricular canal from the cardiac chambers.
Dev Dyn
; 253(1): 157-172, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37083132
4.
Nkx genes establish second heart field cardiomyocyte progenitors at the arterial pole and pattern the venous pole through Isl1 repression.
Development
; 145(3)2018 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29361575
5.
Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.
Am J Hum Genet
; 98(5): 1001-1010, 2016 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27108799
6.
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.
Am J Med Genet A
; 176(11): 2259-2275, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30194818
7.
Nkx2.5 regulates endothelin converting enzyme-1 during pharyngeal arch patterning.
Genesis
; 55(3)2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28109039
8.
An early requirement for nkx2.5 ensures the first and second heart field ventricular identity and cardiac function into adulthood.
Dev Biol
; 400(1): 10-22, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25536398
9.
Nkx genes are essential for maintenance of ventricular identity.
Development
; 140(20): 4203-13, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24026123
10.
Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor.
Front Cell Neurosci
; 17: 1175895, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37275776
11.
Encephalopathy-causing mutations in Gß1 (GNB1) alter regulation of neuronal GIRK channels.
iScience
; 24(9): 103018, 2021 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34522861
12.
Genomic localization of the Z/EG transgene in the mouse genome.
Genesis
; 48(2): 96-100, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20014334
13.
Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood Epilepsy.
Cell Rep
; 33(4): 108303, 2020 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33113364
14.
A caveolin-dependent and PI3K/AKT-independent role of PTEN in ß-catenin transcriptional activity.
Nat Commun
; 6: 8093, 2015 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26307673
15.
A subpopulation of smooth muscle cells, derived from melanocyte-competent precursors, prevents patent ductus arteriosus.
PLoS One
; 8(1): e53183, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382837
16.
Transcriptomic analysis of mouse embryonic skin cells reveals previously unreported genes expressed in melanoblasts.
J Invest Dermatol
; 132(1): 170-8, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21850021
17.
Phosphorylation of BRN2 modulates its interaction with the Pax3 promoter to control melanocyte migration and proliferation.
Mol Cell Biol
; 32(7): 1237-47, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22290434
18.
General strategy to analyse coat colour phenotypes in mice.
Pigment Cell Melanoma Res
; 25(1): 117-9, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22085368
19.
Flanking genomic region of Tyr::Cre mice, rapid genotyping for homozygous mice.
Pigment Cell Res
; 20(4): 305-6, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17630964