Detalhe da pesquisa
1.
Deficient or Excess Folic Acid Supply During Pregnancy Alter Cortical Neurodevelopment in Mouse Offspring.
Cereb Cortex
; 31(1): 635-649, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32995858
2.
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.
Brain
; 142(9): 2617-2630, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31327001
3.
Maternal exposure to carbamazepine at environmental concentrations can cross intestinal and placental barriers.
Biochem Biophys Res Commun
; 474(2): 291-295, 2016 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27105911
4.
Autophagy-linked FYVE containing protein WDFY3 interacts with TRAF6 and modulates RANKL-induced osteoclastogenesis.
J Autoimmun
; 73: 73-84, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27330028
5.
Prenatal folic acid and vitamin B12 imbalance alter neuronal morphology and synaptic density in the mouse neocortex.
Commun Biol
; 6(1): 1133, 2023 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37938221
6.
Corrigendum to "Autophagy-linked FYVE containing protein WDFY3 interacts with TRAF6 and modulates RANKL-induced osteoclastogenesis" [J. Autoimmun. 73C (2016) 73-84].
J Autoimmun
; 84: 132, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28757133
7.
WDFY3 mutation alters laminar position and morphology of cortical neurons.
Mol Autism
; 13(1): 27, 2022 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35733184
8.
A genome-wide CRISPR screen identifies WDFY3 as a regulator of macrophage efferocytosis.
Nat Commun
; 13(1): 7929, 2022 12 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36566259
9.
Wdfy3 regulates glycophagy, mitophagy, and synaptic plasticity.
J Cereb Blood Flow Metab
; 41(12): 3213-3231, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34187232
10.
Pak1ip1 Loss-of-Function Leads to Cell Cycle Arrest, Loss of Neural Crest Cells, and Craniofacial Abnormalities.
Front Cell Dev Biol
; 8: 510063, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32984348
11.
Correction: WDFY3 mutation alters laminar position and morphology of cortical neurons.
Mol Autism
; 14(1): 4, 2023 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36721238
12.
Beyond autophagy: a novel role for autism-linked Wdfy3 in brain mitophagy.
Sci Rep
; 8(1): 11348, 2018 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30054502
13.
Germline Chd8 haploinsufficiency alters brain development in mouse.
Nat Neurosci
; 20(8): 1062-1073, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28671691
14.
Prenatal Neurogenesis in Autism Spectrum Disorders.
Front Chem
; 4: 12, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27014681
15.
The emerging roles of ribosome biogenesis in craniofacial development.
Front Physiol
; 5: 26, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24550838
16.
Neural crest-derived mesenchymal cells require Wnt signaling for their development and drive invagination of the telencephalic midline.
PLoS One
; 9(2): e86025, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24516524
17.
Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology.
Nat Commun
; 5: 4692, 2014 Sep 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25198012
18.
A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting.
PLoS One
; 8(7): e69333, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23935987