Detalhe da pesquisa
1.
Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology.
Annu Rev Neurosci
; 43: 315-336, 2020 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32101484
2.
Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects.
Hum Genet
; 143(3): 263-277, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38451291
3.
ALDH1A2-related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway.
Am J Med Genet A
; 191(1): 90-99, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36263470
4.
Mouse Models of Neural Tube Defects.
Adv Exp Med Biol
; 1236: 39-64, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32304068
5.
Reduced maternal vitamin A status increases the incidence of normal aortic arch variants.
Genesis
; 57(7-8): e23326, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31299141
6.
Supt20 is required for development of the axial skeleton.
Dev Biol
; 421(2): 245-257, 2017 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27894818
7.
Hard to swallow: Developmental biological insights into pediatric dysphagia.
Dev Biol
; 409(2): 329-42, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26554723
8.
Model organisms and mechanisms of gene-environment interactions in structural birth defects.
Genesis
; 59(11): e23461, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34739742
9.
Hectd1 is required for development of the junctional zone of the placenta.
Dev Biol
; 392(2): 368-80, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24855001
10.
Reduced maternal vitamin A status increases the incidence of normal aortic arch variants.
Genesis
; 57(11-12): e23343, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31682315
11.
HectD1 E3 ligase modifies adenomatous polyposis coli (APC) with polyubiquitin to promote the APC-axin interaction.
J Biol Chem
; 288(6): 3753-67, 2013 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23277359
12.
The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure.
Development
; 137(18): 3079-88, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20702562
13.
Mouse as a model for multifactorial inheritance of neural tube defects.
Birth Defects Res C Embryo Today
; 96(2): 193-205, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22692891
14.
Does the cranial mesenchyme contribute to neural fold elevation during neurulation?
Birth Defects Res A Clin Mol Teratol
; 94(10): 841-8, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22945385
15.
Parental obesity-induced changes in developmental programming.
Front Cell Dev Biol
; 10: 918080, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36274855
16.
The visceral yolk sac endoderm provides for absorption of nutrients to the embryo during neurulation.
Birth Defects Res A Clin Mol Teratol
; 88(8): 593-600, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20672346
17.
Hsp90 and complex birth defects: A plausible mechanism for the interaction of genes and environment.
Neurosci Lett
; 716: 134680, 2020 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31821846
18.
Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome.
Birth Defects Res
; 112(16): 1194-1208, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32431076
19.
Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome.
Front Neurol
; 11: 4, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32082240
20.
Cell polarity pathways converge and extend to regulate neural tube closure.
Trends Cell Biol
; 13(9): 451-4, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12946622