Detalhe da pesquisa
1.
AutDB: a platform to decode the genetic architecture of autism.
Nucleic Acids Res
; 46(D1): D1049-D1054, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29186576
2.
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
3.
Role of Cholesterol and Phospholipids in Amylin Misfolding, Aggregation and Etiology of Islet Amyloidosis.
Adv Exp Med Biol
; 855: 95-116, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26149927
4.
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
5.
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
6.
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
7.
A multifaceted approach for analyzing complex phenotypic data in rodent models of autism.
Mol Autism
; 10: 11, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30911366
8.
The ubiquitin ligase HECTD1 promotes retinoic acid signaling required for development of the aortic arch.
Dis Model Mech
; 12(1)2019 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30578278
9.
Polymerase chain reaction-based search for two alpha-globin gene mutations in India.
Hemoglobin
; 32(5): 485-90, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18932074
10.
Striving for Truly Inclusive Collaborations: An Interview with Industry Scientist Cherié Butts, PhD.
J Interferon Cytokine Res
; 42(2): 90-93, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35171705
11.
Perspectives on integration of cell extrinsic and cell intrinsic pathways of signaling required for differentiation of noradrenergic sympathetic ganglion neurons.
Auton Neurosci
; 126-127: 225-31, 2006 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-16647305
12.
Abnormal labyrinthine zone in the Hectd1-null placenta.
Placenta
; 38: 16-23, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26907377
13.
An explant assay for assessing cellular behavior of the cranial mesenchyme.
J Vis Exp
; (71)2013 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23381592
14.
Hectd1 regulates intracellular localization and secretion of Hsp90 to control cellular behavior of the cranial mesenchyme.
J Cell Biol
; 196(6): 789-800, 2012 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22431752
15.
Modeling neural tube defects in the mouse.
Curr Top Dev Biol
; 84: 1-35, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19186242
16.
Expression of Hand2 is sufficient for neurogenesis and cell type-specific gene expression in the enteric nervous system.
Dev Dyn
; 236(1): 93-105, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17075884
17.
Co-inheritance of the Hb Sun Prairie mutation with a point mutation at 5'-UTR in the eastern Indian population.
Br J Haematol
; 129(2): 282-6, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15813858