Detalhe da pesquisa
1.
Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome.
Hum Mol Genet
; 32(12): 1959-1974, 2023 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36790128
2.
Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder.
Dev Neurosci
; 46(1): 1-21, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-37231803
3.
The strengths of the genetic approach to understanding neural systems development and function: Ray Guillery's synthesis.
Eur J Neurosci
; 49(7): 888-899, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29883004
4.
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
5.
Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Cereb Cortex
; 25(10): 3977-93, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25452572
6.
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.
Hum Mol Genet
; 22(2): 300-12, 2013 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23077214
7.
Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome.
Proc Natl Acad Sci U S A
; 109(45): 18601-6, 2012 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23091025
8.
Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium.
Development
; 137(15): 2471-81, 2010 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20573694
9.
Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.
Proc Natl Acad Sci U S A
; 106(38): 16434-45, 2009 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-19805316
10.
Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome.
Dis Model Mech
; 15(2)2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33722956
11.
Developmental and degenerative features in a complicated spastic paraplegia.
Ann Neurol
; 67(4): 516-25, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20437587
12.
Why Does the Face Predict the Brain? Neural Crest Induction, Craniofacial Morphogenesis, and Neural Circuit Development.
Front Physiol
; 11: 610970, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33362582
13.
Disrupted Coordination of Hypoglossal Motor Control in a Mouse Model of Pediatric Dysphagia in DiGeorge/22q11.2 Deletion Syndrome.
eNeuro
; 7(5)2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32855199
14.
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
15.
Molecular specification and patterning of progenitor cells in the lateral and medial ganglionic eminences.
J Neurosci
; 28(38): 9504-18, 2008 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-18799682
16.
In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
J Neurodev Disord
; 11(1): 7, 2019 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31174463
17.
Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment.
Neuron
; 102(6): 1127-1142.e3, 2019 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31079872
18.
Altered neurobiological function of brainstem hypoglossal neurons in DiGeorge/22q11.2 Deletion Syndrome.
Neuroscience
; 359: 1-7, 2017 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28687307
19.
Retinoic acid signaling identifies a distinct precursor population in the developing and adult forebrain.
J Neurosci
; 25(33): 7636-47, 2005 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-16107650
20.
RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.
Mech Dev
; 111(1-2): 177-80, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11804793