Detalhe da pesquisa
1.
Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex.
Cereb Cortex
; 29(9): 3738-3751, 2019 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30307479
2.
Sip1 regulates the generation of the inner nuclear layer retinal cell lineages in mammals.
Development
; 143(15): 2829-41, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27385012
3.
Transcription factor Zeb2 regulates commitment to plasmacytoid dendritic cell and monocyte fate.
Proc Natl Acad Sci U S A
; 113(51): 14775-14780, 2016 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27930303
4.
De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.
Hum Mol Genet
; 24(22): 6390-402, 2015 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26319231
5.
Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease.
Kidney Int
; 90(6): 1262-1273, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27591083
6.
Regulation of trunk neural crest delamination by δEF1 and Sip1 in the chicken embryo.
Dev Growth Differ
; 58(2): 205-14, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26691438
7.
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.
Mutagenesis
; 31(1): 61-7, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26220009
8.
SIP1 expression patterns in brain investigated by generating a SIP1-EGFP reporter knock-in mouse.
Genesis
; 52(1): 56-67, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24243579
9.
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
Eur J Oral Sci
; 122(1): 15-20, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24329876
10.
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice.
PLoS Genet
; 7(9): e1002307, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21980308
11.
Endothelial Zeb2 preserves the hepatic angioarchitecture and protects against liver fibrosis.
Cardiovasc Res
; 118(5): 1262-1275, 2022 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33909875
12.
DeltaEF1 mediates TGF-beta signaling in vascular smooth muscle cell differentiation.
Dev Cell
; 11(1): 93-104, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16824956
13.
Mesenchymal cell remodeling during mouse secondary palate reorientation.
Dev Dyn
; 239(7): 2110-7, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20549719
14.
Down-regulation of TCF8 is involved in the leukemogenesis of adult T-cell leukemia/lymphoma.
Blood
; 112(2): 383-93, 2008 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18467597
15.
Neuroglycan C, a brain-specific chondroitin sulfate proteoglycan, interacts with pleiotrophin, a heparin-binding growth factor.
Neurochem Res
; 35(8): 1131-7, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20369290
16.
Introduction of a de novo Creb-binding protein gene mutation in sperm to produce a Rubinstein-Taybi syndrome model using inbred C57BL/6 mice.
Brain Res
; 1749: 147140, 2020 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33022214
17.
UV-B radiation induces epithelial tumors in mice lacking DNA polymerase eta and mesenchymal tumors in mice deficient for DNA polymerase iota.
Mol Cell Biol
; 26(20): 7696-706, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17015482
18.
The zinc finger transcription factor ZFHX1A is linked to cell proliferation by Rb-E2F1.
Biochem J
; 408(1): 79-85, 2007 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17655524
19.
The transcription factor ZEB1 is aberrantly expressed in aggressive uterine cancers.
Cancer Res
; 66(7): 3893-902, 2006 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16585218
20.
Ndrg1-deficient mice exhibit a progressive demyelinating disorder of peripheral nerves.
Mol Cell Biol
; 24(9): 3949-56, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15082788