Detalhe da pesquisa
1.
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development.
Development
; 148(17)2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34414417
2.
Transcriptomic analysis reveals the role of SIX1 in mouse cranial neural crest patterning and bone development.
Dev Dyn
; 252(10): 1303-1315, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37183792
3.
Mcrs1 is required for branchial arch and cranial cartilage development.
Dev Biol
; 489: 62-75, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35697116
4.
Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome.
Hum Mol Genet
; 29(6): 1002-1017, 2020 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32047912
5.
Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease.
Genesis
; 59(12): e23453, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34664392
6.
The impact of technological endodontic resources on the training of the general dentist.
Eur J Dent Educ
; 25(2): 332-341, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33012127
7.
Negative regulation of endothelin signaling by SIX1 is required for proper maxillary development.
Development
; 144(11): 2021-2031, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28455376
8.
Loss-of-function of Endothelin receptor type A results in Oro-Oto-Cardiac syndrome.
Am J Med Genet A
; 182(5): 1104-1116, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32133772
9.
Runx2-I is an Early Regulator of Epithelial-Mesenchymal Cell Transition in the Chick Embryo.
Dev Dyn
; 247(3): 542-554, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28631378
10.
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia.
Am J Hum Genet
; 96(4): 519-31, 2015 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25772936
11.
Nkx2.5 regulates endothelin converting enzyme-1 during pharyngeal arch patterning.
Genesis
; 55(3)2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28109039
12.
Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome.
Hum Mol Genet
; 29(9): 1580, 2020 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32358605
13.
Cre recombinase-regulated Endothelin1 transgenic mouse lines: novel tools for analysis of embryonic and adult disorders.
Dev Biol
; 400(2): 191-201, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25725491
14.
Ectodermal-derived Endothelin1 is required for patterning the distal and intermediate domains of the mouse mandibular arch.
Dev Biol
; 371(1): 47-56, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22902530
15.
Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies.
Am J Med Genet C Semin Med Genet
; 163C(4): 306-17, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24123988
16.
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation.
Front Cell Dev Biol
; 11: 1274788, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37854072
17.
Advances in Understanding the Pathogenesis of Craniofacial Birth Defects.
J Dev Biol
; 10(3)2022 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35893122
18.
Repressive Interactions Between Transcription Factors Separate Different Embryonic Ectodermal Domains.
Front Cell Dev Biol
; 10: 786052, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35198557
19.
Collagen gel analysis of epithelial-mesenchymal transition in the embryo heart: an in vitro model system for the analysis of tissue interaction, signal transduction, and environmental effects.
Birth Defects Res C Embryo Today
; 93(4): 298-311, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22271679
20.
Mutations in SIX1 Associated with Branchio-oto-Renal Syndrome (BOR) Differentially Affect Otic Expression of Putative Target Genes.
J Dev Biol
; 9(3)2021 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34208995