Detalhe da pesquisa
1.
The cell surface hyaluronidase TMEM2 plays an essential role in mouse neural crest cell development and survival.
PLoS Genet
; 18(7): e1009765, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35839257
2.
Synergistic role of retinoic acid signaling and Gata3 during primitive choanae formation.
Hum Mol Genet
; 30(24): 2383-2392, 2021 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34272563
3.
Craniofacial and dental characteristics of three Japanese individuals with genetically diagnosed SATB2-associated syndrome.
Am J Med Genet A
; 191(7): 1984-1989, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37141439
4.
The Association Between Runx Signaling and Craniofacial Development and Disease.
Curr Osteoporos Rep
; 20(1): 120-126, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34931296
5.
Fork-shaped mandibular incisors as a novel phenotype of LRP5-associated disorder.
Am J Med Genet A
; 185(5): 1544-1549, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33619830
6.
Comprehensive Orthodontic Treatment of a Patient With Prader-Willi Syndrome.
Cleft Palate Craniofac J
; 58(11): 1459-1467, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33272028
7.
Multidisciplinary Approach for Treating Malocclusion of Patient With Basal Cell Nevus Syndrome: A Case Report.
Cleft Palate Craniofac J
; 57(2): 255-262, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31382775
8.
Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresia.
Hum Mol Genet
; 26(7): 1268-1279, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28169399
9.
Orthodontic-Surgical Approach for Treating Skeletal Class III Malocclusion With Severe Maxillary Deficiency in Isolated Cleft Palate.
Cleft Palate Craniofac J
; 56(3): 400-407, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29787302
10.
Ventral neural patterning in the absence of a Shh activity gradient from the floorplate.
Dev Dyn
; 247(1): 170-184, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28891097
11.
Stage- and tissue-specific effect of cyclophosphamide during tooth development.
Eur J Orthod
; 41(5): 519-530, 2019 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30715254
12.
A quantitative method for defining high-arched palate using the Tcof1(+/-) mutant mouse as a model.
Dev Biol
; 415(2): 296-305, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26772999
13.
Loss of function mutation in the palmitoyl-transferase HHAT leads to syndromic 46,XY disorder of sex development by impeding Hedgehog protein palmitoylation and signaling.
PLoS Genet
; 10(5): e1004340, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24784881
14.
Runx/Cbfb signaling regulates postnatal development of granular convoluted tubule in the mouse submandibular gland.
Dev Dyn
; 244(3): 488-96, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25410786
15.
Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects.
PLoS Genet
; 8(10): e1002927, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23055936
16.
Isolation and characterization of SSEA-4-positive subpopulation of human deciduous dental pulp cells.
Clin Oral Investig
; 19(2): 363-71, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24862940
17.
Long-term stability of implant-anchored orthodontics in an adult patient with a Class II Division 2 malocclusion and a unilateral molar scissors-bite.
Am J Orthod Dentofacial Orthop
; 145(4 Suppl): S100-13, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24680017
18.
Characteristic craniofacial defects associated with a novel USP9X truncation mutation.
Hum Genome Var
; 11(1): 21, 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38755172
19.
Roles of heparan sulfate sulfation in dentinogenesis.
J Biol Chem
; 287(15): 12217-29, 2012 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22351753
20.
Stage-specific embryonic antigen-4 identifies human dental pulp stem cells.
Exp Cell Res
; 318(5): 453-63, 2012 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22266579