Detalhe da pesquisa
1.
Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development.
Proc Natl Acad Sci U S A
; 119(31): e2116974119, 2022 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35881792
2.
Revisiting the embryogenesis of lip and palate development.
Oral Dis
; 28(5): 1306-1326, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35226783
3.
A Cyclin A-Myb-MuvB-Aurora B network regulates the choice between mitotic cycles and polyploid endoreplication cycles.
PLoS Genet
; 15(7): e1008253, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31291240
4.
Extending the allelic spectrum at noncoding risk loci of orofacial clefting.
Hum Mutat
; 42(8): 1066-1078, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34004033
5.
Periderm: Life-cycle and function during orofacial and epidermal development.
Semin Cell Dev Biol
; 91: 75-83, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28803895
6.
p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palate.
PLoS Genet
; 13(6): e1006828, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28604778
7.
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.
Hum Mol Genet
; 26(10): 1863-1876, 2017 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334996
8.
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
Hum Mol Genet
; 26(4): 829-842, 2017 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28087736
9.
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
10.
Cleft lip and palate: understanding genetic and environmental influences.
Nat Rev Genet
; 12(3): 167-78, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21331089
11.
Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate.
Hum Mol Genet
; 23(9): 2468-80, 2014 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24362885
12.
Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.
Hum Mol Genet
; 23(10): 2569-79, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24363063
13.
Smad4-Irf6 genetic interaction and TGFß-mediated IRF6 signaling cascade are crucial for palatal fusion in mice.
Development
; 140(6): 1220-30, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23406900
14.
Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptors.
J Virol
; 89(1): 262-74, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25320325
15.
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis.
Genet Med
; 18(11): 1158-1162, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26963285
16.
IRF6 is a mediator of Notch pro-differentiation and tumour suppressive function in keratinocytes.
EMBO J
; 30(22): 4571-85, 2011 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21909072
17.
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus.
Am J Hum Genet
; 90(1): 69-75, 2012 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22197488
18.
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.
Am J Hum Genet
; 91(3): 565-71, 2012 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22901946
19.
Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders.
Am J Med Genet A
; 167A(3): 545-52, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25691407
20.
Mammalian neurogenesis requires Treacle-Plk1 for precise control of spindle orientation, mitotic progression, and maintenance of neural progenitor cells.
PLoS Genet
; 8(3): e1002566, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22479190