Detalhe da pesquisa
1.
Apical expansion of calvarial osteoblasts and suture patency is dependent on fibronectin cues.
Development
; 151(7)2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38602508
2.
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research.
Development
; 147(18)2020 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32958507
3.
Processes and patterns: Insights on cranial covariation from an Apert syndrome mouse model.
Dev Dyn
; 251(10): 1684-1697, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35582939
4.
Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects.
Development
; 145(19)2018 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30228104
5.
The FaceBase Consortium: a comprehensive resource for craniofacial researchers.
Development
; 143(14): 2677-88, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287806
6.
Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1.
Development
; 139(7): 1346-58, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22395741
7.
Transcriptomic landscape of human induced pluripotent stem cell-derived osteogenic differentiation identifies a regulatory role of KLF16.
bioRxiv
; 2024 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38405902
8.
Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome.
Dev Biol
; 368(2): 283-93, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22664175
9.
Apical expansion of calvarial osteoblasts and suture patency is dependent on graded fibronectin cues.
bioRxiv
; 2023 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36711975
10.
The role of vertebrate models in understanding craniosynostosis.
Childs Nerv Syst
; 28(9): 1471-81, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22872264
11.
Mouse models of Apert syndrome.
Childs Nerv Syst
; 28(9): 1505-10, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22872267
12.
Cleft Palate in Apert Syndrome.
J Dev Biol
; 10(3)2022 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35997397
13.
Single-cell analysis identifies a key role for Hhip in murine coronal suture development.
Nat Commun
; 12(1): 7132, 2021 12 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34880220
14.
Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice.
Laryngoscope
; 131(4): E1349-E1356, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32886384
15.
Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology.
Dev Biol
; 328(2): 273-84, 2009 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19389359
16.
Sox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiation.
J Cell Biol
; 168(7): 1065-76, 2005 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-15781477
17.
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex.
J Dev Biol
; 8(4)2020 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33291480
18.
Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis.
Cell Rep
; 32(1): 107871, 2020 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32640236
19.
Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis.
J Vis Exp
; (154)2019 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31904019
20.
C-type natriuretic peptide analog treatment of craniosynostosis in a Crouzon syndrome mouse model.
PLoS One
; 13(7): e0201492, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30048539