Detalhe da pesquisa
1.
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
2.
Phosphotungstic acid-enhanced microCT: Optimized protocols for embryonic and early postnatal mice.
Dev Dyn
; 249(4): 573-585, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31736206
3.
Altered metabolism and resistance to obesity in long-lived mice producing reduced levels of IGF-I.
Am J Physiol Endocrinol Metab
; 308(7): E545-53, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25648834
4.
Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice.
BMC Dev Biol
; 14: 8, 2014 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24580805
5.
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
6.
Embryonic cranial cartilage defects in the Fgfr3Y367C /+ mouse model of achondroplasia.
Anat Rec (Hoboken)
; 2023 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37747411
7.
A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium.
Elife
; 112022 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35704354
8.
Meckel's Cartilage in Mandibular Development and Dysmorphogenesis.
Front Genet
; 13: 871927, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35651944
9.
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
10.
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex.
J Dev Biol
; 8(4)2020 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33291480
11.
Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice.
Dis Model Mech
; 12(5)2019 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-31064775
12.
Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes.
Front Hum Neurosci
; 11: 369, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28790902