Detalhe da pesquisa
1.
Hypomorphic and dominant-negative impact of truncated SOX9 dysregulates Hedgehog-Wnt signaling, causing campomelia.
Proc Natl Acad Sci U S A
; 120(1): e2208623119, 2023 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36584300
2.
SOX9 and SOX10 control fluid homeostasis in the inner ear for hearing through independent and cooperative mechanisms.
Proc Natl Acad Sci U S A
; 119(46): e2122121119, 2022 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36343245
3.
ß1 Integrin regulates convergent extension in mouse notogenesis, ensures notochord integrity and the morphogenesis of vertebrae and intervertebral discs.
Development
; 147(22)2020 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33051257
4.
Fbxo9 functions downstream of Sox10 to determine neuron-glial fate choice in the dorsal root ganglia through Neurog2 destabilization.
Proc Natl Acad Sci U S A
; 117(8): 4199-4210, 2020 02 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32029586
5.
Integrative analysis of metabolomic, genomic, and imaging-based phenotypes identify very-low-density lipoprotein as a potential risk factor for lumbar Modic changes.
Eur Spine J
; 31(3): 735-745, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34564762
6.
Sox2 and FGF20 interact to regulate organ of Corti hair cell and supporting cell development in a spatially-graded manner.
PLoS Genet
; 15(7): e1008254, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31276493
7.
Synergistic co-regulation and competition by a SOX9-GLI-FOXA phasic transcriptional network coordinate chondrocyte differentiation transitions.
PLoS Genet
; 14(4): e1007346, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29659575
8.
Activating the unfolded protein response in osteocytes causes hyperostosis consistent with craniodiaphyseal dysplasia.
Hum Mol Genet
; 26(23): 4572-4587, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28973168
9.
Identification of Genes Associated With Hirschsprung Disease, Based on Whole-Genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development.
Gastroenterology
; 155(6): 1908-1922.e5, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30217742
10.
Quantitative Phase Imaging Flow Cytometry for Ultra-Large-Scale Single-Cell Biophysical Phenotyping.
Cytometry A
; 95(5): 510-520, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31012276
11.
White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathies.
Dev Biol
; 417(2): 229-51, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27059883
12.
Hypertrophic chondrocytes can become osteoblasts and osteocytes in endochondral bone formation.
Proc Natl Acad Sci U S A
; 111(33): 12097-102, 2014 Aug 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25092332
13.
Predicting the spatiotemporal dynamics of hair follicle patterns in the developing mouse.
Proc Natl Acad Sci U S A
; 111(7): 2596-601, 2014 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-24550288
14.
Label-Free Quantitative Proteomics Reveals Survival Mechanisms Developed by Hypertrophic Chondrocytes under ER Stress.
J Proteome Res
; 15(1): 86-99, 2016 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26587667
15.
Kif5b controls the localization of myofibril components for their assembly and linkage to the myotendinous junctions.
Development
; 140(3): 617-26, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23293293
16.
Phosphorylation of Sox9 is required for neural crest delamination and is regulated downstream of BMP and canonical Wnt signaling.
Proc Natl Acad Sci U S A
; 110(8): 2882-7, 2013 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382206
17.
MT1-MMP cleaves Dll1 to negatively regulate Notch signalling to maintain normal B-cell development.
EMBO J
; 30(11): 2281-93, 2011 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21572390
18.
Fate of growth plate hypertrophic chondrocytes: death or lineage extension?
Dev Growth Differ
; 57(2): 179-92, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25714187
19.
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range.
Nature
; 458(7242): 1196-200, 2009 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-19252479
20.
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups.
J Med Genet
; 51(6): 401-6, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24721834