Detalhe da pesquisa
1.
Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish.
Hum Mutat
; 42(4): 392-407, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33382518
2.
Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction.
Genes (Basel)
; 14(4)2023 03 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37107589
3.
Genetic animal modeling for idiopathic scoliosis research: history and considerations.
Spine Deform
; 10(5): 1003-1016, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35430722
4.
Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease.
Genes (Basel)
; 12(6)2021 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34208743
5.
Severity of Idiopathic Scoliosis Is Associated with Differential Methylation: An Epigenome-Wide Association Study of Monozygotic Twins with Idiopathic Scoliosis.
Genes (Basel)
; 12(8)2021 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34440365
6.
Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology.
G3 (Bethesda)
; 8(8): 2663-2672, 2018 07 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-29930198
7.
Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis.
Spine Deform
; 3(4): 288-296, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26120555
8.
Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis.
G3 (Bethesda)
; 5(2): 167-74, 2014 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25504735