Detalhe da pesquisa
1.
Hnrnpk protects against osteoarthritis through targeting WWC1 mRNA and inhibiting Hippo signaling pathway.
Mol Ther
; 32(5): 1461-1478, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38414246
2.
Maslinic acid alleviates intervertebral disc degeneration by inhibiting the PI3K/AKT and NF-κB signaling pathways.
Acta Biochim Biophys Sin (Shanghai)
; 2024 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38495003
3.
Self-amplifying loop of NF-κB and periostin initiated by PIEZO1 accelerates mechano-induced senescence of nucleus pulposus cells and intervertebral disc degeneration.
Mol Ther
; 30(10): 3241-3256, 2022 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35619555
4.
MET promotes the proliferation and differentiation of myoblasts.
Exp Cell Res
; 388(2): 111838, 2020 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31930964
5.
A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud.
Genet Med
; 22(1): 189-198, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31395945
6.
Melatonin prevents bone destruction in mice with retinoic acid-induced osteoporosis.
Mol Med
; 25(1): 43, 2019 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31462213
7.
MTNR1B loss promotes chordoma recurrence by abrogating melatonin-mediated ß-catenin signaling repression.
J Pineal Res
; 67(2): e12588, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31140197
8.
Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous Dysplasia.
Am J Hum Genet
; 97(6): 837-47, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26637977
9.
Mutant MAPK7-Induced Idiopathic Scoliosis is Linked to Impaired Osteogenesis.
Cell Physiol Biochem
; 48(3): 880-890, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30032135
10.
Dual novel mutations in SLC26A2 in two siblings with multiple epiphyseal dysplasia 4 from a Chinese family: a case report.
BMC Med Genet
; 19(1): 70, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29724173
11.
Melatonin-mediated miR-526b-3p and miR-590-5p upregulation promotes chondrogenic differentiation of human mesenchymal stem cells.
J Pineal Res
; 65(1): e12483, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29498095
12.
Successful surgery for a neuromuscular scoliosis patient by pulmonary rehabilitation with forced vital capacity below 30.
Eur Spine J
; 27(9): 2072-2075, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29340778
13.
Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis.
Hum Mutat
; 38(11): 1500-1510, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28714182
14.
What is the Difference in Morphologic Features of the Thoracic Pedicle Between Patients With Adolescent Idiopathic Scoliosis and Healthy Subjects? A CT-based Case-control Study.
Clin Orthop Relat Res
; 475(11): 2765-2774, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28766159
15.
Correction to: Melatonin prevents bone destruction in mice with retinoic acid-induced osteoporosis.
Mol Med
; 27(1): 136, 2021 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34702160
16.
Melatonin reversed tumor necrosis factor-alpha-inhibited osteogenesis of human mesenchymal stem cells by stabilizing SMAD1 protein.
J Pineal Res
; 61(3): 317-27, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27265199
17.
Interspinous spacers versus posterior lumbar interbody fusion for degenerative lumbar spinal diseases: a meta-analysis of prospective studies.
Int Orthop
; 40(6): 1135-42, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26907877
18.
Disclosing the Hidden Structure and Underlying Mutational Mechanism of a Novel Type of Duplication CNV Responsible for Hereditary Multiple Osteochondromas.
Hum Mutat
; 36(8): 758-63, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25990786
19.
Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions.
Hum Genet
; 134(6): 589-603, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25792359
20.
Response to Potuijt et al.
Genet Med
; 22(4): 819-820, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31822852