Detalhe da pesquisa
1.
Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations.
Proc Natl Acad Sci U S A
; 121(18): e2310283121, 2024 Apr 30.
Artigo
Inglês
| MEDLINE | ID: mdl-38669183
2.
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning.
Am J Hum Genet
; 109(2): 270-281, 2022 02 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35063063
3.
PpHY5 is involved in anthocyanin coloration in the peach flesh surrounding the stone.
Plant J
; 114(4): 951-964, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36919360
4.
Circ-FNDC3B Functions as an Oncogenic Factor in Esophageal Squamous Cell Carcinoma via Upregulating MYO5A by Absorbing miR-136-5p and miR-370-3p.
Biochem Genet
; 61(5): 1917-1936, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-36884165
5.
Genome-Wide Analysis of ATP Binding Cassette (ABC) Transporters in Peach (Prunus persica) and Identification of a Gene PpABCC1 Involved in Anthocyanin Accumulation.
Int J Mol Sci
; 24(3)2023 Jan 18.
Artigo
Inglês
| MEDLINE | ID: mdl-36768256
6.
Functional characteristics of a broad spectrum of TBX6 variants in Mayer-Rokitansky-Küster-Hauser syndrome.
Genet Med
; 24(11): 2262-2273, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36112137
7.
T2DM-elicited oxidative stress represses MTA3 expression in mouse Leydig cells.
Reproduction
; 163(5): 267-280, 2022 03 24.
Artigo
Inglês
| MEDLINE | ID: mdl-35239504
8.
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS).
J Med Genet
; 58(1): 41-47, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32381727
9.
Dynamic Maritime Traffic Pattern Recognition with Online Cleaning, Compression, Partition, and Clustering of AIS Data.
Sensors (Basel)
; 22(16)2022 Aug 22.
Artigo
Inglês
| MEDLINE | ID: mdl-36016066
10.
Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosis.
BMC Musculoskelet Disord
; 22(1): 483, 2021 May 25.
Artigo
Inglês
| MEDLINE | ID: mdl-34034738
11.
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.
Hum Mutat
; 41(1): 182-195, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31471994
12.
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.
BMC Med Genet
; 21(1): 115, 2020 05 27.
Artigo
Inglês
| MEDLINE | ID: mdl-32460719
13.
Identification of novel FBN1 variations implicated in congenital scoliosis.
J Hum Genet
; 65(3): 221-230, 2020 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-31827250
14.
Estrogen Receptors (ESRs) Mutations in Adolescent Idiopathic Scoliosis: A Cross-Sectional Study.
Med Sci Monit
; 26: e921611, 2020 Mar 16.
Artigo
Inglês
| MEDLINE | ID: mdl-32218412
15.
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome.
BMC Musculoskelet Disord
; 21(1): 220, 2020 Apr 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32278351
16.
N-myc downstream-regulated gene 4, up-regulated by tumor necrosis factor-α and nuclear factor kappa B, aggravates cardiac ischemia/reperfusion injury by inhibiting reperfusion injury salvage kinase pathway.
Basic Res Cardiol
; 111(2): 11, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26780215
17.
IL-17 mediates inflammatory reactions via p38/c-Fos and JNK/c-Jun activation in an AP-1-dependent manner in human nucleus pulposus cells.
J Transl Med
; 14: 77, 2016 Mar 17.
Artigo
Inglês
| MEDLINE | ID: mdl-26988982
18.
Different locations of RANTES and its receptors on mouse epididymal spermatozoa.
Reprod Fertil Dev
; 2015 Mar 19.
Artigo
Inglês
| MEDLINE | ID: mdl-25786351
19.
ADAMTS-7 exhibits elevated expression in cartilage of osteonecrosis of femoral head and has a positive correlation with TNF- α and NF- κ B P65.
Mediators Inflamm
; 2015: 196702, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25653475
20.
Decoding Macrophage Subtypes to Engineer Modulating Hydrogels for the Alleviation of Intervertebral Disk Degeneration.
Adv Sci (Weinh)
; 11(1): e2304480, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-37939288