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Nanjing Medical University

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Osbpl2 deficiency inhibits Rho/ROCK2/p-ERM signaling and impairs actin cytoskeletal regulation in auditory cells

JOURNAL OF BIOMEDICAL RESEARCH

IF2.4

2025-11-011

PRE

OSBPL2 deficiency impaired cochlear blood-labyrinth barrier via activation of NF-κB signaling pathway

OSBPL2缺乏通过激活NF-κB信号通路损害了耳蜗血-迷路屏障。

Hearing Research

IF2.5

2025-09-150

PRE

APOE4 impairs macrophage lipophagy and promotes demyelination of spiral ganglion neurons in mouse cochleae

APOE4损害小鼠耳蜗螺旋神经节细胞的巨噬细胞脂噬作用，并促进其脱髓鞘。

CELL DEATH DISCOVERY

IF7

2025-04-210

Implication of GPRASP2 in the Proliferation and Hair Cell-Forming of Cochlear Supporting Cells

CELL PROLIFERATION

IF5.6

2024-12-150

OAAI

GPRASP2 deficiency contributes to apoptosis in the spiral ganglion cells via the AMPK/DRP1 signaling pathway

HELIYON

IF3.6

2024-08-010

OAAI

NPC1 Deficiency Contributes to Autophagy-Dependent Ferritinophagy in HEI-OC1 Auditory Cells

FRONTIERS IN MOLECULAR BIOSCIENCES

IF4

2022-07-2213

OAAI

Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling

JCI INSIGHT

IF6.1

2022-02-229

Oxysterol-binding protein-like 2 contributes to the developmental progression of preadipocytes by binding to β-catenin

CELL DEATH DISCOVERY

IF7

2021-05-175

OAAI

OSBPL2 deficiency upregulate SQLE expression increasing intracellular cholesterol and cholesteryl ester by AMPK/SP1 and SREBF2 signalling pathway

OSBPL2缺陷通过AMPK/SP1和SREBF2信号通路上调SQLE表达增加细胞内胆固醇和胆固醇酯

EXPERIMENTAL CELL RESEARCH

IF3.5

2019-10-0130

OAAI

Deletion of OSBPL2 in auditory cells increases cholesterol biosynthesis and drives reactive oxygen species production by inhibiting AMPK activity

CELL DEATH & DISEASE

IF9.6

2019-08-1931

OAAI

OSBPL2-disrupted pigs recapitulate dual features of human hearing loss and hypercholesterolaemia

JOURNAL OF GENETICS AND GENOMICS

IF7.1

2019-08-0128

OAAI

Dynamic expression analysis of armc10, the homologous gene of human GPRASP2, in zebrafish embryos

MOLECULAR MEDICINE REPORTS

IF3.5

2017-08-244

OAAI

GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss

JOURNAL OF MEDICAL GENETICS

IF3.7

2017-01-1715

OAAI

IVS8+1 DelG, a Novel Splice Site Mutation Causing DFNA5 Deafness in a Chinese Family

CHINESE MEDICAL JOURNAL

IF7.3

2015-09-2030

OAAI

Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations

SCIENTIFIC REPORTS

IF3.9

2015-06-027

OAAI

Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing

GENETICS IN MEDICINE

IF6.2

2015-03-0158

OAAI

The association between abnormal microRNA-10b expression and cancer risk: a meta-analysis

SCIENTIFIC REPORTS

IF3.9

2014-12-1615

OAAI

Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

JOURNAL OF TRANSLATIONAL MEDICINE

IF7.5

2014-11-1245

OAAI

Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non-syndromic hearing loss

鉴定导致常染色体显性非综合征性听力损失的新型错义EYA4突变I411K

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

IF5.8

2014-09-1920

OAAI

A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family

GJB2基因中一种新的复合杂合突变导致一个家庭的非综合征性听力损失

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

IF5.8

2013-12-098

OAAI

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