Xin Cao

发表

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

Min Zhang, G. Xing, Cui Zhang, 2019, Experimental cell research.

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

Hongshun Wang, G. Xing, Jun Yao, 2022, JCI insight.

Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblings

X. Qian, Jie Chen, Xia Gao, 2013, International journal of audiology.

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

G. Xing, Cui Zhang, Changsong Lin, 2019, Cell Death & Disease.

Integrative Analyses Identify Potential Key Genes and Calcium-Signaling Pathway in Familial Atrioventricular Nodal Reentrant Tachycardia Using Whole-Exome Sequencing

Y. Zhu, Xiushan Wu, Zhenglin Yang, 2022, Frontiers in cardiovascular medicine.

Identification of a novel MYO6 mutation associated with autosomal dominant non-syndromic hearing loss in a Chinese family by whole-exome sequencing.

T. Tian, Jun Yao, Qinjun Wei, 2018, Genes & genetic systems.

Spatial and temporal expression patterns of Osbpl2a and Osbpl2b during zebrafish embryonic development.

G. Xing, Jun Yao, Qinjun Wei, 2016, International journal of pediatric otorhinolaryngology.

Effect of the tumor suppressor gene ING4 on the proliferation of MCF-7 human breast cancer cells.

Jun Yao, Qinjun Wei, Ya-jie Lu, 2012, Oncology letters.

OSBPL2 Is Required for the Binding of COPB1 to ATGL and the Regulation of Lipid Droplet Lipolysis

Tianming Wang, G. Xing, Jun Yao, 2020, iScience.

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

G. Xing, Changsong Lin, Jun Yao, 2017, Molecular medicine reports.

[Comparative analysis of conservation and regulatory network on core transcription factors in mouse inner ear development].

G. Xing, Xin Cao, Zhi-Qiang Chen, 2013, Yi chuan = Hereditas.

Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss.

G. Xing, Jun Yao, Qinjun Wei, 2018, International journal of pediatric otorhinolaryngology.

Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1

G. Xing, Xin Cao, Luyang Qin, 2015, Scientific Reports.

Metabolic Abnormalities Linked to Auditory Pathways in ApoE-Knockout HEI-OC1 Cells: A Transcription-Metabolism Co-Analysis

Hongshun Wang, Jun Yao, Qinjun Wei, 2022, Biomolecules.

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

G. Xing, Jun Yao, Qinjun Wei, 2015, Scientific Reports.

Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA

G. Xing, Jun Yao, Ya-jie Lu, 2015, Medicine.

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

G. Xing, Jun Yao, Ya-jie Lu, 2015, Chinese medical journal.

Comparative transcriptome analysis of auditory OC-1 cells and zebrafish inner ear tissues in the absence of human OSBPL2 orthologues.

Changsong Lin, Hongshun Wang, Jun Yao, 2019, Biochemical and biophysical research communications.

Inhibition of cell proliferation by siRNA targeting hPRLR in breast cancer MCF-7 cell line

Y. Shu, Qinjun Wei, Ya-jie Lu, 2007 .

Identification of a novel MYO 6 mutation associated with autosomal dominant non-syndromic hearing loss in a Chinese family by whole-exome sequencing

T. Tian, Jun Yao, Qinjun Wei, 2018 .

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

G. Xing, M. Tan, Jun Yao, 2014, International journal of molecular medicine.

Mitochondrial rRNA and tRNA and hearing function

G. Xing, Zhi-bin Chen, Xin Cao, 2007, Cell Research.

Analysis of Carbon Metabolism and Improvement of γ-Polyglutamic Acid Production from Bacillus subtilis NX-2

P. Ouyang, Sha Li, Hong Xu, 2010, Applied biochemistry and biotechnology.

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

G. Xing, Jun Yao, Qinjun Wei, 2014, Journal of Translational Medicine.

Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.

X. Bu, G. Xing, Qinjun Wei, 2006, Biochemical and biophysical research communications.

Gene silencing of hPRLR mRNA by RNA interference in human breast cancer cells.

Qinjun Wei, Ya-jie Lu, Xin Cao, 2008, Molecular medicine reports.

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

Tianming Wang, Hongshun Wang, Jun Yao, 2021, Cell death discovery.

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

Rongfeng Li, Yifan Dai, Min Zhang, 2019, Journal of genetics and genomics = Yi chuan xue bao.

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

C. Liu, Xiaonan Yang, G. Xing, 2014, Genetics in Medicine.

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

Jun Yao, Qinjun Wei, Ya-jie Lu, 2014, Scientific Reports.

Identification and characterization of microRNAs expressed in human breast cancer T-47D cells in response to prolactin treatment by Solexa deep-sequencing technology.

Li Guo, Jun Yao, Qinjun Wei, 2013, Biochemical and biophysical research communications.

The role of receptor‐type protein tyrosine phosphatases in cancer

Xin Cao, Tianming Wang, Yuan Qu, 2023, Precision Medical Sciences.

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

Hongshun Wang, Jun Yao, Qinjun Wei, 2022, Frontiers in Molecular Biosciences.

Expression and promoter methylation of the RASSF1A gene in sporadic breast cancers in Chinese women.

Yongmei Li, Qinjun Wei, Xin Cao, 2008, Oncology reports.

Single nucleotide polymorphisms and haplotypes analysis of DFNB1 locus in Chinese sporadic hearing impairment population.

G. Xing, Ya-jie Lu, Zhi-bin Chen, 2009, Chinese medical journal.

Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China

G. Xing, Jun Yao, Qinjun Wei, 2013, Journal of Translational Medicine.

A systematic review and meta-analysis of 235delC mutation of GJB2 gene

G. Xing, Jun Yao, Qinjun Wei, 2012, Journal of Translational Medicine.

A systematic review and meta-analysis of 235delC mutation of GJB2 gene

G. Xing, Jun Yao, Qinjun Wei, 2012, Journal of Translational Medicine.

Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China

X. Bu, G. Xing, Qinjun Wei, 2011, Journal of biomedical research.

Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.

X. Bu, G. Xing, Qinjun Wei, 2006, Biochemical and biophysical research communications.

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

G. Xing, Qinjun Wei, Ya-jie Lu, 2013, International journal of molecular medicine.

Clinical and Genetic Features in a Chinese Pedigree with Autosomal Dominant Auditory Neuropathy

X. Bu, G. Xing, Qinjun Wei, 2006, ORL.

Promotion of breast cancer cells MDA-MB-231 invasion by di(2-ethylhexyl)phthalate through matrix metalloproteinase-2/-9 overexpression

Z. Fu, Jian Cao, Lei Huang, 2016, Environmental Science and Pollution Research.

G protein-coupled receptor-associated sorting proteins: function and relevant disorders.

Min Zhang, Ya-jie Lu, Xin Cao, 2020, Yi chuan = Hereditas.

Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families

X. Bu, G. Xing, Qinjun Wei, 2013, International journal of audiology.

Inhibition of proliferation induced by anti-sense RNA of HDAC1 in MCF-7 cells.

Jun Yao, Qinjun Wei, Ya-jie Lu, 2009, Molecular medicine reports.

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

G. Xing, Jun Yao, Qinjun Wei, 2014, Journal of Translational Medicine.

Understanding of the molecular evolution of deafness-associated pathogenic mutations of connexin 26

Yi Fan, G. Xing, Xin Cao, 2014, Genetica.

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

G. Xing, Jun Yao, Qinjun Wei, 2017, Journal of Medical Genetics.