Xuechao Zhao

发表

Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X-linked Alport syndrome

X. Kong, Xueliang Shang, Xuechao Zhao, 2020, Biomedical reports.

A method to mathematically determine transduction efficiency of lentivirus in HeLa cells

B. Liu, Xiaohong Kong, Chang Liu, 2014 .

Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing

X. Kong, Ning Liu, Xuechao Zhao, 2022, Neurological Sciences.

Mutation analysis of 419 family and prenatal diagnosis of 339 cases of spinal muscular atrophy in China

X. Kong, Zhen-hua Zhao, Ying-Fang Sun, 2020, BMC Medical Genetics.

Identification of microRNAome in rat bladder reveals miR-1949 as a potential inducer of bladder cancer following spinal cord injury.

B. Liu, Tianci Chu, Hengxing Zhou, 2015, Molecular medicine reports.

Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing

X. Kong, Xuechao Zhao, Conghui Wang, 2022, Neurological Sciences.

Mutation analysis of 419 family and prenatal diagnosis of 339 cases of spinal muscular atrophy in China

X. Kong, Zhen-hua Zhao, Ying-Fang Sun, 2020, BMC Medical Genetics.

A de novo and novel nonsense variants in ASXL2 gene is associated with Shashi-Pena syndrome.

X. Kong, Z. Jiao, Xuechao Zhao, 2022, European journal of medical genetics.

Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China

X. Kong, P. Dai, Xuechao Zhao, 2022, Frontiers in Medicine.

Genetic analysis by targeted next-generation sequencing and novel variation identification of maple syrup urine disease in Chinese Han population

X. Kong, Xiaofan Zhu, Xuechao Zhao, 2021, Scientific Reports.

An Experimental Novel Study: Angelica sinensis Prevents Epidural Fibrosis in Laminectomy Rats via Downregulation of Hydroxyproline, IL-6, and TGF-β1

H. Sharma, Yanhua Su, Hengxing Zhou, 2013, Evidence-based complementary and alternative medicine : eCAM.

Epidural Fibrosis in Laminectomy Rats via Downregulation of Hydroxyproline, Il-6, and Tgf-í Μí»½1

H. Sharma, Yanhua Su, Hengxing Zhou, 2022 .

Identification of two novel SMN1 point mutations associated with a very severe SMA-I phenotype.

X. Kong, Xuechao Zhao, Chen Chen, 2020, European journal of medical genetics.

The 57th amino acid conveys the differential subcellular localization of human immunodeficiency virus-1 Tat derived from subtype B and C

Xiaohong Kong, Chang Liu, Xuechao Zhao, 2016, Virus Genes.

Rapid prenatal diagnosis of Facioscapulohumeral Muscular Dystrophy 1 by combined Bionano optical mapping and karyomapping

Fan Liang, X. Kong, Pidong Li, 2019, Prenatal diagnosis.

Stability of HIV-1 subtype B and C Tat is associated with variation in the carboxyl-terminal region

Xiaohong Kong, Chang Liu, Xuechao Zhao, 2016, Virologica Sinica.

Establishment of a cell line with stable expression of mCherry-EGFP tandem fluorescent-tagged LC3B for studying the impact of HIV-1 infection on autophagic flux.

Yuquan Wei, B. Liu, Xiaohong Kong, 2014, Journal of virological methods.

A novel variant in UBE3A in a family with multigenerational intellectual disability and developmental delay

X. Kong, Xuechao Zhao, Yanhong Wang, 2022, Molecular genetics & genomic medicine.

A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing

X. Kong, P. Dai, Xuechao Zhao, 2019, Molecular Cytogenetics.

A novel NAPB splicing mutation identified by Trio-based exome sequencing is associated with early-onset epileptic encephalopathy.

X. Kong, Xuechao Zhao, Yanhong Wang, 2020, European journal of medical genetics.

Hermansky-Pudlak syndrome: Five Chinese patients with novel variants in HPS1 and HPS6.

X. Kong, Xuechao Zhao, Chen Chen, 2021, European journal of medical genetics.

Evidence for the antisense transcription in the proviral R29-127 strain of bovine immunodeficiency virus

B. Liu, Xiaohong Kong, Xuechao Zhao, 2015, Virologica Sinica.

A novel PCDH19 missense mutation, c.812G>A (p.Gly271Asp), identified using whole‐exome sequencing in a Chinese family with epilepsy female restricted mental retardation syndrome

X. Kong, Xuechao Zhao, Yanhong Wang, 2020, Molecular genetics & genomic medicine.

Novel mutations of COL4A3, COL4A4, and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique

X. Kong, Xuechao Zhao, Chen Chen, 2019, Molecular genetics & genomic medicine.

[Spectrum of pathological genetic variants among 405 Chinese pedigrees affected with oculocutaneous albinism].

X. Kong, Xuechao Zhao, Chen Chen, 2020, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Establishment of a cell line with stable expression of mCherry-EGFP tandem fluorescent-tagged LC3B for studying the impact of HIV-1 infection on autophagic flux.

Yuquan Wei, B. Liu, Xiaohong Kong, 2014, Journal of virological methods.

Identification of microRNAome in rat bladder reveals miR-1949 as a potential inducer of bladder cancer following spinal cord injury.

B. Liu, Tianci Chu, Hengxing Zhou, 2015, Molecular medicine reports.