Gang Liu

发表

PIG11 over-expression predicts good prognosis and induces HepG2 cell apoptosis via reactive oxygen species-dependent mitochondrial pathway.

Xiaomin Liu, Xiao-juan Wang, Yan Wang, 2018, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Clinical Value of Positron Emission Tomography-Computed Tomography Combined with Ultrasound in Detection of Primary Tumors in Patients with Malignant Ascites.

Yan Wang, Gang Liu, Xiaohui Zhu, 2019, Cancer biotherapy & radiopharmaceuticals.

Adenovirus Ad-p53AIP1-mediated gene therapy and its regulation of p53-MDM2 interactions.

Xiaohe Yang, Yan Wang, Yuanji Xu, 2010, Experimental and therapeutic medicine.

Adenovirus Adp 53 AIP 1-mediated gene therapy and its regulation of p 53-MDM 2 interactions

Xiaohe Yang, Yan Wang, Yuanji Xu, 2010 .

Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson’s disease: a case report

Gang Liu, Zhengfeng Xu, Yun Sun, 2018, BMC Medical Genetics.

[Promotion of MAG-1 on Metastasis of Lung Cancer Cells in vitro and Its Expression in Lung Cancer Tissue of 24 Cases.].

Yan Wang, Yuanji Xu, Z. Du, 2009, Zhongguo fei ai za zhi = Chinese journal of lung cancer.

[The proliferation promoting effects of MAG-2 on human lung cancer cell PLA801.].

Yan Wang, Yuanji Xu, Z. Du, 2008, Zhongguo fei ai za zhi = Chinese journal of lung cancer.

A novel and high-strength Ti–Al–V–Fe alloy prepared by spark plasma sintering

Shi-feng Liu, Xin Yang, Gang Liu, 2021, Powder Metallurgy.

A Novel Whole Gene Deletion of BCKDHB by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine Disease

Gang Liu, Zhengfeng Xu, Yun Sun, 2018, Front. Genet..

Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome

Gang Liu, Zhengfeng Xu, P. Hu, 2021, Frontiers in Genetics.

A novel splice site mutation in the UBE2A gene leads to aberrant mRNA splicing in a Chinese patient with X‐linked intellectual disability type Nascimento

Gang Liu, Zhengfeng Xu, D. Ma, 2019, Molecular genetics & genomic medicine.

A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report

Gang Liu, Zhengfeng Xu, P. Hu, 2019, Front. Genet..

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center

Gang Liu, Zhengfeng Xu, P. Hu, 2019, BMC Medical Genetics.

MAG-2 promotes invasion, mobility and adherence capability of lung cancer cells by MMP-2, CD44 and intracellular calcium in vitro.

Gang Liu, Yuhong Meng, Huiyun Lin, 2009, Oncology reports.

Mitogen-activated protein kinase p38 modulates pacemaker ion channels differentiation in P19-derived pluripotent cells

K. Ono, Lin-Ping Kang, Gang Liu, 2020, The journal of physiological sciences : JPS.

Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect

Gang Liu, Zhengfeng Xu, P. Hu, 2015, Molecular Cytogenetics.

A novel COQ8A missense variant associated with a mild form of primary coenzyme Q10 deficiency type 4.

Gang Liu, Zhengfeng Xu, Yun Sun, 2020, Clinical biochemistry.

Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy

Gang Liu, Zhengfeng Xu, D. Ma, 2018, Frontiers in Genetics.

Identification of two novel DNAJC12 gene variants in a patient with mild hyperphenylalaninemia.

Gang Liu, Zhengfeng Xu, Yun Sun, 2023, Gene.

An autofocus algorithm considering wavelength changes for large scale microscopic hyperspectral pathological imaging system

Qingli Li, Gang Liu, X. Tao, 2022, Journal of biophotonics.

Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency

Gang Liu, Zhengfeng Xu, D. Ma, 2022, Journal of clinical laboratory analysis.

Next‐generation sequencing for genetic testing of hearing loss populations

Gang Liu, Zhengfeng Xu, D. Ma, 2023, Clinica Chimica Acta.

High kinesin family member 11 expression predicts poor prognosis in patients with clear cell renal cell carcinoma

S. Zhang, Yan Wang, Gang Liu, 2019, Journal of Clinical Pathology.