Zhiping Tan

发表

Global Survey of Phosphotyrosine Signaling Identifies Oncogenic Kinases in Lung Cancer

Laura A. Sullivan, S. Gygi, J. Kornhauser, 2007, Cell.

Whole‐exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family

Zhiping Tan, Cheng Lei, T. Guo, 2020, Molecular genetics & genomic medicine.

miR‐195 inhibited abnormal activation of osteoblast differentiation in MC3T3‐E1 cells via targeting RAF‐1

Zhiping Tan, Weizhi Zhang, Yifeng Yang, 2018, Experimental cell research.

Mutations of the TGFBR2 gene in Chinese patients with Marfan-related syndrome.

Zhiping Tan, T. Zhao, Jianguo Hu, 2010, Clinical and investigative medicine. Medecine clinique et experimentale.

Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Zhiping Tan, Yifeng Yang, Yi Yin, 2021, BMC medical genomics.

Microduplication of 7q36.3 encompassing the SHH long-range regulator (ZRS) in a patient with triphalangeal thumb-polysyndactyly syndrome and congenital heart disease

Zhiping Tan, Yifeng Yang, Cheng Luo, 2016, Molecular medicine reports.

1q21.1 microduplication in a patient with mental impairment and congenital heart defect

Zhiping Tan, L. Fan, Yifeng Yang, 2015, Molecular medicine reports.

Whole-Exome Sequencing Identifies a Novel Variant (c.1538T > C) of TNNI3K in Arrhythmogenic Right Ventricular Cardiomyopathy

R. Liu, Zhiping Tan, T. Xie, 2022, Frontiers in Cardiovascular Medicine.

High-resolution single nucleotide polymorphism arrays identified an atypical microdeletion of the Williams-Beuren syndrome interval in a patient presenting with a different phenotype.

Zhiping Tan, T. Zhao, Yifeng Yang, 2017, Molecular medicine reports.

[Association of intercellular adhesion molecule-1 gene K469E polymorphism with chronic obstructive pulmonary disease].

Zhiping Tan, Hong Luo, Ping Chen, 2012, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

Case Report: A Young Man With Giant Pericardial Synovial Sarcoma

R. Liu, Zhiping Tan, Hui Guo, 2022, Frontiers in Cardiovascular Medicine.

Identification of KIAA0196 as a novel susceptibility gene for myofibril structural disorganization in cardiac development.

Zhiping Tan, T. Zhao, Yifeng Yang, 2020, International journal of cardiology.

Ehlers-Danlos syndrome type IV is associated with a novel G 984 R COL 3 A 1 mutation

Zhiping Tan, Yifeng Yang, H. Shijun, 2015 .

A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate

Zhiping Tan, T. Zhao, Yifeng Yang, 2017, The Journal of craniofacial surgery.

Ehlers-Danlos syndrome type IV is associated with a novel G984R COL3A1 mutation.

Zhiping Tan, Yifeng Yang, Shijie Wei, 2015, Molecular medicine reports.

A novel mutation in the tropomyosin 1 gene in a Chinese patient with hypertrophic cardiomyopathy

Yong-Heng Luo, Zhiping Tan, Hui Guo, 2022, All Life.

Experimental Study of the Effects of Marrow Mesenchymal Stem Cells Transfected with Hypoxia-Inducible Factor-1α Gene

Wei Zheng, Zhiping Tan, T. Tang, 2009, Journal of biomedicine & biotechnology.

Survey of Tyrosine Kinase Signaling Reveals ROS Kinase Fusions in Human Cholangiocarcinoma

Jian Yu, John Rush, Yi Wang, 2011, PloS one.

Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis

Zhiping Tan, Jianzhong Hu, L. Fan, 2017, Scientific Reports.

Correction: Whole-exome sequencing identifies a novel CCDC151 mutation, c.325GT (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Zhiping Tan, T. Guo, Hong Luo, 2019, Journal of Human Genetics.

Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Zhiping Tan, T. Guo, Hong Luo, 2018, Journal of Human Genetics.

In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans.

H. Horvitz, S. Hoersch, Zhiping Tan, 2011, RNA.

Chemical characterization of Auricularia auricula polysaccharides and its pharmacological effect on heart antioxidant enzyme activities and left ventricular function in aged mice.

Zhiping Tan, Weizhi Zhang, Haidan Liu, 2010, International journal of biological macromolecules.

Current Status and Evaluation of Randomized Clinical Trials of Traditional Chinese Medicine in the Treatment of Cardiovascular Diseases

Zhiping Tan, Yifeng Yang, Xi Guo, 2022, Evidence-based complementary and alternative medicine : eCAM.

Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy

Luyao Wei, Zhiping Tan, Hui Guo, 2023, PloS one.

Neuropeptide Receptors NPR-1 and NPR-2 Regulate Caenorhabditis elegans Avoidance Response to the Plant Stress Hormone Methyl Salicylate

Zhiping Tan, Zhuohua Zhang, Zhiping Tan, 2014, Genetics.

Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome

Luyao Wei, Zhiping Tan, Shijun Hu, 2022, Journal of Genetics.

Targeted next‑generation sequencing for research and diagnostics in congenital heart disease, and cleft lip and/or palate.

Zhiping Tan, Shijun Hu, Lin Liu, 2019, Molecular medicine reports.

CircRNA Microarray Profiling Reveals hsa_circ_0058493 as a Novel Biomarker for Imatinib-Resistant CML

Yinghao Yin, Jie Xiao, Zhiping Tan, 2021, Frontiers in Pharmacology.

The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect

Zhiping Tan, Yifeng Yang, Shijun Hu, 2021, BMC Cardiovascular Disorders.

Identification and Integrate Analysis of Key Biomarkers for Diagnosis and Prognosis of Non-Small Cell Lung Cancer Based on Bioinformatics Analysis

Zhiping Tan, Yifeng Yang, Haidan Liu, 2021, Technology in cancer research & treatment.

Identification of ANKDD1B variants in an ankylosing spondylitis pedigree and a sporadic patient

Jian Wang, G. Ling, Zhiping Tan, 2018, BMC Medical Genetics.

Correction: Whole-exome sequencing identifies a novel CCDC151 mutation, c.325GT (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Zhiping Tan, T. Guo, Weizhi Zhang, 2019, Journal of Human Genetics.

Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Zhiping Tan, T. Guo, Weizhi Zhang, 2018, Journal of Human Genetics.

Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China

Zhiping Tan, T. Guo, Danhui Yang, 2021, Frontiers in Genetics.

Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Zhiping Tan, Yifeng Yang, Yi Yin, 2021, BMC Medical Genomics.

Establishment of a Dihydrofolate Reductase Gene Knock-In Zebrafish Strain to Aid Preliminary Analysis of Congenital Heart Disease Mechanisms

Yong-Heng Luo, Zhiping Tan, Yifeng Yang, 2021, Frontiers in Cardiovascular Medicine.

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice

Y. Liu, Chenyang Lu, Zhiping Tan, 2023, Frontiers of medicine.

A novel mutation of glycogen synthase kinase-3β leads to a reduced level of GSK3β protein in a patient with dilated cardiomyopathy

Xinmin Zhou, Zhiping Tan, Haidan Liu, 2023, Genes & diseases.

Oncogenic K-ras confers SAHA resistance by up-regulating HDAC6 and c-myc expression

Rong Tan, Zhiping Tan, Xin Zhu, 2016, Oncotarget.

Case report: A new de novo mutation of the Troponin T2 gene in a Chinese patient with dilated cardiomyopathy

Zhiping Tan, Ke Gong, Lei Wang, 2023, Frontiers in cardiovascular medicine.

Comprehensive analysis of lncRNA biomarkers in kidney renal clear cell carcinoma by lncRNA-mediated ceRNA network

Yong-Heng Luo, Zhiping Tan, Yifeng Yang, 2021, PloS one.