Z. Tan

发表

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome

Xiu-ying Wang, Haiyun Dong, Hui Zeng, 2016, Molecular Cytogenetics.

Intracellular distribution, assembly and effect of disease-associated connexin 31 mutants in HeLa cells.

K. Xia, Q. Pan, D. Liang, 2005, Acta biochimica et biophysica Sinica.

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

T. Zhao, Jian Wang, Yi-feng Yang, 2014, Molecular Cytogenetics.

Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia

T. Zhao, Li Xie, Jian Wang, 2014, PloS one.

Novel mutation of EXT2 identified in a large family with multiple osteochondromas

Yi-feng Yang, Z. Tan, Xiaojun Chen, 2016, Molecular medicine reports.

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.

Li Xie, Jian Wang, Yi-feng Yang, 2013, Gene.

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome

B. Yin, Cheng Luo, Jian Wang, 2012, American journal of medical genetics. Part A.

A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient

Yi-feng Yang, Z. Tan, Zhuang-zhuang Yuan, 2020, Frontiers in Cardiovascular Medicine.

Taurine transporter is expressed in vascular smooth muscle cells

Jm Li, Xiao-Bo Liao, Lijuan Yuan, 2007, Amino Acids.

Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China.

H. Zhang, H. Luo, Z. Tan, 2012, Genetics and molecular research : GMR.

Whole-exome sequencing reveals doubly novel heterozygous Myosin Binding Protein C and Titin mutations in a Chinese patient with severe dilated cardiomyopathy

L. Fan, Hao Huang, Jing-Jing Li, 2018, Cardiology in the Young.

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Hong Luo, Li Xie, Jian Wang, 2012, European journal of medical genetics.

Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9.

Y. Guo, Z. Tan, X. Shi, 2014, Genetics and molecular research : GMR.

Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome

Xiaohui Xie, Yi-qiao Hu, Yi-feng Yang, 2021, Frontiers in Cardiovascular Medicine.

Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain

Xiaohui Xie, Jian-guang Tang, Yi-qiao Hu, 2021, Frontiers in Neuroscience.

Cx31 is assembled and trafficked to cell surface by ER-Golgi pathway and degraded by proteasomal or lysosomal pathways

K. Xia, Q. Pan, D. Liang, 2005, Cell Research.

Taurine inhibits osteoblastic differentiation of vascular smooth muscle cells via the ERK pathway

Wei Liu, Ling-Qing Yuan, Xiao-Bo Liao, 2008, Amino Acids.

Duplication of 10q22.3–q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability

T. Zhao, Li Xie, Jian Wang, 2015, American journal of medical genetics. Part A.

A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient

Xiaohui Xie, Yi-feng Yang, Z. Tan, 2022, Journal of Human Genetics.

Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies

Jian Wang, Yi-feng Yang, Z. Tan, 2012, American journal of medical genetics. Part A.

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia

Cheng Lei, T. Guo, Shuizi Ding, 2021, Human Genetics.

Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy

T. Guo, Hong Luo, Z. Tan, 2017, Molecular medicine reports.

Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome.

furong dai, Z. Tan, Jian Wang, 2015, Gene.

Mutant CARD10 in a family with progressive immunodeficiency and autoimmunity

Cheng Lei, T. Guo, Shuizi Ding, 2020, Cellular & Molecular Immunology.

Identification of anaplastic lymphoma kinase as a potential therapeutic target in ovarian cancer.

S. Beausoleil, J. Rush, T. Gu, 2012, Cancer research.

Therapeutics , Targets , and Chemical Biology Identi fi cation of Anaplastic Lymphoma Kinase as a Potential Therapeutic Target in Ovarian Cancer

S. Beausoleil, J. Rush, T. Gu, 2012 .

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia

Cheng Lei, T. Guo, Shuizi Ding, 2021, Human Genetics.

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

Jian Wang, Yi-feng Yang, Z. Tan, 2014, Molecular Cytogenetics.

576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy.

Jian Wang, Yi Zhang, Xin Zhu, 2013, Gene.

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death

Li Xie, Jian Wang, Yi-feng Yang, 2014, Scientific Reports.

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome

Xiu-ying Wang, Hui Zeng, Yi-qiao Hu, 2016, Molecular Cytogenetics.

Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy

Hui Zeng, Yi-feng Yang, Z. Tan, 2022, Genes & diseases.

An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families

T. Guo, Hong Luo, Ping Chen, 2017, Scientific Reports.

Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion.

Jian Wang, Yi-feng Yang, Z. Tan, 2012, Gene.

A clinical and molecular analysis of a patient with Emanuel syndrome.

Hong Luo, Ming Tu, Li Xie, 2017, Molecular medicine reports.

Mechanistic study of angiogenesis induced by shh-transfected BMMSC transplantation after myocardial infarction

T. Tang, Xiaoming Wu, Wei Zhang, 2013 .

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Jian-guang Tang, Hui Zeng, Yi-feng Yang, 2017, Cytogenetic and Genome Research.

A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect

Yi-feng Yang, Z. Tan, Jinlan Chen, 2014, Journal of Zhejiang University-SCIENCE B.

Identification of anaplastic lymphoma kinase as a potential therapeutic target in ovarian cancer.

S. Beausoleil, J. Rush, T. Gu, 2012, Cancer research.

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Jian-guang Tang, Hui Zeng, Yi-feng Yang, 2017, Cytogenetic and Genome Research.

Nonmuscle myosin IIA is associated with poor prognosis of esophageal squamous cancer.

Y-C. Yuan, Y. Hu, B. Yin, 2012, Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus.

Identification of a pathogenic SMCHD1 variant in a Chinese patient with bosma arhinia microphthalmia syndrome: a case report

Yi-feng Yang, Z. Tan, Zhuang-zhuang Yuan, 2024, BMC medical genomics.

Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China.

H. Luo, Z. Tan, Can Huang, 2012, Genetics and molecular research : GMR.

Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle

Z. Tan, Can Huang, Jin-fu Yang, 2012, Clinical genetics.