Jian Zeng

发表

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

Ping Fang, Liang Li, Jian Zeng, 2015, BMC Musculoskeletal Disorders.

Premature termination codons in SMN1 leading to spinal muscular atrophy trigger nonsense-mediated mRNA decay.

Jian Zeng, Mengya Zhang, Yan-hong Lin, 2022, Clinica chimica acta; international journal of clinical chemistry.

Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population

Liang Li, Jian Zeng, Tizhen Yan, 2010, European Journal of Human Genetics.

The clinical application of preimplantation genetic diagnosis for X-linked retinitis pigmentosa

Jian Zeng, F. Lan, Yun Liu, 2019, Journal of Assisted Reproduction and Genetics.

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy

Liang Li, Jian Zeng, Wanjun Zhou, 2017, Clinical chemistry and laboratory medicine.

A rapid and sensitive protocol for prenatal molecular diagnosis of X-linked adrenoleukodystrophy.

Jian Zeng, F. Lan, Long-feng Ke, 2010, Clinica chimica acta; international journal of clinical chemistry.

[Genetic diagnosis and analysis of related genes for a pedigree with 2p25 and 12p13 cryptic rearrangements].

Jian Zeng, Xiao Zhang, F. Lan, 2014, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Hybrid minigene splicing assay verified the pathogenicity of a novel splice site variant in the dystrophin gene of a Chinese patient with typical Duchenne muscular dystrophy phenotype

Jian Zeng, Yan-hong Lin, F. Lan, 2016, Clinical chemistry and laboratory medicine.

Establishment of a molecular diagnostic system for spinal muscular atrophy experience from a clinical laboratory in china.

Jian Zeng, Yan-hong Lin, F. Lan, 2011, The Journal of molecular diagnostics : JMD.

Evaluation of an in-house protocol for prenatal molecular diagnosis of SMA in Chinese.

Jian Zeng, F. Lan, Long-feng Ke, 2008, Clinica chimica acta; international journal of clinical chemistry.

Small Supernumerary Ring Chromosome Derived from an Inverted Duplication of 13q11.2q14 in a Fetus with Coarctation of the Aorta

Jian Zeng, Xiao Zhang, F. Lan, 2019, Cytogenetic and Genome Research.

Microarray analysis of gene-expression profile in hepatocellular carcinoma cell, BEL-7402, with stable suppression of hLRH-1 via a DNA vector-based RNA interference.

Jian Zeng, F. Lan, Shui-liang Wang, 2006, Yi chuan xue bao = Acta genetica Sinica.

Increased expression of hLRH-1 in human gastric cancer and its implication in tumorigenesis

Jian Zeng, Rong Wang, F. Lan, 2007, Molecular and Cellular Biochemistry.

The first report showing de novo partial 21q monosomy in an adult woman with occult primary ovarian insufficiency (POI)

Jian Zeng, Mingyan Huang, Zhihong Wang, 2019, Clinical Chemistry and Laboratory Medicine.

[Analysis of small supernumerary marker chromosome 15q11 in four infertile males].

Jian Zeng, Min Zhang, Yan-hong Lin, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.