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张

张文娟 (Wenjuan Zhang)

Central South University

H指数:19

被引数:1,493

个人简介

"2015.11-至今，暨南大学基础医学院公共卫生与预防医学系，公共卫生学教研室、卫生毒理学教研室，副教授 2008.07-2015.10，南方医科大学公共卫生与热带医学学院毒理学系，讲师、副教授； 2005.09-2008.06，中山大学公共卫生学院，卫生毒理学专业攻读医学博士学位 2002.09-2005.07，郑州大学公共卫生学院，劳动卫生与环境卫生学专业攻读医学硕士学位 1997.09-2002.07，郑州大学公共卫生学院，预防医学专业攻读学士学位"

教育背景

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工作经历

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荣誉奖项

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Targeted clearance of extracellular Tau using aptamer-armed monocytes alleviates neuroinflammation in mice with Alzheimer’s disease

利用配体修饰的单核细胞靶向清除阿尔茨海默病小鼠模型中的细胞外Tau，可减轻神经炎症。

Nature Biomedical Engineering

IF26.6

2025-10-010

PRE

Development of a novel nomogram for patients with SCLC and comparison with other models

IF3.4

2024-10-101

OAAI

Emergence of a Novel SARS-CoV-2 Variant in Southern California

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

IF55

2021-04-06254

OA

Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia

IF10.8

2020-12-017

OAAI

Analysis of Genomic Characteristics and Transmission Routes of Patients With Confirmed SARS-CoV-2 in Southern California During the Early Stage of the US COVID-19 Pandemic

JAMA NETWORK OPEN

IF9.7

2020-10-0723

OAAI

Comparison of Large, Medium, and Small Solid Tumor Gene Panels for Detection of Clinically Actionable Mutations in Cancer

TARGETED ONCOLOGY

IF4

2020-08-0810

PREAI

Dominant-negative SOX9 mutations in campomelic dysplasia

campomelic发育异常中的显性阴性SOX9突变

IF3.7

2019-08-2618

OAAI

Tris (2-chloroethyl) phosphate induces senescence-like phenotype of hepatocytes via the p21Waf1/Cip1-Rb pathway in a p53-independent manner

ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY

IF4.2

2017-12-0121

PREAI

Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies

扩大骨骼纤毛病的遗传结构和表型谱

IF3.7

2017-11-0691

OAAI

Cell-free DNA induced apoptosis of granulosa cells by oxidative stress

CLINICA CHIMICA ACTA

IF2.9

2017-10-0128

PREAI

A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis

SCIENTIFIC REPORTS

IF3.9

2017-02-1633

OAAI

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome

SCIENTIFIC REPORTS

IF3.9

2016-09-2641

OAAI

IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome

HUMAN MOLECULAR GENETICS

IF3.2

2016-07-2741

OAAI

Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations

JOURNAL OF MEDICAL GENETICS

IF3.7

2015-12-1539

OAAI

Cell-Cycle Control of Bivalent Epigenetic Domains Regulates the Exit from Pluripotency

STEM CELL REPORTS

IF5.1

2015-09-0178

OAAI

Histone modifications contribute to cellular replicative and hydrogen peroxide-induced premature senescence in human embryonic lung fibroblasts

FREE RADICAL RESEARCH

IF2.9

2014-03-1011

PREAI

Down-regulation of CMTM8 Induces Epithelial-to-Mesenchymal Transition-like Changes via c-MET/Extracellular Signal-regulated Kinase (ERK) Signaling

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2012-04-0162

OAAI

A sandwich assay for quantitative detection of transcription factors in cell lysate

IF3.3

2012-01-014

PREAI

A lateral flow biosensor for rapid detection of DNA-binding protein c-jun

用于快速检测DNA结合蛋白c-6月的侧流生物传感器

BIOSENSORS & BIOELECTRONICS

IF10.5

2011-09-0134

PRE

Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels

IF25.9

2011-05-0345

OAAI