Wenxue Tang

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Aliases
Wenxue Tang, Wen-xue Tang, Wen‐xue Tang
Publication record
67 papers · 2,604 citations · H-index 27

PAPERS

Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants
202316 citationsauthor #9
Geniposide alleviates pressure overload in cardiac fibrosis with suppressed TGF-β1 pathway.
20236 citationsauthor #3
A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient
20225 citationsauthor #7
COVID-19 Resulting in Potential Hearing Damage of Rodents
20221 citationsauthor #5
Application of Nanomedicine in Inner Ear Diseases
202220 citationsauthor #8
Spying on the Peroxynitrite Fluctuation During Hearing Loss Enabled by Rationally Designed Fluorescent Carbon Dots
20227 citationsauthor #1
Defining the Sensitivity Landscape of EGFR Variants to Tyrosine Kinase Inhibitors.
202217 citationsauthor #12
A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
20223 citationsauthor #8
Superoxide dismutase@zeolite Imidazolate Framework-8 Attenuates Noise-Induced Hearing Loss in Rats
202212 citationsauthor #7
Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing
20227 citationsauthor #11
Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome
202114 citationsauthor #7
Detection and clinical significance of circulating tumor cells in colorectal cancer
202147 citationsauthor #8
Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype
20216 citationsauthor #13
Neuroprotective effect of stroke pretreated MSCs against cerebral ischemia/reperfusion injury in rats.
202113 citationsauthor #1
An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease
202112 citationsauthor #20
Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans
20215 citationsauthor #17
An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease
20210 citationsauthor #20
Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene
202111 citationsauthor #23
Lighting up Individual Organelles With Fluorescent Carbon Dots
202112 citationsauthor #8
High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing
202113 citationsauthor #13
Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndrome.
20211 citationsauthor #6
Nanoscale dual-enzyme cascade metal-organic frameworks through biomimetic mineralization as ROS generators for synergistic cancer therapy.
202020 citationsauthor #7
Development of a novel oxidative stress-amplifying nanocomposite capable of supplying intratumoral H2O2 and O2 for enhanced chemodynamic therapy and radiotherapy in patient-derived xenograft (PDX) models.
202021 citationsauthor #3
Perrault syndrome: Clinical report and retrospective analysis
202025 citationsauthor #10
Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma
202096 citationsauthor #12
Thymosin alpha-1 blocks the accumulation of myeloid suppressor cells in NSCLC by inhibiting VEGF production.
202011 citationsauthor #8
Development of MOF “Armor‐Plated” Phycocyanin and Synergistic Inhibition of Cellular Respiration for Hypoxic Photodynamic Therapy in Patient‐Derived Xenograft Models
202041 citationsauthor #4
Myeloid-derived suppressor cells—new and exciting players in lung cancer
2020161 citationsauthor #4
Auditory Neuropathy Spectrum Disorder (ANSD)—Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families
20203 citationsauthor #10
Involvement of Glutathione Depletion in Selective Cytotoxicity of Oridonin to p53-Mutant Esophageal Squamous Carcinoma Cells
202023 citationsauthor #7
Mechanisms of hearing loss and cell death in the cochlea of connexin mutant mice.
20208 citationsauthor #8
Early truncation of the N‐terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype
20207 citationsauthor #9
Roles of HMGB1 in regulating myeloid-derived suppressor cells in the tumor microenvironment
202044 citationsauthor #4
SARS-CoV-2 infecting the inner ear results in potential hearing damage at the early stage or prognosis of COVID-19 in rodents
20200 citationsauthor #5
Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans
202010 citationsauthor #17
Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients
202010 citationsauthor #12
Expression pattern of Connexin 26 and Connexin 30 in mature cochlea of the monkey.
20195 citationsauthor #2
Clinical value of global end-diastolic volume index for fluid resuscitation in cardiac dysfunction patients with septic shock
20180 citationsauthor #7
Localization of Glucose Transporter 10 to Hair Cells' Cuticular Plate in the Mouse Inner Ear
20181 citationsauthor #5
Clinial study on changes of serum creatine kinase brain isoenzyme, ubiquitin carboxy terminal hydrolases L1 and cerebral extraction of oxygen in patients with severe craniocerebral trauma
20170 citationsauthor #8
Inhibition of cyclooxygenase-2 by NS398 attenuates noise-induced hearing loss in mice
201612 citationsauthor #4
Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing.
201538 citationsauthor #2
A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss
20146 citationsauthor #2
Resveratrol Decreases Noise-Induced Cyclooxygenase-2 Expression in the Rat Cochlea
201349 citationsauthor #2
A Low-Cost Exon Capture Method Suitable for Large-Scale Screening of Genetic Deafness by the Massively-Parallel Sequencing Approach
201249 citationsauthor #1
Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.
2012104 citationsauthor #2
Early developmental expression of connexin26 in the cochlea contributes to its dominate functional role in the cochlear gap junctions.
201239 citationsauthor #2
Deoxygedunin, a Natural Product with Potent Neurotrophic Activity in Mice
2010101 citationsauthor #6
Functional Studies Reveal New Mechanisms for Deafness Caused by Connexin Mutations
20098 citationsauthor #2
Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.
200966 citationsauthor #4
Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea
2009107 citationsauthor #2
Targeted connexin26 ablation arrests postnatal development of the organ of Corti.
2009106 citationsauthor #3
Anti‐intercellular adhesion molecule‐1 antibody's effect on noise damage
200921 citationsauthor #2
Pannexins are new molecular candidates for assembling gap junctions in the cochlea
200829 citationsauthor #1
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31
2008108 citationsauthor #7
The Cochlear Pericytes
200867 citationsauthor #4
Gap Junction Mediated Intercellular Metabolite Transfer in the Cochlea Is Compromised in Connexin30 Null Mice
2008109 citationsauthor #2
Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness
2007122 citationsauthor #2
Analysis of connexin subunits required for the survival of vestibular hair cells
200722 citationsauthor #2
Connexin29 Is Highly Expressed in Cochlear Schwann Cells, and It Is Required for the Normal Development and Function of the Auditory Nerve of Mice
200680 citationsauthor #1
Cocaine‐induced alterations in nucleus accumbens ionotropic glutamate receptor subunits in human and non‐human primates
200566 citationsauthor #2
Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts.
2005141 citationsauthor #4
Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions.
2005147 citationsauthor #2
Role of Bcl-2 family of proteins in mediating apoptotic death of PC12 cells exposed to oxygen and glucose deprivation.
200527 citationsauthor #4
Differential regulation of ionotropic glutamate receptor subunits following cocaine self-administration.
200562 citationsauthor #3
Alterations in ionotropic glutamate receptor subunits during binge cocaine self‐administration and withdrawal in rats
200492 citationsauthor #1
Molecular profiling of midbrain dopamine regions in cocaine overdose victims
2003113 citationsauthor #1

TIMELINE

2003 113 citations

2004 92 citations

2005 443 citations

2006 80 citations

2007 144 citations

2008 313 citations

2009 308 citations

2010 101 citations

2012 192 citations

2013 49 citations

2014 6 citations

2015 38 citations

2016 12 citations

2017 0 citations

2018 1 citations

2019 5 citations

2020 480 citations

2021 134 citations

2022 72 citations

2023 22 citations

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