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Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

Nature communications, 2020-07, Vol.11 (1), p.3675-3675, Article 3675

2020

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Identification of MicroRNAs in Human Follicular Fluid: Characterization of MicroRNAs That Govern Steroidogenesis in Vitro and Are Associated With Polycystic Ovary Syndrome in Vivo

The journal of clinical endocrinology and metabolism, 2013-07, Vol.98 (7), p.3068-3079

2013

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The Roles and Features of Genetic Variants in Children with Cerebral Palsy

Journal of bio-X research, 2024-01, Vol.7

2024

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Mutations in TUBB8 and Human Oocyte Meiotic Arrest

The New England journal of medicine, 2016-01, Vol.374 (3), p.223-232

2016

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Src Family Kinases Inhibition Ameliorates Hypoxic-Ischemic Brain Injury in Immature Rats

Frontiers in cellular neuroscience, 2021-12, Vol.15, p.746130-746130

2021

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Metabolomic Profiling to Identify Potential Serum Biomarkers for Schizophrenia and Risperidone Action

Journal of proteome research, 2011-12, Vol.10 (12), p.5433-5443

2011

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The association between HLA-B variants and amoxicillin-induced severe cutaneous adverse reactions in Chinese han population

Frontiers in pharmacology, 2024-05, Vol.15, p.1400239

2024

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Case Report: Novel MFSD8 Variants in a Chinese Family With Neuronal Ceroid Lipofuscinoses 7

Frontiers in genetics, 2022-01, Vol.13, p.807515

2022

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Serum CD203c+ Extracellular Vesicle Serves as a Novel Diagnostic and Prognostic Biomarker for Succinylated Gelatin Induced Perioperative Hypersensitive Reaction

Frontiers in immunology, 2021-09, Vol.12, p.732209-732209

2021

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Serum Extracellular Vesicle–Derived miR-124-3p as a Diagnostic and Predictive Marker for Early-Stage Acute Ischemic Stroke

Frontiers in molecular biosciences, 2021-07, Vol.8, p.685088-685088

2021

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Clinical, Viral and Genetic Characteristics of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) in Shanghai, China

Acta dermato-venereologica, 2018-01, Vol.98 (4), p.401-405

2018

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Long non‐coding RNA ESCCAL‐1/miR‐590/LRP6 signaling pathway participates in the progression of esophageal squamous cell carcinoma

Cancer medicine (Malden, MA), 2023-01, Vol.12 (1), p.445-458

2023

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Establishment of a mathematical prediction model for voriconazole stable maintenance dose: a prospective study

Frontiers in cellular and infection microbiology, 2023-07, Vol.13, p.1157944-1157944

2023

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The Effect of microRNAs in the Regulation of Human CYP3A4: a Systematic Study using a Mathematical Model

Scientific reports, 2014-03, Vol.4 (1), p.4283-4283, Article 4283

2014

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Association of Leukocyte Telomere Length with Type 2 Diabetes in Mainland Chinese Populations

The journal of clinical endocrinology and metabolism, 2012-04, Vol.97 (4), p.1371-1374

2012

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Cryo-EM structure of Mycobacterium tuberculosis 50S ribosomal subunit bound with clarithromycin reveals dynamic and specific interactions with macrolides

Emerging microbes & infections, 2022-12, Vol.11 (1), p.293-305

2022

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Clinical variables and genetic variants associated with perioperative anaphylaxis in Chinese Han population: A pilot study

The World Allergy Organization journal, 2024-01, Vol.17 (1), p.100854-100854, Article 100854

2024

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Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome

PloS one, 2014-02, Vol.9 (2), p.e88013-e88013

2014

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Targeting the metabolic profile of amino acids to identify the key metabolic characteristics in cerebral palsy

Frontiers in molecular neuroscience, 2023-08, Vol.16, p.1237745-1237745

2023

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HLA-A02:01 allele is associated with tanshinone-induced cutaneous drug reactions in Chinese population

The pharmacogenomics journal, 2020-06, Vol.20 (3), p.408-414

2020

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Detection of Turner syndrome using X-chromosome inactivation specific differentially methylated CpG sites: A pilot study

Clinica chimica acta, 2017-05, Vol.468, p.174-179

2017

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Up-regulated expression and aberrant DNA methylation of LEP and SH3PXD2A in pre-eclampsia

PloS one, 2013-03, Vol.8 (3), p.e59753-e59753

2013

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Experimental validation of candidate schizophrenia gene CALN1 as a target for microRNA-137

Neuroscience letters, 2015-08, Vol.602, p.110-114

2015

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An association study of IL2RA polymorphisms with cerebral palsy in a Chinese population

BMC medical genomics, 2022-10, Vol.15 (1), p.1-208, Article 208

2022

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A functional alternative splicing mutation in AIRE gene causes autoimmune polyendocrine syndrome type 1

PloS one, 2013-01, Vol.8 (1), p.e53981-e53981

2013

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Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

Identification of MicroRNAs in Human Follicular Fluid: Characterization of MicroRNAs That Govern Steroidogenesis in Vitro and Are Associated With Polycystic Ovary Syndrome in Vivo

The Roles and Features of Genetic Variants in Children with Cerebral Palsy

Mutations in TUBB8 and Human Oocyte Meiotic Arrest

Src Family Kinases Inhibition Ameliorates Hypoxic-Ischemic Brain Injury in Immature Rats

Metabolomic Profiling to Identify Potential Serum Biomarkers for Schizophrenia and Risperidone Action

The association between HLA-B variants and amoxicillin-induced severe cutaneous adverse reactions in Chinese han population

Case Report: Novel MFSD8 Variants in a Chinese Family With Neuronal Ceroid Lipofuscinoses 7

Serum CD203c+ Extracellular Vesicle Serves as a Novel Diagnostic and Prognostic Biomarker for Succinylated Gelatin Induced Perioperative Hypersensitive Reaction

Serum Extracellular Vesicle–Derived miR-124-3p as a Diagnostic and Predictive Marker for Early-Stage Acute Ischemic Stroke

Clinical, Viral and Genetic Characteristics of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) in Shanghai, China

Long non‐coding RNA ESCCAL‐1/miR‐590/LRP6 signaling pathway participates in the progression of esophageal squamous cell carcinoma

Establishment of a mathematical prediction model for voriconazole stable maintenance dose: a prospective study

The Effect of microRNAs in the Regulation of Human CYP3A4: a Systematic Study using a Mathematical Model

Association of Leukocyte Telomere Length with Type 2 Diabetes in Mainland Chinese Populations

Cryo-EM structure of Mycobacterium tuberculosis 50S ribosomal subunit bound with clarithromycin reveals dynamic and specific interactions with macrolides

Clinical variables and genetic variants associated with perioperative anaphylaxis in Chinese Han population: A pilot study

Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome

Targeting the metabolic profile of amino acids to identify the key metabolic characteristics in cerebral palsy

HLA-A02:01 allele is associated with tanshinone-induced cutaneous drug reactions in Chinese population

Detection of Turner syndrome using X-chromosome inactivation specific differentially methylated CpG sites: A pilot study

Up-regulated expression and aberrant DNA methylation of LEP and SH3PXD2A in pre-eclampsia

Experimental validation of candidate schizophrenia gene CALN1 as a target for microRNA-137

An association study of IL2RA polymorphisms with cerebral palsy in a Chinese population

A functional alternative splicing mutation in AIRE gene causes autoimmune polyendocrine syndrome type 1

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