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Sepsis caused by Phytobacter diazotrophicus complicated with galactosemia type 1 in China: a case report

BMC infectious diseases, 2024-06, Vol.24 (1), p.1-5, Article 599

2024

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A case report: Marfan syndrome with X trisomy and FBN1 and SDHB mutations

BMC medical genomics, 2023-05, Vol.16 (1), p.118-118, Article 118

2023

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Analysis of Fire Resistance of Square-Cased Square Steel Tube Reinforced Concrete (ST-RC) Columns

Materials, 2021-09, Vol.14 (19), p.5541

2021

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Emerging Nano-Based Strategies Against Drug Resistance in Tumor Chemotherapy

Frontiers in bioengineering and biotechnology, 2021-12, Vol.9, p.798882-798882

2021

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A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures

BMC medical genomics, 2023-01, Vol.16 (1), p.3-3, Article 3

2023

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Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Frontiers in genetics, 2022-07, Vol.13

2022

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Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Frontiers in genetics, 2022-03, Vol.13, p.829613

2022

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Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

Frontiers in genetics, 2022-08, Vol.13

2022

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Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome

Molecular genetics & genomic medicine, 2023-10, Vol.11 (10), p.e2242-e2242

2023

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Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview

Molecular cytogenetics, 2022-07, Vol.15 (1), p.1-31, Article 31

2022

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UNC5B-AS1 promotes the proliferation, migration and EMT of hepatocellular carcinoma cells via regulating miR-4306/KDM2A axis

Cell cycle (Georgetown, Tex.), 2021-10, Vol.20 (20), p.2114-2124

2021

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Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population

Clinica chimica acta, 2022-10, Vol.535, p.13-18

2022

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Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare a- and b-Globin Gene Variants in Thalassemia Alleles in the Chinese Population

Archives of pathology & laboratory medicine (1976), 2023-02, Vol.147 (2), p.208-214

2023

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Antitumor effects of the silencing of programmed cell death ligand 1 in colorectal cancer via immunoregulation

Oncology reports, 2018-12, Vol.40 (6), p.3370-3380

2018

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Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population

Archives of pathology & laboratory medicine (1976), 2023-02, Vol.147 (2), p.208-214

2023

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MT1G serves as a tumor suppressor in hepatocellular carcinoma by interacting with p53

Oncogenesis (New York, NY), 2019-11, Vol.8 (12), p.67-11, Article 67

2019

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TROVE2 regulated invasion and migration of hepatocellular carcinoma cells via heparanase

Oncology and translational medicine, 2024-04, Vol.10 (2), p.66-72

2024

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Co-culture system of hepatocytes and endothelial cells: two in vitro approaches for enhancing liver-specific functions of hepatocytes

Cytotechnology (Dordrecht), 2018-08, Vol.70 (4), p.1279-1290

2018

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High Prevalence of Group III-Like Mutations Among BLPACR and First Report of Haemophilus influenzae ST95 Isolated from Blood in China

Infection and drug resistance, 2023-01, Vol.16, p.999-1008

2023

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Long non-coding RNA linc-cdh4-2 inhibits the migration and invasion of HCC cells by targeting R-cadherin pathway

Biochemical and biophysical research communications, 2016-11, Vol.480 (3), p.348-354

2016

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Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare [alpha]- and [beta]-Globin Gene Variants in Thalassemia Alleles in the Chinese Population

Archives of pathology & laboratory medicine (1976), 2023-02, Vol.147 (2), p.208

2023

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Overexpression of galectin-4 promotes cell growth of hepatocellular carcinoma cells in vitro and in vivo

International journal of clinical and experimental pathology, 2017-01, Vol.10 (10), p.10233-10242

2017

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Circular RNA CircEPB4IL2 Functions as Tumor Suppressor in Hepatocellular Carcinoma Through Sponging miR-590-5p

Cancer management and research, 2021-04, p.2969

2021

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Circular RNA CircEPB41L2 Functions as Tumor Suppressor in Hepatocellular Carcinoma Through Sponging miR-590-5p

Cancer management and research, 2021-01, Vol.13, p.2969-2981

2021

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Development of Prognostic Evaluation Model to Predict the Overall Survival and Early Recurrence of Hepatocellular Carcinoma

Journal of hepatocellular carcinoma, 2021-01, Vol.8, p.301-312

2021

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Sepsis caused by Phytobacter diazotrophicus complicated with galactosemia type 1 in China: a case report

A case report: Marfan syndrome with X trisomy and FBN1 and SDHB mutations

Analysis of Fire Resistance of Square-Cased Square Steel Tube Reinforced Concrete (ST-RC) Columns

Emerging Nano-Based Strategies Against Drug Resistance in Tumor Chemotherapy

A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures

Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome

Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview

UNC5B-AS1 promotes the proliferation, migration and EMT of hepatocellular carcinoma cells via regulating miR-4306/KDM2A axis

Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population

Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare a- and b-Globin Gene Variants in Thalassemia Alleles in the Chinese Population

Antitumor effects of the silencing of programmed cell death ligand 1 in colorectal cancer via immunoregulation

Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population

MT1G serves as a tumor suppressor in hepatocellular carcinoma by interacting with p53

TROVE2 regulated invasion and migration of hepatocellular carcinoma cells via heparanase

Co-culture system of hepatocytes and endothelial cells: two in vitro approaches for enhancing liver-specific functions of hepatocytes

High Prevalence of Group III-Like Mutations Among BLPACR and First Report of Haemophilus influenzae ST95 Isolated from Blood in China

Long non-coding RNA linc-cdh4-2 inhibits the migration and invasion of HCC cells by targeting R-cadherin pathway

Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare [alpha]- and [beta]-Globin Gene Variants in Thalassemia Alleles in the Chinese Population

Overexpression of galectin-4 promotes cell growth of hepatocellular carcinoma cells in vitro and in vivo

Circular RNA CircEPB4IL2 Functions as Tumor Suppressor in Hepatocellular Carcinoma Through Sponging miR-590-5p

Circular RNA CircEPB41L2 Functions as Tumor Suppressor in Hepatocellular Carcinoma Through Sponging miR-590-5p

Development of Prognostic Evaluation Model to Predict the Overall Survival and Early Recurrence of Hepatocellular Carcinoma

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