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Magnolol alleviates hypoxia-induced pulmonary vascular remodeling through inhibition of phenotypic transformation in pulmonary arterial smooth muscle cells

Biomedicine & pharmacotherapy, 2022-06, Vol.150, p.113060-113060, Article 113060

2022

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Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

Frontiers in neuroscience, 2021-02, Vol.15, p.604715

2021

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A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease

Molecular genetics & genomic medicine, 2020-12, Vol.8 (12), p.e1545-n/a

2020

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ZPA Regulatory Sequence Variants in Chinese Patients With Preaxial Polydactyly: Genetic and Clinical Characteristics

Frontiers in pediatrics, 2022-05, Vol.10, p.797978-797978

2022

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A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly

Frontiers in pediatrics, 2021-11, Vol.9, p.774575-774575

2021

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GLIS Family Zinc Finger 1 was First Linked With Preaxial Polydactyly I in Humans by Stepwise Genetic Analysis

Frontiers in cell and developmental biology, 2022-01, Vol.9, p.781388-781388

2022

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Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

Frontiers in pediatrics, 2021-08, Vol.9

2021

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Cerebellin-2 promotes endothelial-mesenchymal transition in hypoxic pulmonary hypertension rats by activating NF-κB/HIF-1α/Twist1 pathway

Life sciences (1973), 2023-09, Vol.328, p.121879-121879, Article 121879

2023

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Coordination between NADPH oxidase and vascular peroxidase 1 promotes dysfunctions of endothelial progenitor cells in hypoxia-induced pulmonary hypertensive rats

European journal of pharmacology, 2019-08, Vol.857, p.172459-172459, Article 172459

2019

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Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

Frontiers in neuroscience, 2021-04, Vol.15, p.687435-687435

2021

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Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding

Frontiers in pediatrics, 2021-06, Vol.9

2021

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Application of the Children Neuropsychological and Behavioral Scale-Revision 2016 in young children with autism spectrum disorder

Zhongguo dang dai er ke za zhi, 2020-05, Vol.22 (5), p.494

2020

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Differential diagnosis of autism spectrum disorder and global developmental delay based on machine learning and Children Neuropsychological and Behavioral Scale

Zhongguo dang dai er ke za zhi, 2023-10, Vol.25 (10), p.1028-1033

2023

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Study on anti-osteoporosis effect of Eucommiae Cortex based on GC-MS metabonomics

Zhongguo zhongyao zazhi, 2020-11, Vol.45 (22), p.5555

2020

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基于机器学习和儿童神经心理行为检查量表鉴别孤独症谱系障碍和全面发育迟缓儿童的研究

中国当代儿科杂志, 2023-10, Vol.25 (10), p.1028-1033

2023

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Study on Effects of Concrete Admixtures on Performance of Concrete

Applied Mechanics and Materials, 2011-09, Vol.94-96, p.856-859

Luo, Mei Fang

2011

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Analysis of "solemn, unrefined and great" in word poetry category of hui feng ci hua

Luo, Mei Fang

2010

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Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding

Frontiers in pediatrics, 2021, Vol.9, p.679279-679279

2021

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Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

Frontiers in neuroscience, 2021, Vol.15, p.604715-604715

2021

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Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

Frontiers in pediatrics, 2021, Vol.9, p.687455-687455

2021

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Numerical Simulation on Thermal-Electrical Characteristics and Electrode Patterns of GaN LEDs with Graphene/NiOx Hybrid Electrode

中国物理快报：英文版, 2016-07 (7), p.186-190

Quan-Xi Yan Shu-Fang Zhang Xing-Ming Long Hai-Jun Luo Fang Wu Liang Fang Da-Peng Wei Mei-Yong Liao

2016

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A Coiled‐Coil Domain Containing 50 Splice Variant Is Modulated by Serine/Arginine‐Rich Splicing Factor 3 and Promotes Hepatocellular Carcinoma in Mice by the Ras Signaling Pathway

Hepatology (Baltimore, Md.), 2019-01, Vol.69 (1), p.179-195

2019

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METTL1 overexpression is correlated with poor prognosis and promotes hepatocellular carcinoma via PTEN

Journal of molecular medicine (Berlin, Germany), 2019-11, Vol.97 (11), p.1535-1545

2019

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MMP1 promotes tumor growth and metastasis in esophageal squamous cell carcinoma

Cancer letters, 2016-07, Vol.377 (1), p.97-104

2016

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Ciprofloxacin enhances the biofilm formation of Staphylococcus aureus via an agrC -dependent mechanism

Frontiers in microbiology, 2023-12, Vol.14, p.1328947-1328947

2023

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Magnolol alleviates hypoxia-induced pulmonary vascular remodeling through inhibition of phenotypic transformation in pulmonary arterial smooth muscle cells

Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease

ZPA Regulatory Sequence Variants in Chinese Patients With Preaxial Polydactyly: Genetic and Clinical Characteristics

A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly

GLIS Family Zinc Finger 1 was First Linked With Preaxial Polydactyly I in Humans by Stepwise Genetic Analysis

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

Cerebellin-2 promotes endothelial-mesenchymal transition in hypoxic pulmonary hypertension rats by activating NF-κB/HIF-1α/Twist1 pathway

Coordination between NADPH oxidase and vascular peroxidase 1 promotes dysfunctions of endothelial progenitor cells in hypoxia-induced pulmonary hypertensive rats

Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding

Application of the Children Neuropsychological and Behavioral Scale-Revision 2016 in young children with autism spectrum disorder

Differential diagnosis of autism spectrum disorder and global developmental delay based on machine learning and Children Neuropsychological and Behavioral Scale

Study on anti-osteoporosis effect of Eucommiae Cortex based on GC-MS metabonomics

基于机器学习和儿童神经心理行为检查量表鉴别孤独症谱系障碍和全面发育迟缓儿童的研究

Study on Effects of Concrete Admixtures on Performance of Concrete

Analysis of "solemn, unrefined and great" in word poetry category of hui feng ci hua

Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding

Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

Numerical Simulation on Thermal-Electrical Characteristics and Electrode Patterns of GaN LEDs with Graphene/NiOx Hybrid Electrode

A Coiled‐Coil Domain Containing 50 Splice Variant Is Modulated by Serine/Arginine‐Rich Splicing Factor 3 and Promotes Hepatocellular Carcinoma in Mice by the Ras Signaling Pathway

METTL1 overexpression is correlated with poor prognosis and promotes hepatocellular carcinoma via PTEN

MMP1 promotes tumor growth and metastasis in esophageal squamous cell carcinoma

Ciprofloxacin enhances the biofilm formation of Staphylococcus aureus via an agrC -dependent mechanism

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