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Artemisia pollen allergy in China: Component‐resolved diagnosis reveals allergic asthma patients have significant multiple allergen sensitization

Allergy (Copenhagen), 2019-02, Vol.74 (2), p.284-293

2019

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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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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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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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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

Volltextzugriff (PDF)

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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A Pneumonia Case Associated with Type 2 Polio Vaccine Strains

Chinese medical journal, 2017-01, Vol.130 (1), p.111-112

2017

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Proteomic Analysis of Rice Leaves Shows the Different Regulations to Osmotic Stress and Stress Signals

Journal of integrative plant biology, 2010-11, Vol.52 (11), p.981-995

2010

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Regional brain structural abnormality in ischemic stroke patients： a voxel-based morphometry study

Neural regeneration research, 2016-09, Vol.11 (9), p.1424-1430

2016

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Notch pathway inhibitor DAPT enhances Atoh1 activity to generate new hair cells in situ in rat cochleae

Neural regeneration research, 2017-12, Vol.12 (12), p.2092-2099

2017

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Artemisia pollen allergy in China: Component‐resolved diagnosis reveals allergic asthma patients have significant multiple allergen sensitization

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

Study on Effects of Concrete Admixtures on Performance of Concrete

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

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

A Pneumonia Case Associated with Type 2 Polio Vaccine Strains

Proteomic Analysis of Rice Leaves Shows the Different Regulations to Osmotic Stress and Stress Signals

Regional brain structural abnormality in ischemic stroke patients： a voxel-based morphometry study

Notch pathway inhibitor DAPT enhances Atoh1 activity to generate new hair cells in situ in rat cochleae

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