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METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA

Frontiers in cell and developmental biology, 2022-06, Vol.10, p.894810-894810

2022

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Three-Dimensional Hexagram Gold Nanoparticles: Synthesis and Growth Mechanism

Transactions of Tianjin University, 2019-02, Vol.25 (1), p.31-37

2019

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Effect of soil and topography on vegetation restoration in an opencast coal mine dump in a loess area

Sheng tai xue bao, 2016, Vol.36 (16)

2016

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Front Cover: Urea Electrooxidation in Alkaline Environment: Fundamentals and Applications (ChemElectroChem 13/2023)

ChemElectroChem, 2023-07, Vol.10 (13), p.n/a

2023

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Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene

Zhonghua yi xue yi chuan xue za zhi, 2015-02, Vol.32 (1), p.81

2015

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CircLMBR1 inhibits phenotypic transformation of hypoxia-induced pulmonary artery smooth muscle via the splicing factor PUF60

European journal of pharmacology, 2024-10, Vol.980, p.176855, Article 176855

2024

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Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Zhonghua yi xue yi chuan xue za zhi, 2023-08, Vol.40 (8), p.966

2023

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Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

Zhonghua yi xue yi chuan xue za zhi, 2023-02, Vol.40 (2), p.230

2023

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HNRNPC mediated m 6 A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA

Journal of reproductive immunology, 2023-12, Vol.160, p.104160

2023

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Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Zhonghua yi xue yi chuan xue za zhi, 2021-01, Vol.38 (1), p.52

2021

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Genetic analysis of 90 families affected with spinal muscular atrophy

Zhonghua yi xue yi chuan xue za zhi, 2020-02, Vol.37 (2), p.116

2020

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Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Zhonghua yi xue yi chuan xue za zhi, 2020-01, Vol.37 (1), p.17

2020

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Unveiling the Protonation Kinetics‐Dependent Selectivity in Nitrogen Electroreduction: Achieving 75.05 % Selectivity

Angewandte Chemie, 2022-12, Vol.134 (50), p.n/a

2022

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Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V

Zhonghua yi xue yi chuan xue za zhi, 2019-03, Vol.36 (3), p.207

2019

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Unraveling the Function of Metal–Amorphous Support Interactions in Single‐Atom Electrocatalytic Hydrogen Evolution

Angewandte Chemie, 2022-02, Vol.134 (9), p.n/a

2022

Volltextzugriff (PDF)

Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan

Zhonghua yi xue yi chuan xue za zhi, 2017-04, Vol.34 (2), p.266

2017

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Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia

Zhonghua yi xue yi chuan xue za zhi, 2016-10, Vol.33 (5), p.629

2016

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Prenatal diagnosis and genetic counselingï¿½for Waardenburg syndrome typeï¿½I and II in Chinese families

Molecular medicine reports, 2017-10

2017

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Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion

Zhonghua yi xue yi chuan xue za zhi, 2016-06, Vol.33 (3), p.361

2016

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Phenotypic and genetic analysis of a boy with partial trisomy of 1q

Zhonghua yi xue yi chuan xue za zhi, 2017-06, Vol.34 (3), p.398

2017

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Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21

Zhonghua yi xue yi chuan xue za zhi, 2015-06, Vol.32 (3), p.395

2015

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Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome

Zhonghua yi xue yi chuan xue za zhi, 2015-12, Vol.32 (6), p.823

2015

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Planning and Deployment Method of Electric Vehicle Charging Facilities in a Self-consistent Highway Transportation Energy System

2023 IEEE 6th International Electrical and Energy Conference (CIEEC), 2023, p.466-471

2023

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Improving Current Efficiency Through Optimizing Electrolyte Flow in Zinc Electrowinning Cell

CFD Modeling and Simulation in Materials Processing 2016, p.239-245

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Multimodal Image Fusion based on Improved Pulse-Coupled Neural Network and Convolutional Sparse Representation in NSST Domain

2021 IEEE 5th Advanced Information Technology, Electronic and Automation Control Conference (IAEAC), 2021, Vol.5, p.1295-1300

2021

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METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA

Three-Dimensional Hexagram Gold Nanoparticles: Synthesis and Growth Mechanism

Effect of soil and topography on vegetation restoration in an opencast coal mine dump in a loess area

Front Cover: Urea Electrooxidation in Alkaline Environment: Fundamentals and Applications (ChemElectroChem 13/2023)

Genetic diagnosis for a family without exonic deletions and duplications of dystrophin gene

CircLMBR1 inhibits phenotypic transformation of hypoxia-induced pulmonary artery smooth muscle via the splicing factor PUF60

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation

HNRNPC mediated m 6 A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA

Identification of pathogenic variant in a Chinese pedigree affected with non-syndromic cleft lip and palate

Genetic analysis of 90 families affected with spinal muscular atrophy

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Unveiling the Protonation Kinetics‐Dependent Selectivity in Nitrogen Electroreduction: Achieving 75.05 % Selectivity

Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V

Unraveling the Function of Metal–Amorphous Support Interactions in Single‐Atom Electrocatalytic Hydrogen Evolution

Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan

Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia

Prenatal diagnosis and genetic counselingï¿½for Waardenburg syndrome typeï¿½I and II in Chinese families

Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion

Phenotypic and genetic analysis of a boy with partial trisomy of 1q

Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21

Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome

Planning and Deployment Method of Electric Vehicle Charging Facilities in a Self-consistent Highway Transportation Energy System

Improving Current Efficiency Through Optimizing Electrolyte Flow in Zinc Electrowinning Cell

Multimodal Image Fusion based on Improved Pulse-Coupled Neural Network and Convolutional Sparse Representation in NSST Domain

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