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HnRNPK is involved in stress-induced depression-like behavior via ERK-BDNF pathway in mice

Neurochemistry international, 2023-10, Vol.169, p.105589-105589, Article 105589

2023

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Discussion on the Reproducibility of Precursor Waves in the Water Level Records of Jingle Well

中国地震研究（英文版）, 2013, Vol.27 (2), p.205-222

Zhang Shuliang Liu Ruichun Lv Fang

2013

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In-Situ Water Quality Improvement by Hypolimnion Oxygenation and Artificially Induced Mixing in a Drinking Water Reservoir

Nature environment and pollution technology, 2019-09, Vol.18 (3), p.911-918

2019

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Portal inflow preservation during portal diversion in small-for-size syndrome

World journal of gastroenterology : WJG, 2014-01, Vol.20 (4), p.1021-1029

2014

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1,5-Hydrogen atom transfer of α-iminyl radical cations: a new platform for relay annulation for pyridine derivatives and axially chiral heterobiaryls

Chemical science (Cambridge), 2024-05, Vol.15 (2), p.752-7514

2024

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Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus

Frontiers in genetics, 2023-10, Vol.14

2023

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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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Efficacy and safety of TCMs with anti-inflammatory effect in patients with rheumatoid arthritis: A network meta-analysis

Frontiers in immunology, 2023-03, Vol.14, p.1114930-1114930

2023

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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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Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling

BMC medical genetics, 2019-11, Vol.20 (1), p.169-169, Article 169

2019

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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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The “Hand as Foot” teaching method for the surgical disinfection of hands

Asian journal of surgery, 2023-09, Vol.46 (9), p.3850-3851

2023

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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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Argonaute 2 promotes angiogenesls via the PTEN/ VEGF signaling pathway in human hepatocellular carcinoma

中国药理学报：英文版, 2015 (10), p.1237-1245

Zhen-long YE Yao HUANG Lin-fang LI Hai-li ZHU Hai-xia GAO Hui LIU Sai-qun LV Zeng-hui XU Luo-ningZHENG Tao LIU Jing-lei ZHANG Hua-jun JIN Qi-jun QIAN

2015

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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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Movable Fiber-Integrated Hybrid Plasmonic Waveguide on Metal Film

IEEE photonics technology letters, 2012-03, Vol.24 (6), p.434-436

2012

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IEEE_Xplore

Lateral position intubation followed by endoscopic ultrasound-guided angiotherapy in acute esophageal variceal rupture: A case report

World journal of clinical cases, 2021-01, Vol.9 (2), p.372-378

2021

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Relay Annulation of Ammonium Ylides with Oxindole-Derived α,β-Unsaturated Ketimines: Catalytic Construction of Spiro-polycyclic Oxindoles

Organic letters, 2024-06, Vol.26 (24), p.5115-5119

2024

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Exciton-plasmon-photon conversion in silver nanowire: Polarization dependence

Applied physics letters, 2011-08, Vol.99 (6), p.061103-061103-3

2011

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The clinical and genetic characteristics in children with mitochondrial disease in China

Science China. Life sciences, 2017-07, Vol.60 (7), p.746-757

2017

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The clinical and genetic characteristics in children with mitochondrial disease in China

中国科学：生命科学英文版, 2017 (7), p.746-757

Fang Fang Zhimei Liu Hezhi Fang Jian Wu Danmin Shen Suzhen Sun Changhong Ding Tongli Han Yun Wu Junlan Lv Lei Yang Shufang Li Jianxin Lv Ying Shen

2017

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Combinations of Hd2 and Hd4 genes determine rice adaptability to Heilongjiang Province, northern limit of China

Journal of integrative plant biology, 2015-08, Vol.57 (8), p.698-707

Xiufeng Li Huazhao Liu Maoqing Wang Hualong Liu Xiaojie Tian Wenjia Zhou Tianxiao Lv Zhenyu Wang, Chengcai Chu Jun Fang qingyun Bu

2015

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Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus

Frontiers in genetics, 2023, Vol.14, p.1208540-1208540

2023

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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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HnRNPK is involved in stress-induced depression-like behavior via ERK-BDNF pathway in mice

Discussion on the Reproducibility of Precursor Waves in the Water Level Records of Jingle Well

In-Situ Water Quality Improvement by Hypolimnion Oxygenation and Artificially Induced Mixing in a Drinking Water Reservoir

Portal inflow preservation during portal diversion in small-for-size syndrome

1,5-Hydrogen atom transfer of α-iminyl radical cations: a new platform for relay annulation for pyridine derivatives and axially chiral heterobiaryls

Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus

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

Efficacy and safety of TCMs with anti-inflammatory effect in patients with rheumatoid arthritis: A network meta-analysis

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

Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling

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

The “Hand as Foot” teaching method for the surgical disinfection of hands

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

Argonaute 2 promotes angiogenesls via the PTEN/ VEGF signaling pathway in human hepatocellular carcinoma

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

Movable Fiber-Integrated Hybrid Plasmonic Waveguide on Metal Film

Lateral position intubation followed by endoscopic ultrasound-guided angiotherapy in acute esophageal variceal rupture: A case report

Relay Annulation of Ammonium Ylides with Oxindole-Derived α,β-Unsaturated Ketimines: Catalytic Construction of Spiro-polycyclic Oxindoles

Exciton-plasmon-photon conversion in silver nanowire: Polarization dependence

The clinical and genetic characteristics in children with mitochondrial disease in China

The clinical and genetic characteristics in children with mitochondrial disease in China

Combinations of Hd2 and Hd4 genes determine rice adaptability to Heilongjiang Province, northern limit of China

Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus

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

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