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A data process of human knee joint kinematics obtained by motion-capture measurement

BMC medical informatics and decision making, 2021-04, Vol.21 (1), p.121-121, Article 121

2021

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A pathogenesis related protein, VpPR-10.1, from Vitis pseudoreticulata: an insight of its mode of antifungal activity

PloS one, 2014-04, Vol.9 (4), p.e95102

2014

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Diagnosis of Spinal Muscular Atrophy: A Simple Method for Quantifying the Relative Amount of Survival Motor Neuron Gene 1/2 Using Sanger DNA Sequencing

Chinese medical journal, 2018-12, Vol.131 (24), p.2921-2929

2018

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Associations of serum gamma-linolenic acid levels with erythema severity and anxiety/depression status in patients with rosacea

Anais brasileiros de dermatología, 2024-03, Vol.99 (2), p.189-195

2024

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A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.864-870

2016

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Fast clinical molecular diagnosis of hyperphenylalaninemia using next-generation sequencing-based on a custom AmpliSeq™ panel and Ion Torrent PGM sequencing

Molecular genetics and metabolism, 2014-12, Vol.113 (4), p.261-266

2014

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Numerical simulation of the dolomite in-situ desulfurization in molten iron

Materials research express, 2023-01, Vol.10 (1), p.16512

2023

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Association between SMN2 methylation and disease severity in Chinese children with spinal muscular atrophy

Journal of Zhejiang University. B. Science, 2016, Vol.17 (1), p.76-82

2016

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Mosaicism of Tetrasomy 18p: Clinical and Cytogenetic Findings in a Female Child

Chinese medical journal, 2017-03, Vol.130 (6), p.744-746

2017

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Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7

BMC medical genetics, 2012-09, Vol.13 (1), p.86-86, Article 86

2012

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osaicism of Tetrasomy 18p： Clinical and Cytogenetic Findings in a Female Child

中华医学杂志：英文版, 2017, Vol.130 (6), p.744-746

Jin-Li Bai Yu-Wei Jin Yu-Jin Qu Hong Wang Yan-Yan Cao Fang Song

2017

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The evaluation model of the enterprise energy efficiency based on DPSR

Environmental science and pollution research international, 2019-06, Vol.26 (17), p.16835-16846

2019

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Compound heterozygous mutation in two unrelated cases of Chinese spinal muscular atrophy patients

Chinese medical journal, 2011-02, Vol.124 (3), p.385-389

2011

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Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy

The Journal of molecular diagnostics : JMD, 2016-09, Vol.18 (5), p.741-752

2016

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Association of Copy Numbers of Survival Motor Neuron Gene 2 and Neuronal Apoptosis Inhibitory Protein Gene With the Natural History in a Chinese Spinal Muscular Atrophy Cohort

Journal of child neurology, 2015-03, Vol.30 (4), p.429-436

2015

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Health management of laser rangefinder considering maximum continuous working time

Journal of mechanical science and technology, 2022-10, Vol.36 (10), p.4875-4883

2022

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QTL Mapping for Important Agronomic Traits in Synthetic Hexaploid Wheat Derived from Aegiliops tauschii ssp. tauschii

Journal of Integrative Agriculture, 2014-09, Vol.13 (9), p.1835-1844

YU Ma, CHEN Guo-yue, ZHANG Lian-quan, LIU Ya-xi, LIU Deng-cai, WANG Ji-rui, PU Zhien, ZHANG Li, LAN Xiu-jin, WEI Yu-ming, LIU Chun-ji , ZHENG You-liang (National Key Facility for Crop Gene Resources and Genetic Improvement/Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, P.R.China)

2014

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Green Design for Concurrent Engineering in Agriculture Machinery

Applied Mechanics and Materials, 2013-08, Vol.367, p.151-155

Yu, Jin Wei

2013

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Improved hetero-interface passivation by microcrystalline silicon oxide emitter in silicon heterojunction solar cells

Science bulletin (Beijing), 2016-05, Vol.61 (10), p.787-793

2016

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p.Val19Glyfs21 and p.Leu228 variants in the survival of motor neuron 1 trigger nonsense-mediated mRNA decay causing the SMN1 PTC+ transcripts degradation

Mutation research, 2017-12, Vol.806, p.31-38

2017

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Subtle mutation detection of SMN1 gene in Chinese spinal muscular atrophy patients: implication of molecular diagnostic procedure for SMN1 gene mutations

Genetic testing and molecular biomarkers, 2014-08, Vol.18 (8), p.546-551

2014

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A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome

Journal of Zhejiang University. B. Science, 2015-11, Vol.16 (11), p.957-962

2015

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ntrauterine Cardiac Intervention for Fetal Pulmonary Valve Obstruction Lesion

中华医学杂志：英文版, 2018, Vol.131 (1), p.103-104

2018

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Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene

Journal of Zhejiang University. B. Science, 2014-05, Vol.15 (5), p.474-481

2014

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Determination of phenolic whitening agents in cosmetics by micellar electrokinetic capillary chromatography with amperometric detection

Chinese chemical letters, 2013-07, Vol.24 (7), p.636-638

2013

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A data process of human knee joint kinematics obtained by motion-capture measurement

A pathogenesis related protein, VpPR-10.1, from Vitis pseudoreticulata: an insight of its mode of antifungal activity

Diagnosis of Spinal Muscular Atrophy: A Simple Method for Quantifying the Relative Amount of Survival Motor Neuron Gene 1/2 Using Sanger DNA Sequencing

Associations of serum gamma-linolenic acid levels with erythema severity and anxiety/depression status in patients with rosacea

A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy

Fast clinical molecular diagnosis of hyperphenylalaninemia using next-generation sequencing-based on a custom AmpliSeq™ panel and Ion Torrent PGM sequencing

Numerical simulation of the dolomite in-situ desulfurization in molten iron

Association between SMN2 methylation and disease severity in Chinese children with spinal muscular atrophy

Mosaicism of Tetrasomy 18p: Clinical and Cytogenetic Findings in a Female Child

Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7

osaicism of Tetrasomy 18p： Clinical and Cytogenetic Findings in a Female Child

The evaluation model of the enterprise energy efficiency based on DPSR

Compound heterozygous mutation in two unrelated cases of Chinese spinal muscular atrophy patients

Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy

Association of Copy Numbers of Survival Motor Neuron Gene 2 and Neuronal Apoptosis Inhibitory Protein Gene With the Natural History in a Chinese Spinal Muscular Atrophy Cohort

Health management of laser rangefinder considering maximum continuous working time

QTL Mapping for Important Agronomic Traits in Synthetic Hexaploid Wheat Derived from Aegiliops tauschii ssp. tauschii

Green Design for Concurrent Engineering in Agriculture Machinery

Improved hetero-interface passivation by microcrystalline silicon oxide emitter in silicon heterojunction solar cells

p.Val19Glyfs21 and p.Leu228 variants in the survival of motor neuron 1 trigger nonsense-mediated mRNA decay causing the SMN1 PTC+ transcripts degradation

Subtle mutation detection of SMN1 gene in Chinese spinal muscular atrophy patients: implication of molecular diagnostic procedure for SMN1 gene mutations

A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome

ntrauterine Cardiac Intervention for Fetal Pulmonary Valve Obstruction Lesion

Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene

Determination of phenolic whitening agents in cosmetics by micellar electrokinetic capillary chromatography with amperometric detection

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