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Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease

Brain (London, England : 1878), 2019-08, Vol.142 (8), p.2215-2229

2019

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Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy

Clinical chemistry and laboratory medicine, 2017-03, Vol.55 (3), p.358

2017

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Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma

PloS one, 2011, Vol.6 (9), p.e24779

2011

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A hybrid boundary method for seismic wave propagation problems in slopes

Soil dynamics and earthquake engineering (1984), 2021-08, Vol.147, p.106773, Article 106773

2021

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Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

BMC musculoskeletal disorders, 2015-02, Vol.16 (1), p.11-11, Article 11

2015

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Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Blood cells, molecules, & diseases, 2015-06, Vol.55 (1), p.62-67

2015

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Mathematical Modeling of Drying Kinetics of Salted Otolithes Ruber at the Different Temperature

Advanced materials research, 2013-01, Vol.781-784, p.1347-1352

2013

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Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2012-07, Vol.901, p.53-58

2012

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A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction

Analytical biochemistry, 2012-08, Vol.427 (2), p.144-150

2012

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Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay

Clinical chemistry and laboratory medicine, 2013-05, Vol.51 (5), p.75-77

2013

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Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma

PloS one, 2011-09, Vol.6 (9), p.e24779

2011

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Rapid genotyping of known mutations and polymorphisms in β-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes

Clinical biochemistry, 2008-06, Vol.41 (9), p.681-687

2008

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Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay

Blood cells, molecules, & diseases, 2011-10, Vol.47 (3), p.198-204

2011

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Large-scale population-based genetic screening and prenatal diagnosis for thalassemias in Zhuhai City of Guangdong Province

Chung-hua fu chʿan kʿo tsa chih, 2012-02, Vol.47 (2), p.90-95

2012

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Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda

Zhonghua yi xue yi chuan xue za zhi, 2008-02, Vol.25 (1), p.15

2008

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A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province

Zhonghua yi xue yi chuan xue za zhi, 2008-06, Vol.25 (3), p.256

2008

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Characterization of a Novel 71.8 kb α 0 -Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis

Hemoglobin, 2020-07, Vol.44 (4), p.259-263

2020

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Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis

Hemoglobin, 2020-07, Vol.44 (4), p.259-263

2020

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RNA interference-mediated silencing of a Halloween gene spookier affects nymph performance in the small brown planthopper Laodelphax striatellus

Insect science, 2015-04, Vol.22 (2), p.191-202

2015

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Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous [alpha].sup.0-Thalassemia in Maternal Plasma

PloS one, 2011-09, Vol.6 (9), p.e24779

2011

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Research on Detecting Aluminum in Jellyfish by Flame Atomic Absorption Method

Advanced materials research, 2014-10, Vol.1033-1034, p.732-737

2014

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The Effect of Modified Atmosphere Packaging on the Quality of Sturgeon Caviar at 0°C

Advanced materials research, 2014-06, Vol.941-944, p.1099-1105

2014

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Measuring Microplastic Transport In Lakes: A Methodological Approach

Journal of Pharmaceutical Negative Results, 2022-11, p.2642-2652

Chen Tian , Zhou Jun , Wan Maznah Wan Omar

2022

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Study on Extractiing of Heme from Tilapias Blood by Enzymatic Method

Advanced materials research, 2014-06, Vol.941-944, p.2641-2645

2014

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Cep70 promotes microtubule assembly in vitro by increasing microtubule elongation

Acta biochimica et biophysica Sinica, 2012-05, Vol.44 (5), p.450-454

2012

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Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy

Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma

A hybrid boundary method for seismic wave propagation problems in slopes

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Mathematical Modeling of Drying Kinetics of Salted Otolithes Ruber at the Different Temperature

Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography

A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction

Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay

Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma

Rapid genotyping of known mutations and polymorphisms in β-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes

Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay

Large-scale population-based genetic screening and prenatal diagnosis for thalassemias in Zhuhai City of Guangdong Province

Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda

A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province

Characterization of a Novel 71.8 kb α 0 -Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis

Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis

RNA interference-mediated silencing of a Halloween gene spookier affects nymph performance in the small brown planthopper Laodelphax striatellus

Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous [alpha].sup.0-Thalassemia in Maternal Plasma

Research on Detecting Aluminum in Jellyfish by Flame Atomic Absorption Method

The Effect of Modified Atmosphere Packaging on the Quality of Sturgeon Caviar at 0°C

Measuring Microplastic Transport In Lakes: A Methodological Approach

Study on Extractiing of Heme from Tilapias Blood by Enzymatic Method

Cep70 promotes microtubule assembly in vitro by increasing microtubule elongation

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