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Ectopic expression of NnPER1, a Nelumbo nucifera 1‐cysteine peroxiredoxin antioxidant, enhances seed longevity and stress tolerance in Arabidopsis

The Plant journal : for cell and molecular biology, 2016-11, Vol.88 (4), p.608-619

2016

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Causes of errors in prenatal gene diagnosis and relevant countermeasures

Zhong hua yi xue za zhi, 2008-12, Vol.88 (46), p.3241-3243

Huang, Shang-zhi

2008

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ING4 induces G2/M cell cycle arrest and enhances the chemosensitivity to DNA-damage agents in HepG2 cells

FEBS letters, 2004-07, Vol.570 (1), p.7-12

2004

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Array-MLPA: comprehensive detection of deletions and duplications and its application to DMD patients

Human mutation, 2008, Vol.29 (1), p.190-197

2008

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Association study between candidate genes on transforming growth factor-β signaling pathway and the risk of non-syndromic cleft lip with or without cleft palate in Chinese populations

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2015-06, Vol.47 (3), p.384

2015

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Clinical characterization and mutation identification for multiple sulfatase deficiency patients in China

Zhonghua er ke za zhi, 2013-11, Vol.51 (11), p.836

2013

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Clinical manifestations and mutation study in 16 Chinese patients with Fabry disease

Zhong hua yi xue za zhi, 2010-03, Vol.90 (8), p.551-554

2010

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EDM1： a novel point mutation in cartilage oligomeric matrix protein gene in a Chinese family with multiple epiphyseal dysplasia

Chinese medical journal, 2013-03, Vol.126 (6), p.1103-1107

2013

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Association study for gene polymorphism of folic acid/homocysteine metabolic pathway and nonsyndromic cleft lip with or without cleft palate in Chinese populations

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2013-06, Vol.45 (3), p.352

2013

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Two novel EIF2AK3 mutations in a Chinese boy with Wolcott-Rallison syndrome

Zhonghua er ke za zhi, 2011-04, Vol.49 (4), p.301

2011

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Mutation analysis of the PAH gene in patients with phenylketonuria in Gansu province

Zhonghua yi xue yi chuan xue za zhi, 2009-08, Vol.26 (4), p.419

2009

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Analysis of ITD characteristics in acute myeloid leukemia patients with FLT3-ITD positive

Zhongguo shi yan xue ye xue za zhi, 2011-10, Vol.19 (5), p.1161

2011

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Mutation analysis of PTPN11 gene in Noonan syndrome

Zhonghua yi xue yi chuan xue za zhi, 2010-10, Vol.27 (5), p.554

2010

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Gene mutation analysis of a collodion baby

Zhonghua er ke za zhi, 2009-09, Vol.47 (9), p.654

2009

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Genetic analysis and serum level of cartilage oligomeric matrix protein in patients with pseudoachondroplasia

Chinese medical journal, 2010-08, Vol.123 (16), p.2181-2184

2010

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Novel CHST6 compound heterozygous mutations cause macular corneal dystrophy in a Chinese family

Chung-hua yen k'o tsa chih, 2010-02, Vol.46 (2), p.161

2010

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Detection of microdeletion in Williams syndrome by multiplex ligation-dependent probe amplification

Zhonghua yi xue yi chuan xue za zhi, 2009-08, Vol.26 (4), p.369

2009

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FMS-like tyrosine kinase 3 gene mutation in acute myeloid leukemia detected by denaturing PAGE and its clinical significance

Zhongguo shi yan xue ye xue za zhi, 2010-12, Vol.18 (6), p.1386

2010

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A Chinese girl with fibrodysplasia ossificans progressiva caused by a de novo mutation R206H in ACVR1 gene

Zhonghua er ke za zhi, 2008-03, Vol.46 (3), p.215

2008

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Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a reliable method for detection of non-homozygous patients with spinal muscular atrophy

Zhong hua yi xue za zhi, 2008-05, Vol.88 (18), p.1259-1263

2008

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The power of linkage analysis on PAH gene in prenatal gene diagnosis is improved with three additional short tandem repeat markers

Zhonghua yi xue yi chuan xue za zhi, 2007-08, Vol.24 (4), p.382

2007

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Gene mapping of autosomal dominant retinitis pigmentosa in a Chinese family

Chinese medical journal, 2009-05, Vol.122 (9), p.1097-1101

2009

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TGFBI gene mutation analysis in a Chinese family with Thiel-Behnke corneal dystrophy

Chung-hua yen k'o tsa chih, 2007-08, Vol.43 (8), p.718

2007

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Mutation analysis of glycogen debrancher enzyme gene in five Chinese patients with glycogen storage disease type III

Zhonghua er ke za zhi, 2005-02, Vol.43 (2), p.85

2005

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A research on TGFBI gene mutations in Chinese families with corneal dystrophies

Zhonghua yi xue yi chuan xue za zhi, 2006-06, Vol.23 (3), p.310

2006

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Ectopic expression of NnPER1, a Nelumbo nucifera 1‐cysteine peroxiredoxin antioxidant, enhances seed longevity and stress tolerance in Arabidopsis

Causes of errors in prenatal gene diagnosis and relevant countermeasures

ING4 induces G2/M cell cycle arrest and enhances the chemosensitivity to DNA-damage agents in HepG2 cells

Array-MLPA: comprehensive detection of deletions and duplications and its application to DMD patients

Association study between candidate genes on transforming growth factor-β signaling pathway and the risk of non-syndromic cleft lip with or without cleft palate in Chinese populations

Clinical characterization and mutation identification for multiple sulfatase deficiency patients in China

Clinical manifestations and mutation study in 16 Chinese patients with Fabry disease

EDM1： a novel point mutation in cartilage oligomeric matrix protein gene in a Chinese family with multiple epiphyseal dysplasia

Association study for gene polymorphism of folic acid/homocysteine metabolic pathway and nonsyndromic cleft lip with or without cleft palate in Chinese populations

Two novel EIF2AK3 mutations in a Chinese boy with Wolcott-Rallison syndrome

Mutation analysis of the PAH gene in patients with phenylketonuria in Gansu province

Analysis of ITD characteristics in acute myeloid leukemia patients with FLT3-ITD positive

Mutation analysis of PTPN11 gene in Noonan syndrome

Gene mutation analysis of a collodion baby

Genetic analysis and serum level of cartilage oligomeric matrix protein in patients with pseudoachondroplasia

Novel CHST6 compound heterozygous mutations cause macular corneal dystrophy in a Chinese family

Detection of microdeletion in Williams syndrome by multiplex ligation-dependent probe amplification

FMS-like tyrosine kinase 3 gene mutation in acute myeloid leukemia detected by denaturing PAGE and its clinical significance

A Chinese girl with fibrodysplasia ossificans progressiva caused by a de novo mutation R206H in ACVR1 gene

Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a reliable method for detection of non-homozygous patients with spinal muscular atrophy

The power of linkage analysis on PAH gene in prenatal gene diagnosis is improved with three additional short tandem repeat markers

Gene mapping of autosomal dominant retinitis pigmentosa in a Chinese family

TGFBI gene mutation analysis in a Chinese family with Thiel-Behnke corneal dystrophy

Mutation analysis of glycogen debrancher enzyme gene in five Chinese patients with glycogen storage disease type III

A research on TGFBI gene mutations in Chinese families with corneal dystrophies

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