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Association between DNA variant sites in the apolipoprotein A5 gene and coronary heart disease in Chinese

Metabolism, clinical and experimental, 2005-05, Vol.54 (5), p.568-572

2005

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Putative mutation of PKD1 gene responsible for autosomal dominant polycystic kidney disease in a Chinese family

International journal of urology, 2011-03, Vol.18 (3), p.240-242

2011

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Angiogenesis and cell proliferation in human craniopharyngioma xenografts in nude mice

Journal of neurosurgery, 2006-10, Vol.105 (4 Suppl), p.306-310

2006

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Improvement of HBsAg Gene-Modified Dendritic Cell-Based Vaccine Efficacy by Optimizing Immunization Method or the Application of β-glucosylceramide

Immunological investigations, 2013-01, Vol.42 (2), p.137-155

2013

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Carriers of three polymorphisms of cholesteryl ester transfer protein gene are at increased risk to coronary heart disease in a Chinese population

International journal of cardiology, 2005-09, Vol.103 (3), p.259-265

2005

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The APOC3 SstI polymorphism is weakly associated with sporadic Alzheimer's disease in a Chinese population

Neuroscience letters, 2005-06, Vol.380 (3), p.219-222

2005

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Mutation Screening and Association Study of the Neprilysin Gene in Sporadic Alzheimer's Disease in Chinese Persons

The journals of gerontology. Series A, Biological sciences and medical sciences, 2005-03, Vol.60 (3), p.301-306

2005

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Adiponectin Gene Variation −4522C/T Is Associated with Type 2 Diabetic Obesity and Insulin Resistance in Chinese

Journal of genetics and genomics, 2007-10, Vol.34 (10), p.877-884

2007

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Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer's disease in Chinese

Brain research. Molecular brain research., 2004-01, Vol.120 (2), p.201-204

2004

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Novel P143L polymorphism of the LCAT gene is associated with dyslipidemia in Chinese patients who have coronary atherosclerotic heart disease

Biochemical and biophysical research communications, 2004-05, Vol.318 (1), p.4-10

2004

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The 1239G/C polymorphism in exon 5 of BACE1 gene may be associated with sporadic Alzheimer's disease in Chinese Hans

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-01, Vol.124B (1), p.54-57

2004

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Clustering of variations and haplotype analysis in the highly variable region of exon 11 of BRCA1 in Chinese women with sporadic breast cancer

Human mutation, 2002-11, Vol.20 (5), p.404-405

2002

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Study on the association of lecithin cholesterol acyltransferase gene polymorphisms with the lipid metabolism in coronary atherosclerotic heart disease

Zhonghua yi xue yi chuan xue za zhi, 2003-04, Vol.20 (2), p.135

2003

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A familial chromosomal translocation t(6q;7q) with habitual abortions

Clinical genetics, 1989-07, Vol.36 (1), p.1-4

1989

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A single nucleotide deletion of 293delT in SEDL gene causing spondyloepiphyseal dysplasia tarda in a four-generation Chinese family

Mutation research, 2003-04, Vol.525 (1), p.61-65

2003

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Association between DNA variant sites in the apolipoprotein A5 gene and coronary heart disease in Chinese

Putative mutation of PKD1 gene responsible for autosomal dominant polycystic kidney disease in a Chinese family

Angiogenesis and cell proliferation in human craniopharyngioma xenografts in nude mice

Improvement of HBsAg Gene-Modified Dendritic Cell-Based Vaccine Efficacy by Optimizing Immunization Method or the Application of β-glucosylceramide

Carriers of three polymorphisms of cholesteryl ester transfer protein gene are at increased risk to coronary heart disease in a Chinese population

The APOC3 SstI polymorphism is weakly associated with sporadic Alzheimer's disease in a Chinese population

Mutation Screening and Association Study of the Neprilysin Gene in Sporadic Alzheimer's Disease in Chinese Persons

Adiponectin Gene Variation −4522C/T Is Associated with Type 2 Diabetic Obesity and Insulin Resistance in Chinese

Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer's disease in Chinese

Novel P143L polymorphism of the LCAT gene is associated with dyslipidemia in Chinese patients who have coronary atherosclerotic heart disease

The 1239G/C polymorphism in exon 5 of BACE1 gene may be associated with sporadic Alzheimer's disease in Chinese Hans

Clustering of variations and haplotype analysis in the highly variable region of exon 11 of BRCA1 in Chinese women with sporadic breast cancer

Study on the association of lecithin cholesterol acyltransferase gene polymorphisms with the lipid metabolism in coronary atherosclerotic heart disease

A familial chromosomal translocation t(6q;7q) with habitual abortions

A single nucleotide deletion of 293delT in SEDL gene causing spondyloepiphyseal dysplasia tarda in a four-generation Chinese family

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