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Microarray profiling of microRNAs expressed in testis tissues of developing primates

Journal of assisted reproduction and genetics, 2009-04, Vol.26 (4), p.179-186

2009

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A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion

Human molecular genetics, 2013-04, Vol.22 (8), p.1679-1695

2013

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Human t-Complex Protein 11 (TCP11), a Testis-Specific Gene Product, Is a Potential Determinant of the Sperm Morphology

The Tohoku Journal of Experimental Medicine, 2011, Vol.224(2), pp.111-117

2011

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Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia

Biology of reproduction, 2015-02, Vol.92 (2), p.41-41

2015

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Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment

Human reproduction (Oxford), 2008-09, Vol.23 (9), p.2167-2172

2008

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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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Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment

Human reproduction (Oxford), 2006-03, Vol.21 (3), p.755-759

2006

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The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia

European journal of obstetrics & gynecology and reproductive biology, 2006, Vol.124 (1), p.61-64

2006

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DAZL binds to 3'UTR of Tex19.1 mRNAs and regulates Tex19.1 expression

Molecular biology reports, 2009-11, Vol.36 (8), p.2399-2403

2009

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Preliminary study of the relationship between DAZ gene copy deletions and spermatogenic impairment in Chinese men

Fertility and sterility, 2006-04, Vol.85 (4), p.1061-1063

2006

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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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Cloning and expression analysis of a novel mouse zinc finger protein gene Znf313 abundantly expressed in testis

BMB reports, 2007-03, Vol.40 (2), p.270-276

2007

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Phenotypic Expression of Partial AZFc Deletions Is Independent of the Variations in DAZL and BOULE in a Han Population

Journal of andrology, 2010-03, Vol.31 (2), p.163-168

2010

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A novel allele in the promoter of the hepatic lipase is associated with increased concentration of HDL-C and decreased promoter activity

Journal of lipid research, 2002-10, Vol.43 (10), p.1595-1601

2002

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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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Idiopathic male infertility and partial copy deletion of DAZ gene family

Zhonghua yi xue yi chuan xue za zhi, 2004-10, Vol.21 (5), p.444

2004

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Typing Y Chromosome STR Haplotypes Using Redesigned Primers

Journal of forensic sciences, 2002-01, Vol.47 (1), p.215-217

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 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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Microarray profiling of microRNAs expressed in testis tissues of developing primates

A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion

Human t-Complex Protein 11 (TCP11), a Testis-Specific Gene Product, Is a Potential Determinant of the Sperm Morphology

Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia

Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment

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

Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment

The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia

DAZL binds to 3'UTR of Tex19.1 mRNAs and regulates Tex19.1 expression

Preliminary study of the relationship between DAZ gene copy deletions and spermatogenic impairment in Chinese men

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

Cloning and expression analysis of a novel mouse zinc finger protein gene Znf313 abundantly expressed in testis

Phenotypic Expression of Partial AZFc Deletions Is Independent of the Variations in DAZL and BOULE in a Han Population

A novel allele in the promoter of the hepatic lipase is associated with increased concentration of HDL-C and decreased promoter activity

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

Idiopathic male infertility and partial copy deletion of DAZ gene family

Typing Y Chromosome STR Haplotypes Using Redesigned Primers

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

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

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