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Vascular Endothelial Growth Factor Polymorphisms in Relation to Breast Cancer Development and Prognosis

Clinical cancer research, 2005-05, Vol.11 (10), p.3647-3653

2005

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Association of Prolactin and Its Receptor Gene Regions with Familial Breast Cancer

The journal of clinical endocrinology and metabolism, 2006-04, Vol.91 (4), p.1513-1519

2006

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Polymorphisms and haplotype structures in genes for transforming growth factor β1 and its receptors in familial and unselected breast cancers

International journal of cancer, 2004-10, Vol.112 (1), p.94-99

2004

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Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant

Carcinogenesis (New York), 2006-03, Vol.27 (3), p.606-609

2006

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Association of NCOA3 Polymorphisms with Breast Cancer Risk

Clinical cancer research, 2005-03, Vol.11 (6), p.2169-2174

2005

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Association of death receptor 4 haplotype 626C–683C with an increased breast cancer risk

Carcinogenesis (New York), 2005-11, Vol.26 (11), p.1975-1977

2005

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Re: Association of a Common Variant of the CASP8 Gene With Reduced Risk of Breast Cancer

JNCI : Journal of the National Cancer Institute, 2005-07, Vol.97 (13), p.1012-1012

2005

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Breast cancer in young women (≤35 years): Genomic aberrations detected by comparative genomic hybridization

International journal of cancer, 2003-11, Vol.107 (4), p.583-592

2003

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The insulin-like growth factor-1 pathway mediator genes: SHC1 Met300Val shows a protective effect in breast cancer

Carcinogenesis (New York), 2004-12, Vol.25 (12), p.2473-2478

2004

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The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk

Carcinogenesis (New York), 2005-03, Vol.26 (3), p.643-647

2005

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Polyglutamine repeat length in the NCOA3 does not affect risk in familial breast cancer

Cancer epidemiology, biomarkers & prevention, 2005, Vol.14 (1), p.291-292

2005

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Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer

Carcinogenesis (New York), 2006-03, Vol.27 (3), p.593-598

2006

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The single nucleotide polymorphism IVS1+309 in Mouse Double Minute 2 does not affect risk of familial breast cancer

Cancer research (Chicago, Ill.), 2006-01, Vol.66 (2), p.646-648

2006

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p16INK4a immunohistochemistry improves interobserver agreement in the diagnosis of cervical intraepithelial neoplasia

The American journal of surgical pathology, 2002-11, Vol.26 (11), p.1389-1399

2002

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Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families

Human mutation, 2004-12, Vol.24 (6), p.534-534

2004

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Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer

Carcinogenesis (New York), 2006-08, Vol.27 (8), p.1655-1660

2006

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Polymorphisms in genes involved in GH1 release and their association with breast cancer risk

Carcinogenesis (New York), 2006-09, Vol.27 (9), p.1867-1875

2006

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Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk

International journal of cancer, 2006-05, Vol.118 (10), p.2505-2508

2006

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Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer

International journal of cancer, 2006-06, Vol.118 (11), p.2917-2918

2006

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c‐MYC Asn11Ser is associated with increased risk for familial breast cancer

International journal of cancer, 2005-11, Vol.117 (4), p.638-642

2005

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TP53-binding protein variants and breast cancer risk: a case-control study

Breast cancer research : BCR, 2005-01, Vol.7 (4), p.R502-R505, Article R502

2005

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Polymorphisms and haplotype structures in genes for transforming growth factor beta1 and its receptors in familial and unselected breast cancers

International journal of cancer, 2004-10, Vol.112 (1), p.94-99

2004

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Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer

JNCI : Journal of the National Cancer Institute, 2004-02, Vol.96 (3), p.234-5; author reply 235

2004

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Re: Integrin 3 Leu33Pro Homozygosity and Risk of Cancer

JNCI : Journal of the National Cancer Institute, 2004-02, Vol.96 (3), p.234-235

2004

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Detection of isolated disseminated tumor cells in bone marrow and blood samples of patients with hepatocellular carcinoma

Archives of surgery (Chicago. 1960), 2000-02, Vol.135 (2), p.213

2000

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Vascular Endothelial Growth Factor Polymorphisms in Relation to Breast Cancer Development and Prognosis

Association of Prolactin and Its Receptor Gene Regions with Familial Breast Cancer

Polymorphisms and haplotype structures in genes for transforming growth factor β1 and its receptors in familial and unselected breast cancers

Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant

Association of NCOA3 Polymorphisms with Breast Cancer Risk

Association of death receptor 4 haplotype 626C–683C with an increased breast cancer risk

Re: Association of a Common Variant of the CASP8 Gene With Reduced Risk of Breast Cancer

Breast cancer in young women (≤35 years): Genomic aberrations detected by comparative genomic hybridization

The insulin-like growth factor-1 pathway mediator genes: SHC1 Met300Val shows a protective effect in breast cancer

The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk

Polyglutamine repeat length in the NCOA3 does not affect risk in familial breast cancer

Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer

The single nucleotide polymorphism IVS1+309 in Mouse Double Minute 2 does not affect risk of familial breast cancer

p16INK4a immunohistochemistry improves interobserver agreement in the diagnosis of cervical intraepithelial neoplasia

Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer

Polymorphisms in genes involved in GH1 release and their association with breast cancer risk

Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk

Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer

c‐MYC Asn11Ser is associated with increased risk for familial breast cancer

TP53-binding protein variants and breast cancer risk: a case-control study

Polymorphisms and haplotype structures in genes for transforming growth factor beta1 and its receptors in familial and unselected breast cancers

Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer

Re: Integrin 3 Leu33Pro Homozygosity and Risk of Cancer

Detection of isolated disseminated tumor cells in bone marrow and blood samples of patients with hepatocellular carcinoma

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