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Pathogenesis of DNA repair-deficient cancers: a statistical meta-analysis of putative Real Common Target genes

Oncogene, 2003-04, Vol.22 (15), p.2226-2235

2003

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Mechanisms of inactivation of the receptor tyrosine kinase EPHB2 in colorectal tumors

Cancer research (Chicago, Ill.), 2005-11, Vol.65 (22), p.10170-10173

2005

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Microsatellite instability in the development of DNA mismatch repair deficient tumors

Cancer biomarkers : section A of Disease markers, 2006, Vol.2 (1-2), p.69-86

2006

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Microsatellite instability of selective target genes in HNPCC-associated colon adenomas

Oncogene, 2005-04, Vol.24 (15), p.2525-2535

2005

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Molecular testing for microsatellite instability and its value in tumor characterization

Expert review of molecular diagnostics, 2005-07, Vol.5 (4), p.599-611

2005

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Cytosine deaminase gene as a potential tool for the genetic therapy of colorectal cancer

Journal of surgical oncology, 1996-01, Vol.61 (1), p.42-48

1996

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Combined molecular and clinical approaches for the identification of families with familial adenomatous polyposis coli

Annals of surgery, 1999-03, Vol.229 (3), p.350-361

1999

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High frequency of retinoic acid receptor beta abnormalities in human lung cancer

Oncogene, 1991-10, Vol.6 (10), p.1859-1868

1991

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Multiple endocrine neoplasia type 2–associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors

Surgery, 1998-09, Vol.124 (3), p.484-490

1998

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Identification of a novel germline mutation in a FAP family

Human molecular genetics, 1994-07, Vol.3 (7), p.1167-1168

1994

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Expression of an endogenous retroviral sequence from the HERV‐H group in gastrointestinal cancers

International journal of cancer, 2007-10, Vol.121 (7), p.1417-1423

2007

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A large MSH2 Alu insertion mutation causes HNPCC in a German kindred

Human genetics, 2004-10, Vol.115 (5), p.432-438

2004

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Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor

European journal of human genetics : EJHG, 2006-05, Vol.14 (5), p.561-566

2006

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Analysis of somatic APC mutations in rare extracolonic tumors of patients with familial adenomatous polyposis coli

Genes chromosomes & cancer, 2004-10, Vol.41 (2), p.93-98

2004

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Acceptance of and attitude toward genetic testing for hereditary nonpolyposis colorectal cancer: A comparison of participants and nonparticipants in genetic counseling

Diseases of the colon & rectum, 2004-02, Vol.47 (2), p.153-162

2004

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Microsatellite Analysis of Hereditary Nonpolyposis Colorectal Cancer-Associated Colorectal Adenomas by Laser-Assisted Microdissection: Correlation with Mismatch Repair Protein Expression Provides New Insights in Early Steps of Tumorigenesis

The Journal of molecular diagnostics : JMD, 2005-05, Vol.7 (2), p.160-170

2005

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Monitoring Gene Therapy with Cytosine Deaminase: In Vitro Studies Using Tritiated-5-Fluorocytosine

The Journal of nuclear medicine (1978), 1996-01, Vol.37 (1), p.87-94

1996

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Evaluation of bethesda guidelines in relation to microsatellite instability

Diseases of the colon & rectum, 2001-09, Vol.44 (9), p.1281-1289

2001

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Frequent Allelic Imbalance of Tumor Suppressor Gene Loci in Cervical Dysplasia

International journal of gynecological pathology, 1999-10, Vol.18 (4), p.374-380

1999

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Pathogenesis of DNA repair-deficient cancers: a statistical meta-analysis of putative Real Common Target genes

Mechanisms of inactivation of the receptor tyrosine kinase EPHB2 in colorectal tumors

Microsatellite instability in the development of DNA mismatch repair deficient tumors

Microsatellite instability of selective target genes in HNPCC-associated colon adenomas

Molecular testing for microsatellite instability and its value in tumor characterization

Cytosine deaminase gene as a potential tool for the genetic therapy of colorectal cancer

Combined molecular and clinical approaches for the identification of families with familial adenomatous polyposis coli

High frequency of retinoic acid receptor beta abnormalities in human lung cancer

Multiple endocrine neoplasia type 2–associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors

Identification of a novel germline mutation in a FAP family

Expression of an endogenous retroviral sequence from the HERV‐H group in gastrointestinal cancers

A large MSH2 Alu insertion mutation causes HNPCC in a German kindred

Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor

Analysis of somatic APC mutations in rare extracolonic tumors of patients with familial adenomatous polyposis coli

Acceptance of and attitude toward genetic testing for hereditary nonpolyposis colorectal cancer: A comparison of participants and nonparticipants in genetic counseling

Microsatellite Analysis of Hereditary Nonpolyposis Colorectal Cancer-Associated Colorectal Adenomas by Laser-Assisted Microdissection: Correlation with Mismatch Repair Protein Expression Provides New Insights in Early Steps of Tumorigenesis

Monitoring Gene Therapy with Cytosine Deaminase: In Vitro Studies Using Tritiated-5-Fluorocytosine

Evaluation of bethesda guidelines in relation to microsatellite instability

Frequent Allelic Imbalance of Tumor Suppressor Gene Loci in Cervical Dysplasia

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