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Genetic susceptibility for breast cancer: How many more genes to be found?

Critical reviews in oncology/hematology, 2007-08, Vol.63 (2), p.125-149

2007

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High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands

Clinical genetics, 2012-03, Vol.81 (3), p.284-288

2012

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Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma

Science (American Association for the Advancement of Science), 2000-02, Vol.287 (5454), p.848-851

2000

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Quantifying measures to limit wind-driven resuspension of sediments for improvement of the ecological quality in some shallow Dutch lakes

Hydrobiologia, 2013-06, Vol.710 (1), p.279-295

2013

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Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients

Clinical endocrinology (Oxford), 2011-11, Vol.75 (5), p.650-655

2011

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Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK21100delC variant

Journal of medical genetics, 2004-10, Vol.41 (10), p.731-735

2004

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Micrometastases and Survival in Stage II Colorectal Cancer

The New England journal of medicine, 1998-07, Vol.339 (4), p.223-228

1998

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A new method to detect apoptosis in paraffin sections: in situ end- labeling of fragmented DNA

The journal of histochemistry and cytochemistry, 1993-01, Vol.41 (1), p.7-12

1993

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Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

Journal of medical genetics, 2001-05, Vol.38 (5), p.318-322

2001

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E-cadherin inactivation in lobular carcinoma in situ of the breast: an early event in tumorigenesis

British journal of cancer, 1997-11, Vol.76 (9), p.1131-1133

1997

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SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology

The Journal of pathology, 2003-11, Vol.201 (3), p.480-486

2003

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EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas

American journal of human genetics, 1999-09, Vol.65 (3), p.689-698

1999

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Genetic alterations on chromosome 16 and 17 are important features of ductal carcinoma in situ of the breast and are associated with histologic type

British Journal of Cancer, 1999-12, Vol.81 (8), p.1410-1418

1999

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Simultaneous loss of E-cadherin and catenins in invasive lobular breast cancer and lobular carcinoma in situ

The Journal of pathology, 1997-12, Vol.183 (4), p.404-411

1997

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Instability of short tandem repeats (microsatellites) in human cancers

Nature genetics, 1994-02, Vol.6 (2), p.152-156

1994

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Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas

European journal of endocrinology, 2005-01, Vol.152 (1), p.87

2005

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E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines

British journal of cancer, 2006-03, Vol.94 (5), p.661-671

2006

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Rapid detection of BRCA1 mutations by the protein truncation test

Nature genetics, 1995-06, Vol.10 (2), p.208-212

1995

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Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis

The Journal of pathology, 1999-12, Vol.189 (4), p.454-462

1999

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Glucocorticoid therapy and the risk of equine laminitis

Equine veterinary education, 2013-01, Vol.25 (1), p.39-46

2013

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Cell-cycle-related staining patterns of anti-proliferating cell nuclear antigen monoclonal antibodies. Comparison with BrdUrd labeling and Ki- 67 staining

The American journal of pathology, 1991-05, Vol.138 (5), p.1165-1172

1991

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Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families

Oncogene, 2004-05, Vol.23 (23), p.4076-4083

2004

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Efficacy of oral and intravenous dexamethasone in horses with recurrent airway obstruction

Equine veterinary journal, 2004-07, Vol.36 (5), p.426-430

2004

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Molecular genetic evidence for the conversion hypothesis of the origin of malignant mixed Müllerian tumours

The Journal of pathology, 1997-12, Vol.183 (4), p.424-431

1997

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

JNCI : Journal of the National Cancer Institute, 1998-08, Vol.90 (15), p.1138-1145

1998

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Genetic susceptibility for breast cancer: How many more genes to be found?

High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands

Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma

Quantifying measures to limit wind-driven resuspension of sediments for improvement of the ecological quality in some shallow Dutch lakes

Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients

Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK21100delC variant

Micrometastases and Survival in Stage II Colorectal Cancer

A new method to detect apoptosis in paraffin sections: in situ end- labeling of fragmented DNA

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

E-cadherin inactivation in lobular carcinoma in situ of the breast: an early event in tumorigenesis

SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology

EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas

Genetic alterations on chromosome 16 and 17 are important features of ductal carcinoma in situ of the breast and are associated with histologic type

Simultaneous loss of E-cadherin and catenins in invasive lobular breast cancer and lobular carcinoma in situ

Instability of short tandem repeats (microsatellites) in human cancers

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas

E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines

Rapid detection of BRCA1 mutations by the protein truncation test

Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis

Glucocorticoid therapy and the risk of equine laminitis

Cell-cycle-related staining patterns of anti-proliferating cell nuclear antigen monoclonal antibodies. Comparison with BrdUrd labeling and Ki- 67 staining

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families

Efficacy of oral and intravenous dexamethasone in horses with recurrent airway obstruction

Molecular genetic evidence for the conversion hypothesis of the origin of malignant mixed Müllerian tumours

Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

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