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Inactivation of the von Hippel-Lindau tumor suppressor leads to selective expression of a human endogenous retrovirus in kidney cancer

Oncogene, 2011-11, Vol.30 (47), p.4697-4706

2011

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Epigenetic Inactivation of RASSF1A in Lung and Breast Cancers and Malignant Phenotype Suppression

JNCI : Journal of the National Cancer Institute, 2001-05, Vol.93 (9), p.691-699

2001

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Hypoxic repression of STAT1 and its downstream genes by a pVHL HIF-1 target DEC1 STRA13

Oncogene, 2007-02, Vol.26 (6), p.802-812

2007

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Hypermethylation of Ron proximal promoter associates with lack of full-length Ron and transcription of oncogenic short-Ron from an internal promoter

Oncogene, 2007-07, Vol.26 (31), p.4499-4512

2007

Volltextzugriff (PDF)

Expression of cell surface transmembrane carbonic anhydrase genes CA9 and CA12 in the human eye: overexpression of CA12 (CAXII) in glaucoma

Journal of medical genetics, 2003-04, Vol.40 (4), p.257-261

2003

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Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer

JAMA : the journal of the American Medical Association, 1995-02, Vol.273 (7), p.564

1995

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STRA13 expression and subcellular localisation in normal and tumour tissues: implications for use as a diagnostic and differentiation marker

Journal of medical genetics, 2005-07, Vol.42 (7), p.565-576

2005

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Loss of PL6 protein expression in renal clear cell carcinomas and other VHL-deficient tumours

The Journal of pathology, 2008, Vol.214 (1), p.46-57

2008

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Genetic and functional analysis of the von Hippel-Lindau (VHL) tumour suppressor gene promoter

Journal of medical genetics, 2002-07, Vol.39 (7), p.463-472

2002

Volltextzugriff (PDF)

Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene

Oncogene, 1998-06, Vol.16 (24), p.3151-3157

1998

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Identification of intragenic mutations in the Von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

Human molecular genetics, 1994-08, Vol.3 (8), p.1303-1308

1994

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Characterization and Chromosomal Localization of a cDNA Encoding Brain Amyloid of Alzheimer's Disease

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4791), p.877-880

1987

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Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours

Oncogene, 2001-03, Vol.20 (12), p.1509-1518

2001

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Molecular analysis of the von Hippel-Lindau disease tumor suppressor gene in human lung cancer cell lines

Oncogene, 1994-06, Vol.9 (6), p.1599-1604

1994

Volltextzugriff (PDF)

Autoimmunity, spontaneous tumourigenesis, and IL-15 insufficiency in mice with a targeted disruption of the tumour suppressor gene FusI

The Journal of pathology, 2007-04, Vol.211 (5), p.591-601

2007

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Gene structure of the human MET proto-oncogene

Oncogene, 1997-09, Vol.15 (13), p.1583-1586

1997

Volltextzugriff (PDF)

Genetic Changes in Human Adrenocortical Carcinomas

JNCI : Journal of the National Cancer Institute, 1989-04, Vol.81 (7), p.518-519

1989

Volltextzugriff (PDF)

Three tetranucleotide polymorphisms for loci: D3S1352; D3S1358; D3S1359

Human molecular genetics, 1993-08, Vol.2 (8), p.1327-1327

1993

Volltextzugriff (PDF)

Detailed mapping of germline deletions of the von Hippel—Lindau disease tumour suppressor gene

Human molecular genetics, 1994-04, Vol.3 (4), p.595-598

1994

Volltextzugriff (PDF)

Detection of germline mutations in the von Hippel-Lindau disease gene by the primer specified restriction map modification method

Journal of medical genetics, 1995-12, Vol.32 (12), p.938-941

1995

Volltextzugriff (PDF)

Two single nucleotide polymorphisms (SNPs) in the CALL gene for association studies with IQ

Psychiatric genetics, 1999-09, Vol.9 (3), p.165-167

1999

Volltextzugriff (PDF)

Mapping the Von Hippel — Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis

Human molecular genetics, 1993-07, Vol.2 (7), p.879-882

1993

Volltextzugriff (PDF)

Fourteen new polymorphic dinucleotide repeats on human chromosome 3: D3S1432, D3S1433, D3S1434, D3S1483, D3S1484, D3S1485, D3S1486, D3S1487, D3S1488, D3S1489, D3S1490, D3S1496, D3S1497 and D3S1498

Human molecular genetics, 1994-05, Vol.3 (5), p.837-837

1994

Volltextzugriff (PDF)

Gene structure of the human receptor tyrosine kinase RON and mutation analysis in lung cancer samples

Genes chromosomes & cancer, 2000-10, Vol.29 (2), p.147-156

2000

Volltextzugriff (PDF)

A novel donor splice site mutation associated with two mRNAs in von Hippel — Lindau disease

Human molecular genetics, 1994-07, Vol.3 (7), p.1191-1192

1994

Volltextzugriff (PDF)

1 – 25 von 1.264

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Inactivation of the von Hippel-Lindau tumor suppressor leads to selective expression of a human endogenous retrovirus in kidney cancer

Epigenetic Inactivation of RASSF1A in Lung and Breast Cancers and Malignant Phenotype Suppression

Hypoxic repression of STAT1 and its downstream genes by a pVHL HIF-1 target DEC1 STRA13

Hypermethylation of Ron proximal promoter associates with lack of full-length Ron and transcription of oncogenic short-Ron from an internal promoter

Expression of cell surface transmembrane carbonic anhydrase genes CA9 and CA12 in the human eye: overexpression of CA12 (CAXII) in glaucoma

Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer

STRA13 expression and subcellular localisation in normal and tumour tissues: implications for use as a diagnostic and differentiation marker

Loss of PL6 protein expression in renal clear cell carcinomas and other VHL-deficient tumours

Genetic and functional analysis of the von Hippel-Lindau (VHL) tumour suppressor gene promoter

Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene

Identification of intragenic mutations in the Von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

Characterization and Chromosomal Localization of a cDNA Encoding Brain Amyloid of Alzheimer's Disease

Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours

Molecular analysis of the von Hippel-Lindau disease tumor suppressor gene in human lung cancer cell lines

Autoimmunity, spontaneous tumourigenesis, and IL-15 insufficiency in mice with a targeted disruption of the tumour suppressor gene FusI

Gene structure of the human MET proto-oncogene

Genetic Changes in Human Adrenocortical Carcinomas

Three tetranucleotide polymorphisms for loci: D3S1352; D3S1358; D3S1359

Detailed mapping of germline deletions of the von Hippel—Lindau disease tumour suppressor gene

Detection of germline mutations in the von Hippel-Lindau disease gene by the primer specified restriction map modification method

Two single nucleotide polymorphisms (SNPs) in the CALL gene for association studies with IQ

Mapping the Von Hippel — Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis

Fourteen new polymorphic dinucleotide repeats on human chromosome 3: D3S1432, D3S1433, D3S1434, D3S1483, D3S1484, D3S1485, D3S1486, D3S1487, D3S1488, D3S1489, D3S1490, D3S1496, D3S1497 and D3S1498

Gene structure of the human receptor tyrosine kinase RON and mutation analysis in lung cancer samples

A novel donor splice site mutation associated with two mRNAs in von Hippel — Lindau disease

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