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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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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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Genetic Changes in Human Adrenocortical Carcinomas

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

1989

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Three tetranucleotide polymorphisms for loci: D3S1352; D3S1358; D3S1359

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

1993

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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

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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

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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

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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

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Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3:D3S587; D3S1317; D3S1435

Human molecular genetics, 1993-08, Vol.2 (8), p.1326-1326

1993

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Sequence and chromosomal assignment of a novel cDNA identified by immunoscreening of a thyroid expression library: similarity to a family of mitochondrial solute carrier proteins

Molecular endocrinology (Baltimore, Md.), 1989-09, Vol.3 (9), p.1498-1508

1989

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Six dinucleotide microsatellite polymorphisms on human chromosome 3

Human molecular genetics, 1993-06, Vol.2 (6), p.817-818

1993

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A centromeric microsatellite probe on chromosome 3: LIB 9-95ca (D3S1338)

Human molecular genetics, 1993-03, Vol.2 (3), p.335-335

1993

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A polymorphic dinucleotide repeat probe on chromosome 3p: LIB 44-36ca (D3S769)

Human molecular genetics, 1993-01, Vol.2 (1), p.89-89

1993

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DNA sequences in human nasopharyngeal carcinoma cells that specify susceptibility to tumor promoter-induced neoplastic transformation

Carcinogenesis (New York), 1987-01, Vol.8 (1), p.121-127

1987

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Molecular genetic analysis of the 3p — syndrome

Human molecular genetics, 1994-06, Vol.3 (6), p.903-908

1994

Volltextzugriff (PDF)

Taql and Pstl RFLPs in the von Hippel–Lindau disease gene (VHL)

Human molecular genetics, 1993-10, Vol.2 (10), p.1750-1750

1993

Volltextzugriff (PDF)

Three tetrameric repeat polymorphisms on human chromosome 3: D3S1349; D3S1350; D3S1351

Human molecular genetics, 1993-06, Vol.2 (6), p.819-819

1993

Volltextzugriff (PDF)

A MspI polymorphism and linkage mapping of the human protein-tyrosine phosphatase G (PTPRG) gene

Human molecular genetics, 1993-01, Vol.2 (1), p.91-91

1993

Volltextzugriff (PDF)

Specific Genetic Change in Tumors Associated With von Hippel-Lindau Disease

JNCI : Journal of the National Cancer Institute, 1989-07, Vol.81 (14), p.1097-1101

1989

Volltextzugriff (PDF)

TaqI and PstI RFLPs in the von Hippel-Lindau disease gene (VHL)

Human molecular genetics, 1993-10, Vol.2 (10), p.1750-1750

1993

Volltextzugriff (PDF)

A Mspl polymorphism and linkage mapping of the human proteintyrosine phosphatase G (PTPRG) gene

Human molecular genetics, 1993-01, Vol.2 (1), p.91-91

1993

Volltextzugriff (PDF)

Three tetrameric repeat polymorphisms on human chromosome. III: D3S1349; D3S1350; D3S1351

Human molecular genetics, 1993, Vol.2 (6)

1993

Volltextzugriff (PDF)

A MspI polymorphism and linkage mapping of the human protein-tyrosine phosphate G (PTRG) gene

Human molecular genetics, 1993, Vol.2 (1)

1993

Volltextzugriff (PDF)

A microsatellite polymorphic probe on chromosome 3p: λLIB12–2CATT (D3S1244)

Human molecular genetics, 1992-09, Vol.1 (6), p.452-452

1992

Volltextzugriff (PDF)

Assessment of endothelial function by non-invasive peripheral arterial tonometry predicts late cardiovascular adverse events

European heart journal, 2010-05, Vol.31 (9), p.1142-1148

2010

Volltextzugriff (PDF)

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

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

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

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

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

Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3:D3S587; D3S1317; D3S1435

Sequence and chromosomal assignment of a novel cDNA identified by immunoscreening of a thyroid expression library: similarity to a family of mitochondrial solute carrier proteins

Six dinucleotide microsatellite polymorphisms on human chromosome 3

A centromeric microsatellite probe on chromosome 3: LIB 9-95ca (D3S1338)

A polymorphic dinucleotide repeat probe on chromosome 3p: LIB 44-36ca (D3S769)

DNA sequences in human nasopharyngeal carcinoma cells that specify susceptibility to tumor promoter-induced neoplastic transformation

Molecular genetic analysis of the 3p — syndrome

Taql and Pstl RFLPs in the von Hippel–Lindau disease gene (VHL)

Three tetrameric repeat polymorphisms on human chromosome 3: D3S1349; D3S1350; D3S1351

A MspI polymorphism and linkage mapping of the human protein-tyrosine phosphatase G (PTPRG) gene

Specific Genetic Change in Tumors Associated With von Hippel-Lindau Disease

TaqI and PstI RFLPs in the von Hippel-Lindau disease gene (VHL)

A Mspl polymorphism and linkage mapping of the human proteintyrosine phosphatase G (PTPRG) gene

Three tetrameric repeat polymorphisms on human chromosome. III: D3S1349; D3S1350; D3S1351

A MspI polymorphism and linkage mapping of the human protein-tyrosine phosphate G (PTRG) gene

A microsatellite polymorphic probe on chromosome 3p: λLIB12–2CATT (D3S1244)

Assessment of endothelial function by non-invasive peripheral arterial tonometry predicts late cardiovascular adverse events

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