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HRAS1 oncogene

Known as: v-Ha-RAS Harvey Rat Sarcoma Viral Oncogene Homolog, Oncogene H-Ras, HRAS 
The oncogene (v-ras-Ha or v-Ha-ras) of Harvey murine sarcoma virus (Ha-MuSV) encodes a transforming protein.
National Institutes of Health

Related topics

Related topics

8 relations
11p15.5HRAS geneHRAS wt AlleleHomo sapiens
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Papers overview

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Highly Cited
2009
Highly Cited
2009
Male‐to‐male transmission of Costello syndrome: G12S HRAS germline mutation inherited from a father with somatic mosaicism
Costello syndrome is a rare congenital anomaly syndrome associated with mental retardation and predisposition to benign and… Expand
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2005
2005
Testing and improving predictions of scour and fill depths in a northern California coastal stream
Seasonal scour and fill from bankfull flows were measured in Freshwater Creek, a gravel-bed coastal stream of northern California… Expand
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2002
2002
An allele of HRAS1 3'variable number of tandem repeats is a frailty allele: implication for an evolutionarily-conserved pathway involved in longevity.
The human HRAS1 belongs to an evolutionarily-conserved family of genes which enrolls among its members the yeast RAS2, a gene… Expand
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2001
2001
Rare HRAS1 alleles are a risk factor for the development of brain tumors
The highly polymorphic HRAS1 minisatellite locus, located 1 kilobase downstream from the H‐ras1 gene, has been associated with… Expand
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Highly Cited
2000
Highly Cited
2000
The latent nuclear antigen of Kaposi sarcoma-associated herpesvirus targets the retinoblastoma–E2F pathway and with the oncogene Hras transforms primary rat cells
Kaposi sarcoma-associated herpesvirus (KSHV) is involved in the etiopathogenesis of Kaposi sarcoma and certain… Expand
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Highly Cited
2000
Highly Cited
2000
Mutations and copy number increase of HRAS in Spitz nevi with distinctive histopathological features.
Spitz nevus is a benign melanocytic neoplasm that can be difficult or impossible to histologically distinguish from melanoma. We… Expand
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Highly Cited
2000
Highly Cited
2000
The HRAS1 minisatellite locus and risk of ovarian cancer.
Approximately 10% of ovarian cancers are due to mutations in highly penetrant inherited cancer susceptibility genes. The highly… Expand
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1999
1999
Genetic susceptibility associated with rare HRAS1 variable number of tandem repeats alleles in Spanish non-small cell lung cancer patients.
The highly polymorphic HRAS1 variable number of tandem repeats (VNTR), which maps 1 kb downstream from the human H-ras1 gene, has… Expand
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1992
1992
The HRAS1 gene cluster: two upstream regions recognizing transcripts and a third encoding a gene with a leucine zipper domain.
We have cloned and characterized a 55-kb region of DNA surrounding HRAS1. It contains a cluster of two, and possibly three, genes… Expand
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1991
1991
Allele Loss on Chromosome 11 in a Pituitary Tumor from a Patient with Multiple Endocrine Neoplasia Type 1
We have examined the allele loss of chromosome 11 in a pituitary tumor from a patient with familial multiple endocrine neoplasia… Expand
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