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HRAS1 oncogene
Known as:
v-Ha-RAS Harvey Rat Sarcoma Viral Oncogene Homolog
, Oncogene H-Ras
, HRAS
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The oncogene (v-ras-Ha or v-Ha-ras) of Harvey murine sarcoma virus (Ha-MuSV) encodes a transforming protein.
National Institutes of Health
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Related topics
Related topics
8 relations
11p15.5
HRAS gene
HRAS wt Allele
Homo sapiens
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
HRAS Mutations in Epithelial–Myoepithelial Carcinoma
S. Chiosea
,
Megan Miller
,
R. Seethala
Head and Neck Pathology
2013
Corpus ID: 5580805
The molecular profile of epithelial–myoepithelial carcinomas (EMCa) has not been well studied, though a recent association with…
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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
K. Sol‐Church
,
D. Stabley
,
+5 authors
K. Gripp
American journal of medical genetics. Part A
2009
Corpus ID: 1844487
Costello syndrome is a rare congenital anomaly syndrome associated with mental retardation and predisposition to benign and…
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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.
M. Bonafè
,
C. Barbi
,
+8 authors
C. Franceschi
Gene
2002
Corpus ID: 35365757
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
S. A. Radkov
,
P. Kellam
,
C. Boshoff
Nature Medicine
2000
Corpus ID: 3067895
Kaposi sarcoma-associated herpesvirus (KSHV) is involved in the etiopathogenesis of Kaposi sarcoma and certain…
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Highly Cited
2000
Highly Cited
2000
Mutations and copy number increase of HRAS in Spitz nevi with distinctive histopathological features.
B. Bastian
,
P. Leboit
,
D. Pinkel
The American journal of pathology
2000
Corpus ID: 45269794
Highly Cited
2000
Highly Cited
2000
The HRAS1 minisatellite locus and risk of ovarian cancer.
J. Weitzel
,
S. Ding
,
+5 authors
T. Krontiris
Cancer research
2000
Corpus ID: 40789857
Approximately 10% of ovarian cancers are due to mutations in highly penetrant inherited cancer susceptibility genes. The highly…
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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.
R. Rosell
,
R. Calvo
,
+5 authors
A. Barnadas
Clinical cancer research : an official journal of…
1999
Corpus ID: 7806791
The highly polymorphic HRAS1 variable number of tandem repeats (VNTR), which maps 1 kb downstream from the human H-ras1 gene, has…
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1991
1991
Allele Loss on Chromosome 11 in a Pituitary Tumor from a Patient with Multiple Endocrine Neoplasia Type 1
K. Yoshimoto
,
H. Iwahana
,
Katsuyuki Kubo
,
S. Saito
,
M. Itakura
Japanese journal of cancer research : Gann
1991
Corpus ID: 2093690
We have examined the allele loss of chromosome 11 in a pituitary tumor from a patient with familial multiple endocrine neoplasia…
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1988
1988
Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers
W. Bickmore
,
S. Christie
,
V. Heyningen
,
N. Hastie
,
D. Porteous
Nucleic Acids Res.
1988
Corpus ID: 15053129
The clinical association of Wilms' tumour with aniridia, genitourinary abnormalities and mental retardation (WAGR syndrome) is…
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1987
1987
HRAS1 proto-oncogene polymorphisms in human malignant melanoma: TaqI defined alleles significantly associated with the disease.
P. Radice
,
M. Pierotti
,
M. Borrello
,
M. T. Illeni
,
D. Rovini
,
G. Della Porta
Oncogene
1987
Corpus ID: 33837330
We have analysed the DNA of peripheral blood leukocytes (PBL) from 55 melanoma patients and 53 healthy individuals and failed to…
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