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N-ras Genes
Known as:
Oncogene N-RAS
, N ras Oncogenes
, Neuroblastoma RAS Viral Oncogene Homolog
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Human Oncogene N-RAS is a mutated variant of NRAS Gene (RAS Family), which encodes p21 N-Ras Protein, a monomeric GTPase involved in transmembrane…
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National Institutes of Health
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Related topics
Related topics
9 relations
1p13
Colorectal Carcinoma
Homo sapiens
NRAS gene
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Broader (1)
Genes, ras
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
SP174 Antibody Lacks Specificity for NRAS Q61R and Cross-Reacts With HRAS and KRAS Q61R Mutant Proteins in Malignant Melanoma
Anna Felisiak-Golabek
,
Shingo Inaguma
,
+10 authors
M. Miettinen
Applied immunohistochemistry & molecular…
2018
Corpus ID: 13768058
HRAS, KRAS, and NRAS, highly homologous proteins, are often mutationally activated in cancer. Usually, mutations cluster in…
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2014
2014
Mutational status of KRAS, NRAS, and BRAF in primary clear cell ovarian carcinoma
G. Zannoni
,
G. Improta
,
+5 authors
F. Fraggetta
Virchows Archiv
2014
Corpus ID: 24764490
Ovarian clear cell carcinoma (OCCC) is a subtype of epithelial ovarian cancer with characteristic biological features and…
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2014
2014
Lack of KRAS, NRAS, BRAF and TP53 mutations improves outcome of elderly metastatic colorectal cancer patients treated with cetuximab, oxaliplatin and UFT
M. Di Bartolomeo
,
F. Pietrantonio
,
+11 authors
O. B. O. T. M. Group
Targeted oncology
2014
Corpus ID: 51312
There is conflicting evidence on the predictive role of KRAS status when cetuximab is added to oxaliplatin-based regimens. This…
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2012
2012
NRAS Mutations in Noonan Syndrome
Ellen Denayer
,
H. Peeters
,
L. Sevenants
,
M. Derbent
,
J. Fryns
,
E. Legius
Molecular Syndromology
2012
Corpus ID: 38686307
Noonan syndrome is a genetically heterogeneous disorder caused by mutations in PTPN11, SOS1, RAF1 and less frequently in KRAS…
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2012
2012
Constitutional NRAS mutations are rare among patients with Noonan syndrome or juvenile myelomonocytic leukemia
L. Kraoua
,
H. Journel
,
+5 authors
H. Cavé
American Journal of Medical Genetics. Part A
2012
Corpus ID: 25494737
Recently, germline mutations of NRAS have been shown to be associated with Noonan syndrome (NS), a relatively common…
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2012
2012
Clinicopathologic Features of V600E and V600K Melanoma—Letter
Rosalyn Jewell
,
P. Chambers
,
+7 authors
J. Newton-Bishop
Clinical Cancer Research
2012
Corpus ID: 12715079
The presence of a BRAF mutation in a melanoma tumor predicts response to BRAF inhibitors; however, the biological characteristics…
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2010
2010
Retroviral insertional mutagenesis identifies Zeb2 activation as a novel leukemogenic collaborating event in CALM-AF10 transgenic mice.
D. Caudell
,
David P. Harper
,
+4 authors
P. Aplan
Blood
2010
Corpus ID: 206880401
The t(10;11) translocation results in a CALM-AF10 fusion gene in a subset of leukemia patients. Expression of a CALM-AF10…
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2009
2009
Characterization of candidate gene copy number alterations in the 11q13 region along with BRAF and NRAS mutations in human melanoma
Viktória Lázár
,
Szilvia Ecsedi
,
+6 authors
M. Balázs
Modern Pathology
2009
Corpus ID: 21444768
Amplification of the 11q13 chromosomal region is a common event in primary melanomas. Several candidate genes are localized at…
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Highly Cited
1992
Highly Cited
1992
Detection of RAS mutations in archival testicular germ cell tumors by polymerase chain reaction and oligonucleotide hybridization
J. Moul
,
S. Theune
,
E. Chang
Genes, Chromosomes and Cancer
1992
Corpus ID: 46443961
Preliminary studies of RAS mutational activation in human testicular germ cell neoplasms have yielded conflicting results…
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1990
1990
Detection of preferential NRAS mutations in human male germ cell tumors by the polymerase chain reaction
S. Ganguly
,
V. Murty
,
F. Samaniego
,
V. Reuter
,
G. Bosl
,
R. Chaganti
Genes, Chromosomes and Cancer
1990
Corpus ID: 31588408
We have studied 31 male germ cell tumors (GCTs) for probable mutations in codons 12, 13, and 61 of HRAS, KRAS, and NRAS oncogenes…
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