Citations for
1EPCAM, HRAS, ZEB1
Cytosolic EpCAM cooperates with H-Ras to regulate epithelial to mesenchymal transition through ZEB1
Omar FA, Brown TC, Gillanders WE, Fleming TP, Smith MA, Bremner RM, Sankpal NV.
PLoS One. May 16;18(5):e0285707. doi: 10.1371/journal.pone.0285707. 2023
2HRAS, KRAS, LZTR1, MRAS, NRAS
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases.
Abe T, Umeki I, Kanno SI, Inoue SI, Niihori T, Aoki Y.
Cell Death Differ. Mar;27(3):1023-1035. doi: 10.1038/s41418-019-0395-5. Epub 2019 Jul 23 2020
3HRAS, KRAS, LZTR1
LZTR1 is a regulator of RAS ubiquitination and signaling.
Bigenzahn JW, Collu GM, Kartnig F, Pieraks M, Vladimer GI, Heinz LX, Sedlyarov V, Schischlik F, Fauster A, Rebsamen M, Parapatics K, Blomen VA, Müller AC, Winter GE, Kralovics R, Brummelkamp TR, Mlodzik M, Superti-Furga G.
Science Dec 7;362(6419):1171-1177. doi: 10.1126/science.aap8210. Epub 2018 Nov 15 2018
4CIB1, HRAS, PAPSS1
CIB1 contributes to oncogenic signalling by Ras via modulating the subcellular localisation of sphingosine kinase 1.
Zhu W, Gliddon BL, Jarman KE, Moretti PAB, Tin T, Parise LV, Woodcock JM, Powell JA, Ruszkiewicz A, Pitman MR, Pitson SM.
Oncogene 36(18):2619-2627. doi: 10.1038/onc.2016.428. Epub 2016 Dec 12. 2017
5CIP2A, HRAS
CIP2A cooperates with H-Ras to promote epithelial-mesenchymal transition in cervical-cancer progression.
Wu Y, Gu TT, Zheng PS.
Cancer Lett 356(2 Pt B):646-55. doi: 10.1016/j.canlet.2014.10.013. 2015
6HRAS, ING4, TDG
Oncogenic Ras suppresses ING4-TDG-Fas axis to promote apoptosis resistance.
Sun J, Shen Q, Lu H, Jiang Z, Xu W, Feng L, Li L, Wang X, Cai X, Jin H.
Oncotarget 6(39):41997-2007. doi: 10.18632/oncotarget.6015. 2015
7HRAS, NOS3
Endomembrane H-Ras controls vascular endothelial growth factor-induced nitric-oxide synthase-mediated endothelial cell migration.
Haeussler DJ, Pimentel DR, Hou X, Burgoyne JR, Cohen RA, Bachschmid MM.
J Biol Chem 288(21):15380-9. doi: 10.1074/jbc.M112.427765. Epub 2013 Apr 2. 2013
8COSTS, HRAS
Two cases with severe lethal course of Costello syndrome associated with HRAS p.G12C and p.G12D.
Lorenz S, Petersen C, Kordaß U, Seidel H, Zenker M, Kutsche K.
Eur J Med Genet 55(11):615-9. doi: 10.1016/j.ejmg.2012.07.007. Epub 2012 Aug 7. 2012
9HRAS, TP53BP2
Autophagic activity dictates the cellular response to oncogenic RAS.
Wang Y, Wang XD, Lapi E, Sullivan A, Jia W, He YW, Ratnayaka I, Zhong S, Goldin RD, Goemans CG, Tolkovsky AM, Lu X.
Proc Natl Acad Sci U S A 109(33):13325-30. doi: 10.1073/pnas.1120193109. Epub 2012 Jul 30. 2012
10HRAS
Oncogene Ras/phosphatidylinositol 3-kinase signaling targets histone H3 acetylation at lysine 56.
Liu Y, Wang DL, Chen S, Zhao L, Sun FL.
J Biol Chem 287(49):41469-80. doi: 10.1074/jbc.M112.367847. Epub 2012 Sep 16. 2012
11HRAS, KRAS
Interplay between oncogenic K-Ras and wild-type H-Ras in Caco2 cell transformation.
Ikonomou G, Kostourou V, Shirasawa S, Sasazuki T, Samiotaki M, Panayotou G.
J Proteomics 75(17):5356-69. doi: 10.1016/j.jprot.2012.06.038. Epub 2012 Jul 16. 2012
12HRAS
Methylation pattern of oncogene HRAS gene promoter region and its clinical relevance to urocystic tumorigenesis.
Sun XF, Li L, Li XJ, Shen W.
Mol Biol Rep 39(8):8431-7. doi: 10.1007/s11033-012-1696-7. Epub 2012 Jun 19. 2012
13COSTS, HRAS
Neonatal lethal Costello syndrome and unusual dinucleotide deletion/insertion mutations in HRAS predicting p.Gly12Val.
Burkitt-Wright EM, Bradley L, Shorto J, McConnell VP, Gannon C, Firth HV, Park SM, D'Amore A, Munyard PF, Turnpenny PD, Charlton A, Wilson M, Kerr B.
Am J Med Genet A 158A(5):1102-10. doi: 10.1002/ajmg.a.35296. Epub 2012 Apr 11. 2012
14COSTS, HRAS
Costello syndrome: a Ras/mitogen activated protein kinase pathway syndrome (rasopathy) resulting from HRAS germline mutations.
Gripp KW, Lin AE.
Genet Med 14(3):285-92. doi: 10.1038/gim.0b013e31822dd91f. Review. 2012
15HRAS, PEA15, PLD1
PEA-15 potentiates H-Ras-mediated epithelial cell transformation through phospholipase D.
Sulzmaier FJ, Valmiki MK, Nelson DA, Caliva MJ, Geerts D, Matter ML, White EP, Ramos JW.
Oncogene 31(30):3547-60. doi: 10.1038/onc.2011.514. Epub 2011 Nov 21. 2012
16HRAS
H-Ras isoform modulates extracellular matrix synthesis, proliferation, and migration in fibroblasts.
Fuentes-Calvo I, Blázquez-Medela AM, Eleno N, Santos E, López-Novoa JM, Martínez-Salgado C.
Am J Physiol Cell Physiol 302(4):C686-97. doi: 10.1152/ajpcell.00103.2011. Epub 2011 Nov 16. 2012
17DIRAS3, HRAS, RAF1
The tumor suppressor DiRas3 forms a complex with H-Ras and C-RAF proteins and regulates localization, dimerization, and kinase activity of C-RAF.
Baljuls A, Beck M, Oenel A, Robubi A, Kroschewski R, Hekman M, Rudel T, Rapp UR.
J Biol Chem 287(27):23128-40. doi: 10.1074/jbc.M112.343780. Epub 2012 May 17. 2012
18HRAS, KRAS, SMPS1, SMPS2
Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome.
Groesser L, Herschberger E, Ruetten A, Ruivenkamp C, Lopriore E, Zutt M, Langmann T, Singer S, Klingseisen L, Schneider-Brachert W, Toll A, Real FX, Landthaler M, Hafner C.
Nat Genet at Genet. 2012 2012
19BECN1, HRAS, PMAIP1
Oncogenic Ras-induced expression of Noxa and Beclin-1 promotes autophagic cell death and limits clonogenic survival.
Elgendy M, Sheridan C, Brumatti G, Martin SJ.
Mol Cell 42(1):23-35. Epub 2011 Feb 25. 2011
20COSTS, HRAS
Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome.
Gripp KW, Stabley DL, Geller PL, Hopkins E, Stevenson DA, Carey JC, Sol-Church K.
Am J Med Genet A 155A(9):2263-8. doi: 10.1002/ajmg.a.34150. Epub 2011 Aug 10. 2011
21COSTS, HRAS
HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome.
Niihori T, Aoki Y, Okamoto N, Kurosawa K, Ohashi H, Mizuno S, Kawame H, Inazawa J, Ohura T, Arai H, Nabatame S, Kikuchi K, Kuroki Y, Miura M, Tanaka T, Ohtake A, Omori I, Ihara K, Mabe H, Watanabe K, Niijima S, Okano E, Numabe H, Matsubara Y.
J Hum Genet 56(10):707-15. doi: 10.1038/jhg.2011.85. Epub 2011 Aug 18. 2011
22BRIP1, HRAS, KRAS
Oncogenic RAS regulates BRIP1 expression to induce dissociation of BRCA1 from chromatin, inhibit DNA repair, and promote senescence.
Tu Z, Aird KM, Bitler BG, Nicodemus JP, Beeharry N, Xia B, Yen TJ, Zhang R.
Dev Cell 21(6):1077-91. doi: 10.1016/j.devcel.2011.10.010. Epub 2011 Dec 1. 2011
23BNIP3, HRAS
H-ras up-regulates expression of BNIP3.
Kalas W, Swiderek E, Rapak A, Kopij M, Rak J, Strzadala L.
Anticancer Res 31(9):2869-75. 2011
24HRAS
Identification of H-Ras-specific motif for the activation of invasive signaling program in human breast epithelial cells.
Yong HY, Hwang JS, Son H, Park HI, Oh ES, Kim HH, Kim do K, Choi WS, Lee BJ, Kim HR, Moon A.
Neoplasia 13(2):98-107. 2011
25HRAS
Current evidence on the relationship between HRAS1 polymorphism and breast cancer risk: a meta-analysis.
Zhang C, Lv GQ, Yu XM, Gu YL, Li JP, Du LF, Zhou P.
Breast Cancer Res Treat 128(2):467-72. doi: 10.1007/s10549-011-1344-2. Epub 2011 Jan 9. 2011
26DPP8, DPP9, HRAS
A novel role of dipeptidyl peptidase 9 in epidermal growth factor signaling.
Yao TW, Kim WS, Yu DM, Sharbeen G, McCaughan GW, Choi KY, Xia P, Gorrell MD.
Mol Cancer Res 9(7):948-59. doi: 10.1158/1541-7786.MCR-10-0272. Epub 2011 May 26. 2011
27COSTS, HRAS
Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation.
Gremer L, De Luca A, Merbitz-Zahradnik T, Dallapiccola B, Morlot S, Tartaglia M, Kutsche K, Ahmadian MR, Rosenberger G.
Hum Mol Genet 19(5):790-802. Epub 2009 Dec 8.PMID: 19995790 2010
28DYRK1B, HRAS
DYRK1B-dependent autocrine-to-paracrine shift of Hedgehog signaling by mutant RAS.
Lauth M, Bergström A, Shimokawa T, Tostar U, Jin Q, Fendrich V, Guerra C, Barbacid M, Toftgård R.
Nat Struct Mol Biol 17(6):718-25. Epub 2010 May 30. 2010
29CSTS, HRAS
Oncogenic HRAS mutations cause prolonged PI3K signaling in response to epidermal growth factor in fibroblasts of patients with Costello syndrome.
Rosenberger G, Meien S, Kutsche K.
Hum Mutat 30(3):352-62. 2009
30FGFR3, HRAS
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors.
Goriely A, Hansen RM, Taylor IB, Olesen IA, Jacobsen GK, McGowan SJ, Pfeifer SP, McVean GA, Meyts ER, Wilkie AO.
Nat Genet 41(11):1247-52. Epub 2009 Oct 25.PMID: 19855393 2009
31COSTS, HRAS
Longitudinal course of cognitive, adaptive, and behavioral characteristics in Costello syndrome.
Axelrad ME, Schwartz DD, Fehlis JE, Hopkins E, Stabley DL, Sol-Church K, Gripp KW.
Am J Med Genet A 149A(12):2666-72.PMID: 19919001 2009
32HRAS, KRAS, BRAF, CFC2, COSTS, CFC3, MAP2K1, MAP2K2, CFC4, CFC5
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
Schulz AL, Albrecht B, Arici C, van der Burgt I, Buske A, Gillessen-Kaesbach G, Heller R, Horn D, HŸbner CA, Korenke GC, Kšnig R, Kress W, KrŸger G, Meinecke P, MŸcke J, Plecko B, Rossier E, Schinzel A, Schulze A, Seemanova E, Seidel H, Spranger S, Tuysuz B, Uhrig S, Wieczorek D, Kutsche K, Zenker M.
Clin Genet 73(1):62-70. Epub 2007 Nov 27. 2008
33COSTS, HRAS
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation.
Denayer E, Parret A, Chmara M, Schubbert S, Vogels A, Devriendt K, Frijns JP, Rybin V, de Ravel TJ, Shannon K, Cools J, Scheffzek K, Legius E.
Hum Mutat 29(2):232-9. 2008
34HRAS, COSTS
Costello syndrome associated with novel germline HRAS mutations: an attenuated phenotype?
Gripp KW, Innes AM, Axelrad ME, Gillan TL, Parboosingh JS, Davies C, Leonard NJ, Lapointe M, Doyle D, Catalano S, Nicholson L, Stabley DL, Sol-Church K.
Am J Med Genet A 146(6):683-90. 2008
35COSTS, HRAS
The diagnosis of Costello syndrome: nomenclature in Ras/MAPK pathway disorders.
Kerr B, Allanson J, Delrue MA, Gripp KW, Lacombe D, Lin AE, Rauen KA.
Am J Med Genet A 146A(9):1218-20. Review. No abstract available. 2008
36BRAF, CFC2, CFC3, CFC4, CFC5, COSTS, HRAS, KRAS, MAP2K1, MAP2K2, NS3
The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders.
Aoki Y, Niihori T, Narumi Y, Kure S, Matsubara Y.
Hum Mutat 29(8):992-1006. 2008
37BRAF, CFC2, CFC3, COSTS, HRAS, KRAS, LEOPS, MAP2K1, MAPK1, MTOR, NF1, NFNS, NS1, NS3, NS4, NS5, PTPN11, RAF1, SOS1
Oncogenes on my mind: ERK and MTOR signaling in cognitive diseases.
Krab LC, Goorden SM, Elgersma Y.
Trends Genet 24(10):498-510. Epub 2008 Sep 4. 2008
38HRAS
p21 Ras/impedes mitogenic signal propagation regulates cytokine production and migration in CD4 T cells.
Czyzyk J, Chen HC, Bottomly K, Flavell RA.
J Biol Chem 283(34):23004-15. Epub 2008 Jun 24. 2008
39HRAS, KRAS, NRAS
Kras and Hras--what is the difference?
Berns A.
Nat Genet 40(10):1149-50. No abstract available. 2008
40CFC5, COSTS, HRAS, KRAS, NS3
Clinical and molecular aspects of RAS related disorders.
Denayer E, de Ravel T, Legius E.
J Med Genet 45(11):695-703. Epub 2008 Jun 11. Review. 2008
41HRAS, COSTS
HRAS and the Costello syndrome.
Rauen K.
Clin Genet 71(2):101-8. 2007
42NS3, KRAS, COSTS, HRAS
The neoplastic risk in children with Noonan syndrome and Costello syndrome.
Lopez-Rangel E.
Clin Genet 71(1):44-5. 2007
43HRAS, COSTS
Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome.
Zampino G, Pantaleoni F, Carta C, Cobellis G, Vasta I, Neri C, Pogna EA, De Feo E, Delogu A, Sarkozy A, Atzeri F, Selicorni A, Rauen KA, Cytrynbaum CS, Weksberg R, Dallapiccola B, Ballabio A, Gelb BD, Neri G, Tartaglia M.
Hum Mutat 28(3):265-72. 2007
44CFC2, CFC3, CFC4, CFC5, KRAS, MAP2K1, MAP2K2, BRAF, COSTS, HRAS
Molecular and clinical characterization of cardio-facio-cutaneous (CFC) syndrome: overlapping clinical manifestations with Costello syndrome.
Narumi Y, Aoki Y, Niihori T, Neri G, Cave H, Verloes A, Nava C, Kavamura MI, Okamoto N, Kurosawa K, Hennekam RC, Wilson LC, Gillessen-Kaesbach G, Wieczorek D, Lapunzina P, Ohashi H, Makita Y, Kondo I, Tsuchiya S, Ito E, Sameshima K, Kato K, Kure S, Matsubara Y.
Am J Med Genet A 143(8):799-807. 2007
45COSTS,HRAS
Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation.
van der Burgt I, Kupsky W, Stassou S, Nadroo A, Barroso C, Diem A, Kratz CP, Dvorsky R, Ahmadian MR, Zenker M.
J Med Genet 44(7):459-62. Epub 2007 Apr 5. 2007
46CFC2, BRAF, CFC3, MAP21K1, CFC3, MAP2K2, CFC5, KRAS, COSTS, HRAS
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome.
Nava C, Hanna N, Michot C, Pereira S, Pouvreau N, Niihori T, Aoki Y, Matsubara Y, Arveiler B, Lacombe D, Pasmant E, Parfait B, Baumann C, HŽron D, Sigaudy S, Toutain A, Rio M, Goldenberg A, Leheup B, Verloes A, CavŽ H.
J Med Genet 44(12):763-71. Epub 2007 Aug 17. 2007
47HRAS, COSTS
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlation.
Gripp KW, Lin AE, Stabley DL, Nicholson L, Scott CI Jr, Doyle D, Aoki Y, Matsubara Y, Zackai EH, Lapunzina P, Gonzalez-Meneses A, Holbrook J, Agresta CA, Gonzalez IL, Sol-Church K.
Am J Med Genet A 140(1):1-7. 2006
48HRAS, COSTS
HRAS mutations in Costello syndrome: detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy.
Estep AL, Tidyman WE, Teitell MA, Cotter PD, Rauen KA.
Am J Med Genet A 140(1):8-16. 2006
49HRAS, COSTS
Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases.
Kerr B, Delrue MA, Sigaudy S, Perveen R, Marche M, Burgelin I, Stef M, Tang B, Eden OB, O'Sullivan J, De Sandre-Giovannoli A, Reardon W, Brewer C, Bennett C, Quarell O, M'Cann E, Donnai D, Stewart F, Hennekam R, Cave H, Verloes A, Philip N, Lacombe D, Levy N, Arveiler B, Black G.
J Med Genet 43(5):401-5. Epub 2006 Jan 27. 2006
50CFC2, BRAF, CFC3, MAP2K1, CFC4, MAP2K2, COSTS, HRAS
Distinguishing Costello versus cardio-facio-cutaneous syndrome: BRAF mutations in patients with a Costello phenotype.
Rauen KA.
Am J Med Genet A 140(15):1681-3. No abstract available. 2006
51HRAS, COSTS
Somatic mosaicism for an HRAS mutation causes Costello syndrome.
Gripp KW, Stabley DL, Nicholson L, Hoffman JD, Sol-Church K.
Am J Med Genet A 140(20):2163-9. 2006
52HRAS, CLU
Oncogenic HRAS suppresses clusterin expression through promoter hypermethylation.
Lund P, Weisshaupt K, Mikeska T, Jammas D, Chen X, Kuban RJ, UngethŸm U, Krapfenbauer U, Herzel HP, SchŠfer R, Walter J, Sers C.
Oncogene 25(35):4890-903. Epub 2006 Mar 27. 2006
53HRAS, COSTS
Germline mutations in HRAS proto-oncogene cause Costello syndrome.
Aoki Y, Niihori T, Kawame H, Kurosawa K, Ohashi H, Tanaka Y, Filocamo M, Kato K, Suzuki Y, Kure S, Matsubara Y.
Nat Genet 37(10):1038-40. Epub 2005 Sep 18. 2005
54ZDHHC9, GOLGA7, HRAS
DHHC9 and GCP16 constitute a human protein fatty acyltransferase with specificity for H- and N-Ras.
Swarthout JT, Lobo S, Farh L, Croke MR, Greentree WK, Deschenes RJ, Linder ME.
J Biol Chem 280(35):31141-8. Epub 2005 Jul 6. 2005
55HRAS, RAP1A
Identification of a novel domain of Ras and Rap1 that directs their differential subcellular localizations.
Nomura K, Kanemura H, Satoh T, Kataoka T.
J Biol Chem 279(21):22664-73. Epub 2004 Mar 18. 2004
56NRAS, KRAS, HRAS
ras mutations are associated with aggressive tumor phenotypes and poor prognosis in thyroid cancer.
Garcia-Rostan G, Zhao H, Camp RL, Pollan M, Herrero A, Pardo J, Wu R, Carcangiu ML, Costa J, Tallini G.
J Clin Oncol 21(17):3226-35. 2003
57HRAS, KRAS, RCE1
Human Ras converting enzyme endoproteolytic specificity at the P2' and P3' positions of K-Ras-derived peptides.
Hollander IJ, Frommer E, Aulabaugh A, Mallon R.
Biochim Biophys Acta 1649(1):24-9. 2003
58HRAS
H-ras oncogene mutation in dedifferentiated liposarcoma. Polymerase chain reaction-restriction fragment length polymorphism analysis.
Sakamoto A, Oda Y, Adachi T, Tamiya S, Matsuda S, Tanaka K, Iwamoto Y, Tsuneyoshi M.
Am J Clin Pathol 115(2):235-42. 2001
59HRAS
Additional characterization of a hexanucleotide polymorphic site in the first intron of human H-ras gene: comparative study of its alterations in non-small cell lung carcinomas and sporadic invasive breast carcinomas.
Kotsinas A, Gorgoulis VG, Zacharatos P, Mariatos G, Kokotas S, Liloglou T, Ikonomopoulos J, Zoumpourlis V, Kyroudi A, Field JK, Asimacopoulos PJ, Kittas C.
Cancer Genet Cytogenet 126(2):147-54. 2001
60HRAS
Distinct mutation patterns of breast cancer-associated alleles of the HRAS1 minisatellite locus.
Ding S, et al.
Hum Mol Genet 8 : 515-521. 1999
61RASSF7, D11S4893, D11S4894, D11S4895, HRAS
A 500-kb physical map and contig from the Harvey ras-1 gene to the 11p telomere.
Russell MW, et al.
Genomics 35 : 353-360. 1996
62HRAS, LQT1
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome.
Schulze-Bahr E, et al.
J Mol Med 73 : 565-569. 1995
63HRAS, LQT1
Exclusion of HRAS from long QT locus.
Roy N, et al.
Nat Genet 8 : 113-114. 1994
64HRAS
Polymerase chain reaction analysis of allele frequency and loss at the Harvey ras locus in myeloid malignancies.
Ardern JC, et al.
Leukemia 7 : 258-262. 1993
65HRAS
H-ras-1 gene mutations in basal cell carcinoma : automated direct sequencing of clinical specimens.
Wilke WW, et al.
Mod Pathol 6 : 15-19. 1993
66HRAS
PCR detection of an insertion/deletion polymorphism in intron 1 of the HRAS1 locus.
Tanci P, et al.
Nucleic Acids Res 20 : 1157. 1992
67HRAS
CGG repeat polymorphism at the c-Ha-ras oncogene locus.
Riggins GJ, et al.
Hum Mol Genet 1 : 775. 1992
68HRAS
Prevalence of RAS oncogene mutation in head and neck carcinomas.
Anderson JA, et al.
J Otolaryngol 21 : 321-326. 1992
69HRAS, KRAS, NRAS
Infrequent point mutations in codons 12 and 61 of ras oncogenes in human hepatocellular carcinomas.
Challen C, et al.
J Hepatol 14 : 342-346. 1992
70HRAS
Point mutations in the Ha-ras oncogene are detectable in formalin-fixed tissues of oral squamous cell carcinomas, but are infrequent in British cases.
Warnakulasuriya KAAS, et al.
J Oral Pathol Med 21 : 225-229. 1992
71HRAS
Polymorphism in exon 1 of the c-Ha-ras gene, (HRAS).
Hoban PR, et al.
Nucleic Acids Res 19 : 6976. 1991
72HRAS
Correlation of mutations of oncogene C-Ha-ras at codon 12 with metastasis and survival of gastric cancer patients.
Deng G, et al.
Oncogene Res 6 : 33-38. 1991
73HRAS
A new RFLP in intron 1 of the human c-Ha-ras1 gene and its close relationship with the variable tandem repeats inthe region 3' to the gene.
Iwahana H, et al.
Oncogene 5 : 1049-1053. 1990
74HRAS
A cosmid clone map derived from a small region of human chromosome 11.
Harrison-Lavoie KJ, John RM, Porteous DJ, Little PF.
Genomics 5 : 501-509. 1989
75HRAS
RAS oncogene mutation in multiple myeloma.
Neri A, et al.
J Exp Med 170 : 1715-1725. 1989
76HRAS
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.
Orita M, et al.
Genomics 5 : 874-879. 1989
77HRAS, KRAS
Analysis of RAS oncogene mutations in human lymphoid malignancies.
Neri A, et al.
Proc Natl Acad Sci U S A 85 : 9268-9272. 1988
78HRAS
HinfI RFLP downstream to the human HRAS1 gene.
Harumoto T, et al.
Nucleic Acids Res 16 : 2366. 1988
79HRAS
HRAS1-selected chromosome transfer generates markers which co-localize aniridia and genitourinary dysplasia associated translocation breakpoints and the Wilms' tumour gene within band 11p13.
Porteous DJ, et al.
(HGM9) Cytogenet Cell Genet 46 : 676. 1987
80HRAS, D11S99, D11S100, D11S101, D11S105, D11S106, D11S108, D11S109, D11S110, D11S111, D11S113, D11S115, D11S116, D11S117, D11S119, D11S169, D11S170, D11S171, D11S172, D11S173, D11S175, D11S176, D11S177, D11S178, D11S181
Co-transfer of defined genes and cloning of anonymous DNA markers following HRAS1-selected chromosome mediated gene transfer.
Porteous DJ, et al.
(HGM9) Cytogenet Cell Genet 46 : 676. 1987
81HRAS
Evidence against Ha-ras-1 involvement in sporadic and familial melanoma.
Gerhard DS, et al.
Nature 325 : 73-75. 1987
82HRAS
Two RFLPs generated by Taq I at the human HRSA1 locus.
Pierotti MA, et al.
Nucleic Acids Res 14 : 4379. 1986
83HRAS
Detection of two TaqI polymorphisms in the VTR region of the human HRAS1 oncogene.
Pierotti MA, et al.
Cytogenet Cell Genet 43 : 174-180. 1986
84INS, HRAS
DNA polymorphisms indicate loss of heterozygosity for chromosome 11 of D98AH2 cells.
Kaelbling M, et al.
Cytogenet Cell Genet 41 : 240-244. 1986
85HRAS
A dot-blot screening procedure for mutated ras oncogenes using synthetic oligodeoxynucleotides.
Verlaan de Vries M, et al.
Gene 50 : 313-320. 1986
86HB-NA@, HBB, HBBP1, HBD, HBE1, HBG1, HBG2, HRAS, INS, MODY10, PTH
Germ-line chromosomal localization of genes in chromosome 11p linkage: parathyroid hormone, beta-globin, c-H-ras-1, and insulin.
Chaganti RSK, et al.
Somat Cell Mol Genet 11 : 197-202. 1985
87HRAS
c-Ha-ras1 is not deleted in del(11p13) Wilms' tumor (WAGR) and maps to 11p15.1->11p15.5.
Junien C, et al.
(HGM7) Cytogenet Cell Genet 37 : 503. 1984
88HB-NA@, INS, WAGR, HRAS
Wilms tumor-aniridia association : segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene.
Fisher JH, et al.
Somat Cell Mol Genet 10 : 455-464. 1984
89HRAS, INS
HRAS 1, insulin, and beta-globin map outside of 11p11.2-->p14.1
de Martinville B, et al.
(HGM7) Cytogenet Cell Genet 37 : 530. 1984
90HRAS, ERAS, KRAS1P, KRAS
Dispersion of the ras family of transforming genes to four different chromosomes in man.
O'Brien SJ, et al.
Nature 302 : 839-842. 1983
91HRAS
The c-Ha-ras 1, insulin, and beta-globin loci map outside the deletion associated with aniridia-Wilms' tumour.
de Martinville B, et al.
Nature 305 : 641-643. 1983
92HRAS
Oncogene from human EJ bladder carcinoma is located on the short arm of chromosome 11.
de Martinville B, et al.
Science 219 : 498-501. 1983
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