ID   LAU-T618A
AC   CVCL_DI23
SY   LAU618
DR   cancercelllines; CVCL_DI23
DR   Cosmic; 1675362
DR   GEO; GSM566252
DR   GEO; GSM568789
DR   Progenetix; CVCL_DI23
DR   Wikidata; Q54901980
RX   PubMed=20862285;
RX   PubMed=21494657;
RX   PubMed=22197931;
CC   From: Ludwig Institute for Cancer Research, Lausanne Branch; Lausanne; Switzerland.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Transcriptomics; Microarray.
CC   Omics: Variations; Array-based CGH.
CC   Omics: Variations; CNV analysis.
CC   Derived from site: Metastatic; Cutaneous; UBERON=UBERON_0000014.
DI   NCIt; C3510; Cutaneous melanoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
CA   Cancer cell line
DT   Created: 13-07-16; Last updated: 10-04-25; Version: 8
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RX   PubMed=20862285; DOI=10.1371/journal.pone.0012773; PMCID=PMC2940856;
RA   Caballero O.L., Zhao Q., Rimoldi D., Stevenson B.J., Svobodova S.,
RA   Devalle S., Rohrig U.F., Pagotto A., Michielin O., Speiser D.E.,
RA   Wolchok J.D., Liu C.-L., Pejovic T., Odunsi K., Brasseur F.,
RA   van den Eynde B.J., Old L.J., Lu X., Cebon J.S., Strausberg R.L.,
RA   Simpson A.J.G.;
RT   "Frequent MAGE mutations in human melanoma.";
RL   PLoS ONE 5:e12773.1-e12773.7(2010).
//
RX   PubMed=21494657; DOI=10.1371/journal.pone.0018369; PMCID=PMC3072964;
RA   Valsesia A., Rimoldi D., Martinet D., Ibberson M., Benaglio P.,
RA   Quadroni M., Waridel P., Gaillard M., Pidoux M., Rapin B., Rivolta C.,
RA   Xenarios I., Simpson A.J.G., Antonarakis S.E., Beckmann J.S.,
RA   Jongeneel C.V., Iseli C., Stevenson B.J.;
RT   "Network-guided analysis of genes with altered somatic copy number and
RT   gene expression reveals pathways commonly perturbed in metastatic
RT   melanoma.";
RL   PLoS ONE 6:e18369.1-e18369.12(2011).
//
RX   PubMed=22197931; DOI=10.1038/ng.1026;
RA   Nikolaev S.I., Rimoldi D., Iseli C., Valsesia A., Robyr D., Gehrig C.,
RA   Harshman K., Guipponi M., Bukach O.V., Zoete V., Michielin O.,
RA   Muehlethaler K., Speiser D.E., Beckmann J.S., Xenarios I.,
RA   Halazonetis T.D., Jongeneel C.V., Stevenson B.J., Antonarakis S.E.;
RT   "Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2
RT   mutations in melanoma.";
RL   Nat. Genet. 44:133-139(2011).
//