ID   AG10107
AC   CVCL_2I86
DR   CLO; CLO_0021867
DR   Coriell; AG10107
DR   Wikidata; Q54743237
RX   CelloPub=CLPUB00597;
RX   PubMed=9804340;
RX   PubMed=11511294;
RX   PubMed=18368133;
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   56Y
CA   Transformed cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 10
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RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994).
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RX   PubMed=9804340; DOI=10.1046/j.1523-1747.1998.00391.x;
RA   Khan S.G., Levy H.L., Legerski R.J., Quackenbush E., Reardon J.T.,
RA   Emmert S., Sancar A., Li L., Schneider T.D., Cleaver J.E.,
RA   Kraemer K.H.;
RT   "Xeroderma pigmentosum group C splice mutation associated with autism
RT   and hypoglycinemia.";
RL   J. Invest. Dermatol. 111:791-796(1998).
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RX   PubMed=11511294; DOI=10.1046/j.1523-1747.2001.01424.x;
RA   Gozukara E.M., Khan S.G., Metin A., Emmert S., Busch D.B.,
RA   Shahlavi T., Coleman D.M., Miller M., Chinsomboon N., Stefanini M.,
RA   Kraemer K.H.;
RT   "A stop codon in xeroderma pigmentosum group C families in Turkey and
RT   Italy: molecular genetic evidence for a common ancestor.";
RL   J. Invest. Dermatol. 117:197-204(2001).
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RX   PubMed=18368133; DOI=10.1038/jid.2008.48; PMCID=PMC2562952;
RA   Inui H., Oh K.-S., Nadem C., Ueda T., Khan S.G., Metin A., Gozukara E.M.,
RA   Emmert S., Slor H., Busch D.B., Baker C.C., DiGiovanna J.J.,
RA   Tamura D., Seitz C.S., Gratchev A., Wu W.-H., Chung K.Y., Chung H.J.,
RA   Azizi E., Woodgate R., Schneider T.D., Kraemer K.H.;
RT   "Xeroderma pigmentosum-variant patients from America, Europe, and
RT   Asia.";
RL   J. Invest. Dermatol. 128:2055-2068(2008).
//