ID   NHSF46
AC   CVCL_G283
SY   NHSF-46; Normal Human Skin Fibroblast 46 year old
DR   CLO; CLO_0050707
DR   BioSample; SAMN03472341
DR   RCB; RCB0162
DR   Wikidata; Q54930531
RX   PubMed=4011712;
RX   PubMed=4031543;
RX   PubMed=4083160;
RX   PubMed=7300843;
CC   Population: Japanese.
CC   Senescence: Senesces at 37 PDL (PubMed=4083160); 45 PDL (RCB=RCB0162).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): RCB
ST   Amelogenin: X,Y
ST   CSF1PO: 10,12
ST   D13S317: 9,10
ST   D16S539: 10,14
ST   D5S818: 12,13
ST   D7S820: 8,10
ST   TH01: 7,9
ST   TPOX: 11
ST   vWA: 16,18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   46Y
CA   Finite cell line
DT   Created: 11-02-13; Last updated: 29-06-23; Version: 12
//
RX   PubMed=4011712; DOI=10.1111/j.1751-1097.1985.tb03538.x;
RA   Fujiwara Y., Uehara Y., Ichihashi M., Nishioka K.;
RT   "Xeroderma pigmentosum complementation group F: more assignments and
RT   repair characteristics.";
RL   Photochem. Photobiol. 41:629-634(1985).
//
RX   PubMed=4031543; DOI=10.1111/1523-1747.ep12276776;
RA   Ichihashi M., Fujiwara Y., Uehara Y., Matsumoto A.;
RT   "A mild form of xeroderma pigmentosum assigned to complementation
RT   group G and its repair heterogeneity.";
RL   J. Invest. Dermatol. 85:284-287(1985).
//
RX   PubMed=4083160; DOI=10.1007/978-1-4684-7853-2_23;
RA   Fujiwara Y., Kano Y., Ichihashi M., Nakao Y., Matsumura T.;
RT   "Abnormal fibroblast aging and DNA replication in the Werner
RT   syndrome.";
RL   Adv. Exp. Med. Biol. 190:459-477(1985).
//
RX   PubMed=7300843; DOI=10.1016/0027-5107(81)90123-8;
RA   Kano Y., Fujiwara Y.;
RT   "Roles of DNA interstrand crosslinking and its repair in the induction
RT   of sister-chromatid exchange and a higher induction in Fanconi's
RT   anemia cells.";
RL   Mutat. Res. 81:365-375(1976).
//