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For information, get in touch with: Dott.ssa Barbara Parodi
Email: barbara.parodi@hsanmartino.it
  P. Romano, A. Manniello et al. Nucl Acids Res 2009 37:D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105

Short description of cell lines
Species: human, Caucasian


- By clicking on the cell line name, you will retrieve the detailed description of the cell line
- By clicking on one of the terms between parentheses, you will retrieve the list of all relevant cell line

1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

D-A92a (amnion, trisomy 21 / Down syndrome) - GGB
D-A92f (fibroblast, trisomy 21 / Down syndrome) - GGB
D-B87 (amnion) - GGB
D-C95 (amnion) - GGB
D-F92 (fibroblast, trisomy 21 / Down syndrome) - GGB
D-F94 (amnion, trisomy 21 / Down syndrome) - GGB
D-G92 (fibroblast, trisomy 21 / Down syndrome) - GGB
D-M89 (amnion, Patau syndrome / trisomy 13) - GGB
D-R86 (amnion, Edwards' syndrome / trisomy 18) - GGB
D-T93 (amnion) - GGB
D0994 (fibroblast) - GGB
D1589 (fibroblast) - GGB
D2085 (fibroblast) - GGB
D2187 (fibroblast, anencephaly) - GGB
D94 (fibroblast, Miller-Dieker syndrome) - GGB
D96 (fibroblast) - GGB
Da Mo (skin, fibroblast, Ehlers-Danlos syndrome, type V) - BGEBS
DA94 (fibroblast, Patau syndrome / trisomy 13) - GGB
DB-R95 (amnion) - GGB
DBC95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
DBM96 (lymphocyte, neurofibromatosis type I) - GGB
DBV95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
DC-P87 (amnion, trisomy 21 / Down syndrome) - GGB
DC96 (lymphocyte, familial epylepsy) - GGB
DCi96 (lymphocyte, familial epylepsy) - GGB
DCo96 (lymphocyte, familial epylepsy) - GGB
DCon96 (lymphocyte, familial epylepsy) - GGB
DDC95 (lymphocyte, T, trisomy 21 / Down syndrome) - GGB
DE96P (lymphocyte) - GGB
Detroit 510 (skin, fibroblast, galactosemia) - ECACC
Detroit 510 (skin, fibroblast, galactosemia) - IZSBS
Detroit 525 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - ECACC
Detroit 525 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - IZSBS
Detroit 529 (skin, fibroblast, trisomy 21 / Down syndrome) - ECACC
Detroit 529 (skin, fibroblast, trisomy 21 / Down syndrome) - IZSBS
Detroit 532 (skin, trisomy 21 / Down syndrome) - ECACC
Detroit 532 (foreskin, trisomy 21 / Down syndrome) - IZSBS
Detroit 539 (skin, fibroblast, trisomy 21 / Down syndrome) - ECACC
Detroit 539 (skin, fibroblast, trisomy 21 / Down syndrome) - IZSBS
Detroit 548 (skin, fibroblast, partial D trisomy) - IZSBS
Detroit 551 (skin, embryonic) - ECACC
Detroit 551 (skin, embryonic) - IZSBS
Detroit 562 (pharynx, carcinoma) - ECACC
Detroit 562 (pharynx, carcinoma) - IZSBS
Detroit 573 (skin, fibroblast, B/D translocation) - ECACC
Detroit 573 (skin, fibroblast, B/D translocation) - IZSBS
DFA96M (lymphocyte) - GGB
DFC96 (lymphocyte, familial epylepsy) - GGB
DFF87 (lymphocyte, trisomy 21 / Down syndrome) - GGB
DFGe96 (lymphocyte, familial epylepsy) - GGB
DFGi96 (lymphocyte, familial epylepsy) - GGB
DG96 (lymphocyte, familial epylepsy) - GGB
DL86 (fibroblast, severe combined immunodeficiency disease) - GGB
DL87 (fibroblast) - GGB
DLF87 (fibroblast) - GGB
DLG96f (fibroblast, Down syndrome, mosaic) - GGB
DLG96IL2 (lymphocyte, Down syndrome, mosaic) - GGB
DLL87S (fibroblast) - GGB
DM94 (lymphocyte, Angelman syndrome) - GGB
DMM87 (lymphocyte) - GGB
DMS 153 (lung, carcinoma, small cell) - ECACC
DMS 454 (lung, carcinoma, small cell) - ECACC
DMS 53 (lung, carcinoma, small cell) - ECACC
DMS 92 (lung, carcinoma, small cell) - ECACC
DOK (tongue, carcinoma) - ECACC
DP-LL95 (amnion, trisomy 21 / Down syndrome) - GGB
DPS84 (fibroblast, osteogenesis imperfecta) - GGB
DR89P (lymphocyte) - GGB
DS 92 (fibroblast, trisomy 21 / Down syndrome) - GGB
DSH1PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DSH2PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DSH3PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DSH4PV (skin, fibroblast, dyschromatosis symmetrica hereditaria) - PVCGU
DU 145 (prostate, carcinoma) - IZSBS
DU 145 (prostate, carcinoma) - MIUEP
DU-145 (prostate, carcinoma) - ICLC
DVA96 (lymphocyte, familial epylepsy) - GGB


For information, get in touch with:
IRCCS Ospedale Policlinico San Martino
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Barbara Parodi
Email: barbara.parodi@hsanmartino.it

If you want to cite CLDB and HyperCLDB, please use the following reference:

P. Romano, A. Manniello, O. Aresu, M. Armento, M. Cesaro, B. Parodi.
Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines.
Nucleic Acids Research 2009 37(Database issue):D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105