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For information, get in touch with: Dott.ssa Assunta Manniello
Email: mariaassunta.manniello@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
Tissue/organ: chorionic villi


- 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 lines

A-B92v (human, Caucasian, chromosome mosaic) - GGB
IGV001/92 (human, Caucasian, glycogen storage disease II) - GEIMM
IGV001/96 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGV001/99 (human, Caucasian, mucolipidosis II) - GEIMM
IGV003/90 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGV003/93 (human, Caucasian, fucosidosis) - GEIMM
IGV005/93 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGV005/94 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGV006/99 (human, Caucasian, Gaucher disease type II) - GEIMM
IGV008/94 (human, Caucasian, mucolipidosis II) - GEIMM
IGV009/90 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGV009/96 (human, Caucasian, Gaucher disease type II) - GEIMM
IGV009/99 (human, Caucasian, Krabbe disease) - GEIMM
IGV011/92 (human, Caucasian, Sjogren-Larsson syndrome) - GEIMM
IGV017/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGV025/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGV028/91 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGV029/91 (human, Caucasian, glycogen storage disease II) - GEIMM
IGV030/84 (human, Caucasian, gangliosidosis, generalized GM1, type I) - GEIMM
IGV032/91 (human, Caucasian, Sandhoff disease) - GEIMM
M1191 (human, Caucasian, trisomy 9) - GGB
O1192 (human, Caucasian, trisomy 4) - GGB
P1095 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
P1392 (human, Caucasian, chromosome aberration) - GGB
P1393 (human, Caucasian, chromosome aberration) - GGB
P2594 (human, Caucasian) - GGB
S-D92v (human, Caucasian) - GGB
S1088 (human, Caucasian) - GGB
S1295 (human, Caucasian, trisomy 16) - GGB
V1790 (human, Caucasian, chromosome aberration) - GGB


For information, get in touch with:
IRCCS AOU San Martino IST,
c/o Centro Biotecnologie Avanzate, Torre D - Piano 2

Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Assunta Manniello
Email: mariaassunta.manniello@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