Version 4.0.200811





Short description of cell lines.
Tissue/organ: chorionic villi


- By selecting the cell line name, you will receive the detailed description of the cell line
- By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
- You can search any term of the list by using the 'Find' utility of your browser

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:

Istituto Nazionale per la Ricerca sul Cancro,
c/o Centro Biotecnologie Avanzate, Torre B - Piano 2
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy Tel: +39-0105558-289, Fax: +39-0105558-295
Email: assunta.manniello@istge.it