Searching the RRID Resource Information Network
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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
https://web.expasy.org/cellosaurus/CVCL_HQ23
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25407, RRID:CVCL_HQ23 Copy
https://web.expasy.org/cellosaurus/CVCL_BW49
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25309, RRID:CVCL_BW49 Copy
https://web.expasy.org/cellosaurus/CVCL_5K79
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25361, RRID:CVCL_5K79 Copy
https://web.expasy.org/cellosaurus/CVCL_5K94
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25380, RRID:CVCL_5K94 Copy
https://web.expasy.org/cellosaurus/CVCL_BA18
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25370, RRID:CVCL_BA18 Copy
https://web.expasy.org/cellosaurus/CVCL_5K72
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25350, RRID:CVCL_5K72 Copy
https://web.expasy.org/cellosaurus/CVCL_5K91
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25377, RRID:CVCL_5K91 Copy
https://web.expasy.org/cellosaurus/CVCL_5K89
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25374, RRID:CVCL_5K89 Copy
https://web.expasy.org/cellosaurus/CVCL_5K92
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25378, RRID:CVCL_5K92 Copy
https://web.expasy.org/cellosaurus/CVCL_5K84
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25367, RRID:CVCL_5K84 Copy
https://web.expasy.org/cellosaurus/CVCL_5K76
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25354, RRID:CVCL_5K76 Copy
https://web.expasy.org/cellosaurus/CVCL_BW50
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25334, RRID:CVCL_BW50 Copy
https://web.expasy.org/cellosaurus/CVCL_HL84
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25408, RRID:CVCL_HL84 Copy
https://web.expasy.org/cellosaurus/CVCL_5K87
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM25372, RRID:CVCL_5K87 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ19
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25402, RRID:CVCL_HQ19 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ22
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25406, RRID:CVCL_HQ22 Copy
https://web.expasy.org/cellosaurus/CVCL_5K86
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25369, RRID:CVCL_5K86 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ44
Organism: Homo sapiens (Human)
Disease: Argininosuccinic aciduria
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25500, RRID:CVCL_AZ44 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ50
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25544, RRID:CVCL_HQ50 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ45
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25483, RRID:CVCL_HQ45 Copy
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