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_5T63
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5T63 Copy
https://web.expasy.org/cellosaurus/CVCL_0H55
Organism: Homo sapiens (Human)
Disease: Deletion 18q syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM50186, RRID:CVCL_0H55 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5T55
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM50182, RRID:CVCL_5T55 Copy
https://web.expasy.org/cellosaurus/CVCL_5T56
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Comments: Population: Lebanese.
Proper citation: RRID:CVCL_5T56 Copy
https://web.expasy.org/cellosaurus/CVCL_5L35
Organism: Homo sapiens (Human)
Disease: Deletion 18q syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5L35 Copy
https://web.expasy.org/cellosaurus/CVCL_5T60
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM50248, RRID:CVCL_5T60 Copy
https://web.expasy.org/cellosaurus/CVCL_5T62
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM50276, RRID:CVCL_5T62 Copy
https://web.expasy.org/cellosaurus/CVCL_5L35
Organism: Homo sapiens (Human)
Disease: Deletion 18q syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM50180, RRID:CVCL_5L35 Copy
https://web.expasy.org/cellosaurus/CVCL_5T59
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM50215, RRID:CVCL_5T59 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5T55
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5T55 Copy
https://web.expasy.org/cellosaurus/CVCL_0G72
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_0G72 Copy
https://web.expasy.org/cellosaurus/CVCL_5T58
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5T58 Copy
https://web.expasy.org/cellosaurus/CVCL_7351
Organism: Homo sapiens (Human)
Disease: Xeroderma pigmentosum, complementation group C
Category: Finite cell line
Comments: Senescence: Senesces at 24 PDL (PubMed=3003928; PubMed=6492896)., Population: African American.
Proper citation: RRID:CVCL_7351 Copy
https://web.expasy.org/cellosaurus/CVCL_X222
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM00017, RRID:CVCL_X222 Copy
https://web.expasy.org/cellosaurus/CVCL_7267
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_7267 Copy
https://web.expasy.org/cellosaurus/CVCL_X224
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM00088, RRID:CVCL_X224 Copy
https://web.expasy.org/cellosaurus/CVCL_V746
Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00072, RRID:CVCL_V746 Copy
https://web.expasy.org/cellosaurus/CVCL_H959
Organism: Homo sapiens (Human)
Disease: Nephropathic cystinosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_H959 Copy
https://web.expasy.org/cellosaurus/CVCL_X225
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00137, RRID:CVCL_X225 Copy
https://web.expasy.org/cellosaurus/CVCL_H959
Organism: Homo sapiens (Human)
Disease: Nephropathic cystinosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00090, RRID:CVCL_H959 Copy
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