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_HQ26
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HQ26 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ33
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25434, RRID:CVCL_HQ33 Copy
https://web.expasy.org/cellosaurus/CVCL_CX88
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Chinese.
Proper citation: Coriell Cat# GM25441, RRID:CVCL_CX88 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ43
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25454, RRID:CVCL_HQ43 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ33
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HQ33 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ37
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HQ37 Copy
https://web.expasy.org/cellosaurus/CVCL_LN95
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal dominant 1
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_LN95 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ39
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25450, RRID:CVCL_HQ39 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ42
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25453, RRID:CVCL_HQ42 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ25
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HQ25 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ32
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HQ32 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ26
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25413, RRID:CVCL_HQ26 Copy
https://web.expasy.org/cellosaurus/CVCL_HK65
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HK65 Copy
https://web.expasy.org/cellosaurus/CVCL_BA16
Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_BA16 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ43
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HQ43 Copy
https://web.expasy.org/cellosaurus/CVCL_HL86
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HL86 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ32
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25433, RRID:CVCL_HQ32 Copy
https://web.expasy.org/cellosaurus/CVCL_HL85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25409, RRID:CVCL_HL85 Copy
https://web.expasy.org/cellosaurus/CVCL_JF33
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_JF33 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ35
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25436, RRID:CVCL_HQ35 Copy
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