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_H991
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; cell lines from neonatal foreskins.
Proper citation: Coriell Cat# GM21808, RRID:CVCL_H991 Copy
https://web.expasy.org/cellosaurus/CVCL_H988
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Senescence: Senesces at 29 PDL (Coriell=GM21807)., Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; cell lines from neonatal foreskins.
Proper citation: RRID:CVCL_H988 Copy
https://web.expasy.org/cellosaurus/CVCL_HL14
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type I
Category: Finite cell line
Proper citation: RRID:CVCL_HL14 Copy
https://web.expasy.org/cellosaurus/CVCL_5R41
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_5R41 Copy
https://web.expasy.org/cellosaurus/CVCL_U543
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM21890, RRID:CVCL_U543 Copy
https://web.expasy.org/cellosaurus/CVCL_F109
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_F109 Copy
https://web.expasy.org/cellosaurus/CVCL_H992
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Senescence: Senesces at 25 PDL (Coriell=GM21810)., Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; cell lines from neonatal foreskins.
Proper citation: RRID:CVCL_H992 Copy
https://web.expasy.org/cellosaurus/CVCL_7663
Organism: Homo sapiens (Human)
Disease: Roberts-SC phocomelia syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_7663 Copy
https://web.expasy.org/cellosaurus/CVCL_5R40
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: Coriell Cat# GM21874, RRID:CVCL_5R40 Copy
https://web.expasy.org/cellosaurus/CVCL_H989
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Senescence: Senesces at 27 PDL (Coriell=GM21811)., Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; cell lines from neonatal foreskins.
Proper citation: RRID:CVCL_H989 Copy
https://web.expasy.org/cellosaurus/CVCL_5R40
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_5R40 Copy
https://web.expasy.org/cellosaurus/CVCL_BT55
Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Finite cell line
Proper citation: RRID:CVCL_BT55 Copy
https://web.expasy.org/cellosaurus/CVCL_H992
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Senescence: Senesces at 25 PDL (Coriell=GM21810)., Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; cell lines from neonatal foreskins.
Proper citation: Coriell Cat# GM21810, RRID:CVCL_H992 Copy
https://web.expasy.org/cellosaurus/CVCL_HK04
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: Coriell Cat# GM21881, RRID:CVCL_HK04 Copy
https://web.expasy.org/cellosaurus/CVCL_HL15
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type III
Category: Finite cell line
Proper citation: Coriell Cat# GM21819, RRID:CVCL_HL15 Copy
https://web.expasy.org/cellosaurus/CVCL_HL17
Organism: Homo sapiens (Human)
Disease: Campomelic dysplasia
Category: Finite cell line
Proper citation: Coriell Cat# GM21894, RRID:CVCL_HL17 Copy
https://web.expasy.org/cellosaurus/CVCL_H990
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Senescence: Senesces at 18 PDL (Coriell=GM21806)., Population: Caucasian., Part of: NIGMS collection of multiple cell lines from the same individual; cell lines from neonatal foreskins.
Proper citation: RRID:CVCL_H990 Copy
https://web.expasy.org/cellosaurus/CVCL_HK10
Organism: Homo sapiens (Human)
Disease: Marfan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_HK10 Copy
https://web.expasy.org/cellosaurus/CVCL_HK36
Organism: Homo sapiens (Human)
Disease: Marfan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_HK36 Copy
https://web.expasy.org/cellosaurus/CVCL_HK13
Organism: Homo sapiens (Human)
Disease: Marfan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_HK13 Copy
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