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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_HL10
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type III
Category: Finite cell line
Proper citation: Coriell Cat# GM21673, RRID:CVCL_HL10 Copy
https://web.expasy.org/cellosaurus/CVCL_HL10
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type III
Category: Finite cell line
Proper citation: RRID:CVCL_HL10 Copy
https://web.expasy.org/cellosaurus/CVCL_HL08
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type IV
Category: Finite cell line
Proper citation: RRID:CVCL_HL08 Copy
https://web.expasy.org/cellosaurus/CVCL_HL65
Organism: Homo sapiens (Human)
Disease: Fibromuscular dysplasia
Category: Finite cell line
Proper citation: Coriell Cat# GM21671, RRID:CVCL_HL65 Copy
https://web.expasy.org/cellosaurus/CVCL_HL63
Organism: Homo sapiens (Human)
Disease: Fibromuscular dysplasia
Category: Finite cell line
Proper citation: RRID:CVCL_HL63 Copy
https://web.expasy.org/cellosaurus/CVCL_HL03
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type I
Category: Finite cell line
Proper citation: Coriell Cat# GM21604, RRID:CVCL_HL03 Copy
https://web.expasy.org/cellosaurus/CVCL_HL12
Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Finite cell line
Proper citation: Coriell Cat# GM21675, RRID:CVCL_HL12 Copy
https://web.expasy.org/cellosaurus/CVCL_HL63
Organism: Homo sapiens (Human)
Disease: Fibromuscular dysplasia
Category: Finite cell line
Proper citation: Coriell Cat# GM21669, RRID:CVCL_HL63 Copy
https://web.expasy.org/cellosaurus/CVCL_DR33
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type IV
Category: Finite cell line
Proper citation: Coriell Cat# GM21788, RRID:CVCL_DR33 Copy
https://web.expasy.org/cellosaurus/CVCL_1J84
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Proper citation: RRID:CVCL_1J84 Copy
https://web.expasy.org/cellosaurus/CVCL_HL31
Organism: Homo sapiens (Human)
Disease: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_HL31 Copy
https://web.expasy.org/cellosaurus/CVCL_1J85
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Proper citation: RRID:CVCL_1J85 Copy
https://web.expasy.org/cellosaurus/CVCL_DR36
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type II
Category: Finite cell line
Proper citation: RRID:CVCL_DR36 Copy
https://web.expasy.org/cellosaurus/CVCL_BT53
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_BT53 Copy
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: RRID:CVCL_H991 Copy
https://web.expasy.org/cellosaurus/CVCL_U542
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_U542 Copy
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
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