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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.
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_U701
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# AG01437, RRID:CVCL_U701 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B48
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8B48 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B53
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8B53 Copy
Possibly Discontinued Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_V551
Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_V551 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE20
Organism: Homo sapiens (Human)
Disease: Oculocerebrorenal syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# AG01756, RRID:CVCL_JE20 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE42
Organism: Homo sapiens (Human)
Disease: Kidney Wilms tumor
Category: Finite cell line
Comments: Donor information: Established from the irradiated skin of a nephroblastoma patient.
Proper citation: RRID:CVCL_JE42 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE21
Organism: Homo sapiens (Human)
Disease: Cowden syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# AG01964, RRID:CVCL_JE21 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE27
Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JE27 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B51
Organism: Homo sapiens (Human)
Disease: Alagille syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90081517, RRID:CVCL_8B51 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE37
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# AG01485, RRID:CVCL_JE37 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B52
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90082301, RRID:CVCL_8B52 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE41
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JE41 Copy
Contaminated Discontinued
https://web.expasy.org/cellosaurus/CVCL_D101
Organism: Homo sapiens (Human)
Disease: Childhood T acute lymphoblastic leukemia
Category: Cancer cell line
Comments: Population: Caucasian., Problematic cell line: Contaminated. Shown to be a CCRF-CEM derivative (PubMed=12592342; PubMed=20143388). Originally thought to originates from the bone marrow of a patient suffering from neuroblastoma that evolved into a Hodgkin lymphoma.., Group: Patented cell line.
Proper citation: RRID:CVCL_D101 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE28
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: South American (Brazil, Guyana, Venezuela).
Proper citation: RRID:CVCL_JE28 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B50
Organism: Homo sapiens (Human)
Disease: Alagille syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8B50 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B50
Organism: Homo sapiens (Human)
Disease: Alagille syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90081516, RRID:CVCL_8B50 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JE28
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: South American (Brazil, Guyana, Venezuela).
Proper citation: Coriell Cat# AG01839, RRID:CVCL_JE28 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8B47
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90052207, RRID:CVCL_8B47 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_W842
Organism: Homo sapiens (Human)
Disease: Progeria
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_W842 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_A2KS
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_A2KS Copy
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