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_5Q03
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5Q03 Copy
https://web.expasy.org/cellosaurus/CVCL_5P82
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P82 Copy
https://web.expasy.org/cellosaurus/CVCL_5P98
Organism: Homo sapiens (Human)
Disease: Williams syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P98 Copy
https://web.expasy.org/cellosaurus/CVCL_5K11
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5K11 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q08
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM13554, RRID:CVCL_5Q08 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q09
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM13590, RRID:CVCL_5Q09 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q08
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5Q08 Copy
https://web.expasy.org/cellosaurus/CVCL_U537
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_U537 Copy
https://web.expasy.org/cellosaurus/CVCL_U539
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM13556, RRID:CVCL_U539 Copy
https://web.expasy.org/cellosaurus/CVCL_U538
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_U538 Copy
https://web.expasy.org/cellosaurus/CVCL_W965
Organism: Homo sapiens (Human)
Disease: Klinefelter syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM17867, RRID:CVCL_W965 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q82
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM17938, RRID:CVCL_5Q82 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q82
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5Q82 Copy
https://web.expasy.org/cellosaurus/CVCL_5K19
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5K19 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q96
Organism: Homo sapiens (Human)
Disease: Azoospermia
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5Q96 Copy
https://web.expasy.org/cellosaurus/CVCL_5K15
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM18322, RRID:CVCL_5K15 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q86
Organism: Homo sapiens (Human)
Disease: Holoprosencephaly
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM18311, RRID:CVCL_5Q86 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q88
Organism: Homo sapiens (Human)
Disease: Azoospermia
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5Q88 Copy
https://web.expasy.org/cellosaurus/CVCL_5K12
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM18319, RRID:CVCL_5K12 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q96
Organism: Homo sapiens (Human)
Disease: Azoospermia
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM18340, RRID:CVCL_5Q96 Copy
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