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.
| Name | Proper Citation | Organism | Disease |
Comments |
Defining Citation | Category | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
ND31038 Resource Report Resource Website Discontinued |
RRID:CVCL_EY71 | Homo sapiens (Human) | Huntington's disease | PMID:22952635 | Finite cell line | Female | Coriell:ND31038, NHCDR:ND31038, Wikidata:Q54929453 |
CVCL_EY71 | 2026-09-03 06:52:35 | 0 | ||||||
|
ND31846 Resource Report Resource Website Discontinued |
RRID:CVCL_EY76 | Homo sapiens (Human) | Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). | PMID:22952635 | Finite cell line | Female | Coriell:ND31846, NHCDR:ND31846, Wikidata:Q54929518 |
CVCL_EY76 | 2026-09-03 06:52:37 | 0 | ||||||
|
ND31508 Resource Report Resource Website Discontinued |
Coriell Cat# ND31508, RRID:CVCL_EY72 | Homo sapiens (Human) | Parkinson disease | PMID:22952635 | Finite cell line | Male | Coriell | ND31508 | BioSample:SAMN00805617, Coriell:ND31508, NHCDR:ND31508, Wikidata:Q54929483 |
CVCL_EY72 | 2026-09-03 06:52:36 | 0 | ||||
|
ND31551 Resource Report Resource Website Discontinued |
RRID:CVCL_EY73 | Homo sapiens (Human) | Huntington's disease | PMID:22952635 | Finite cell line | Male | Coriell:ND31551, NHCDR:ND31551, Wikidata:Q54929491 |
CVCL_EY73 | 2026-09-03 06:52:36 | 0 | ||||||
|
ND31630 Resource Report Resource Website Discontinued Possibly Discontinued |
RRID:CVCL_DD53 | Homo sapiens (Human) | Parkinson disease |
PMID:22952635 PMID:27191603 |
Finite cell line | Male | BioSample:SAMN00805625, Coriell:ND31630, NHCDR:ND31630, Wikidata:Q54929499 |
CVCL_DD53 | 2026-09-03 06:52:36 | 0 | ||||||
|
ND31717 Resource Report Resource Website Discontinued |
Coriell Cat# ND31717, RRID:CVCL_EY74 | Homo sapiens (Human) | Parkinson disease | PMID:22952635 | Finite cell line | Female | Coriell | ND31717 | BioSample:SAMN00805627, Coriell:ND31717, NHCDR:ND31717, Wikidata:Q54929512 |
CVCL_EY74 | 2026-09-03 06:52:36 | 0 | ||||
|
ND32462 Resource Report Resource Website Discontinued |
NHCDR Cat# ND32462, RRID:CVCL_EY78 | Homo sapiens (Human) | Parkinson disease | Population: Caucasian. | PMID:22952635 | Finite cell line | Male | NHCDR | ND32462 | BioSample:SAMN00805655, Coriell:ND32462, NHCDR:ND32462, Wikidata:Q54929554 |
CVCL_EY78 | 2026-09-03 06:52:38 | 0 | |||
|
ND32157 Resource Report Resource Website Discontinued |
RRID:CVCL_EY77 | Homo sapiens (Human) | Parkinson disease | Population: Caucasian. | PMID:22952635 | Finite cell line | Female | BioSample:SAMN00805647, Coriell:ND32157, NHCDR:ND32157, Wikidata:Q54929544 |
CVCL_EY77 | 2026-09-03 06:52:37 | 0 | |||||
|
ND32603 Resource Report Resource Website Discontinued |
Coriell Cat# ND32603, RRID:CVCL_EY79 | Homo sapiens (Human) | PMID:22952635 | Finite cell line | Female | Coriell | ND32603 | Coriell:ND32603, NHCDR:ND32603, Wikidata:Q54929572 |
CVCL_EY79 | 2026-09-03 06:52:38 | 0 | |||||
|
ND32603 Resource Report Resource Website Discontinued |
RRID:CVCL_EY79 | Homo sapiens (Human) | PMID:22952635 | Finite cell line | Female | Coriell:ND32603, NHCDR:ND32603, Wikidata:Q54929572 |
CVCL_EY79 | 2026-09-03 06:52:38 | 0 | |||||||
|
ND32697 Resource Report Resource Website Discontinued |
NHCDR Cat# ND32697, RRID:CVCL_EY80 | Homo sapiens (Human) | Parkinson disease | Population: Caucasian. | PMID:22952635 | Finite cell line | Male | NHCDR | ND32697 | BioSample:SAMN00805659, Coriell:ND32697, NHCDR:ND32697, Wikidata:Q54929587 |
CVCL_EY80 | 2026-09-03 06:52:38 | 0 | |||
|
ND32970 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_EY41 | Homo sapiens (Human) | Parkinson disease 8, autosomal dominant | PMID:22952635 | Finite cell line | Coriell:ND32970, Wikidata:Q54929630 |
CVCL_EY41 | 2026-09-03 06:52:39 | 0 | |||||||
|
ND32949 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_EY38 | Homo sapiens (Human) | Parkinson disease 8, autosomal dominant | PMID:22952635 | Finite cell line | Male | Coriell:ND32949, Wikidata:Q54929623 |
CVCL_EY38 | 2026-09-03 06:52:39 | 0 | ||||||
|
ND32944 Resource Report Resource Website Discontinued |
RRID:CVCL_EY28 | Homo sapiens (Human) | Parkinson disease 8, autosomal dominant | Donor information: At sampling donor was not affected with Parkinson disease but at risk for disease., Population: Caucasian. | Finite cell line | Male | Coriell:ND32944, NHCDR:ND32944, Wikidata:Q54929619 |
CVCL_EY28 | 2026-09-03 06:52:39 | 0 | ||||||
|
ND32951 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_EY39 | Homo sapiens (Human) | Frontotemporal dementia-1 |
PMID:22952635 PMID:26143746 |
Finite cell line | Female | FTDP-17-2 | Coriell:ND32951, Wikidata:Q54929624 |
CVCL_EY39 | 2026-09-03 06:52:39 | 0 | |||||
|
ND32948 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A9R0 | Homo sapiens (Human) | Parkinson disease 8, autosomal dominant | Population: Caucasian. | Finite cell line | Male | Coriell:ND32948, Wikidata:Q102114585 |
CVCL_A9R0 | 2026-09-03 06:52:39 | 0 | ||||||
|
ND33391 Resource Report Resource Website Discontinued |
Coriell Cat# ND33391, RRID:CVCL_EY91 | Homo sapiens (Human) | PMID:22952635 | Finite cell line | Female | Coriell | ND33391 | Coriell:ND33391, NHCDR:ND33391, Wikidata:Q54929675 |
CVCL_EY91 | 2026-09-03 06:52:40 | 0 | |||||
|
ND32976 Resource Report Resource Website Discontinued |
RRID:CVCL_EY90 | Homo sapiens (Human) | Parkinson disease 8, autosomal dominant | Population: Caucasian; Spanish. | PMID:22952635 | Finite cell line | Female | BioSample:SAMN00805675, Coriell:ND32976, NHCDR:ND32976, Wikidata:Q54929634 |
CVCL_EY90 | 2026-09-03 06:52:39 | 0 | |||||
|
ND23017 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# ND23017, RRID:CVCL_FF81 | Homo sapiens (Human) | Transformed cell line | Male | Coriell | ND23017 | Coriell:ND23017, Wikidata:Q54928600 |
CVCL_FF81 | 2026-09-03 06:52:17 | 0 | ||||||
|
ND26512 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_FG66 | Homo sapiens (Human) | Transformed cell line | Male | Coriell:ND26512, Wikidata:Q54929009 |
CVCL_FG66 | 2026-09-03 06:52:26 | 0 |
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