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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.

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  • References:pmid:23665875 (facet)

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1,669 Results - per page

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GM18339
 
Resource Report
Resource Website 		RRID:CVCL_5Q95 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031065,
Coriell:GM18339,
Wikidata:Q54849507		 CVCL_5Q95 2026-09-12 05:35:52 0
GM18339
 
Resource Report
Resource Website 		Coriell Cat# GM18339, RRID:CVCL_5Q95 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM18339 CLO:CLO_0031065,
Coriell:GM18339,
Wikidata:Q54849507		 CVCL_5Q95 2026-09-12 05:35:52 0
GM18320
 
Resource Report
Resource Website 		Coriell Cat# GM18320, RRID:CVCL_5K13 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Female Coriell GM18320 CLO:CLO_0031077,
Coriell:GM18320,
Wikidata:Q54849492		 CVCL_5K13 2026-09-12 05:35:52 0
GM18336
 
Resource Report
Resource Website 		Coriell Cat# GM18336, RRID:CVCL_5Q92 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM18336 CLO:CLO_0031068,
Coriell:GM18336,
Wikidata:Q54849504		 CVCL_5Q92 2026-09-12 05:35:52 0
GM18338
 
Resource Report
Resource Website 		RRID:CVCL_5Q94 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0031066,
Coriell:GM18338,
Wikidata:Q54849506		 CVCL_5Q94 2026-09-12 05:35:52 0
GM18334
 
Resource Report
Resource Website 		RRID:CVCL_5Q90 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male CLO:CLO_0031070,
Coriell:GM18334,
Wikidata:Q54849502		 CVCL_5Q90 2026-09-12 05:35:52 0
GM18323
 
Resource Report
Resource Website 		RRID:CVCL_5K16 Homo sapiens (Human) Smith-Magenis syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0031075,
Coriell:GM18323,
Wikidata:Q54849495		 CVCL_5K16 2026-09-12 05:35:52 0
GM18381
 
Resource Report
Resource Website 		RRID:CVCL_5Q99 Homo sapiens (Human) Pseudotrisomy 13 syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0031096,
Coriell:GM18381,
Wikidata:Q54849519		 CVCL_5Q99 2026-09-12 05:35:53 0
GM18378
 
Resource Report
Resource Website 		Coriell Cat# GM18378, RRID:CVCL_5Q97 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female Coriell GM18378 Coriell:GM18378,
Wikidata:Q54849517		 CVCL_5Q97 2026-09-12 05:35:53 0
GM18825
 
Resource Report
Resource Website 		RRID:CVCL_2U51 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0026217,
Coriell:GM18825,
Wikidata:Q54849859		 CVCL_2U51 2026-09-12 05:36:00 0
GM18828
 
Resource Report
Resource Website 		Coriell Cat# GM18828, RRID:CVCL_2U54 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM18828 CLO:CLO_0026216,
Coriell:GM18828,
Wikidata:Q54849862		 CVCL_2U54 2026-09-12 05:36:00 0
GM18826
 
Resource Report
Resource Website 		RRID:CVCL_2U52 Homo sapiens (Human) Developmental delay Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0026218,
Coriell:GM18826,
Wikidata:Q54849860		 CVCL_2U52 2026-09-12 05:36:00 0
GM19155
 
Resource Report
Resource Website 		Coriell Cat# GM19155, RRID:CVCL_0X57 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM19155 CLO:CLO_0027370,
Coriell:GM19155,
Wikidata:Q54850221		 CVCL_0X57 2026-09-12 05:36:08 0
GM19344
 
Resource Report
Resource Website 		Coriell Cat# GM19344, RRID:CVCL_2U55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM19344 CLO:CLO_0027438,
Coriell:GM19344,
Wikidata:Q54850390		 CVCL_2U55 2026-09-12 05:36:12 0
GM19715
 
Resource Report
Resource Website 		Coriell Cat# GM19715, RRID:CVCL_5R00 Homo sapiens (Human) Shprintzen-Goldberg craniosynostosis syndrome PMID:23665875 Transformed cell line Female Coriell GM19715 Coriell:GM19715,
Wikidata:Q54850620		 CVCL_5R00 2026-09-12 05:36:17 0
GM07158
 
Resource Report
Resource Website 		Coriell Cat# GM07158, RRID:CVCL_0L58 Homo sapiens (Human) Intellectual developmental disorder PMID:23665875 Transformed cell line Male Coriell GM07158 CLO:CLO_0036896,
Coriell:GM07158,
Wikidata:Q54842560		 CVCL_0L58 2026-09-12 05:33:16 0
GM07148
 
Resource Report
Resource Website 		Coriell Cat# GM07148, RRID:CVCL_5N56 Homo sapiens (Human) Population: Native North American. PMID:23665875 Finite cell line Female Coriell GM07148 CLO:CLO_0036817,
Coriell:GM07148,
Wikidata:Q54842544		 CVCL_5N56 2026-09-12 05:33:15 0
GM07213
 
Resource Report
Resource Website 		RRID:CVCL_F610 Homo sapiens (Human) Karyotypic information: 46,X,i(X)(q28) (PubMed=10377420)., Population: African American. PMID:10377420
PMID:23665875 		Finite cell line Female GM7213 CLO:CLO_0036924,
Coriell:GM07213,
Wikidata:Q54842580		 CVCL_F610 2026-09-12 05:33:16 0
GM07150
 
Resource Report
Resource Website 		Coriell Cat# GM07150, RRID:CVCL_2T29 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM07150 CLO:CLO_0036885,
Coriell:GM07150,
Wikidata:Q54842546		 CVCL_2T29 2026-09-12 05:33:15 0
GM07158
 
Resource Report
Resource Website 		RRID:CVCL_0L58 Homo sapiens (Human) Intellectual developmental disorder PMID:23665875 Transformed cell line Male CLO:CLO_0036896,
Coriell:GM07158,
Wikidata:Q54842560		 CVCL_0L58 2026-09-12 05:33:16 0

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