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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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GM22624
 
Resource Report
Resource Website 		RRID:CVCL_1K37 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell:GM22624,
Wikidata:Q54852665		 CVCL_1K37 2026-02-07 08:10:39 0
GM22633
 
Resource Report
Resource Website 		RRID:CVCL_1P95 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell:GM22633,
Wikidata:Q54852675		 CVCL_1P95 2026-02-07 08:10:39 0
GM50142
 
Resource Report
Resource Website 		RRID:CVCL_5T49 Homo sapiens (Human) PMID:23665875 Transformed cell line Male JL263 CLO:CLO_0014676,
Coriell:GM50142,
Wikidata:Q54854217		 CVCL_5T49 2026-02-07 08:11:32 0
GM50168
 
Resource Report
Resource Website 		RRID:CVCL_5L31 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL339 CLO:CLO_0015018,
Coriell:GM50168,
Wikidata:Q54854241		 CVCL_5L31 2026-02-07 08:11:44 0
GM50152
 
Resource Report
Resource Website 		Coriell Cat# GM50152, RRID:CVCL_5L26 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Female JL280 Coriell GM50152 CLO:CLO_0014709,
Coriell:GM50152,
Wikidata:Q54854225		 CVCL_5L26 2026-02-07 08:11:44 0
GM50150
 
Resource Report
Resource Website 		Coriell Cat# GM50150, RRID:CVCL_5T52 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female JL278 Coriell GM50150 CLO:CLO_0014715,
Coriell:GM50150,
Wikidata:Q54854224		 CVCL_5T52 2026-02-07 08:11:33 0
GM50154
 
Resource Report
Resource Website 		RRID:CVCL_0G59 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL285 CLO:CLO_0014718,
Coriell:GM50154,
Wikidata:Q54854227		 CVCL_0G59 2026-02-07 08:11:44 0
GM50116
 
Resource Report
Resource Website 		Coriell Cat# GM50116, RRID:CVCL_0F96 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Male JL156 Coriell GM50116 CLO:CLO_0014761,
Coriell:GM50116,
Wikidata:Q54854204		 CVCL_0F96 2026-02-07 08:11:43 0
GM50122
 
Resource Report
Resource Website 		Coriell Cat# GM50122, RRID:CVCL_0F92 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Male JL184 Coriell GM50122 CLO:CLO_0014752,
Coriell:GM50122,
Wikidata:Q54854208		 CVCL_0F92 2026-02-07 08:11:37 0
GM50112
 
Resource Report
Resource Website 		RRID:CVCL_0G48 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875 		Transformed cell line Female JL137 CLO:CLO_0014757,
Coriell:GM50112,
Wikidata:Q54854200		 CVCL_0G48 2026-02-07 08:11:43 0
GM50113
 
Resource Report
Resource Website 		Coriell Cat# GM50113, RRID:CVCL_0F90 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Female JL143 Coriell GM50113 CLO:CLO_0014755,
Coriell:GM50113,
Wikidata:Q54854201		 CVCL_0F90 2026-02-07 08:11:43 0
GM50147
 
Resource Report
Resource Website 		Coriell Cat# GM50147, RRID:CVCL_5T50 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL273 Coriell GM50147 CLO:CLO_0014683,
Coriell:GM50147,
Wikidata:Q54854221		 CVCL_5T50 2026-02-07 08:11:32 0
GM50175
 
Resource Report
Resource Website 		Coriell Cat# GM50175, RRID:CVCL_5L33 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL366 Coriell GM50175 CLO:CLO_0015010,
Coriell:GM50175,
Wikidata:Q54854247		 CVCL_5L33 2026-02-07 08:11:33 0
GM50118
 
Resource Report
Resource Website 		Coriell Cat# GM50118, RRID:CVCL_0F98 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Male JL172 Coriell GM50118 CLO:CLO_0014758,
Coriell:GM50118,
Wikidata:Q54854205		 CVCL_0F98 2026-02-07 08:11:37 0
GM50164
 
Resource Report
Resource Website 		Coriell Cat# GM50164, RRID:CVCL_5L29 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL325 Coriell GM50164 CLO:CLO_0014721,
Coriell:GM50164,
Wikidata:Q54854236		 CVCL_5L29 2026-02-07 08:11:38 0
GM50150
 
Resource Report
Resource Website 		RRID:CVCL_5T52 Homo sapiens (Human) Holoprosencephaly PMID:23665875 Transformed cell line Female JL278 CLO:CLO_0014715,
Coriell:GM50150,
Wikidata:Q54854224		 CVCL_5T52 2026-02-07 08:11:44 0
GM50139
 
Resource Report
Resource Website 		Coriell Cat# GM50139, RRID:CVCL_0G55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL259 Coriell GM50139 CLO:CLO_0014675,
Coriell:GM50139,
Wikidata:Q54854216		 CVCL_0G55 2026-02-07 08:11:44 0
GM50122
 
Resource Report
Resource Website 		RRID:CVCL_0F92 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Male JL184 CLO:CLO_0014752,
Coriell:GM50122,
Wikidata:Q54854208		 CVCL_0F92 2026-02-07 08:11:32 0
GM50116
 
Resource Report
Resource Website 		RRID:CVCL_0F96 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Male JL156 CLO:CLO_0014761,
Coriell:GM50116,
Wikidata:Q54854204		 CVCL_0F96 2026-02-07 08:11:37 0
GM50175
 
Resource Report
Resource Website 		RRID:CVCL_5L33 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL366 CLO:CLO_0015010,
Coriell:GM50175,
Wikidata:Q54854247		 CVCL_5L33 2026-02-07 08:11:44 0

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Welcome to the Resource Identification Portal Community.

Please see Force11 for more detailed information

We thank the NIH for their support of the RRID portal Award# R24GM144308, U24DK097771, U24DA039832, HHSN276201700124P, 75N97021P00135

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