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19,458 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
AG15868
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG15868, RRID:CVCL_2Q52 Chelonoidis niger (Galapagos giant tortoise) Group: Reptilian cell line., Group: Endangered species/breed cell line. Finite cell line Female Coriell AG15868 CLO:CLO_0019545,
Coriell:AG15868,
Wikidata:Q54745892
CVCL_2Q52 2026-09-12 06:20:40 0
AG18356
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_V983 Pan troglodytes (Chimpanzee) Group: Non-human primate cell line. PMID:22720000 Transformed cell line Female Coriell:AG18356,
Wikidata:Q54746766
CVCL_V983 2026-09-12 06:20:49 0
AG18357
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_V984 Pan troglodytes (Chimpanzee) Group: Non-human primate cell line. PMID:22720000 Transformed cell line Female Coriell:AG18357,
Wikidata:Q54746770
CVCL_V984 2026-09-12 06:20:49 0
AG18358
 
Resource Report
Resource Website
Discontinued
Coriell Cat# AG18358, RRID:CVCL_V985 Pan troglodytes (Chimpanzee) Group: Non-human primate cell line. PMID:22720000
PMID:22797897
PMID:24136357
PMID:25468404
Transformed cell line Female Min18358, Min 18358 Coriell AG18358 Coriell:AG18358,
GEO:GSM945680,
GEO:GSM1204870,
GEO:GSM1468858,
GEO:GSM1468866,
GEO:GSM1468874,
GEO:GSM1468882,
GEO:GSM1468890,
GEO:GSM1468898,
PRIDE:PXD000419,
Wikidata:Q54746772
CVCL_V985 2026-09-12 06:20:49 0
AG18355
 
Resource Report
Resource Website
Discontinued
Coriell Cat# AG18355, RRID:CVCL_V982 Pan troglodytes (Chimpanzee) Group: Non-human primate cell line. PMID:22720000 Transformed cell line Male Coriell AG18355 Coriell:AG18355,
Wikidata:Q54746765
CVCL_V982 2026-09-12 06:20:49 0
AG18359
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_V986 Pan troglodytes (Chimpanzee) Group: Non-human primate cell line. PMID:22720000
PMID:22797897
PMID:24136357
PMID:24380390
PMID:25468404
Transformed cell line Female Min18359, Min 18359 ArrayExpress:E-MTAB-1511,
Coriell:AG18359,
GEO:GSM945678,
GEO:GSM1204869,
GEO:GSM1468859,
GEO:GSM1468867,
GEO:GSM1468875,
GEO:GSM1468883,
GEO:GSM1468891,
GEO:GSM1468899,
PRIDE:PXD000419,
Wikidata:Q54746775
CVCL_V986 2026-09-12 06:20:49 0
AG0425
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B59 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:91082128,
Wikidata:Q54609958
CVCL_8B59 2026-09-12 06:19:43 0
AG0441
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B63 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:91092607,
Wikidata:Q54610105
CVCL_8B63 2026-09-12 06:19:44 0
AG0422
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B57 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:91081203,
Wikidata:Q54609953
CVCL_8B57 2026-09-12 06:19:43 0
AG0438
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B60 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:91091602,
Wikidata:Q54610071
CVCL_8B60 2026-09-12 06:19:43 0
AG0441
 
Resource Report
Resource Website
Discontinued
ECACC Cat# 91092607, RRID:CVCL_8B63 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91092607 ECACC:91092607,
Wikidata:Q54610105
CVCL_8B63 2026-09-12 06:19:44 0
AG0423
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B58 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:91081204,
Wikidata:Q54609956
CVCL_8B58 2026-09-12 06:19:43 0
AG0449
 
Resource Report
Resource Website
Discontinued
ECACC Cat# 91100411, RRID:CVCL_8B66 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91100411 ECACC:91100411,
Wikidata:Q54610270
CVCL_8B66 2026-09-12 06:19:45 0
AG04459
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_2A96 Homo sapiens (Human) Population: Caucasian., Part of: Baltimore Longitudinal Study of Aging (BLSA) cell line collection. PMID:7307581 Finite cell line Male GRC#0198 CLO:CLO_0034661,
Coriell:AG04459,
Wikidata:Q54610258
CVCL_2A96 2026-09-12 06:19:45 0
AG0479
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B67 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:91102207,
Wikidata:Q54739756
CVCL_8B67 2026-09-12 06:19:46 0
AG04459
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG04459, RRID:CVCL_2A96 Homo sapiens (Human) Population: Caucasian., Part of: Baltimore Longitudinal Study of Aging (BLSA) cell line collection. PMID:7307581 Finite cell line Male GRC#0198 Coriell AG04459 CLO:CLO_0034661,
Coriell:AG04459,
Wikidata:Q54610258
CVCL_2A96 2026-09-12 06:19:45 0
AG0448
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_8B65 Homo sapiens (Human) 22q11.2 deletion syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:91100410,
Wikidata:Q54610268
CVCL_8B65 2026-09-12 06:19:45 0
AG05307
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A2PA Semnopithecus entellus (Northern plains gray langur) Group: Non-human primate cell line. Finite cell line Female Coriell:AG05307,
Wikidata:Q105506283
CVCL_A2PA 2026-09-12 06:19:47 0
AG05187
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG05187, RRID:CVCL_A2CX Homo sapiens (Human) Population: Caucasian., Part of: Baltimore Longitudinal Study of Aging (BLSA) cell line collection. Finite cell line Male AG05187A, GRC#0214 Coriell AG05187 Coriell:AG05187,
Wikidata:Q105506277
CVCL_A2CX 2026-09-12 06:19:46 0
AG05230
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG05230, RRID:CVCL_A2DZ Homo sapiens (Human) Werner syndrome Population: Japanese. Finite cell line Female Coriell AG05230 Coriell:AG05230,
Wikidata:Q105506280
CVCL_A2DZ 2026-09-12 06:19:47 0

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