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256,031 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
GM09489
 
Resource Report
Resource Website
Coriell Cat# GM09489, RRID:CVCL_8A39 Homo sapiens (Human) Transformed cell line Female Coriell GM09489 CLO:CLO_0011542,
Coriell:GM09489,
Wikidata:Q54843797
CVCL_8A39 2026-08-01 05:05:44 0
GM09471
 
Resource Report
Resource Website
RRID:CVCL_AU73 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian; Acadian. Transformed cell line Male CLO:CLO_0011525,
Coriell:GM09471,
Wikidata:Q54843781
CVCL_AU73 2026-08-01 05:05:44 0
GM09507
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM09507, RRID:CVCL_N110 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Male GM18039 Coriell GM09507 CLO:CLO_0015608,
Coriell:GM09507,
Coriell:GM18039,
Wikidata:Q54843809
CVCL_N110 2026-08-01 05:05:45 0
GM09523
 
Resource Report
Resource Website
RRID:CVCL_8A43 Homo sapiens (Human) Transformed cell line Female GM09523A CLO:CLO_0011514,
Coriell:GM09523,
Wikidata:Q54843813
CVCL_8A43 2026-08-01 05:05:45 0
GM09488
 
Resource Report
Resource Website
Coriell Cat# GM09488, RRID:CVCL_8A38 Homo sapiens (Human) Transformed cell line Female Coriell GM09488 CLO:CLO_0011541,
Coriell:GM09488,
Wikidata:Q54843796
CVCL_8A38 2026-08-01 05:05:45 0
GM09494
 
Resource Report
Resource Website
Coriell Cat# GM09494, RRID:CVCL_U716 Homo sapiens (Human) Osteogenesis imperfecta type II Population: Caucasian. Finite cell line Male Coriell GM09494 CLO:CLO_0011539,
Coriell:GM09494,
Wikidata:Q54843798
CVCL_U716 2026-08-01 05:05:44 0
GM09502
 
Resource Report
Resource Website
RRID:CVCL_N109 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18038 CLO:CLO_0011457,
CLO:CLO_0015635,
Coriell:GM09502,
Coriell:GM18038,
Wikidata:Q54843806
CVCL_N109 2026-08-01 05:05:45 0
GM09464
 
Resource Report
Resource Website
RRID:CVCL_AU69 Homo sapiens (Human) Population: Caucasian; Acadian. Transformed cell line Female GM09464A CLO:CLO_0011530,
Coriell:GM09464,
Wikidata:Q54843776
CVCL_AU69 2026-08-01 05:05:44 0
GM09535
 
Resource Report
Resource Website
RRID:CVCL_9Z64 Homo sapiens (Human) Neurofibromatosis type 1 Population: Caucasian; English/Irish/Scottish. Transformed cell line Female GM09535A CLO:CLO_0011489,
Coriell:GM09535,
Wikidata:Q54843827
CVCL_9Z64 2026-08-01 05:05:45 0
GM09595
 
Resource Report
Resource Website
RRID:CVCL_8A46 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0026607,
Coriell:GM09595,
Wikidata:Q54843877
CVCL_8A46 2026-08-01 05:05:47 0
GM09572
 
Resource Report
Resource Website
Coriell Cat# GM09572, RRID:CVCL_5M05 Homo sapiens (Human) Transformed cell line Male Coriell GM09572 CLO:CLO_0011443,
Coriell:GM09572,
Wikidata:Q54843850
CVCL_5M05 2026-08-01 05:05:46 0
GM09589
 
Resource Report
Resource Website
Coriell Cat# GM09589, RRID:CVCL_GT51 Homo sapiens (Human) Hereditary factor II deficiency Transformed cell line Female Coriell GM09589 CLO:CLO_0011396,
Coriell:GM09589,
Wikidata:Q54843865
CVCL_GT51 2026-08-01 05:05:47 0
GM09548
 
Resource Report
Resource Website
RRID:CVCL_F211 Homo sapiens (Human) Transformed cell line Female GM09548A CLO:CLO_0011419,
Coriell:GM09548,
Wikidata:Q54843839
CVCL_F211 2026-08-01 05:05:45 0
GM09591
 
Resource Report
Resource Website
Coriell Cat# GM09591, RRID:CVCL_FV47 Homo sapiens (Human) Junctional epidermolysis bullosa Population: Belizean. Transformed cell line Female Coriell GM09591 CLO:CLO_0011402,
Coriell:GM09591,
Wikidata:Q54843867
CVCL_FV47 2026-08-01 05:05:46 0
GM09616
 
Resource Report
Resource Website
Coriell Cat# GM09616, RRID:CVCL_9Z67 Homo sapiens (Human) Neurofibromatosis type 1 Population: Caucasian. Transformed cell line Female Coriell GM09616 CLO:CLO_0026651,
Coriell:GM09616,
Wikidata:Q54843886
CVCL_9Z67 2026-08-01 05:05:47 0
GM09608
 
Resource Report
Resource Website
Coriell Cat# GM09608, RRID:CVCL_8A56 Homo sapiens (Human) Hereditary factor VII deficiency Transformed cell line Female Coriell GM09608 CLO:CLO_0026621,
Coriell:GM09608,
Wikidata:Q54843880
CVCL_8A56 2026-08-01 05:05:47 0
GM09588
 
Resource Report
Resource Website
RRID:CVCL_N318 Homo sapiens (Human) Transformed cell line Female GM09588A CLO:CLO_0011395,
Coriell:GM09588,
Wikidata:Q54843864
CVCL_N318 2026-08-01 05:05:47 0
GM09582
 
Resource Report
Resource Website
RRID:CVCL_7494 Homo sapiens (Human) Ataxia telangiectasia syndrome PMID:16166284
PMID:23943852
Transformed cell line Female CLO:CLO_0011435,
Coriell:GM09582,
GEO:GSM1116633,
GEO:GSM1116634,
GEO:GSM1116635,
GEO:GSM1116636,
Lonza:973,
Wikidata:Q54843858
CVCL_7494 2026-08-01 05:05:46 0
GM09567
 
Resource Report
Resource Website
Coriell Cat# GM09567, RRID:CVCL_N112 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Male GM18041 Coriell GM09567 CLO:CLO_0011455,
CLO:CLO_0015614,
Coriell:GM09567,
Coriell:GM18041,
Wikidata:Q54843847
CVCL_N112 2026-08-01 05:05:46 0
GM09614
 
Resource Report
Resource Website
RRID:CVCL_FV48 Homo sapiens (Human) Epidermolysis bullosa dystrophica Population: African American. Transformed cell line Female CLO:CLO_0026614,
Coriell:GM09614,
Wikidata:Q54843884
CVCL_FV48 2026-08-01 05:05:46 0

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