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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
GM15012
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5V23 Homo sapiens (Human) Angelman syndrome PMID:23665875 Transformed cell line Male Coriell:GM15012,
Wikidata:Q54847566
CVCL_5V23 2026-08-01 05:07:30 0
GM1500-6TG-A12
 
Resource Report
Resource Website
Misclassified
Misclassified
Possibly Discontinued
RRID:CVCL_H616 Homo sapiens (Human) Characteristics: Secretes IgG2 kappa., Population: Caucasian., Problematic cell line: Misclassified. Parent cell line (GM01500) was originally thought to be a myeloma cell line but is a B-lymphoblastoid cell line.., Group: Patented cell line., Group: Hybridoma fusion partner cell line. PMID:6969366 Transformed cell line Male GM1500 6TG-A12, GM 1500 6TG-A12, GM 1500 6TG-A1 2, GM 1500 6 TG-A12, GM1500TG-A12 Wikidata:Q54847546 cvcl_d870 CVCL_H616 2026-08-01 05:07:30 0
GM22232
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM22232, RRID:CVCL_1U26 Homo sapiens (Human) Population: Jewish; Ashkenazi., Part of: National Laboratory for the Genetics of Israeli Populations (NLGIP) collection. Transformed cell line Male NLGIP-6630, NLGIP6630 Coriell GM22232 CLO:CLO_0014821,
Coriell:GM22232,
Wikidata:Q54852442
CVCL_1U26 2026-08-01 05:09:31 0
GM15789
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_0Q31 Homo sapiens (Human) Nijmegen breakage syndrome Population: Caucasian; Czechoslovakian. Finite cell line Male Coriell:GM15789,
Wikidata:Q54848201
CVCL_0Q31 2026-08-01 05:07:47 0
GM15776
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM15776, RRID:CVCL_1S97 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line Coriell GM15776 Coriell:GM15776,
Wikidata:Q54848196
cvcl_1q37 CVCL_1S97 2026-08-01 05:07:47 0
GM16098
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5Q62 Homo sapiens (Human) Nijmegen breakage syndrome PMID:23665875 Finite cell line Female Coriell:GM16098,
Wikidata:Q54848320
CVCL_5Q62 2026-08-01 05:07:54 0
GM16101
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WN Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell:GM16101,
Wikidata:Q107115128
CVCL_A5WN 2026-08-01 05:07:49 0
GM16292
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WI Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell:GM16292,
Wikidata:Q107115152
CVCL_A5WI 2026-08-01 05:07:52 0
GM16289
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WF Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell:GM16289,
Wikidata:Q107115145
CVCL_A5WF 2026-08-01 05:07:52 0
GM16292
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16292, RRID:CVCL_A5WI Homo sapiens (Human) PMID:28161093 Transformed cell line Female Coriell GM16292 Coriell:GM16292,
Wikidata:Q107115152
CVCL_A5WI 2026-08-01 05:07:52 0
GM16295
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16295, RRID:CVCL_A5WL Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell GM16295 Coriell:GM16295,
Wikidata:Q107115158
CVCL_A5WL 2026-08-01 05:07:52 0
GM16294
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WK Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16294,
Wikidata:Q107115156
CVCL_A5WK 2026-08-01 05:07:52 0
GM16286
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WC Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16286,
Wikidata:Q107115138
CVCL_A5WC 2026-08-01 05:07:51 0
GM16287
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WD Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Male Coriell:GM16287,
Wikidata:Q107115140
CVCL_A5WD 2026-08-01 05:07:51 0
GM16291
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WH Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16291,
Wikidata:Q107115150
CVCL_A5WH 2026-08-01 05:07:55 0
GM16295
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WL Homo sapiens (Human) PMID:28161093 Transformed cell line Male Coriell:GM16295,
Wikidata:Q107115158
CVCL_A5WL 2026-08-01 05:07:55 0
GM16333
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_A5WM Homo sapiens (Human) Facioscapulohumeral muscular dystrophy 1 PMID:28161093 Transformed cell line Female Coriell:GM16333,
Wikidata:Q107115161
CVCL_A5WM 2026-08-01 05:07:53 0
GM16330
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16330, RRID:CVCL_A5WR Homo sapiens (Human) PMID:28161093 Transformed cell line Sex unspecified Coriell GM16330 Coriell:GM16330,
Wikidata:Q107115159
CVCL_A5WR 2026-08-01 05:07:56 0
GM16436
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_0H58 Homo sapiens (Human) Tourette syndrome Transformed cell line Male JL281 Coriell:GM16436,
Wikidata:Q54848558
CVCL_0H58 2026-08-01 05:07:57 0
GM16434
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM16434, RRID:CVCL_0H57 Homo sapiens (Human) Transformed cell line Male JL203 Coriell GM16434 Coriell:GM16434,
Wikidata:Q54848556
CVCL_0H57 2026-08-01 05:07:57 0

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