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1,669 Results - per page

Show More Columns | Download Top 1000 Results

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
GM06047
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_5U19 Homo sapiens (Human) Miller-Dieker syndrome PMID:23665875
PMID:24413397
Finite cell line Male MDS1r(17) Fib CLO:CLO_0023537,
Coriell:GM06047,
GEO:GSM1274192,
Wikidata:Q54842128
CVCL_5U19 2026-09-12 05:33:01 1
GM06061
 
Resource Report
Resource Website
RRID:CVCL_F655 Homo sapiens (Human) Karyotypic information: 49,XXXXX.arr(X)x4 (Coriell=GM06061)., Population: Caucasian. PMID:23665875 Transformed cell line Female GM6061, GM06061B, GM6061B CLO:CLO_0023541,
Coriell:GM06061,
Wikidata:Q54842141
CVCL_F655 2026-09-12 05:33:02 0
GM06136
 
Resource Report
Resource Website
Coriell Cat# GM06136, RRID:CVCL_X331 Homo sapiens (Human) PMID:6661932
PMID:23665875
Transformed cell line Male GM 6136 Coriell GM06136 CLO:CLO_0023662,
Coriell:GM06136,
Wikidata:Q54842188
CVCL_X331 2026-09-12 05:33:03 0
GM06111
 
Resource Report
Resource Website
RRID:CVCL_7447 Homo sapiens (Human) Population: African American. PMID:23665875 Finite cell line Female GM6111, GM 06111 CLO:CLO_0023644,
Coriell:GM06111,
Wikidata:Q54842170
CVCL_7447 2026-09-12 05:33:03 0
GM06111
 
Resource Report
Resource Website
Coriell Cat# GM06111, RRID:CVCL_7447 Homo sapiens (Human) Population: African American. PMID:23665875 Finite cell line Female GM6111, GM 06111 Coriell GM06111 CLO:CLO_0023644,
Coriell:GM06111,
Wikidata:Q54842170
CVCL_7447 2026-09-12 05:33:03 0
GM06222
 
Resource Report
Resource Website
Coriell Cat# GM06222, RRID:CVCL_X332 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 6222 Coriell GM06222 CLO:CLO_0023145,
Coriell:GM06222,
Wikidata:Q54842223
CVCL_X332 2026-09-12 05:33:04 0
GM06226
 
Resource Report
Resource Website
RRID:CVCL_1P96 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0023092,
Coriell:GM06226,
Wikidata:Q54842230
CVCL_1P96 2026-09-12 05:33:04 0
GM06222
 
Resource Report
Resource Website
RRID:CVCL_X332 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 6222 CLO:CLO_0023145,
Coriell:GM06222,
Wikidata:Q54842223
CVCL_X332 2026-09-12 05:33:04 0
GM06326
 
Resource Report
Resource Website
Coriell Cat# GM06326, RRID:CVCL_1Q23 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM06326 CLO:CLO_0023060,
Coriell:GM06326,
Wikidata:Q54842254
CVCL_1Q23 2026-09-12 05:33:05 0
GM06226
 
Resource Report
Resource Website
Coriell Cat# GM06226, RRID:CVCL_1P96 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM06226 CLO:CLO_0023092,
Coriell:GM06226,
Wikidata:Q54842230
CVCL_1P96 2026-09-12 05:33:04 0
GM06228
 
Resource Report
Resource Website
RRID:CVCL_2T20 Homo sapiens (Human) PMID:10577914
PMID:23665875
Transformed cell line Female CLO:CLO_0023094,
Coriell:GM06228,
Wikidata:Q54842232
CVCL_2T20 2026-09-12 05:33:04 0
GM06473
 
Resource Report
Resource Website
RRID:CVCL_5N43 Homo sapiens (Human) Population: Hispanic. PMID:23665875 Finite cell line Female CLO:CLO_0023251,
Coriell:GM06473,
Wikidata:Q54842293
CVCL_5N43 2026-09-12 05:33:07 0
GM06803
 
Resource Report
Resource Website
RRID:CVCL_5N46 Homo sapiens (Human) WAGR syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0036543,
Coriell:GM06803,
Wikidata:Q54842334
CVCL_5N46 2026-09-12 05:33:10 0
GM06802
 
Resource Report
Resource Website
Coriell Cat# GM06802, RRID:CVCL_5N45 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM06802 CLO:CLO_0036542,
Coriell:GM06802,
Wikidata:Q54842333
CVCL_5N45 2026-09-12 05:33:10 0
GM06801
 
Resource Report
Resource Website
RRID:CVCL_5N44 Homo sapiens (Human) Intellectual developmental disorder Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell:GM06801,
Wikidata:Q54842332
CVCL_5N44 2026-09-12 05:33:10 0
GM06802
 
Resource Report
Resource Website
RRID:CVCL_5N45 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0036542,
Coriell:GM06802,
Wikidata:Q54842333
CVCL_5N45 2026-09-12 05:33:10 0
GM06918
 
Resource Report
Resource Website
Coriell Cat# GM06918, RRID:CVCL_5N49 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM06918 CLO:CLO_0036467,
Coriell:GM06918,
Wikidata:Q54842389
CVCL_5N49 2026-09-12 05:33:11 0
GM06936
 
Resource Report
Resource Website
Coriell Cat# GM06936, RRID:CVCL_5N50 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM06936 CLO:CLO_0036463,
Coriell:GM06936,
Wikidata:Q54842397
CVCL_5N50 2026-09-12 05:33:11 0
GM06918
 
Resource Report
Resource Website
RRID:CVCL_5N49 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0036467,
Coriell:GM06918,
Wikidata:Q54842389
CVCL_5N49 2026-09-12 05:33:11 0
GM00496
 
Resource Report
Resource Website
Coriell Cat# GM00496, RRID:CVCL_X231 Homo sapiens (Human) Trisomy 8 PMID:694721
PMID:6661932
PMID:23665875
Finite cell line Male GM-496, GM-0496, GM 496, GM496 Coriell GM00496 CLO:CLO_0025949,
Coriell:GM00496,
Wikidata:Q54836262
CVCL_X231 2026-09-12 05:31:44 0

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