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236,573 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 Authority Record Last Update Mentions Count
GM13419
 
Resource Report
Resource Website
Coriell Cat# GM13419, RRID:CVCL_1N85 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Male Coriell GM13419 CLO:CLO_0012646,
BioSample:SAMN00802356,
Coriell:GM13419,
Wikidata:Q54846515
CVCL_1N85 Cellosaurus 2026-09-26 06:51:14 0
GM13331
 
Resource Report
Resource Website
Coriell Cat# GM13331, RRID:CVCL_1K73 Homo sapiens (Human) Glycogen storage disease type II Transformed cell line Male Coriell GM13331 CLO:CLO_0013253,
BioSample:SAMN00802311,
Coriell:GM13331,
Wikidata:Q54846467
CVCL_1K73 Cellosaurus 2026-09-26 06:51:13 0
GM13360
 
Resource Report
Resource Website
RRID:CVCL_AD77 Homo sapiens (Human) X-linked centronuclear myopathy Transformed cell line Male CLO:CLO_0012843,
BioSample:SAMN00802330,
Coriell:GM13360,
Wikidata:Q54846481
CVCL_AD77 Cellosaurus 2026-09-26 06:51:14 0
GM13411
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_8A61 Homo sapiens (Human) Leigh disease Population: Chinese. PMID:8042671
PMID:30471880
Finite cell line Male CLO:CLO_0012853,
BioSample:SAMN00802348,
Coriell:GM13411,
Wikidata:Q54846509
CVCL_8A61 Cellosaurus 2026-09-26 06:51:14 1
GM13336
 
Resource Report
Resource Website
Coriell Cat# GM13336, RRID:CVCL_7532 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male Coriell GM13336 CLO:CLO_0012886,
BioSample:SAMN00802316,
Coriell:GM13336,
Wikidata:Q54846469
CVCL_7532 Cellosaurus 2026-09-26 06:51:13 0
GM13313
 
Resource Report
Resource Website
Coriell Cat# GM13313, RRID:CVCL_4F09 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13313 CLO:CLO_0013217,
BioSample:SAMN00802291,
Coriell:GM13313,
Wikidata:Q54846453
CVCL_4F09 Cellosaurus 2026-09-26 06:51:13 0
GM13410
 
Resource Report
Resource Website
Coriell Cat# GM13410, RRID:CVCL_2U27 Homo sapiens (Human) PMID:23665875 Transformed cell line Sex ambiguous Coriell GM13410 CLO:CLO_0012856,
BioSample:SAMN00802346,
Coriell:GM13410,
Wikidata:Q54846508
CVCL_2U27 Cellosaurus 2026-09-26 06:51:14 0
GM13437
 
Resource Report
Resource Website
RRID:CVCL_5P78 Homo sapiens (Human) Pelizaeus-Merzbacher disease Transformed cell line Male CLO:CLO_0012665,
Coriell:GM13437,
Wikidata:Q54846528
CVCL_5P78 Cellosaurus 2026-09-26 06:51:14 0
GM13445
 
Resource Report
Resource Website
Coriell Cat# GM13445, RRID:CVCL_1S74 Homo sapiens (Human) Group: Human/rodent somatic cell hybrid. PMID:1559705 Hybrid cell line 5184-4 Coriell GM13445 CLO:CLO_0012182,
Coriell:GM13445,
Wikidata:Q54846532
CVCL_1S74 Cellosaurus 2026-09-26 06:51:14 0
GM13448
 
Resource Report
Resource Website
Coriell Cat# GM13448, RRID:CVCL_1S75 Homo sapiens (Human) Group: Human/rodent somatic cell hybrid. PMID:1559705 Hybrid cell line HAL26-12 Coriell GM13448 CLO:CLO_0012167,
Coriell:GM13448,
Wikidata:Q54846534
cvcl_f739 CVCL_1S75 Cellosaurus 2026-09-26 06:51:14 0
GM13347
 
Resource Report
Resource Website
Coriell Cat# GM13347, RRID:CVCL_4W22 Homo sapiens (Human) Rubinstein-Taybi syndrome Transformed cell line Female Coriell GM13347 CLO:CLO_0012891,
BioSample:SAMN00802322,
Coriell:GM13347,
Wikidata:Q54846476
CVCL_4W22 Cellosaurus 2026-09-26 06:51:14 0
GM13430
 
Resource Report
Resource Website
Coriell Cat# GM13430, RRID:CVCL_2U28 Homo sapiens (Human) Transformed cell line Male Coriell GM13430 CLO:CLO_0012673,
BioSample:SAMN00802368,
Coriell:GM13430,
Wikidata:Q54846522
CVCL_2U28 Cellosaurus 2026-09-26 06:51:14 0
GM13415
 
Resource Report
Resource Website
Coriell Cat# GM13415, RRID:CVCL_1N83 Homo sapiens (Human) Beckwith-Wiedemann syndrome PMID:23665875 Transformed cell line Female Coriell GM13415 CLO:CLO_0012653,
BioSample:SAMN00802350,
Coriell:GM13415,
Wikidata:Q54846512
CVCL_1N83 Cellosaurus 2026-09-26 06:51:14 0
GM13352
 
Resource Report
Resource Website
RRID:CVCL_1K74 Homo sapiens (Human) Glycogen storage disease type II Population: Indian. Finite cell line Female CLO:CLO_0012903,
BioSample:SAMN00802326,
Coriell:GM13352,
Wikidata:Q54846478
CVCL_1K74 Cellosaurus 2026-09-26 06:51:14 0
GM13363
 
Resource Report
Resource Website
RRID:CVCL_Y602 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1B Transformed cell line Female CLO:CLO_0012844,
BioSample:SAMN00802332,
Coriell:GM13363,
Wikidata:Q54846482
CVCL_Y602 Cellosaurus 2026-09-26 06:51:14 0
GM13441
 
Resource Report
Resource Website
RRID:CVCL_5P79 Homo sapiens (Human) Shprintzen-Goldberg craniosynostosis syndrome Population: Caucasian. PMID:22639450 Finite cell line Male CLO:CLO_0012669,
BioSample:SAMN00802380,
Coriell:GM13441,
Wikidata:Q54846531
CVCL_5P79 Cellosaurus 2026-09-26 06:51:14 0
GM13355
 
Resource Report
Resource Website
RRID:CVCL_5F65 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Male CLO:CLO_0012841,
BioSample:SAMN00802328,
Coriell:GM13355,
GEO:GSM421153,
Wikidata:Q54846479
CVCL_5F65 Cellosaurus 2026-09-26 06:51:14 0
GM13439
 
Resource Report
Resource Website
RRID:CVCL_CX12 Homo sapiens (Human) Glycine encephalopathy Population: Jordanian. Transformed cell line Female CLO:CLO_0012666,
BioSample:SAMN00802376,
Coriell:GM13439,
Wikidata:Q54846529
CVCL_CX12 Cellosaurus 2026-09-26 06:51:14 0
GM13315
 
Resource Report
Resource Website
Coriell Cat# GM13315, RRID:CVCL_4F11 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female Coriell GM13315 CLO:CLO_0013219,
BioSample:SAMN00802295,
Coriell:GM13315,
Wikidata:Q54846456
CVCL_4F11 Cellosaurus 2026-09-26 06:51:13 0
GM13445
 
Resource Report
Resource Website
RRID:CVCL_1S74 Homo sapiens (Human) Group: Human/rodent somatic cell hybrid. PMID:1559705 Hybrid cell line 5184-4 CLO:CLO_0012182,
Coriell:GM13445,
Wikidata:Q54846532
CVCL_1S74 Cellosaurus 2026-09-26 06:51:14 0

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