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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
GM13412
 
Resource Report
Resource Website
Coriell Cat# GM13412, RRID:CVCL_1S72 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:2045096 Hybrid cell line 1HL35-5, 1HL35 subclone 5 Coriell GM13412 CLO:CLO_0012655,
Coriell:GM13412,
Wikidata:Q54846510
cvcl_1n51 CVCL_1S72 2026-09-12 05:34:49 0
GM13343
 
Resource Report
Resource Website
Coriell Cat# GM13343, RRID:CVCL_GS85 Homo sapiens (Human) Pancreatic lipase deficiency PMID:11393534 Transformed cell line Male Coriell GM13343 CLO:CLO_0012899,
BioSample:SAMN00802318,
Coriell:GM13343,
Wikidata:Q54846474
CVCL_GS85 2026-09-12 05:34:49 0
GM13324
 
Resource Report
Resource Website
Coriell Cat# GM13324, RRID:CVCL_2N05 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13323 (Cellosaurus=CVCL_2N04). PMID:23665875 Transformed cell line Female Coriell GM13324 CLO:CLO_0013274,
Coriell:GM13324,
Wikidata:Q54846461
CVCL_2N05 2026-09-12 05:34:48 0
GM13446
 
Resource Report
Resource Website
Coriell Cat# GM13446, RRID:CVCL_DE53 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. PMID:1559705 Hybrid cell line 640-5A Coriell GM13446 CLO:CLO_0012181,
Coriell:GM13446,
Wikidata:Q54846533
CVCL_DE53 2026-09-12 05:34:50 0
GM13436
 
Resource Report
Resource Website
RRID:CVCL_5P77 Homo sapiens (Human) Pelizaeus-Merzbacher disease Transformed cell line Male CLO:CLO_0012664,
BioSample:SAMN00802374,
Coriell:GM13436,
Wikidata:Q54846527
CVCL_5P77 2026-09-12 05:34:49 0
GM13356
 
Resource Report
Resource Website
RRID:CVCL_0I46 Homo sapiens (Human) Part of: CEPH/Venezuelan pedigree cell line collection. Transformed cell line Female CLO:CLO_0012842,
Coriell:GM13356,
Wikidata:Q54846480
CVCL_0I46 2026-09-12 05:34:49 0
GM13430
 
Resource Report
Resource Website
RRID:CVCL_2U28 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0012673,
BioSample:SAMN00802368,
Coriell:GM13430,
Wikidata:Q54846522
CVCL_2U28 2026-09-12 05:34:49 0
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 2026-09-12 05:34:49 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 2026-09-12 05:34:48 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 2026-09-12 05:34:49 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 2026-09-12 05:34:49 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 2026-09-12 05:34:48 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 2026-09-12 05:34:48 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 2026-09-12 05:34:49 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 2026-09-12 05:34:49 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 2026-09-12 05:34:49 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 2026-09-12 05:34:50 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 2026-09-12 05:34:49 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 2026-09-12 05:34:49 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 2026-09-12 05:34:49 0

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