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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
GM16456
 
Resource Report
Resource Website
Coriell Cat# GM16456, RRID:CVCL_0H33 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH468 Coriell GM16456 CLO:CLO_0017808,
Coriell:GM16456,
Wikidata:Q54848576
CVCL_0H33 2026-09-05 10:58:02 0
GM16440
 
Resource Report
Resource Website
RRID:CVCL_0H53 Homo sapiens (Human) Bipolar disorder PMID:23665875 Transformed cell line Female JL481 CLO:CLO_0017791,
Coriell:GM16440,
Wikidata:Q54848562
CVCL_0H53 2026-09-05 10:58:01 0
GM16450
 
Resource Report
Resource Website
Coriell Cat# GM16450, RRID:CVCL_0H30 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH466 Coriell GM16450 CLO:CLO_0017801,
Coriell:GM16450,
Wikidata:Q54848570
CVCL_0H30 2026-09-05 10:58:02 0
GM16491
 
Resource Report
Resource Website
Coriell Cat# GM16491, RRID:CVCL_9Z48 Homo sapiens (Human) Refsum disease Finite cell line Female Coriell GM16491 CLO:CLO_0017519,
Coriell:GM16491,
Wikidata:Q54848605
CVCL_9Z48 2026-09-05 10:58:02 0
GM16514
 
Resource Report
Resource Website
Coriell Cat# GM16514, RRID:CVCL_4F74 Homo sapiens (Human) Zellweger syndrome Finite cell line Male Coriell GM16514 CLO:CLO_0017489,
Coriell:GM16514,
Wikidata:Q54848617
CVCL_4F74 2026-09-05 10:58:02 0
GM16449
 
Resource Report
Resource Website
Coriell Cat# GM16449, RRID:CVCL_0H48 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL314 Coriell GM16449 CLO:CLO_0017800,
Coriell:GM16449,
Wikidata:Q54848569
CVCL_0H48 2026-09-05 10:58:02 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 2026-09-05 10:58:01 0
GM16514
 
Resource Report
Resource Website
RRID:CVCL_4F74 Homo sapiens (Human) Zellweger syndrome Finite cell line Male CLO:CLO_0017489,
Coriell:GM16514,
Wikidata:Q54848617
CVCL_4F74 2026-09-05 10:58:02 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 2026-09-05 10:58:01 0
GM16452
 
Resource Report
Resource Website
RRID:CVCL_0H31 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH458 CLO:CLO_0017807,
Coriell:GM16452,
Wikidata:Q54848572
CVCL_0H31 2026-09-05 10:58:02 0
GM16481
 
Resource Report
Resource Website
RRID:CVCL_0E67 Homo sapiens (Human) Cystinuria Population: Caucasian. Transformed cell line Male CLO:CLO_0017523,
Coriell:GM16481,
Wikidata:Q54848588
CVCL_0E67 2026-09-05 10:58:02 0
GM16437
 
Resource Report
Resource Website
Coriell Cat# GM16437, RRID:CVCL_0H27 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH429 Coriell GM16437 CLO:CLO_0017781,
Coriell:GM16437,
Wikidata:Q54848559
CVCL_0H27 2026-09-05 10:58:01 0
GM16438
 
Resource Report
Resource Website
RRID:CVCL_0H47 Homo sapiens (Human) PMID:23665875 Transformed cell line Male JL480 CLO:CLO_0017782,
Coriell:GM16438,
Wikidata:Q54848560
CVCL_0H47 2026-09-05 10:58:01 0
GM16460
 
Resource Report
Resource Website
Coriell Cat# GM16460, RRID:CVCL_0H34 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH406 Coriell GM16460 CLO:CLO_0017822,
Coriell:GM16460,
Wikidata:Q54848579
CVCL_0H34 2026-09-05 10:58:02 0
GM16439
 
Resource Report
Resource Website
RRID:CVCL_0H28 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH556 CLO:CLO_0017783,
Coriell:GM16439,
Wikidata:Q54848561
CVCL_0H28 2026-09-05 10:58:01 0
GM16444
 
Resource Report
Resource Website
Coriell Cat# GM16444, RRID:CVCL_0H29 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line JH478 Coriell GM16444 CLO:CLO_0017787,
Coriell:GM16444,
Wikidata:Q54848565
CVCL_0H29 2026-09-05 10:58:01 0
GM16447
 
Resource Report
Resource Website
Coriell Cat# GM16447, RRID:CVCL_5L23 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL288 Coriell GM16447 CLO:CLO_0017803,
Coriell:GM16447,
Wikidata:Q54848567
CVCL_5L23 2026-09-05 10:58:01 0
GM16455
 
Resource Report
Resource Website
RRID:CVCL_0H51 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL401 CLO:CLO_0017811,
Coriell:GM16455,
Wikidata:Q54848575
CVCL_0H51 2026-09-05 10:58:02 0
GM16510
 
Resource Report
Resource Website
RRID:CVCL_9R35 Homo sapiens (Human) Neonatal adrenoleukodystrophy Finite cell line Female CLO:CLO_0017483,
Coriell:GM16510,
Wikidata:Q54848614
CVCL_9R35 2026-09-05 10:58:02 0
GM16445
 
Resource Report
Resource Website
RRID:CVCL_5L22 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Male JL439 CLO:CLO_0017802,
Coriell:GM16445,
Wikidata:Q54848566
CVCL_5L22 2026-09-05 10:58:01 0

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