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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
GM10719
 
Resource Report
Resource Website
RRID:CVCL_1Y46 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0023708,
BioSample:SAMN00800178,
Coriell:GM10719,
Wikidata:Q54844622
CVCL_1Y46 2026-09-12 05:34:05 0
GM10660
 
Resource Report
Resource Website
Coriell Cat# GM10660, RRID:CVCL_1R99 Homo sapiens (Human) Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:9441767 Hybrid cell line GM10660A, DCR-1 Coriell GM10660 CLO:CLO_0024583,
Coriell:GM10660,
Wikidata:Q54844577
cvcl_f739 CVCL_1R99 2026-09-12 05:34:04 0
GM10702
 
Resource Report
Resource Website
RRID:CVCL_HJ78 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male Coriell:GM10702,
Wikidata:Q54844605
CVCL_HJ78 2026-09-12 05:34:05 0
GM10695
 
Resource Report
Resource Website
Coriell Cat# GM10695, RRID:CVCL_0Q21 Homo sapiens (Human) Marfan syndrome Transformed cell line Female Coriell GM10695 CLO:CLO_0023752,
BioSample:SAMN00800166,
Coriell:GM10695,
Wikidata:Q54844596
CVCL_0Q21 2026-09-12 05:34:05 0
GM10672
 
Resource Report
Resource Website
Coriell Cat# GM10672, RRID:CVCL_DA33 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 2 Population: Caucasian. Finite cell line Female Coriell GM10672 CLO:CLO_0024603,
BioSample:SAMN00800146,
Coriell:GM10672,
Wikidata:Q54844586
CVCL_DA33 2026-09-12 05:34:04 0
GM10662
 
Resource Report
Resource Website
Coriell Cat# GM10662, RRID:CVCL_1S00 Cricetulus griseus (Chinese hamster) Group: Human/rodent somatic cell hybrid. Hybrid cell line 8121-A1, GM10662A Coriell GM10662 CLO:CLO_0024586,
Coriell:GM10662,
Wikidata:Q54844578
CVCL_1S00 2026-09-12 05:34:04 0
GM10714
 
Resource Report
Resource Website
Coriell Cat# GM10714, RRID:CVCL_GT64 Homo sapiens (Human) Hereditary hemorrhagic telangiectasia Donor information: At sampling donor was not affected with hereditary hemorrhagic telangiectasia but at risk for disease. Transformed cell line Female Coriell GM10714 CLO:CLO_0023730,
Coriell:GM10714,
Wikidata:Q54844617
CVCL_GT64 2026-09-12 05:34:05 0
GM10667
 
Resource Report
Resource Website
RRID:CVCL_N154 Homo sapiens (Human) Population: Indian., Part of: Human variation panel. PMID:10051646 Finite cell line Male GM17027 CLO:CLO_0014700,
CLO:CLO_0024610,
BioSample:SAMN00800142,
Coriell:GM10667,
Coriell:GM17027,
Wikidata:Q54844583
CVCL_N154 2026-09-12 05:34:04 0
GM10672
 
Resource Report
Resource Website
RRID:CVCL_DA33 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 2 Population: Caucasian. Finite cell line Female CLO:CLO_0024603,
BioSample:SAMN00800146,
Coriell:GM10672,
Wikidata:Q54844586
CVCL_DA33 2026-09-12 05:34:04 0
GM10660
 
Resource Report
Resource Website
RRID:CVCL_1R99 Homo sapiens (Human) Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:9441767 Hybrid cell line GM10660A, DCR-1 CLO:CLO_0024583,
Coriell:GM10660,
Wikidata:Q54844577
cvcl_f739 CVCL_1R99 2026-09-12 05:34:04 0
GM10722
 
Resource Report
Resource Website
RRID:CVCL_6G97 Homo sapiens (Human) Karyotypic information: 46,XY,del(4)(qter->p15.2) (Coriell=GM10722). Finite cell line Male CLO:CLO_0023704,
Coriell:GM10722,
Wikidata:Q54844624
CVCL_6G97 2026-09-12 05:34:05 0
GM10695
 
Resource Report
Resource Website
RRID:CVCL_0Q21 Homo sapiens (Human) Marfan syndrome Transformed cell line Female CLO:CLO_0023752,
BioSample:SAMN00800166,
Coriell:GM10695,
Wikidata:Q54844596
CVCL_0Q21 2026-09-12 05:34:05 0
GM10732
 
Resource Report
Resource Website
Coriell Cat# GM10732, RRID:CVCL_DB78 Homo sapiens (Human) Transformed cell line Male Coriell GM10732 CLO:CLO_0023695,
Coriell:GM10732,
Wikidata:Q54844629
CVCL_DB78 2026-09-12 05:34:05 0
GM10708
 
Resource Report
Resource Website
RRID:CVCL_4I33 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male CLO:CLO_0023724,
Coriell:GM10708,
Wikidata:Q54844612
CVCL_4I33 2026-09-12 05:34:05 0
GM10725
 
Resource Report
Resource Website
Coriell Cat# GM10725, RRID:CVCL_AJ43 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female Coriell GM10725 CLO:CLO_0023701,
Coriell:GM10725,
Wikidata:Q54844627
CVCL_AJ43 2026-09-12 05:34:05 0
GM10701
 
Resource Report
Resource Website
Coriell Cat# GM10701, RRID:CVCL_4I28 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM10701A Coriell GM10701 CLO:CLO_0023734,
Coriell:GM10701,
Wikidata:Q54844599
CVCL_4I28 2026-09-12 05:34:05 0
GM10729
 
Resource Report
Resource Website
Coriell Cat# GM10729, RRID:CVCL_0Q22 Homo sapiens (Human) Transformed cell line Female GM10729A Coriell GM10729 CLO:CLO_0023700,
BioSample:SAMN00800182,
Coriell:GM10729,
Wikidata:Q54844628
CVCL_0Q22 2026-09-12 05:34:05 0
GM10649
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UR80 Homo sapiens (Human) Osteochondrodysplasia PMID:1897572 Finite cell line Female Coriell:GM10649,
Wikidata:Q93810070
CVCL_UR80 2026-09-12 05:34:04 0
GM10669
 
Resource Report
Resource Website
Coriell Cat# GM10669, RRID:CVCL_AE15 Homo sapiens (Human) Cowden syndrome Population: Caucasian. Finite cell line Female Coriell GM10669 CLO:CLO_0024605,
BioSample:SAMN00800144,
Coriell:GM10669,
Wikidata:Q54844585
CVCL_AE15 2026-09-12 05:34:04 0
GM10838
 
Resource Report
Resource Website
Coriell Cat# GM10838, RRID:CVCL_R598 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:17122850
PMID:19043577
PMID:20856902
PMID:21397061
PMID:21418647
PMID:24924344
PMID:26621101
Transformed cell line Male Coriell GM10838 CLO:CLO_0023778,
BioSample:SAMN00800240,
Coriell:GM10838,
GEO:GSM112497,
GEO:GSM112777,
GEO:GSM188774,
GEO:GSM291606,
GEO:GSM316402,
GEO:GSM316403,
GEO:GSM316404,
GEO:GSM420606,
GEO:GSM649293,
GEO:GSM651077,
GEO:GSM651078,
GEO:GSM957434,
IGSR:NA10838,
Wikidata:Q54844671
CVCL_R598 2026-09-12 05:34:06 0

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