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95,747 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
GM10703
 
Resource Report
Resource Website
Coriell Cat# GM10703, RRID:CVCL_4I29 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female Coriell GM10703 CLO:CLO_0023735,
Coriell:GM10703,
Wikidata:Q54844606
CVCL_4I29 2026-09-05 10:56:28 0
GM10711
 
Resource Report
Resource Website
RRID:CVCL_W906 Homo sapiens (Human) Hereditary hemorrhagic telangiectasia Transformed cell line Female CLO:CLO_0023728,
Coriell:GM10711,
Wikidata:Q54844615
CVCL_W906 2026-09-05 10:56:28 0
GM10712
 
Resource Report
Resource Website
Coriell Cat# GM10712, RRID:CVCL_DB77 Homo sapiens (Human) Transformed cell line Female Coriell GM10712 CLO:CLO_0023732,
Coriell:GM10712,
Wikidata:Q54844616
CVCL_DB77 2026-09-05 10:56:28 0
GM10723
 
Resource Report
Resource Website
Coriell Cat# GM10723, RRID:CVCL_AJ41 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female GM10723A Coriell GM10723 CLO:CLO_0023703,
Coriell:GM10723,
Wikidata:Q54844625
CVCL_AJ41 2026-09-05 10:56:28 0
GM10705
 
Resource Report
Resource Website
Coriell Cat# GM10705, RRID:CVCL_4I31 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female Coriell GM10705 CLO:CLO_0023737,
Coriell:GM10705,
Wikidata:Q54844609
CVCL_4I31 2026-09-05 10:56:28 0
GM10684
 
Resource Report
Resource Website
RRID:CVCL_W564 Homo sapiens (Human) Werdnig-Hoffmann disease Population: Caucasian. PMID:28284873 Transformed cell line Female GM10684B CLO:CLO_0024611,
CLO:CLO_0037445,
BioSample:SAMN00800154,
Coriell:GM10684,
LINCS_LDP:LPC-1046,
Wikidata:Q54844590
CVCL_W564 2026-09-05 10:56:27 0
GM10650
 
Resource Report
Resource Website
RRID:CVCL_AT09 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0024572,
BioSample:SAMN00800132,
Coriell:GM10650,
Wikidata:Q54844572
CVCL_AT09 2026-09-05 10:56:27 0
GM10705
 
Resource Report
Resource Website
RRID:CVCL_4I31 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female CLO:CLO_0023737,
Coriell:GM10705,
Wikidata:Q54844609
CVCL_4I31 2026-09-05 10:56:28 0
GM10707
 
Resource Report
Resource Website
RRID:CVCL_4J02 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female CLO:CLO_0023727,
Coriell:GM10707,
Wikidata:Q54844611
CVCL_4J02 2026-09-05 10:56:28 0
GM10710
 
Resource Report
Resource Website
RRID:CVCL_AD73 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0023729,
BioSample:SAMN00800170,
Coriell:GM10710,
Wikidata:Q54844614
CVCL_AD73 2026-09-05 10:56:28 0
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 2026-09-05 10:56:28 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 2026-09-05 10:56:28 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 2026-09-05 10:56:27 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 2026-09-05 10:56:28 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 2026-09-05 10:56:27 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 2026-09-05 10:56:28 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 2026-09-05 10:56:28 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 2026-09-05 10:56:28 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 2026-09-05 10:56:27 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 2026-09-05 10:56:27 0

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