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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
GM03910
 
Resource Report
Resource Website
Coriell Cat# GM03910, RRID:CVCL_AK94 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03910 CLO:CLO_0015996,
Coriell:GM03910,
Wikidata:Q54838317
CVCL_AK94 2026-07-25 04:32:53 0
GM03870
 
Resource Report
Resource Website
RRID:CVCL_1H75 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM03870A CLO:CLO_0016028,
BioSample:SAMN00808582,
Coriell:GM03870,
Wikidata:Q54838289
CVCL_1H75 2026-07-25 04:32:52 0
GM03863
 
Resource Report
Resource Website
RRID:CVCL_1H68 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Transformed cell line Female CLO:CLO_0015734,
BioSample:SAMN00808575,
Coriell:GM03863,
Wikidata:Q54838282
CVCL_1H68 2026-07-25 04:32:52 0
GM03890
 
Resource Report
Resource Website
RRID:CVCL_W304 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. Transformed cell line Male GM03890A CLO:CLO_0016007,
BioSample:SAMN00808595,
Coriell:GM03890,
Wikidata:Q54838303
CVCL_W304 2026-07-25 04:32:53 0
GM03836
 
Resource Report
Resource Website
Coriell Cat# GM03836, RRID:CVCL_AK87 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Female GM 3836 Coriell GM03836 CLO:CLO_0015642,
BioSample:SAMN00808560,
Coriell:GM03836,
Wikidata:Q54838264
CVCL_AK87 2026-07-25 04:32:52 0
GM03889
 
Resource Report
Resource Website
Coriell Cat# GM03889, RRID:CVCL_W303 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. PMID:6726265 Finite cell line Male GM 3889 Coriell GM03889 CLO:CLO_0016010,
BioSample:SAMN00808594,
Coriell:GM03889,
Wikidata:Q54838302
CVCL_W303 2026-07-25 04:32:53 0
GM03866
 
Resource Report
Resource Website
Coriell Cat# GM03866, RRID:CVCL_1H71 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Finite cell line Female Coriell GM03866 CLO:CLO_0015710,
BioSample:SAMN00808578,
Coriell:GM03866,
Wikidata:Q54838285
CVCL_1H71 2026-07-25 04:32:52 0
GM03869
 
Resource Report
Resource Website
Coriell Cat# GM03869, RRID:CVCL_1H74 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female Coriell GM03869 CLO:CLO_0016026,
BioSample:SAMN00808581,
Coriell:GM03869,
Wikidata:Q54838288
CVCL_1H74 2026-07-25 04:32:52 0
GM03850
 
Resource Report
Resource Website
Coriell Cat# GM03850, RRID:CVCL_AM66 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:7094393 Finite cell line Female GM3850 Coriell GM03850 CLO:CLO_0015631,
BioSample:SAMN00808564,
Coriell:GM03850,
Wikidata:Q54838268
CVCL_AM66 2026-07-25 04:32:52 0
GM03891
 
Resource Report
Resource Website
Coriell Cat# GM03891, RRID:CVCL_W305 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. PMID:6726265 Finite cell line Male GM 3891 Coriell GM03891 CLO:CLO_0016008,
BioSample:SAMN00808596,
Coriell:GM03891,
Wikidata:Q54838304
CVCL_W305 2026-07-25 04:32:53 0
GM03882
 
Resource Report
Resource Website
RRID:CVCL_2S97 Homo sapiens (Human) Karyotypic information: 46,XX,t(3;10)(3pter->3q25::10p15->10pter;10qter->10p15::3q25->3qter) (Coriell=GM03882)., Population: Caucasian. Finite cell line Female CLO:CLO_0016041,
BioSample:SAMN00808589,
Coriell:GM03882,
Wikidata:Q54838297
CVCL_2S97 2026-07-25 04:32:53 0
GM03894
 
Resource Report
Resource Website
Coriell Cat# GM03894, RRID:CVCL_AK91 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Male GM 3894 Coriell GM03894 CLO:CLO_0016018,
BioSample:SAMN00808599,
Coriell:GM03894,
Wikidata:Q54838307
CVCL_AK91 2026-07-25 04:32:53 0
GM03861
 
Resource Report
Resource Website
Coriell Cat# GM03861, RRID:CVCL_1H66 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM03861 CLO:CLO_0015730,
BioSample:SAMN00808573,
Coriell:GM03861,
Wikidata:Q54838280
CVCL_1H66 2026-07-25 04:32:52 0
GM03847
 
Resource Report
Resource Website
Coriell Cat# GM03847, RRID:CVCL_2S96 Homo sapiens (Human) Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11.2->22qter;22pter->22q11.2::11q23->11qter)mat (Coriell=GM03847)., Population: Caucasian. PMID:10577914 Finite cell line Female Coriell GM03847 CLO:CLO_0015633,
BioSample:SAMN00808563,
Coriell:GM03847,
Wikidata:Q54838267
CVCL_2S96 2026-07-25 04:32:52 0
GM03865
 
Resource Report
Resource Website
RRID:CVCL_1H70 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female CLO:CLO_0015737,
BioSample:SAMN00808577,
Coriell:GM03865,
Wikidata:Q54838284
CVCL_1H70 2026-07-25 04:32:52 0
GM03892
 
Resource Report
Resource Website
Coriell Cat# GM03892, RRID:CVCL_W306 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. PMID:6726265 Transformed cell line Male GM 3892, GM03892A Coriell GM03892 CLO:CLO_0016022,
BioSample:SAMN00808597,
Coriell:GM03892,
Wikidata:Q54838305
CVCL_W306 2026-07-25 04:32:53 0
GM03889
 
Resource Report
Resource Website
RRID:CVCL_W303 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. PMID:6726265 Finite cell line Male GM 3889 CLO:CLO_0016010,
BioSample:SAMN00808594,
Coriell:GM03889,
Wikidata:Q54838302
CVCL_W303 2026-07-25 04:32:53 0
GM03877
 
Resource Report
Resource Website
RRID:CVCL_EF94 Homo sapiens (Human) Glutathione synthetase deficiency Population: Caucasian. PMID:8896573 Finite cell line Male GM03877A CLO:CLO_0016037,
BioSample:SAMN00808587,
Coriell:GM03877,
Wikidata:Q54838294
CVCL_EF94 2026-07-25 04:32:52 0
GM03853
 
Resource Report
Resource Website
RRID:CVCL_W307 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian; German. PMID:6726265 Transformed cell line Male GM 3853 CLO:CLO_0015624,
BioSample:SAMN00808567,
Coriell:GM03853,
Wikidata:Q54838271
CVCL_W307 2026-07-25 04:32:52 0
GM03851
 
Resource Report
Resource Website
RRID:CVCL_GY19 Homo sapiens (Human) Leber congenital amaurosis Population: Caucasian. Transformed cell line Female CLO:CLO_0015629,
BioSample:SAMN00808565,
Coriell:GM03851,
Wikidata:Q54838269
CVCL_GY19 2026-07-25 04:32:52 0

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