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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
GM01017
 
Resource Report
Resource Website
Coriell Cat# GM01017, RRID:CVCL_6B41 Homo sapiens (Human) Metachromatic leukodystrophy Transformed cell line Female GM-1017 Coriell GM01017 CLO:CLO_0029493,
BioSample:SAMN00803561,
Coriell:GM01017,
Wikidata:Q54836603
CVCL_6B41 2026-08-15 04:28:55 0
GM01022
 
Resource Report
Resource Website
Coriell Cat# GM01022, RRID:CVCL_V790 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: Caucasian. PMID:806052
PMID:826372
Transformed cell line Female GM-1022, GM01022A Coriell GM01022 CLO:CLO_0029494,
BioSample:SAMN00803567,
Coriell:GM01022,
Wikidata:Q54836607
CVCL_V790 2026-08-15 04:28:55 0
GM01070
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01070, RRID:CVCL_CX38 Homo sapiens (Human) Finite cell line Female GM-1070 Coriell GM01070 Coriell:GM01070,
Wikidata:Q54836631
CVCL_CX38 2026-08-15 04:28:56 0
GM01082
 
Resource Report
Resource Website
Coriell Cat# GM01082, RRID:CVCL_GS53 Homo sapiens (Human) Erythropoietic porphyria Population: Caucasian. Finite cell line Male GM-1082, GM01082A Coriell GM01082 CLO:CLO_0030364,
BioSample:SAMN00803610,
Coriell:GM01082,
Wikidata:Q54836633
CVCL_GS53 2026-08-15 04:28:56 0
GM01096
 
Resource Report
Resource Website
Coriell Cat# GM01096, RRID:CVCL_0M00 Homo sapiens (Human) Population: Caucasian. PMID:24555846
PMID:25326100
Finite cell line Male GM-1096 Coriell GM01096 CLO:CLO_0030184,
BioSample:SAMN00803624,
Coriell:GM01096,
GEO:GSM1257682,
GEO:GSM1266957,
GEO:GSM1267040,
GEO:GSM1288426,
Wikidata:Q54836643
CVCL_0M00 2026-08-15 04:28:56 0
GM01058
 
Resource Report
Resource Website
Coriell Cat# GM01058, RRID:CVCL_H141 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM1058, GM-1058 Coriell GM01058 CLO:CLO_0030366,
BioSample:SAMN00803598,
Coriell:GM01058,
Wikidata:Q54836625
CVCL_H141 2026-08-15 04:28:56 0
GM01007
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01007, RRID:CVCL_JB65 Homo sapiens (Human) Refsum disease Finite cell line Female GM-1007 Coriell GM01007 Coriell:GM01007,
Wikidata:Q54836596
CVCL_JB65 2026-08-15 04:28:55 0
GM01018
 
Resource Report
Resource Website
Coriell Cat# GM01018, RRID:CVCL_M980 Homo sapiens (Human) Metachromatic leukodystrophy Population: Puerto Rican., Part of: Human variation panel. PMID:7313555 Transformed cell line Female GM-1018, GM 1018, GM01018A, GM17072 Coriell GM01018 CLO:CLO_0014601,
CLO:CLO_0029492,
BioSample:SAMN00803563,
Coriell:GM01018,
Coriell:GM17072,
Wikidata:Q54836604
CVCL_M980 2026-08-15 04:28:55 0
GM00993
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD83 Homo sapiens (Human) Finite cell line Female GM-993 Coriell:GM00993,
Wikidata:Q54836585
CVCL_JD83 2026-08-15 04:28:55 0
GM01070
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX38 Homo sapiens (Human) Finite cell line Female GM-1070 Coriell:GM01070,
Wikidata:Q54836631
CVCL_CX38 2026-08-15 04:28:56 0
GM01109
 
Resource Report
Resource Website
RRID:CVCL_1V05 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1109, GM01109A CLO:CLO_0030177,
BioSample:SAMN00803634,
Coriell:GM01109,
Wikidata:Q54836648
CVCL_1V05 2026-08-15 04:28:56 0
GM01093
 
Resource Report
Resource Website
RRID:CVCL_DD66 Homo sapiens (Human) Osteogenesis imperfecta Population: Caucasian. Finite cell line Male GM-1093 CLO:CLO_0030195,
BioSample:SAMN00803618,
Coriell:GM01093,
Wikidata:Q54836640
CVCL_DD66 2026-08-15 04:28:56 0
GM01017
 
Resource Report
Resource Website
RRID:CVCL_6B41 Homo sapiens (Human) Metachromatic leukodystrophy Transformed cell line Female GM-1017 CLO:CLO_0029493,
BioSample:SAMN00803561,
Coriell:GM01017,
Wikidata:Q54836603
CVCL_6B41 2026-08-15 04:28:55 0
GM00995
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00995, RRID:CVCL_CX41 Homo sapiens (Human) Finite cell line Male GM-995 Coriell GM00995 Coriell:GM00995,
Wikidata:Q54836587
CVCL_CX41 2026-08-15 04:28:55 0
GM00995
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX41 Homo sapiens (Human) Finite cell line Male GM-995 Coriell:GM00995,
Wikidata:Q54836587
CVCL_CX41 2026-08-15 04:28:55 0
GM01087
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD76 Homo sapiens (Human) Finite cell line Female GM-1087 Coriell:GM01087,
Wikidata:Q54836638
CVCL_JD76 2026-08-15 04:28:56 0
GM01031
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_0R30 Homo sapiens (Human) PMID:19815695 Transformed cell line Male GM-1031 CLO:CLO_0030375,
BioSample:SAMN00803583,
Coriell:GM01031,
Wikidata:Q54836615
CVCL_0R30 2026-08-15 04:28:56 0
GM01059
 
Resource Report
Resource Website
RRID:CVCL_X079 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-1059, GM 1059, GM01059A CLO:CLO_0030365,
BioSample:SAMN00803600,
Coriell:GM01059,
Wikidata:Q54836626
CVCL_X079 2026-08-15 04:28:56 0
GM01028
 
Resource Report
Resource Website
RRID:CVCL_V431 Homo sapiens (Human) Galactosemia Population: Caucasian. Transformed cell line Female GM-1028, GM01028A CLO:CLO_0030378,
BioSample:SAMN00803577,
Coriell:GM01028,
Wikidata:Q54836612
CVCL_V431 2026-08-15 04:28:56 0
GM01012
 
Resource Report
Resource Website
RRID:CVCL_L744 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. PMID:20715179 Finite cell line Male GM-1012, GM1012A CLO:CLO_0029469,
BioSample:SAMN00803553,
Coriell:GM01012,
Wikidata:Q54836599
CVCL_L744 2026-08-15 04:28:55 0

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