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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
GM04374
 
Resource Report
Resource Website
RRID:CVCL_GS63 Homo sapiens (Human) Tyrosinemia type II Population: Native North American. Finite cell line Female CLO:CLO_0019341,
Coriell:GM04374,
Wikidata:Q54838504
CVCL_GS63 2026-09-12 05:32:39 0
GM04372
 
Resource Report
Resource Website
RRID:CVCL_2Z50 Homo sapiens (Human) Krabbe disease PMID:3926002 Finite cell line Male GM 4372 CLO:CLO_0019303,
Coriell:GM04372,
Wikidata:Q54838503
CVCL_2Z50 2026-09-12 05:32:39 0
GM04420
 
Resource Report
Resource Website
Coriell Cat# GM04420, RRID:CVCL_AI32 Homo sapiens (Human) Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Finite cell line Female Coriell GM04420 CLO:CLO_0019710,
Coriell:GM04420,
Wikidata:Q54838519
CVCL_AI32 2026-09-12 05:32:40 0
GM04285
 
Resource Report
Resource Website
RRID:CVCL_Y867 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male CLO:CLO_0019593,
Coriell:GM04285,
Wikidata:Q54838466
CVCL_Y867 2026-09-12 05:32:38 0
GM04411
 
Resource Report
Resource Website
RRID:CVCL_9Y77 Homo sapiens (Human) Albright's hereditary osteodystrophy Transformed cell line Female GM04411A CLO:CLO_0019709,
Coriell:GM04411,
Wikidata:Q54838518
CVCL_9Y77 2026-09-12 05:32:40 0
GM04285
 
Resource Report
Resource Website
Coriell Cat# GM04285, RRID:CVCL_Y867 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male Coriell GM04285 CLO:CLO_0019593,
Coriell:GM04285,
Wikidata:Q54838466
CVCL_Y867 2026-09-12 05:32:38 0
GM04346
 
Resource Report
Resource Website
RRID:CVCL_0M32 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. Finite cell line Male CLO:CLO_0019560,
Coriell:GM04346,
Wikidata:Q54838496
CVCL_0M32 2026-09-12 05:32:39 0
GM04375
 
Resource Report
Resource Website
Coriell Cat# GM04375, RRID:CVCL_W622 Homo sapiens (Human) Klinefelter syndrome Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM04375A Coriell GM04375 CLO:CLO_0019338,
Coriell:GM04375,
Wikidata:Q54838507
CVCL_W622 2026-09-12 05:32:39 0
GM04394
 
Resource Report
Resource Website
RRID:CVCL_0R33 Homo sapiens (Human) Gaucher disease Population: African American., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:2464926
PMID:6593712
PMID:19815695
Finite cell line Male GM4394 CLO:CLO_0019702,
Coriell:GM04394,
Wikidata:Q54838511
CVCL_0R33 2026-09-12 05:32:40 0
GM04263
 
Resource Report
Resource Website
RRID:CVCL_GT50 Homo sapiens (Human) Hypophosphatasia Population: Caucasian. Finite cell line Female CLO:CLO_0019612,
Coriell:GM04263,
Wikidata:Q54838456
CVCL_GT50 2026-09-12 05:32:38 0
GM04364
 
Resource Report
Resource Website
RRID:CVCL_5M95 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Finite cell line Male CLO:CLO_0019314,
Coriell:GM04364,
Wikidata:Q54838499
CVCL_5M95 2026-09-12 05:32:39 0
GM04280
 
Resource Report
Resource Website
Coriell Cat# GM04280, RRID:CVCL_H153 Mus musculus (Mouse) Hybridoma KE2 Coriell GM04280 CLO:CLO_0019601,
Coriell:GM04280,
Wikidata:Q54838462
cvcl_3411 CVCL_H153 2026-09-12 05:32:38 0
GM04307
 
Resource Report
Resource Website
RRID:CVCL_CZ83 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0019625,
Coriell:GM04307,
Wikidata:Q54838476
CVCL_CZ83 2026-09-12 05:32:39 0
GM04425
 
Resource Report
Resource Website
RRID:CVCL_9Y78 Homo sapiens (Human) Albright's hereditary osteodystrophy Transformed cell line Female CLO:CLO_0019684,
Coriell:GM04425,
Wikidata:Q54838522
CVCL_9Y78 2026-09-12 05:32:40 0
FH34
 
Resource Report
Resource Website
RRID:CVCL_E619 Homo sapiens (Human) Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel. PMID:30844424 Transformed cell line Female dbMHC:48808,
IHW:IHW09415,
IPD-IMGT/HLA:26019,
Wikidata:Q54834822
CVCL_E619 2026-09-12 05:31:05 0
FH07
 
Resource Report
Resource Website
RRID:CVCL_E593 Homo sapiens (Human) Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel. PMID:30844424 Transformed cell line Male FH7, TER317, TER-317, Ter 317, TER391, TER-391, Ter 391, Extract 466 dbMHC:48847,
IHW:IHW09381,
IPD-IMGT/HLA:14085,
Wikidata:Q54834795
CVCL_E593 2026-09-12 05:31:04 0
FH17
 
Resource Report
Resource Website
RRID:CVCL_E603 Homo sapiens (Human) Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel. PMID:30844424 Transformed cell line Female dbMHC:48790,
IHW:IHW09391,
IPD-IMGT/HLA:25998,
Wikidata:Q54834805
CVCL_E603 2026-09-12 05:31:04 0
FH37
 
Resource Report
Resource Website
RRID:CVCL_E622 Homo sapiens (Human) Population: Caucasian., Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel. PMID:30844424 Transformed cell line Female dbMHC:48811,
IHW:IHW09424,
IPD-IMGT/HLA:26027,
Wikidata:Q54834825
CVCL_E622 2026-09-12 05:31:05 0
FH21
 
Resource Report
Resource Website
RRID:CVCL_E607 Homo sapiens (Human) Population: Caucasian., Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel. PMID:30844424 Transformed cell line Male dbMHC:48795,
IHW:IHW09403,
IPD-IMGT/HLA:26007,
Wikidata:Q54834809
CVCL_E607 2026-09-12 05:31:05 0
FH64
 
Resource Report
Resource Website
RRID:CVCL_E649 Homo sapiens (Human) Part of: 13th International Histocompatibility Workshop (13IHW) cell line panel. PMID:30844424 Transformed cell line Sex unspecified dbMHC:48841,
IHW:IHW09452,
IPD-IMGT/HLA:26049,
Wikidata:Q54834854
CVCL_E649 2026-09-12 05:31:05 0

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