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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
GM04206
 
Resource Report
Resource Website
RRID:CVCL_1H98 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian. PMID:6316146 Finite cell line Female CLO:CLO_0019496,
Coriell:GM04206,
Wikidata:Q54838422
CVCL_1H98 2026-07-25 04:32:56 0
GM04219
 
Resource Report
Resource Website
RRID:CVCL_1I05 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6316146 Transformed cell line Male GM04219B CLO:CLO_0019511,
Coriell:GM04219,
Wikidata:Q54838431
CVCL_1I05 2026-07-25 04:32:56 0
GM04211
 
Resource Report
Resource Website
RRID:CVCL_X455 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6316146 Transformed cell line Male CLO:CLO_0019517,
Coriell:GM04211,
Wikidata:Q54838427
CVCL_X455 2026-07-25 04:32:56 0
GM04226
 
Resource Report
Resource Website
Coriell Cat# GM04226, RRID:CVCL_1I11 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian. PMID:6316146 Finite cell line Male Coriell GM04226 CLO:CLO_0019461,
Coriell:GM04226,
Wikidata:Q54838437
CVCL_1I11 2026-07-25 04:32:56 0
GM04213
 
Resource Report
Resource Website
Coriell Cat# GM04213, RRID:CVCL_1I03 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6316146 Transformed cell line Female Coriell GM04213 CLO:CLO_0019515,
Coriell:GM04213,
Wikidata:Q54838429
CVCL_1I03 2026-07-25 04:32:56 0
GM04205
 
Resource Report
Resource Website
Coriell Cat# GM18015, RRID:CVCL_M949 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:6316146 Transformed cell line Male GM18015 Coriell GM18015 CLO:CLO_0016021,
CLO:CLO_0019497,
Coriell:GM04205,
Coriell:GM18015,
Wikidata:Q54838421
CVCL_M949 2026-07-25 04:32:56 0
GM04189
 
Resource Report
Resource Website
Coriell Cat# GM04189, RRID:CVCL_1H84 Homo sapiens (Human) Population: Caucasian. PMID:6316146 Transformed cell line Female Coriell GM04189 CLO:CLO_0015926,
Coriell:GM04189,
Wikidata:Q54838401
CVCL_1H84 2026-07-25 04:32:55 0
GM04235
 
Resource Report
Resource Website
RRID:CVCL_W029 Homo sapiens (Human) Hypophosphatasia Population: Caucasian. PMID:1409720
PMID:2705456
PMID:8675582
Finite cell line Male GM 4235, GM4235 CLO:CLO_0019477,
Coriell:GM04235,
Wikidata:Q54838446
CVCL_W029 2026-07-25 04:32:56 0
GM04192
 
Resource Report
Resource Website
RRID:CVCL_1H87 Homo sapiens (Human) Population: Caucasian. PMID:6316146 Finite cell line Male CLO:CLO_0015921,
Coriell:GM04192,
Wikidata:Q54838405
CVCL_1H87 2026-07-25 04:32:55 0
GM04232
 
Resource Report
Resource Website
Coriell Cat# GM04232, RRID:CVCL_1I16 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian. PMID:6316146 Finite cell line Male Coriell GM04232 CLO:CLO_0019454,
Coriell:GM04232,
Wikidata:Q54838443
CVCL_1I16 2026-07-25 04:32:56 0
GM04250
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM17052, RRID:CVCL_N015 Homo sapiens (Human) Sporadic retinoblastoma Population: Japanese., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:23665875
PMID:29959025
Finite cell line Female GM17052, AG04250, AG4250, RB9T Coriell GM17052 CLO:CLO_0014647,
CLO:CLO_0019479,
Coriell:AG04250,
Coriell:GM04250,
Coriell:GM17052,
JCRB:KURB2685,
Wikidata:Q54838453
CVCL_N015 2026-07-25 04:32:56 0
GM04195
 
Resource Report
Resource Website
Coriell Cat# GM04195, RRID:CVCL_1H90 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6316146 Transformed cell line Female Coriell GM04195 CLO:CLO_0015923,
Coriell:GM04195,
Wikidata:Q54838408
CVCL_1H90 2026-07-25 04:32:55 0
GM04205
 
Resource Report
Resource Website
RRID:CVCL_M949 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:6316146 Transformed cell line Male GM18015 CLO:CLO_0016021,
CLO:CLO_0019497,
Coriell:GM04205,
Coriell:GM18015,
Wikidata:Q54838421
CVCL_M949 2026-07-25 04:32:56 0
GM04225
 
Resource Report
Resource Website
Coriell Cat# GM04225, RRID:CVCL_1I10 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. PMID:6316146 Transformed cell line Male Coriell GM04225 CLO:CLO_0019458,
Coriell:GM04225,
Wikidata:Q54838436
CVCL_1I10 2026-07-25 04:32:56 0
GM04198
 
Resource Report
Resource Website
RRID:CVCL_1H93 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6316146 Finite cell line Female CLO:CLO_0019499,
Coriell:GM04198,
Wikidata:Q54838411
CVCL_1H93 2026-07-25 04:32:55 0
GM04233
 
Resource Report
Resource Website
Coriell Cat# GM04233, RRID:CVCL_1I17 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian. PMID:6316146 Transformed cell line Male Coriell GM04233 CLO:CLO_0019484,
Coriell:GM04233,
Wikidata:Q54838444
CVCL_1I17 2026-07-25 04:32:56 0
GM04222
 
Resource Report
Resource Website
RRID:CVCL_1I08 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6316146 Finite cell line Male CLO:CLO_0019456,
Coriell:GM04222,
Wikidata:Q54838434
CVCL_1I08 2026-07-25 04:32:56 0
GM04178
 
Resource Report
Resource Website
RRID:CVCL_DD77 Homo sapiens (Human) Osteogenesis imperfecta type II Population: Caucasian. Finite cell line Female CLO:CLO_0016178,
Coriell:GM04178,
Wikidata:Q54838396
CVCL_DD77 2026-07-25 04:32:55 0
GM04250
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM04250, RRID:CVCL_N015 Homo sapiens (Human) Sporadic retinoblastoma Population: Japanese., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:23665875
PMID:29959025
Finite cell line Female GM17052, AG04250, AG4250, RB9T Coriell GM04250 CLO:CLO_0014647,
CLO:CLO_0019479,
Coriell:AG04250,
Coriell:GM04250,
Coriell:GM17052,
JCRB:KURB2685,
Wikidata:Q54838453
CVCL_N015 2026-07-25 04:32:56 0
GM04207
 
Resource Report
Resource Website
Coriell Cat# GM04207, RRID:CVCL_1H99 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian. PMID:6316146 Transformed cell line Female Coriell GM04207 CLO:CLO_0019524,
Coriell:GM04207,
Wikidata:Q54838423
CVCL_1H99 2026-07-25 04:32:56 0

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