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117,735 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
GM01016
 
Resource Report
Resource Website
Coriell Cat# GM01016, RRID:CVCL_6B40 Homo sapiens (Human) Transformed cell line Male GM-1016 Coriell GM01016 CLO:CLO_0029497,
BioSample:SAMN00803559,
Coriell:GM01016,
Wikidata:Q54836602
CVCL_6B40 2026-07-25 04:32:11 0
GM01053
 
Resource Report
Resource Website
RRID:CVCL_V531 Homo sapiens (Human) Hurler syndrome Population: Caucasian. Finite cell line Male GM-1053, GM01053A CLO:CLO_0030370,
BioSample:SAMN00803592,
Coriell:GM01053,
Wikidata:Q54836622
CVCL_V531 2026-07-25 04:32:11 0
GM01061
 
Resource Report
Resource Website
RRID:CVCL_V036 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:2973075
PMID:6220707
PMID:6458814
Finite cell line Male GM-1061, GM 1061, GM1061, GM01061A CLO:CLO_0030368,
BioSample:SAMN00803602,
Coriell:GM01061,
Wikidata:Q54836627
CVCL_V036 2026-07-25 04:32:11 0
GM01208
 
Resource Report
Resource Website
RRID:CVCL_M982 Homo sapiens (Human) Population: Latino or Hispanic; Dominican., Part of: Human variation panel. Finite cell line Male GM-1208, GM17350 CLO:CLO_0013724,
CLO:CLO_0030252,
BioSample:SAMN00803714,
Coriell:GM01208,
Coriell:GM17350,
Wikidata:Q54836703
CVCL_M982 2026-07-25 04:32:14 0
GM01202
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V799 Homo sapiens (Human) Karyotypic information: 49,XXXXY (Coriell=GM01202)., Population: Caucasian. PMID:62390
PMID:6661932
PMID:23665875
Transformed cell line Male GM-1202, GM 1202, GM1202, GM1202A, GM01202C CLO:CLO_0030260,
BioSample:SAMN00803702,
Coriell:GM01202,
Wikidata:Q54836697
CVCL_V799 2026-07-25 04:32:14 1
GM01179
 
Resource Report
Resource Website
Coriell Cat# GM01179, RRID:CVCL_4J28 Homo sapiens (Human) Porphyria cutanea tarda Population: Caucasian. Finite cell line Male GM-1179 Coriell GM01179 CLO:CLO_0030262,
BioSample:SAMN00803688,
Coriell:GM01179,
Wikidata:Q54836690
CVCL_4J28 2026-07-25 04:32:13 0
GM01150
 
Resource Report
Resource Website
Coriell Cat# GM01150, RRID:CVCL_4J20 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1150 Coriell GM01150 CLO:CLO_0030226,
BioSample:SAMN00803662,
Coriell:GM01150,
Wikidata:Q54836666
CVCL_4J20 2026-07-25 04:32:13 0
GM01188
 
Resource Report
Resource Website
RRID:CVCL_4J29 Homo sapiens (Human) Glucose-6-phosphate dehydrogenase deficiency Karyotypic information: 46,XY,inv(9) (Coriell=GM01188)., Population: Caucasian; Sardinian. PMID:7803800 Finite cell line Male GM-1188 CLO:CLO_0030265,
BioSample:SAMN00803694,
Coriell:GM01188,
Wikidata:Q54836693
CVCL_4J29 2026-07-25 04:32:13 0
GM01153
 
Resource Report
Resource Website
Coriell Cat# GM01153, RRID:CVCL_4J23 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1153 Coriell GM01153 CLO:CLO_0030234,
BioSample:SAMN00803668,
Coriell:GM01153,
Wikidata:Q54836669
CVCL_4J23 2026-07-25 04:32:12 0
GM01178
 
Resource Report
Resource Website
RRID:CVCL_CV40 Homo sapiens (Human) Progeria From: Montreal Children's Hospital cell repository; Montreal; Canada. PMID:7253718 Finite cell line Male GM-1178, GM 1178, GM1178, GM01178B, AG01178, AG-1178, AG1178, AG01178B, WG0380, WG380 CLO:CLO_0030204,
CLO:CLO_0036894,
Coriell:AG01178,
Coriell:GM01178,
Wikidata:Q54836689
CVCL_CV40 2026-07-25 04:32:13 0
GM01159
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01159, RRID:CVCL_CX14 Homo sapiens (Human) Finite cell line Male GM-1159 Coriell GM01159 Coriell:GM01159,
Wikidata:Q54836673
CVCL_CX14 2026-07-25 04:32:14 0
GM01136
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB92 Homo sapiens (Human) Huntington's disease Finite cell line Male GM-1136 Coriell:GM01136,
Wikidata:Q54836660
CVCL_JB92 2026-07-25 04:32:12 0
GM01187
 
Resource Report
Resource Website
Coriell Cat# GM01187, RRID:CVCL_8516 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6220707 Finite cell line Male GM-1187, GM 1187 Coriell GM01187 CLO:CLO_0030264,
BioSample:SAMN00803692,
Coriell:GM01187,
Wikidata:Q54836692
CVCL_8516 2026-07-25 04:32:14 0
GM01206
 
Resource Report
Resource Website
RRID:CVCL_H142 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male GM-1206, GM01206A CLO:CLO_0030254,
BioSample:SAMN00803710,
Coriell:GM01206,
Wikidata:Q54836701
CVCL_H142 2026-07-25 04:32:13 0
GM01151
 
Resource Report
Resource Website
RRID:CVCL_4J21 Homo sapiens (Human) Glucose-6-phosphate dehydrogenase deficiency Population: Caucasian; Sardinian. Finite cell line Male GM-1151 CLO:CLO_0030228,
BioSample:SAMN00803664,
Coriell:GM01151,
Wikidata:Q54836667
CVCL_4J21 2026-07-25 04:32:12 0
GM01138
 
Resource Report
Resource Website
RRID:CVCL_V798 Homo sapiens (Human) Population: African American. PMID:862431
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-1138, GM 1138, GM1138 CLO:CLO_0030239,
BioSample:SAMN00803654,
Coriell:GM01138,
Wikidata:Q54836662
CVCL_V798 2026-07-25 04:32:12 0
GM01140
 
Resource Report
Resource Website
RRID:CVCL_CX03 Homo sapiens (Human) Glycine encephalopathy Population: Caucasian. Finite cell line Male GM1140, GM-1140 CLO:CLO_0030243,
BioSample:SAMN00803658,
Coriell:GM01140,
Wikidata:Q54836664
CVCL_CX03 2026-07-25 04:32:13 0
GM01209
 
Resource Report
Resource Website
RRID:CVCL_1Y23 Homo sapiens (Human) Galactosemia Donor information: Established from monozygotic twin of GM01210 (Cellosaurus=CVCL_1Y24)., Population: Latino or Hispanic; Dominican. PMID:1766867 Finite cell line Male GM-1209, GM 1209 CLO:CLO_0030257,
BioSample:SAMN00803716,
Coriell:GM01209,
Wikidata:Q54836704
CVCL_1Y23 2026-07-25 04:32:13 0
GM01206
 
Resource Report
Resource Website
Coriell Cat# GM01206, RRID:CVCL_H142 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male GM-1206, GM01206A Coriell GM01206 CLO:CLO_0030254,
BioSample:SAMN00803710,
Coriell:GM01206,
Wikidata:Q54836701
CVCL_H142 2026-07-25 04:32:14 0
GM01219
 
Resource Report
Resource Website
RRID:CVCL_H967 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Finite cell line Male GM-1219 CLO:CLO_0030288,
Coriell:GM01219,
Wikidata:Q54836712
CVCL_H967 2026-07-25 04:32:14 0

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