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10,882 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
GM07492
 
Resource Report
Resource Website
1+ mentions
Possibly Discontinued
Coriell Cat# GM07492, RRID:CVCL_7467 Homo sapiens (Human) Population: Caucasian. PMID:29125828
PMID:30567591
PMID:32291635
PMID:35850241
Finite cell line Male C7492 Coriell GM07492 CLO:CLO_0016480,
Coriell:GM07492,
GEO:GSM2794412,
GEO:GSM3124644,
Wikidata:Q54842796
CVCL_7467 2026-09-12 05:33:21 3
GM07545
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F165 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0016386,
Coriell:GM07545,
Wikidata:Q54842848
CVCL_F165 2026-09-12 05:33:23 2
GM13976
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM13976, RRID:CVCL_L266 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM13977 (Cellosaurus=CVCL_L267)., Part of: ENCODE project common cell types; tier 3. Transformed cell line Female Coriell GM13976 CLO:CLO_0033830,
EFO:EFO_0005345,
BioSample:SAMN00802796,
Coriell:GM13976,
ENCODE:ENCBS220AAA,
GEO:GSM1008591,
Wikidata:Q54846966
CVCL_L266 2026-09-12 05:34:59 1
GM08333
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM08333, RRID:CVCL_7477 Homo sapiens (Human) Population: African American. PMID:17668376 Finite cell line Male GM8333, GM008333A Coriell GM08333 CLO:CLO_0010582,
Coriell:GM08333,
Wikidata:Q54843149
CVCL_7477 2026-09-12 05:33:30 1
GM08330
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM08330, RRID:CVCL_N044 Homo sapiens (Human) Population: Caucasian. PMID:24271013 Finite cell line Male GM8330 Coriell GM08330 CLO:CLO_0010567,
Coriell:GM08330,
Wikidata:Q54843147
CVCL_N044 2026-09-12 05:33:29 1
GM08447
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM08447, RRID:CVCL_7487 Homo sapiens (Human) Population: Caucasian. PMID:17668376 Finite cell line Female Coriell GM08447 CLO:CLO_0010544,
BioSample:SAMN00798072,
Coriell:GM08447,
Wikidata:Q54843213
CVCL_7487 2026-09-12 05:33:31 3
GM08399
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7482 Homo sapiens (Human) PMID:1690734
PMID:7847674
PMID:8643543
PMID:22152194
PMID:29125828
PMID:30567591
PMID:32291635
Finite cell line Female GM8399, GM 8399, C8399 CLO:CLO_0010527,
Coriell:GM08399,
GEO:GSM2794415,
GEO:GSM3124645,
Wikidata:Q54843197
CVCL_7482 2026-09-12 05:33:31 3
GM08399
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM08399, RRID:CVCL_7482 Homo sapiens (Human) PMID:1690734
PMID:7847674
PMID:8643543
PMID:22152194
PMID:29125828
PMID:30567591
PMID:32291635
Finite cell line Female GM8399, GM 8399, C8399 Coriell GM08399 CLO:CLO_0010527,
Coriell:GM08399,
GEO:GSM2794415,
GEO:GSM3124645,
Wikidata:Q54843197
CVCL_7482 2026-09-12 05:33:31 3
GM08398
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7481 Homo sapiens (Human) Population: Caucasian. PMID:15268757
PMID:16126733
PMID:30567591
PMID:33038742
Finite cell line Male GM8398, GM08398C CLO:CLO_0010526,
BioSample:SAMN00798056,
Coriell:GM08398,
GEO:GSM88295,
GEO:GSM88296,
GEO:GSM88297,
GEO:GSM88313,
GEO:GSM88314,
GEO:GSM88315,
GEO:GSM1316986,
GEO:GSM1317025,
GEO:GSM3124634,
Wikidata:Q54843196
CVCL_7481 2026-09-12 05:33:31 2
GM08402
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7485 Homo sapiens (Human) PMID:1690734
PMID:26984941
PMID:28444186
PMID:30567591
Finite cell line Male GM 8402, GM-8402, GM 08402 CLO:CLO_0010530,
Coriell:GM08402,
GEO:GSM1316987,
GEO:GSM3124653,
Wikidata:Q54843200
CVCL_7485 2026-09-12 05:33:31 1
GM09497
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_AY35 Homo sapiens (Human) Fragile X syndrome Karyotypic information: 46,XY,t(1;3)(3pter->3p22::1p32->1qter;1pter->1p32::3p22->3qter) [3]; 46,XY,t(3;12)(3pter->3q12::12q24.1->12qter;12pter->12q24.1:;3q12->3qter) [3]; 46,XY [13] (Coriell=GM09497)., Population: Caucasian. Finite cell line Male CLO:CLO_0011480,
Coriell:GM09497,
Wikidata:Q54843801
CVCL_AY35 2026-09-12 05:33:44 1
GM09497
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM09497, RRID:CVCL_AY35 Homo sapiens (Human) Fragile X syndrome Karyotypic information: 46,XY,t(1;3)(3pter->3p22::1p32->1qter;1pter->1p32::3p22->3qter) [3]; 46,XY,t(3;12)(3pter->3q12::12q24.1->12qter;12pter->12q24.1:;3q12->3qter) [3]; 46,XY [13] (Coriell=GM09497)., Population: Caucasian. Finite cell line Male Coriell GM09497 CLO:CLO_0011480,
Coriell:GM09497,
Wikidata:Q54843801
CVCL_AY35 2026-09-12 05:33:44 1
GM15223
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM15223, RRID:CVCL_5W53 Homo sapiens (Human) Part of: DNA polymorphism discovery resource collection. PMID:9872978
PMID:18805990
Transformed cell line Sex unspecified Coriell GM15223 CLO:CLO_0027483,
Coriell:GM15223,
GEO:GSM260565,
GEO:GSM260566,
GEO:GSM260567,
GEO:GSM260568,
Wikidata:Q54847743
CVCL_5W53 2026-09-12 05:35:17 1
GM15245
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM15245, RRID:CVCL_5W71 Homo sapiens (Human) Part of: DNA polymorphism discovery resource collection. PMID:9872978
PMID:12160888
PMID:18805990
PMID:31401124
PMID:35931342
Transformed cell line Sex unspecified Coriell GM15245 CLO:CLO_0027391,
Coriell:GM15245,
GEO:GSM260569,
GEO:GSM260570,
GEO:GSM260571,
GEO:GSM260572,
Wikidata:Q54847766
CVCL_5W71 2026-09-12 05:35:18 1
GM15385
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_5Y77 Homo sapiens (Human) Part of: DNA polymorphism discovery resource collection. PMID:9872978
PMID:12160888
PMID:18805990
Transformed cell line Sex unspecified CLO:CLO_0026789,
Coriell:GM15385,
GEO:GSM260597,
GEO:GSM260598,
GEO:GSM260599,
GEO:GSM260600,
Wikidata:Q54847889
CVCL_5Y77 2026-09-12 05:35:22 1
GM15385
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM15385, RRID:CVCL_5Y77 Homo sapiens (Human) Part of: DNA polymorphism discovery resource collection. PMID:9872978
PMID:12160888
PMID:18805990
Transformed cell line Sex unspecified Coriell GM15385 CLO:CLO_0026789,
Coriell:GM15385,
GEO:GSM260597,
GEO:GSM260598,
GEO:GSM260599,
GEO:GSM260600,
Wikidata:Q54847889
CVCL_5Y77 2026-09-12 05:35:22 1
GM15850
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_U734 Homo sapiens (Human) Friedreich ataxia Population: Caucasian. PMID:18485778 Transformed cell line Female CLO:CLO_0027780,
EFO:EFO_0006276,
ChEMBL-Cells:CHEMBL4295474,
ChEMBL-Targets:CHEMBL4296416,
Coriell:GM15850,
GEO:GSM113813,
GEO:GSM113814,
GEO:GSM113815,
GEO:GSM113816,
GEO:GSM113817,
GEO:GSM113818,
GEO:GSM113819,
GEO:GSM113820,
GEO:GSM113821,
GEO:GSM113822,
GEO:GSM113823,
GEO:GSM113824,
PubChem_Cell_line:CVCL_U734,
Wikidata:Q54848235
CVCL_U734 2026-09-12 05:35:29 1
GM15871
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM15871, RRID:CVCL_AM76 Homo sapiens (Human) Population: Caucasian. Finite cell line Male Coriell GM15871 CLO:CLO_0018546,
Coriell:GM15871,
Wikidata:Q54848245
CVCL_AM76 2026-09-12 05:35:29 1
GM16209
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_U739 Homo sapiens (Human) Friedreich ataxia Transformed cell line Female CLO:CLO_0019325,
Coriell:GM16209,
Wikidata:Q54848365
CVCL_U739 2026-09-12 05:35:32 1
GM16214
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_U742 Homo sapiens (Human) Friedreich ataxia Transformed cell line Male CLO:CLO_0019333,
Coriell:GM16214,
Wikidata:Q54848377
CVCL_U742 2026-09-12 05:35:32 1

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