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10,163 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
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 2026-07-25 04:33:53 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 2026-07-25 04:33:53 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 2026-07-25 04:33:54 1
GM11997
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM11997, RRID:CVCL_5C55 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:20856902
PMID:21418647
Transformed cell line Female Coriell GM11997 CLO:CLO_0020503,
Coriell:GM11997,
GEO:GSM316267,
GEO:GSM316268,
GEO:GSM316269,
GEO:GSM420731,
GEO:GSM651081,
GEO:GSM651082,
GEO:GSM957436,
Wikidata:Q54845432
CVCL_5C55 2026-07-25 04:34:45 1
GM11997
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_5C55 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:20856902
PMID:21418647
Transformed cell line Female CLO:CLO_0020503,
Coriell:GM11997,
GEO:GSM316267,
GEO:GSM316268,
GEO:GSM316269,
GEO:GSM420731,
GEO:GSM651081,
GEO:GSM651082,
GEO:GSM957436,
Wikidata:Q54845432
CVCL_5C55 2026-07-25 04:34:45 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 2026-07-25 04:34:07 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 2026-07-25 04:34:07 1
GM03868
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM03868, RRID:CVCL_1H73 Homo sapiens (Human) Huntington's disease Population: Caucasian. Finite cell line Female Coriell GM03868 CLO:CLO_0016025,
BioSample:SAMN00808580,
Coriell:GM03868,
Wikidata:Q54838287
CVCL_1H73 2026-07-25 04:32:52 1
GM04078
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_T820 Homo sapiens (Human) Friedreich ataxia Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian. PMID:27002638
PMID:28444186
PMID:29125828
Finite cell line Male GM-4078, F4078, 4078 CLO:CLO_0016228,
ChEMBL-Cells:CHEMBL4802059,
Coriell:GM04078,
GEO:GSM2794424,
PubChem_Cell_line:CVCL_T820,
Wikidata:Q54838382
CVCL_T820 2026-07-25 04:32:54 1
GM04592
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V473 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 4592, GM04592A CLO:CLO_0018882,
Coriell:GM04592,
Wikidata:Q54838578
CVCL_V473 2026-07-25 04:32:59 1
GM04506
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7413 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian. PMID:21490598 Finite cell line Female GM04506A, HF25 CLO:CLO_0018815,
Coriell:GM04506,
Wikidata:Q54838546
CVCL_7413 2026-07-25 04:32:59 3
GM04506
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04506, RRID:CVCL_7413 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian. PMID:21490598 Finite cell line Female GM04506A, HF25 Coriell GM04506 CLO:CLO_0018815,
Coriell:GM04506,
Wikidata:Q54838546
CVCL_7413 2026-07-25 04:32:59 3
GM04616
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04616, RRID:CVCL_V475 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:17668376
Finite cell line Female GM 4616, GM04616A Coriell GM04616 CLO:CLO_0018955,
Coriell:GM04616,
Wikidata:Q54838601
CVCL_V475 2026-07-25 04:33:00 3
GM04626
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04626, RRID:CVCL_X310 Homo sapiens (Human) PMID:6661932
PMID:21177337
PMID:23665875
Finite cell line Female GM 4626 Coriell GM04626 CLO:CLO_0018940,
Coriell:GM04626,
GEO:GSM608319,
GEO:GSM608320,
Wikidata:Q54838608
CVCL_X310 2026-07-25 04:33:00 1
GM04626
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_X310 Homo sapiens (Human) PMID:6661932
PMID:21177337
PMID:23665875
Finite cell line Female GM 4626 CLO:CLO_0018940,
Coriell:GM04626,
GEO:GSM608319,
GEO:GSM608320,
Wikidata:Q54838608
CVCL_X310 2026-07-25 04:33:00 1
GM04616
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V475 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:17668376
Finite cell line Female GM 4616, GM04616A CLO:CLO_0018955,
Coriell:GM04616,
Wikidata:Q54838601
CVCL_V475 2026-07-25 04:33:00 3
GM05131
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_AX78 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male CLO:CLO_0025352,
Coriell:GM05131,
Wikidata:Q54838877
CVCL_AX78 2026-07-25 04:33:07 1
GM05131
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM05131, RRID:CVCL_AX78 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male Coriell GM05131 CLO:CLO_0025352,
Coriell:GM05131,
Wikidata:Q54838877
CVCL_AX78 2026-07-25 04:33:07 1
GM05565
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7432 Homo sapiens (Human) Population: Latino or Hispanic. PMID:24119401
PMID:30567591
Finite cell line Male GM5565, GM 05565 CLO:CLO_0024544,
Coriell:GM05565,
GEO:GSM3124627,
Wikidata:Q54841872
CVCL_7432 2026-07-25 04:33:12 1
GM05659
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7434 Homo sapiens (Human) Population: Caucasian. PMID:1652892
PMID:2475503
PMID:2705456
PMID:2837086
PMID:3745952
PMID:8605078
PMID:17668376
PMID:18973801
PMID:24119401
PMID:25732146
PMID:27543334
PMID:30220252
PMID:30497978
PMID:30567591
PMID:33038742
Finite cell line Male GM5659, GM-5659, GM 5659, GM05659B, GM5659B, GM05659C, GM 5659C, GM05659D, GM5659D CLO:CLO_0024626,
EFO:EFO_0006278,
Coriell:GM05659,
GEO:GSE11919,
GEO:GSM3124625,
Wikidata:Q54841910
CVCL_7434 2026-07-25 04:33:14 5

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