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  • References:pmid:23665875 (facet)

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Click the to add this resource to an Authentication Report or Collection

1,669 Results - per page

Show More Columns | Download Top 1000 Results

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
GM03435
 
Resource Report
Resource Website
RRID:CVCL_X286 Homo sapiens (Human) PMID:6661932
PMID:23665875
Finite cell line Male GM 3435 CLO:CLO_0017049,
Coriell:GM03435,
Wikidata:Q54838067
CVCL_X286 2026-02-07 08:05:15 0
GM03462
 
Resource Report
Resource Website
RRID:CVCL_X287 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 3462 CLO:CLO_0017032,
BioSample:SAMN00808411,
Coriell:GM03462,
Wikidata:Q54838078
CVCL_X287 2026-02-07 08:05:15 0
GM03493
 
Resource Report
Resource Website
Coriell Cat# GM03493, RRID:CVCL_X288 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 3493 Coriell GM03493 CLO:CLO_0017327,
BioSample:SAMN00808428,
Coriell:GM03493,
Wikidata:Q54838096
CVCL_X288 2026-02-07 08:05:16 0
GM03470
 
Resource Report
Resource Website
Coriell Cat# GM03470, RRID:CVCL_F108 Homo sapiens (Human) PMID:6617268
PMID:6661932
PMID:23665875
Transformed cell line Female GM 3470 Coriell GM03470 CLO:CLO_0017010,
BioSample:SAMN00808418,
Coriell:GM03470,
Wikidata:Q54838085
CVCL_F108 2026-02-07 08:05:15 0
GM03479
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_2Y96 Homo sapiens (Human) 22q11.2 deletion syndrome PMID:23665875 Finite cell line Male CLO:CLO_0017004,
BioSample:SAMN00808420,
Coriell:GM03479,
Wikidata:Q54838087
CVCL_2Y96 2026-02-07 08:05:15 0
GM03501
 
Resource Report
Resource Website
RRID:CVCL_1N77 Homo sapiens (Human) Population: Caucasian. PMID:2535035
PMID:23665875
Finite cell line Male GM3501 CLO:CLO_0017334,
BioSample:SAMN00808431,
Coriell:GM03501,
Wikidata:Q54838105
CVCL_1N77 2026-02-07 08:05:16 0
GM03577
 
Resource Report
Resource Website
Coriell Cat# GM03577, RRID:CVCL_X294 Homo sapiens (Human) 22q11.2 deletion syndrome Karyotypic information: 45,XY,der(3)(3pter->3q29::22q11->22qter),-22 (Coriell=GM03577)., Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM 3577 Coriell GM03577 CLO:CLO_0017255,
BioSample:SAMN00808457,
Coriell:GM03577,
Wikidata:Q54838139
CVCL_X294 2026-02-07 08:05:17 0
GM03501
 
Resource Report
Resource Website
Coriell Cat# GM03501, RRID:CVCL_1N77 Homo sapiens (Human) Population: Caucasian. PMID:2535035
PMID:23665875
Finite cell line Male GM3501 Coriell GM03501 CLO:CLO_0017334,
BioSample:SAMN00808431,
Coriell:GM03501,
Wikidata:Q54838105
CVCL_1N77 2026-02-07 08:05:16 0
GM03493
 
Resource Report
Resource Website
RRID:CVCL_X288 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 3493 CLO:CLO_0017327,
BioSample:SAMN00808428,
Coriell:GM03493,
Wikidata:Q54838096
CVCL_X288 2026-02-07 08:05:23 0
GM03469
 
Resource Report
Resource Website
RRID:CVCL_7390 Homo sapiens (Human) Population: Mexican., Part of: Human variation panel. PMID:16244288
PMID:23665875
Transformed cell line Male GM03469A, GM17066 CLO:CLO_0014565,
CLO:CLO_0017026,
BioSample:SAMN00808417,
Coriell:GM03469,
Coriell:GM17066,
Wikidata:Q54838084
CVCL_7390 2026-02-07 08:05:15 0
GM01416
 
Resource Report
Resource Website
RRID:CVCL_F657 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Transformed cell line Female GM-1416, GM 1416, GM1416, GM01416B CLO:CLO_0030788,
BioSample:SAMN00803874,
Coriell:GM01416,
Wikidata:Q54836816
CVCL_F657 2026-02-07 08:04:40 0
GM01414
 
Resource Report
Resource Website
RRID:CVCL_X246 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American. PMID:6661932
PMID:10377420
PMID:23665875
Finite cell line Female GM-1414, GM 1414, GM1414 CLO:CLO_0030794,
BioSample:SAMN00803870,
Coriell:GM01414,
Wikidata:Q54836814
CVCL_X246 2026-02-07 08:04:39 0
GM01416
 
Resource Report
Resource Website
Coriell Cat# GM01416, RRID:CVCL_F657 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Transformed cell line Female GM-1416, GM 1416, GM1416, GM01416B Coriell GM01416 CLO:CLO_0030788,
BioSample:SAMN00803874,
Coriell:GM01416,
Wikidata:Q54836816
CVCL_F657 2026-02-07 08:04:43 0
GM01414
 
Resource Report
Resource Website
Coriell Cat# GM01414, RRID:CVCL_X246 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American. PMID:6661932
PMID:10377420
PMID:23665875
Finite cell line Female GM-1414, GM 1414, GM1414 Coriell GM01414 CLO:CLO_0030794,
BioSample:SAMN00803870,
Coriell:GM01414,
Wikidata:Q54836814
CVCL_X246 2026-02-07 08:04:40 0
GM01359
 
Resource Report
Resource Website
RRID:CVCL_X080 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18.arr(18)x3 (Coriell=GM01359)., Population: Caucasian. PMID:6661932
PMID:7329430
PMID:23665875
Finite cell line Male GM-1359, GM 1359 CLO:CLO_0030907,
BioSample:SAMN00803814,
Coriell:GM01359,
Wikidata:Q54836780
CVCL_X080 2026-02-07 08:04:38 0
GM01564
 
Resource Report
Resource Website
RRID:CVCL_X251 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM-1564, GM 1564 CLO:CLO_0031457,
BioSample:SAMN00806916,
Coriell:GM01564,
Wikidata:Q54836908
CVCL_X251 2026-02-07 08:04:45 0
GM01535
 
Resource Report
Resource Website
Coriell Cat# GM01535, RRID:CVCL_X250 Homo sapiens (Human) Population: African American. PMID:6661932
PMID:11687795
PMID:23665875
Finite cell line Female GM-1535, GM 1535, GM1535 Coriell GM01535 CLO:CLO_0031488,
BioSample:SAMN00806900,
Coriell:GM01535,
GEO:GSM797,
Wikidata:Q54836891
CVCL_X250 2026-02-07 08:04:45 0
GM01549
 
Resource Report
Resource Website
Coriell Cat# GM01549, RRID:CVCL_X081 Homo sapiens (Human) PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-1549, GM 1549 Coriell GM01549 CLO:CLO_0031485,
Coriell:GM01549,
Wikidata:Q54836893
CVCL_X081 2026-02-07 08:04:42 0
GM01484
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_F130 Homo sapiens (Human) Sporadic retinoblastoma Population: Caucasian. PMID:7253718
PMID:23665875
Transformed cell line Female GM1484, AG01484, AG-1484, AG 1484, AG1484 CLO:CLO_0031433,
BioSample:SAMN00806866,
Coriell:AG01484,
Coriell:GM01484,
Wikidata:Q54836853
CVCL_F130 2026-02-07 08:04:41 0
GM01641
 
Resource Report
Resource Website
RRID:CVCL_5M69 Homo sapiens (Human) Neurofibromatosis type 1 Population: African American. PMID:23665875 Transformed cell line Female GM-1641 CLO:CLO_0031523,
BioSample:SAMN00807013,
Coriell:GM01641,
Wikidata:Q54836975
CVCL_5M69 2026-02-07 08:04:43 0

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