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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 Authority Record Last Update Mentions Count
GM03136
 
Resource Report
Resource Website
RRID:CVCL_GS60 Homo sapiens (Human) Adenosine deaminase deficiency Population: Jewish; Sephardic. PMID:1346349
PMID:1680289
PMID:2567118
Finite cell line Female GM 3136 CLO:CLO_0013522,
BioSample:SAMN00808266,
Coriell:GM03136,
Wikidata:Q54837896
CVCL_GS60 Cellosaurus 2026-09-26 06:49:03 0
GM03237
 
Resource Report
Resource Website
Coriell Cat# GM03237, RRID:CVCL_F072 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:7438795 Transformed cell line Male GM3237, GM18010 Coriell GM03237 CLO:CLO_0016000,
CLO:CLO_0016730,
BioSample:SAMN00808316,
Coriell:GM03237,
Coriell:GM18010,
Wikidata:Q54837958
CVCL_F072 Cellosaurus 2026-09-26 06:49:04 0
GM03216
 
Resource Report
Resource Website
Coriell Cat# GM03216, RRID:CVCL_HQ60 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Female Coriell GM03216 CLO:CLO_0013374,
BioSample:SAMN00808301,
Coriell:GM03216,
Wikidata:Q54837943
CVCL_HQ60 Cellosaurus 2026-09-26 06:49:04 0
GM03233
 
Resource Report
Resource Website
RRID:CVCL_4D83 Homo sapiens (Human) Supernumerary circular chromosome Finite cell line Male CLO:CLO_0016472,
BioSample:SAMN00808312,
Coriell:GM03233,
Wikidata:Q54837954
CVCL_4D83 Cellosaurus 2026-09-26 06:49:04 0
GM03224
 
Resource Report
Resource Website
RRID:CVCL_CY30 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Transformed cell line Male CLO:CLO_0016475,
BioSample:SAMN00808309,
Coriell:GM03224,
Wikidata:Q54837951
CVCL_CY30 Cellosaurus 2026-09-26 06:49:04 0
GM03193
 
Resource Report
Resource Website
RRID:CVCL_AB29 Homo sapiens (Human) Dyskeratosis congenita Transformed cell line Male CLO:CLO_0013390,
BioSample:SAMN00808286,
Coriell:GM03193,
Wikidata:Q54837928
CVCL_AB29 Cellosaurus 2026-09-26 06:49:03 0
GM03196
 
Resource Report
Resource Website
RRID:CVCL_V819 Homo sapiens (Human) Karyotypic information: 46,XX,inv(5)(pter->p13::q13->p13::q13->qter),t(17;22)(17qter->17p13::22q11->22qter;22pter->22q11::17p13->17pter) (Coriell=GM03196)., Population: Caucasian. PMID:6617268
PMID:7438788
Finite cell line Female GM-3196, GM 3196, GM3196 CLO:CLO_0013398,
BioSample:SAMN00808289,
Coriell:GM03196,
Wikidata:Q54837931
CVCL_V819 Cellosaurus 2026-09-26 06:49:03 0
GM03214
 
Resource Report
Resource Website
RRID:CVCL_HQ58 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Male CLO:CLO_0013378,
BioSample:SAMN00808299,
Coriell:GM03214,
Wikidata:Q54837941
CVCL_HQ58 Cellosaurus 2026-09-26 06:49:04 0
GM03196
 
Resource Report
Resource Website
Coriell Cat# GM03196, RRID:CVCL_V819 Homo sapiens (Human) Karyotypic information: 46,XX,inv(5)(pter->p13::q13->p13::q13->qter),t(17;22)(17qter->17p13::22q11->22qter;22pter->22q11::17p13->17pter) (Coriell=GM03196)., Population: Caucasian. PMID:6617268
PMID:7438788
Finite cell line Female GM-3196, GM 3196, GM3196 Coriell GM03196 CLO:CLO_0013398,
BioSample:SAMN00808289,
Coriell:GM03196,
Wikidata:Q54837931
CVCL_V819 Cellosaurus 2026-09-26 06:49:03 0
GM03333
 
Resource Report
Resource Website
Coriell Cat# GM03333, RRID:CVCL_H147 Homo sapiens (Human) Population: African American. Transformed cell line Female GM03333A Coriell GM03333 CLO:CLO_0016592,
BioSample:SAMN00808359,
Coriell:GM03333,
Wikidata:Q54838011
CVCL_H147 Cellosaurus 2026-09-26 06:49:05 0
GM03265
 
Resource Report
Resource Website
RRID:CVCL_9Q84 Homo sapiens (Human) Oculocerebrorenal syndrome Donor information: At sampling donor was not affected with oculocerebrorenal syndrome but has a 50% risk., Population: Caucasian. PMID:19700499 Finite cell line Male GM 03265, GM3265, Lowe 3265 CLO:CLO_0016705,
BioSample:SAMN00808329,
Coriell:GM03265,
Wikidata:Q54837980
CVCL_9Q84 Cellosaurus 2026-09-26 06:49:04 0
GM03347
 
Resource Report
Resource Website
Coriell Cat# GM03347, RRID:CVCL_N006 Homo sapiens (Human) Wolman disease Population: Mexican., Part of: Human variation panel. Finite cell line Female GM17065 Coriell GM03347 CLO:CLO_0014571,
CLO:CLO_0016540,
BioSample:SAMN00808362,
Coriell:GM03347,
Coriell:GM17065,
Wikidata:Q54838015
CVCL_N006 Cellosaurus 2026-09-26 06:49:05 0
GM03314
 
Resource Report
Resource Website
RRID:CVCL_L948 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian; British. PMID:3374507 Finite cell line Female GM3314 CLO:CLO_0016755,
BioSample:SAMN00808343,
Coriell:GM03314,
Wikidata:Q54837996
CVCL_L948 Cellosaurus 2026-09-26 06:49:05 0
GM03333
 
Resource Report
Resource Website
RRID:CVCL_H147 Homo sapiens (Human) Population: African American. Transformed cell line Female GM03333A CLO:CLO_0016592,
BioSample:SAMN00808359,
Coriell:GM03333,
Wikidata:Q54838011
CVCL_H147 Cellosaurus 2026-09-26 06:49:05 0
GM03255
 
Resource Report
Resource Website
Coriell Cat# GM03255, RRID:CVCL_X282 Homo sapiens (Human) PMID:6661932
PMID:8530005
PMID:23665875
Finite cell line Male GM-3255, GM 3255 Coriell GM03255 CLO:CLO_0016709,
BioSample:SAMN00808327,
Coriell:GM03255,
Wikidata:Q54837977
CVCL_X282 Cellosaurus 2026-09-26 06:49:04 0
GM03332
 
Resource Report
Resource Website
RRID:CVCL_7381 Homo sapiens (Human) Ataxia telangiectasia syndrome Population: African American. PMID:23943852 Transformed cell line Male GM03332A CLO:CLO_0016595,
BioSample:SAMN00808358,
Coriell:GM03332,
GEO:GSM1116571,
GEO:GSM1116572,
GEO:GSM1116625,
GEO:GSM1116626,
GEO:GSM1116627,
GEO:GSM1116628,
Wikidata:Q54838010
CVCL_7381 Cellosaurus 2026-09-26 06:49:05 0
GM03242
 
Resource Report
Resource Website
Coriell Cat# GM03242, RRID:CVCL_JB91 Homo sapiens (Human) Idiopathic basal ganglia calcification 1 Finite cell line Female Coriell GM03242 CLO:CLO_0016740,
Coriell:GM03242,
Wikidata:Q54837963
CVCL_JB91 Cellosaurus 2026-09-26 06:49:04 0
GM03324
 
Resource Report
Resource Website
RRID:CVCL_F091 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0016575,
BioSample:SAMN00808352,
Coriell:GM03324,
Wikidata:Q54838004
CVCL_F091 Cellosaurus 2026-09-26 06:49:05 0
GM03246
 
Resource Report
Resource Website
Coriell Cat# GM03246, RRID:CVCL_AT04 Homo sapiens (Human) Multiple sulfatase deficiency disease Transformed cell line Male Coriell GM03246 CLO:CLO_0016745,
BioSample:SAMN00808322,
Coriell:GM03246,
Wikidata:Q54837971
CVCL_AT04 Cellosaurus 2026-09-26 06:49:04 0
GM03299
 
Resource Report
Resource Website
Coriell Cat# GM03299, RRID:CVCL_7380 Homo sapiens (Human) PMID:6173245
PMID:6330733
PMID:6667451
PMID:23943852
Transformed cell line Female GM-3299, GM 3299, GM3299, GMO3299, GM03299B Coriell GM03299 BTO:BTO_0005027,
CLO:CLO_0016805,
Coriell:GM03299,
GEO:GSM1116597,
GEO:GSM1116598,
GEO:GSM1116599,
GEO:GSM1116600,
Wikidata:Q54837991
CVCL_7380 Cellosaurus 2026-09-26 06:49:05 0

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