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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
GM02037
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02037, RRID:CVCL_7349 Homo sapiens (Human) Karyotypic information: 46,XY [45]; 46,XY,t(4;16)(4qter->4p14::16q24->16qter;16pter->16q24::4p14->4pter) [5] (Coriell=GM02037)., Population: Caucasian. PMID:6223188
PMID:8643543
PMID:30567591
Finite cell line Male GM2037, GM-2037, GM 2037, GM02037A, GM2037A, GM 2037A, GM02037B, GM 2037B, GM02037C Coriell GM02037 BTO:BTO_0003842,
CLO:CLO_0032574,
BioSample:SAMN00807416,
Coriell:GM02037,
GEO:GSM3124641,
Wikidata:Q54837256
CVCL_7349 Cellosaurus 2026-09-26 06:48:51 1
GM02028
 
Resource Report
Resource Website
Coriell Cat# GM02028, RRID:CVCL_CZ13 Homo sapiens (Human) Finite cell line Male GM-2028, GM02028A Coriell GM02028 CLO:CLO_0032575,
Coriell:GM02028,
Wikidata:Q54837247
CVCL_CZ13 Cellosaurus 2026-09-26 06:48:51 0
GM02060
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM02060, RRID:CVCL_ZP42 Homo sapiens (Human) Senescence: Senesces at 22 PDL (PubMed=6492896). PMID:6492896 Finite cell line Sex unspecified GM2060 Coriell GM02060 Coriell:GM02060,
Wikidata:Q98126373
CVCL_ZP42 Cellosaurus 2026-09-26 06:48:52 0
GM02095
 
Resource Report
Resource Website
Coriell Cat# GM02095, RRID:CVCL_H178 Homo sapiens (Human) Metachromatic leukodystrophy Finite cell line Female GM-2095 Coriell GM02095 CLO:CLO_0031822,
BioSample:SAMN00807482,
Coriell:GM02095,
Wikidata:Q54837299
CVCL_H178 Cellosaurus 2026-09-26 06:48:52 0
GM02079
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02079, RRID:CVCL_1H41 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6220707 Finite cell line Female GM-2079, GM 2079, GM02079A Coriell GM02079 CLO:CLO_0032509,
BioSample:SAMN00807468,
Coriell:GM02079,
Wikidata:Q54837291
CVCL_1H41 Cellosaurus 2026-09-26 06:48:52 1
GM02052
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7350 Homo sapiens (Human) Ataxia telangiectasia syndrome Population: Jewish; Moroccan. PMID:761484
PMID:11313956
PMID:12446774
PMID:19896956
Finite cell line Female GM-2052, GM 2052, GM2052, GM02052A, AT19IJE-F CLO:CLO_0032553,
BioSample:SAMN00807434,
Coriell:GM02052,
Wikidata:Q54837268
CVCL_7350 Cellosaurus 2026-09-26 06:48:52 1
GM02057
 
Resource Report
Resource Website
RRID:CVCL_X448 Homo sapiens (Human) Aspartylglycosaminuria Population: Caucasian; Finnish. PMID:1904874 Finite cell line Female GM-2057 CLO:CLO_0032533,
BioSample:SAMN00807442,
Coriell:GM02057,
Wikidata:Q54837276
CVCL_X448 Cellosaurus 2026-09-26 06:48:52 0
GM02066
 
Resource Report
Resource Website
RRID:CVCL_CW97 Homo sapiens (Human) Nephropathic cystinosis Population: Caucasian. PMID:9792862
PMID:28649545
Finite cell line Female GM2066, GM-2066, GM 2066 CLO:CLO_0032516,
BioSample:SAMN00807454,
Coriell:GM02066,
Wikidata:Q54837283
CVCL_CW97 Cellosaurus 2026-09-26 06:48:52 0
GM02065
 
Resource Report
Resource Website
RRID:CVCL_9R68 Homo sapiens (Human) Mucolipidosis type IIIA Population: Caucasian. PMID:16465621 Finite cell line Male GM-2065 CLO:CLO_0032530,
BioSample:SAMN00807452,
Coriell:GM02065,
Wikidata:Q54837282
CVCL_9R68 Cellosaurus 2026-09-26 06:48:52 0
GM02026
 
Resource Report
Resource Website
RRID:CVCL_4J44 Homo sapiens (Human) Population: Caucasian. PMID:7803800 Finite cell line Female GM-2026, GM02026A CLO:CLO_0032578,
BioSample:SAMN00807402,
Coriell:GM02026,
Wikidata:Q54837245
CVCL_4J44 Cellosaurus 2026-09-26 06:48:51 0
GM02058
 
Resource Report
Resource Website
RRID:CVCL_V466 Homo sapiens (Human) Down syndrome Karyotypic information: 46,XX,i(21)(qter->q10::q10->qter) [13]; 46,XX [87] (Coriell=GM02058)., Population: Jewish; Ashkenazi. Finite cell line Female GM-2058 CLO:CLO_0032534,
BioSample:SAMN00807444,
Coriell:GM02058,
Wikidata:Q54837277
CVCL_V466 Cellosaurus 2026-09-26 06:48:52 0
GM02027
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB69 Homo sapiens (Human) Finite cell line Female GM-2027 Coriell:GM02027,
Wikidata:Q54837246
CVCL_JB69 Cellosaurus 2026-09-26 06:48:51 0
GM02054
 
Resource Report
Resource Website
Coriell Cat# GM02054, RRID:CVCL_X087 Homo sapiens (Human) PMID:6617268
PMID:6661932
Transformed cell line Male GM-2054, GM 2054 Coriell GM02054 CLO:CLO_0032538,
BioSample:SAMN00807438,
Coriell:GM02054,
Wikidata:Q54837273
CVCL_X087 Cellosaurus 2026-09-26 06:48:52 0
GM02030
 
Resource Report
Resource Website
Coriell Cat# GM02030, RRID:CVCL_X259 Homo sapiens (Human) Trisomy 8 Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-2030, GM 2030 Coriell GM02030 CLO:CLO_0032576,
BioSample:SAMN00807404,
Coriell:GM02030,
Wikidata:Q54837249
CVCL_X259 Cellosaurus 2026-09-26 06:48:51 0
GM02048
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_M927 Homo sapiens (Human) Mucolipidosis type IV Population: Jewish; Ashkenazi. Finite cell line Female GM-2048 CLO:CLO_0032549,
BioSample:SAMN00807426,
Coriell:GM02048,
Wikidata:Q54837263
CVCL_M927 Cellosaurus 2026-09-26 06:48:52 2
GM02067
 
Resource Report
Resource Website
Coriell Cat# GM02067, RRID:CVCL_V467 Homo sapiens (Human) Down syndrome Karyotypic information: 47,XY,+21 [44]; 47,XY,t(1;16)(q21;p13.3],+21 [4]; 46,XY [2] (Coriell=GM02067)., Population: Caucasian. PMID:6661932 Finite cell line Male GM-2067, GM 2067, GM02067A Coriell GM02067 CLO:CLO_0032517,
BioSample:SAMN00807456,
Coriell:GM02067,
Wikidata:Q54837284
CVCL_V467 Cellosaurus 2026-09-26 06:48:52 0
GM02044
 
Resource Report
Resource Website
RRID:CVCL_1D93 Homo sapiens (Human) Karyotypic information: 45,XY,-16,t(14;16)(16;18)(14qter->14p12::16p11->16pter;18qter->18p1::16q12->16qter) (Coriell=GM02044). PMID:2095701 Finite cell line Male GM-2044, GM2044 CLO:CLO_0032556,
Coriell:GM02044,
Wikidata:Q54837259
CVCL_1D93 Cellosaurus 2026-09-26 06:48:51 0
GM02099
 
Resource Report
Resource Website
RRID:CVCL_2Z73 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Transformed cell line Male GM-2099 CLO:CLO_0031823,
BioSample:SAMN00807488,
Coriell:GM02099,
Wikidata:Q54837302
CVCL_2Z73 Cellosaurus 2026-09-26 06:48:52 0
GM02124
 
Resource Report
Resource Website
RRID:CVCL_4J45 Homo sapiens (Human) Acute intermittent porphyria Population: Caucasian. Transformed cell line Female GM-2124 CLO:CLO_0031847,
BioSample:SAMN00807498,
Coriell:GM02124,
Wikidata:Q54837308
CVCL_4J45 Cellosaurus 2026-09-26 06:48:52 0
GM02068
 
Resource Report
Resource Website
RRID:CVCL_1N60 Homo sapiens (Human) Karyotypic information: 46,XX,t(6;7)(6pter->6q27::7q22->7qter;7pter->7q22::6q27->6qter) (Coriell=GM02068)., Population: Caucasian. Finite cell line Female GM-2068 CLO:CLO_0032518,
BioSample:SAMN00807458,
Coriell:GM02068,
Wikidata:Q54837285
CVCL_1N60 Cellosaurus 2026-09-26 06:48:52 0

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