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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
GM02670
 
Resource Report
Resource Website
Coriell Cat# GM02670, RRID:CVCL_5M77 Homo sapiens (Human) XX male Population: Caucasian. PMID:23665875 Finite cell line Male Coriell GM02670 CLO:CLO_0015007,
Coriell:GM02670,
Wikidata:Q54837614
CVCL_5M77 Cellosaurus 2026-09-26 06:48:58 0
GM02673
 
Resource Report
Resource Website
Coriell Cat# GM02673, RRID:CVCL_7361 Homo sapiens (Human) Population: Caucasian. PMID:15450399
PMID:30567591
Finite cell line Male GM2673 Coriell GM02673 CLO:CLO_0015004,
Coriell:GM02673,
GEO:GSM3124655,
Wikidata:Q54837617
CVCL_7361 Cellosaurus 2026-09-26 06:48:58 0
GM02645
 
Resource Report
Resource Website
Coriell Cat# GM02645, RRID:CVCL_DD71 Homo sapiens (Human) Osteogenesis imperfecta Population: Caucasian. Finite cell line Male Coriell GM02645 CLO:CLO_0015039,
Coriell:GM02645,
Wikidata:Q54837603
CVCL_DD71 Cellosaurus 2026-09-26 06:48:58 0
GM02670
 
Resource Report
Resource Website
RRID:CVCL_5M77 Homo sapiens (Human) XX male Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0015007,
Coriell:GM02670,
Wikidata:Q54837614
CVCL_5M77 Cellosaurus 2026-09-26 06:48:58 0
GM02617
 
Resource Report
Resource Website
RRID:CVCL_CY08 Homo sapiens (Human) Population: Caucasian. PMID:7438795 Finite cell line Female GM2617 CLO:CLO_0032678,
Coriell:GM02617,
Wikidata:Q54837583
CVCL_CY08 Cellosaurus 2026-09-26 06:48:57 0
GM02664
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L977 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Male GM02643 CLO:CLO_0014990,
Coriell:GM02643,
Coriell:GM02664,
Wikidata:Q54837609
CVCL_L977 Cellosaurus 2026-09-26 06:48:58 0
DD2521
 
Resource Report
Resource Website
ECACC Cat# 96010950, RRID:CVCL_9K22 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 96010950 ECACC:96010950,
Wikidata:Q54830286
CVCL_9K22 Cellosaurus 2026-09-26 06:46:44 0
DD2513
 
Resource Report
Resource Website
RRID:CVCL_9K20 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95122209,
Wikidata:Q54830283
CVCL_9K20 Cellosaurus 2026-09-26 06:46:44 0
DD2522
 
Resource Report
Resource Website
ECACC Cat# 96010956, RRID:CVCL_AR06 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 96010956 ECACC:96010956,
Wikidata:Q54830287
CVCL_AR06 Cellosaurus 2026-09-26 06:46:44 0
DD2634
 
Resource Report
Resource Website
RRID:CVCL_9K47 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:96042602,
Wikidata:Q54830321
CVCL_9K47 Cellosaurus 2026-09-26 06:46:45 0
DD2609
 
Resource Report
Resource Website
ECACC Cat# 96032944, RRID:CVCL_AR10 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 96032944 ECACC:96032944,
Wikidata:Q54830318
CVCL_AR10 Cellosaurus 2026-09-26 06:46:45 0
DD2586
 
Resource Report
Resource Website
RRID:CVCL_AR09 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:96030703,
Wikidata:Q54830312
CVCL_AR09 Cellosaurus 2026-09-26 06:46:44 0
DD2553
 
Resource Report
Resource Website
ECACC Cat# 96020520, RRID:CVCL_9K31 Homo sapiens (Human) Type 1 diabetes mellitus Karyotypic information: 46,XY,der(2),ins(2;6) (ECACC=96020520)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 96020520 ECACC:96020520,
Wikidata:Q54830297
CVCL_9K31 Cellosaurus 2026-09-26 06:46:44 0
DD2530
 
Resource Report
Resource Website
ECACC Cat# 96011601, RRID:CVCL_9K24 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 96011601 ECACC:96011601,
Wikidata:Q54830289
CVCL_9K24 Cellosaurus 2026-09-26 06:46:44 0
DD2644
 
Resource Report
Resource Website
RRID:CVCL_9K50 Homo sapiens (Human) Smith-Lemli-Opitz syndrome Karyotypic information: 46,XY.ish 22q11-2(cH748x2) (ECACC=96050810)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:96050810,
Wikidata:Q54830324
CVCL_9K50 Cellosaurus 2026-09-26 06:46:45 0
DD2553
 
Resource Report
Resource Website
RRID:CVCL_9K31 Homo sapiens (Human) Type 1 diabetes mellitus Karyotypic information: 46,XY,der(2),ins(2;6) (ECACC=96020520)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:96020520,
Wikidata:Q54830297
CVCL_9K31 Cellosaurus 2026-09-26 06:46:44 0
DD2456
 
Resource Report
Resource Website
ECACC Cat# 95110314, RRID:CVCL_9K09 Homo sapiens (Human) Klippel-Feil syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 95110314 ECACC:95110314,
Wikidata:Q54830271
CVCL_9K09 Cellosaurus 2026-09-26 06:46:43 0
DD2470
 
Resource Report
Resource Website
RRID:CVCL_9K12 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95112009,
Wikidata:Q54830275
CVCL_9K12 Cellosaurus 2026-09-26 06:46:44 0
DD2565
 
Resource Report
Resource Website
RRID:CVCL_9K35 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:96022001,
Wikidata:Q54830303
CVCL_9K35 Cellosaurus 2026-09-26 06:46:44 0
DD2489
 
Resource Report
Resource Website
RRID:CVCL_9K16 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:95120417,
Wikidata:Q54830279
CVCL_9K16 Cellosaurus 2026-09-26 06:46:44 0

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