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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 Record Last Update Mentions Count
GM18367
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_6G81 Homo sapiens (Human) Seckel syndrome Caution: Could be identical to DK0064 (Cellosaurus=CVCL_R778)., Population: Pakistani. Transformed cell line Male CLO:CLO_0031109,
Coriell:GM18367,
Wikidata:Q54849516
CVCL_6G81 2026-08-29 04:32:04 0
GM15989
 
Resource Report
Resource Website
RRID:CVCL_F626 Homo sapiens (Human) Nijmegen breakage syndrome Caution: Could be identical to GM07166VA7 (Cellosaurus=CVCL_WL44)., Population: Caucasian. Transformed cell line Female CLO:CLO_0018690,
Coriell:GM15989,
Wikidata:Q54848287
cvcl_7464 CVCL_F626 2026-08-29 04:31:35 0
GM15912
 
Resource Report
Resource Website
Coriell Cat# GM15912, RRID:CVCL_DR49 Homo sapiens (Human) Childhood absence epilepsy Donor information: Established from monozygotic twin of GM15911 (Cellosaurus=CVCL_DR48). Transformed cell line Female Coriell GM15912 CLO:CLO_0018730,
Coriell:GM15912,
Wikidata:Q54848274
CVCL_DR49 2026-08-29 04:31:34 0
GM15912
 
Resource Report
Resource Website
RRID:CVCL_DR49 Homo sapiens (Human) Childhood absence epilepsy Donor information: Established from monozygotic twin of GM15911 (Cellosaurus=CVCL_DR48). Transformed cell line Female CLO:CLO_0018730,
Coriell:GM15912,
Wikidata:Q54848274
CVCL_DR49 2026-08-29 04:31:38 0
GM16363
 
Resource Report
Resource Website
Coriell Cat# GM16363, RRID:CVCL_5Q67 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM16362 (Cellosaurus=CVCL_5Q66). Transformed cell line Male Coriell GM16363 Coriell:GM16363,
Wikidata:Q54848472
CVCL_5Q67 2026-08-29 04:31:39 0
GM16362
 
Resource Report
Resource Website
Coriell Cat# GM16362, RRID:CVCL_5Q66 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM16363 (Cellosaurus=CVCL_5Q67). PMID:23665875 Transformed cell line Male Coriell GM16362 Coriell:GM16362,
Wikidata:Q54848471
CVCL_5Q66 2026-08-29 04:31:40 0
GM13323
 
Resource Report
Resource Website
Coriell Cat# GM13323, RRID:CVCL_2N04 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13324 (Cellosaurus=CVCL_2N05). PMID:23665875 Transformed cell line Female Coriell GM13323 CLO:CLO_0013275,
Coriell:GM13323,
Wikidata:Q54846460
CVCL_2N04 2026-08-29 04:30:48 0
GM13324
 
Resource Report
Resource Website
RRID:CVCL_2N05 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13323 (Cellosaurus=CVCL_2N04). PMID:23665875 Transformed cell line Female CLO:CLO_0013274,
Coriell:GM13324,
Wikidata:Q54846461
CVCL_2N05 2026-08-29 04:30:48 0
GM13323
 
Resource Report
Resource Website
RRID:CVCL_2N04 Homo sapiens (Human) Turner syndrome Donor information: Established from monozygotic twin of GM13324 (Cellosaurus=CVCL_2N05). PMID:23665875 Transformed cell line Female CLO:CLO_0013275,
Coriell:GM13323,
Wikidata:Q54846460
CVCL_2N04 2026-08-29 04:30:53 0
MTSV1-7 neo
 
Resource Report
Resource Website
RRID:CVCL_A8R7 Homo sapiens (Human) Characteristics: Control cell line for MTSV1-7 ce1 (Cellosaurus=CVCL_3033). PMID:8099725 Transformed cell line Female MTSV1-7neo Wikidata:Q102114566 cvcl_8645 CVCL_A8R7 2026-08-29 04:47:12 0
HQ00406
 
Resource Report
Resource Website
Coriell Cat# HQ00406, RRID:CVCL_3D99 Homo sapiens (Human) Huntington's disease Donor information: Established from monozygotic twin of HQ00405 (Cellosaurus=CVCL_3D98). Transformed cell line Female Coriell HQ00406 Coriell:HQ00406,
Wikidata:Q54892195
CVCL_3D99 2026-08-29 04:40:52 0
HQ00406
 
Resource Report
Resource Website
RRID:CVCL_3D99 Homo sapiens (Human) Huntington's disease Donor information: Established from monozygotic twin of HQ00405 (Cellosaurus=CVCL_3D98). Transformed cell line Female Coriell:HQ00406,
Wikidata:Q54892195
CVCL_3D99 2026-08-29 04:40:53 0
QIMR-WW1-LCL
 
Resource Report
Resource Website
RRID:CVCL_W930 Homo sapiens (Human) Caution: Could be identical to WeWak1 (Cellosaurus=CVCL_E871)., Population: Papuan. PMID:2898508
PMID:3037521
PMID:7601573
Transformed cell line Male WW1-LCL, WW1 LCL, WW-1-LCL Wikidata:Q54948841 CVCL_W930 2026-08-29 04:57:03 0
XP2OS(SV)
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_3242 Homo sapiens (Human) Xeroderma pigmentosum, complementation group A Caution: Could be identical to GM04312 (Cellosaurus=CVCL_ZN80)., Population: Japanese. PMID:2039995
PMID:7000335
Transformed cell line Female XP2OS (SV), XP2OS-SV, XP20S-SV40, XP20s(SV40) JCRB:JCRB0301,
JCRB:KURB1008,
Wikidata:Q54994913
cvcl_f510 CVCL_3242 2026-08-29 05:03:54 1
NH50328
 
Resource Report
Resource Website
RRID:CVCL_B6HL Homo sapiens (Human) Frontotemporal dementia Characteristics: Non-edited control for NH50327 (Cellosaurus=CVCL_B6HK)., Population: Caucasian. Induced pluripotent stem cell Female NHCDR:NH50328,
Wikidata:Q112129423
cvcl_a9rn CVCL_B6HL 2026-08-29 04:54:27 0
NH50336
 
Resource Report
Resource Website
RRID:CVCL_B6HV Homo sapiens (Human) Frontotemporal dementia-1 Characteristics: Non-edited control for NH50337 (Cellosaurus=CVCL_B6HW)., Population: Caucasian. Induced pluripotent stem cell Male NHCDR:NH50336,
Wikidata:Q112129431
cvcl_ux23 CVCL_B6HV 2026-08-29 04:54:41 0
NH50325
 
Resource Report
Resource Website
RRID:CVCL_B6HI Homo sapiens (Human) Frontotemporal dementia-1 Characteristics: Non-edited control for NH50326 (Cellosaurus=CVCL_B6HJ)., Population: Caucasian. Induced pluripotent stem cell Male NHCDR:NH50325,
Wikidata:Q112129420
cvcl_ux04 CVCL_B6HI 2026-08-29 04:54:27 0
NH50141
 
Resource Report
Resource Website
RRID:CVCL_UW85 Homo sapiens (Human) Amyotrophic lateral sclerosis 1 Characteristics: Non-edited control for NH50140 (Cellosaurus=CVCL_UW84)., Population: Hispanic. Induced pluripotent stem cell Female NHCDR:NH50141,
Wikidata:Q98127565
cvcl_ry49 CVCL_UW85 2026-08-29 04:54:22 0
ND33438
 
Resource Report
Resource Website
RRID:CVCL_DR50 Homo sapiens (Human) Seizure disorder Donor information: Established from monozygotic twin of ND33439 (Cellosaurus=CVCL_DR51). Transformed cell line Male Coriell:ND33438,
Wikidata:Q54929679
CVCL_DR50 2026-08-29 04:54:05 0
ND33439
 
Resource Report
Resource Website
RRID:CVCL_DR51 Homo sapiens (Human) Seizure disorder Donor information: Established from monozygotic twin of ND33438 (Cellosaurus=CVCL_DR50). Transformed cell line Male Coriell:ND33439,
Wikidata:Q54929680
CVCL_DR51 2026-08-29 04:54:00 0

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