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19,458 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
ND30047
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY61 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). PMID:22952635 Finite cell line Female Coriell:ND30047,
NHCDR:ND30047,
Wikidata:Q54929315
CVCL_EY61 2026-08-29 04:53:51 0
ND30015
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY59 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). PMID:22952635 Finite cell line Female Coriell:ND30015,
NHCDR:ND30015,
Wikidata:Q54929313
CVCL_EY59 2026-08-29 04:53:54 0
ND29968
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY55 Homo sapiens (Human) Parkinson disease 2, autosomal recessive juvenile PMID:22952635 Finite cell line Male BioSample:SAMN00805499,
Coriell:ND29968,
NHCDR:ND29968,
Wikidata:Q54929295
CVCL_EY55 2026-08-29 04:53:53 0
ND30260
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY66 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Female Coriell:ND30260,
NHCDR:ND30260,
Wikidata:Q54929342
CVCL_EY66 2026-08-29 04:53:55 0
ND29969
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY56 Homo sapiens (Human) Parkinson disease 2, autosomal recessive juvenile PMID:22952635 Finite cell line Female BioSample:SAMN00805501,
Coriell:ND29969,
NHCDR:ND29969,
Wikidata:Q54929296
CVCL_EY56 2026-08-29 04:53:51 0
ND30159
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY63 Homo sapiens (Human) Parkinson disease PMID:22952635 Finite cell line Female BioSample:SAMN00805543,
Coriell:ND30159,
NHCDR:ND30159,
Wikidata:Q54929326
CVCL_EY63 2026-08-29 04:53:54 0
ND30626
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y896 Homo sapiens (Human) Huntington's disease Caution: Patient indicated as not affected with HD in HQ01462, but as affected in ND30626. PMID:22952635 Finite cell line Male Coriell:ND30626,
NHCDR:ND30626,
Wikidata:Q54929408
CVCL_Y896 2026-08-29 04:53:53 0
ND30625
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND30625, RRID:CVCL_Y895 Homo sapiens (Human) Population: Caucasian. PMID:22952635
PMID:34746695
Finite cell line Male Coriell ND30625 CLO:CLO_0037415,
Coriell:ND30625,
LINCS_LDP:LPC-1016,
NHCDR:ND30625,
Wikidata:Q54929407
CVCL_Y895 2026-08-29 04:53:56 0
ND30327
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_EY36 Homo sapiens (Human) Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia PMID:22952635 Finite cell line Coriell:ND30327,
Wikidata:Q54929357
CVCL_EY36 2026-08-29 04:53:52 0
ND30364
 
Resource Report
Resource Website
Discontinued
Discontinued
RRID:CVCL_EY67 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Female Coriell:ND30364,
NHCDR:ND30364,
Wikidata:Q54929359
CVCL_EY67 2026-08-29 04:53:52 0
ND30625
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND30625, RRID:CVCL_Y895 Homo sapiens (Human) Population: Caucasian. PMID:22952635
PMID:34746695
Finite cell line Male NHCDR ND30625 CLO:CLO_0037415,
Coriell:ND30625,
LINCS_LDP:LPC-1016,
NHCDR:ND30625,
Wikidata:Q54929407
CVCL_Y895 2026-08-29 04:53:53 0
ND31037
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND31037, RRID:CVCL_EY70 Homo sapiens (Human) PMID:22952635 Finite cell line Male Coriell ND31037 Coriell:ND31037,
NHCDR:ND31037,
Wikidata:Q54929452
CVCL_EY70 2026-08-29 04:53:54 0
ND31009
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_2Y35 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Male Coriell:ND31009,
NHCDR:ND31009,
Wikidata:Q54929450
CVCL_2Y35 2026-08-29 04:53:58 0
ND31008
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND31008, RRID:CVCL_2Y36 Homo sapiens (Human) PMID:22952635 Finite cell line Female NHCDR ND31008 Coriell:ND31008,
NHCDR:ND31008,
Wikidata:Q54929449
CVCL_2Y36 2026-08-29 04:53:54 0
ND31008
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND31008, RRID:CVCL_2Y36 Homo sapiens (Human) PMID:22952635 Finite cell line Female Coriell ND31008 Coriell:ND31008,
NHCDR:ND31008,
Wikidata:Q54929449
CVCL_2Y36 2026-08-29 04:53:54 0
ND31038
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY71 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Female Coriell:ND31038,
NHCDR:ND31038,
Wikidata:Q54929453
CVCL_EY71 2026-08-29 04:53:58 0
ND31846
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY76 Homo sapiens (Human) Donor information: At sampling donor was not affected with Huntington's disease but at risk for disease (HTT has CAG repeat length greater than or equal to 36). PMID:22952635 Finite cell line Female Coriell:ND31846,
NHCDR:ND31846,
Wikidata:Q54929518
CVCL_EY76 2026-08-29 04:54:00 0
ND31508
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND31508, RRID:CVCL_EY72 Homo sapiens (Human) Parkinson disease PMID:22952635 Finite cell line Male Coriell ND31508 BioSample:SAMN00805617,
Coriell:ND31508,
NHCDR:ND31508,
Wikidata:Q54929483
CVCL_EY72 2026-08-29 04:53:59 0
ND31551
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY73 Homo sapiens (Human) Huntington's disease PMID:22952635 Finite cell line Male Coriell:ND31551,
NHCDR:ND31551,
Wikidata:Q54929491
CVCL_EY73 2026-08-29 04:53:55 0
ND31630
 
Resource Report
Resource Website
Discontinued
Possibly Discontinued
RRID:CVCL_DD53 Homo sapiens (Human) Parkinson disease PMID:22952635
PMID:27191603
Finite cell line Male BioSample:SAMN00805625,
Coriell:ND31630,
NHCDR:ND31630,
Wikidata:Q54929499
CVCL_DD53 2026-08-29 04:53:59 0

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