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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
ND40600
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UF63 Homo sapiens (Human) Parkinson disease PMID:27264186 Induced pluripotent stem cell Coriell:ND40600,
Wikidata:Q98127489
CVCL_UF63 2026-07-25 04:57:02 0
ND40061
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ41 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Male Coriell:ND40061,
NHCDR:ND40061,
Wikidata:Q54930144
CVCL_EZ41 2026-07-25 04:57:01 0
ND40067
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ45 Homo sapiens (Human) Parkinson disease 2, autosomal recessive juvenile Population: Caucasian; Polish. Finite cell line Female Coriell:ND40067,
NHCDR:ND40067,
Wikidata:Q54930148
CVCL_EZ45 2026-07-25 04:57:01 0
ND40068
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EY29 Homo sapiens (Human) Parkinson disease 6, early onset Population: Caucasian; Polish. Finite cell line Female Coriell:ND40068,
NHCDR:ND40068,
Wikidata:Q54930149
CVCL_EY29 2026-07-25 04:57:01 0
ND39896
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND39896, RRID:CVCL_Y828 Homo sapiens (Human) Parkinson disease Population: Caucasian. PMID:27264186 Induced pluripotent stem cell Male ND39896*C NHCDR ND39896 Coriell:ND39896,
NHCDR:ND39896,
SKIP:SKIP001377,
SKIP:SKIP004716,
Wikidata:Q54930133
CVCL_Y828 2026-07-25 04:57:01 0
ND39955
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND39955, RRID:CVCL_EZ38 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Male NHCDR ND39955 Coriell:ND39955,
NHCDR:ND39955,
Wikidata:Q54930134
CVCL_EZ38 2026-07-25 04:57:01 0
ND40077
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ53 Homo sapiens (Human) Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia Population: Caucasian. Finite cell line Female Coriell:ND40077,
NHCDR:ND40077,
Wikidata:Q54930158
CVCL_EZ53 2026-07-25 04:57:02 0
ND40599
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UF62 Homo sapiens (Human) Parkinson disease 8, autosomal dominant PMID:27264186 Induced pluripotent stem cell Male Coriell:ND40599,
Wikidata:Q98127487
CVCL_UF62 2026-07-25 04:57:02 0
ND40064
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ42 Homo sapiens (Human) Friedreich ataxia Population: Caucasian. Finite cell line Male Coriell:ND40064,
NHCDR:ND40064,
Wikidata:Q54930145
CVCL_EZ42 2026-07-25 04:57:01 0
ND39957
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND39957, RRID:CVCL_EZ39 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Female NHCDR ND39957 Coriell:ND39957,
NHCDR:ND39957,
Wikidata:Q54930135
CVCL_EZ39 2026-07-25 04:57:01 0
ND40069
 
Resource Report
Resource Website
Discontinued
Discontinued
RRID:CVCL_EZ46 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Female Coriell:ND40069,
NHCDR:ND40069,
Wikidata:Q54930150
CVCL_EZ46 2026-07-25 04:57:02 0
ND40019
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y830 Homo sapiens (Human) Parkinson disease 8, autosomal dominant Donor information: At sampling donor was not affected with Parkinson disease but at risk for disease. PMID:26651604 Induced pluripotent stem cell Male ND40019*C Coriell:ND40019,
NHCDR:ND40019,
SKIP:SKIP001373,
SKIP:SKIP004718,
Wikidata:Q54930140
CVCL_Y830 2026-07-25 04:57:01 0
ND40082
 
Resource Report
Resource Website
Discontinued
Discontinued
RRID:CVCL_EZ58 Homo sapiens (Human) Frontotemporal dementia Population: Caucasian. Finite cell line Female Coriell:ND40082,
NHCDR:ND40082,
Wikidata:Q54930163
CVCL_EZ58 2026-07-25 04:57:02 0
ND40074
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ50 Homo sapiens (Human) Frontotemporal dementia-1 Population: Caucasian. Finite cell line Male Coriell:ND40074,
NHCDR:ND40074,
Wikidata:Q54930155
CVCL_EZ50 2026-07-25 04:57:02 0
ND42229
 
Resource Report
Resource Website
Discontinued
Discontinued
RRID:CVCL_Y846 Homo sapiens (Human) Huntington's disease Induced pluripotent stem cell Female Coriell:ND42229,
NHCDR:ND42229,
Wikidata:Q54930214
cvcl_8519 CVCL_Y846 2026-07-25 04:57:03 0
ND41180
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UF69 Homo sapiens (Human) Parkinson disease 8, autosomal dominant PMID:27264186 Induced pluripotent stem cell Male Coriell:ND41180,
Wikidata:Q98127497
CVCL_UF69 2026-07-25 04:57:03 0
ND41864
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_1N97 Homo sapiens (Human) PMID:23063362 Induced pluripotent stem cell Male 2L16, Control #16 Coriell:ND41864,
NHCDR:ND41864,
Wikidata:Q54584597
CVCL_1N97 2026-07-25 04:57:03 0
ND41869
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND41869, RRID:CVCL_Y840 Homo sapiens (Human) Frontotemporal dementia Induced pluripotent stem cell Male ND41869*C NHCDR ND41869 Coriell:ND41869,
NHCDR:ND41869,
SKIP:SKIP001564,
SKIP:SKIP004726,
Wikidata:Q54930206
CVCL_Y840 2026-07-25 04:57:03 0
ND41864
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND41864, RRID:CVCL_1N97 Homo sapiens (Human) PMID:23063362 Induced pluripotent stem cell Male 2L16, Control #16 Coriell ND41864 Coriell:ND41864,
NHCDR:ND41864,
Wikidata:Q54584597
CVCL_1N97 2026-07-25 04:57:03 0
ND41657
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y835 Homo sapiens (Human) Huntington's disease Induced pluripotent stem cell Female Coriell:ND41657,
NHCDR:ND41657,
SKIP:SKIP001562,
SKIP:SKIP004722,
Wikidata:Q54930200
cvcl_y897 CVCL_Y835 2026-07-25 04:57:03 0

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