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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
ND36091
 
Resource Report
Resource Website
Discontinued
Discontinued
Coriell Cat# ND36091, RRID:CVCL_EZ15 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell ND36091 Coriell:ND36091,
NHCDR:ND36091,
Wikidata:Q54929931
CVCL_EZ15 2026-08-29 04:54:07 0
ND35976
 
Resource Report
Resource Website
1+ mentions
Discontinued
Coriell Cat# ND35976, RRID:CVCL_EZ14 Homo sapiens (Human) Parkinson disease Population: Caucasian. PMID:22952635 Finite cell line Male Coriell ND35976 Coriell:ND35976,
NHCDR:ND35976,
Wikidata:Q54929919
CVCL_EZ14 2026-08-29 04:54:07 1
ND35976
 
Resource Report
Resource Website
1+ mentions
Discontinued
RRID:CVCL_EZ14 Homo sapiens (Human) Parkinson disease Population: Caucasian. PMID:22952635 Finite cell line Male Coriell:ND35976,
NHCDR:ND35976,
Wikidata:Q54929919
CVCL_EZ14 2026-08-29 04:54:14 1
ND36997
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y808 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Induced pluripotent stem cell Female ND36997*C, HD 21 Coriell:ND36997,
NHCDR:ND36997,
SKIP:SKIP001087,
SKIP:SKIP004699,
Wikidata:Q54930006
cvcl_w557 CVCL_Y808 2026-08-29 04:54:09 0
ND37132
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND37132, RRID:CVCL_EZ17 Homo sapiens (Human) Parkinson disease Population: Caucasian. PMID:22952635 Finite cell line Male Coriell ND37132 Coriell:ND37132,
NHCDR:ND37132,
Wikidata:Q54930016
CVCL_EZ17 2026-08-29 04:54:17 0
ND36999
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_W577 Homo sapiens (Human) Huntington's disease Population: Caucasian. Induced pluripotent stem cell Male ND36999*F, HD 6 Coriell:ND36999,
NHCDR:ND36999,
SKIP:SKIP001089,
SKIP:SKIP004701,
Wikidata:Q54930008
cvcl_w576 CVCL_W577 2026-08-29 04:54:09 0
ND37132
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND37132, RRID:CVCL_EZ17 Homo sapiens (Human) Parkinson disease Population: Caucasian. PMID:22952635 Finite cell line Male NHCDR ND37132 Coriell:ND37132,
NHCDR:ND37132,
Wikidata:Q54930016
CVCL_EZ17 2026-08-29 04:54:09 0
ND36998
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y807 Homo sapiens (Human) Huntington's disease Population: Caucasian. Induced pluripotent stem cell Female ND36998*G, HD 29 Coriell:ND36998,
NHCDR:ND36998,
SKIP:SKIP001088,
SKIP:SKIP004700,
Wikidata:Q54930007
cvcl_f063 CVCL_Y807 2026-08-29 04:54:17 0
ND38549
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND38549, RRID:CVCL_Y818 Homo sapiens (Human) Induced pluripotent stem cell Female Coriell ND38549 Coriell:ND38549,
NHCDR:ND38549,
SKIP:SKIP001092,
SKIP:SKIP004707,
Wikidata:Q54930071
cvcl_y964 CVCL_Y818 2026-08-29 04:54:11 0
ND37609
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ20 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Male Coriell:ND37609,
NHCDR:ND37609,
Wikidata:Q54930041
CVCL_EZ20 2026-08-29 04:54:10 0
ND38020
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ24 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Male Coriell:ND38020,
NHCDR:ND38020,
Wikidata:Q54930052
CVCL_EZ24 2026-08-29 04:54:18 0
ND38477
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y812 Homo sapiens (Human) Parkinson disease 2, autosomal recessive juvenile PMID:27264186 Induced pluripotent stem cell Male Coriell:ND38477,
NHCDR:ND38477,
SKIP:SKIP001371,
SKIP:SKIP004702,
Wikidata:Q54930063
cvcl_y811 CVCL_Y812 2026-08-29 04:54:19 0
ND38549
 
Resource Report
Resource Website
Discontinued
NHCDR Cat# ND38549, RRID:CVCL_Y818 Homo sapiens (Human) Induced pluripotent stem cell Female NHCDR ND38549 Coriell:ND38549,
NHCDR:ND38549,
SKIP:SKIP001092,
SKIP:SKIP004707,
Wikidata:Q54930071
cvcl_y964 CVCL_Y818 2026-08-29 04:54:19 0
ND37609
 
Resource Report
Resource Website
Discontinued
Coriell Cat# ND37609, RRID:CVCL_EZ20 Homo sapiens (Human) Parkinson disease Population: Caucasian. Finite cell line Male Coriell ND37609 Coriell:ND37609,
NHCDR:ND37609,
Wikidata:Q54930041
CVCL_EZ20 2026-08-29 04:54:10 0
ND38552
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_Y820 Homo sapiens (Human) Huntington's disease Induced pluripotent stem cell Female Coriell:ND38552,
NHCDR:ND38552,
SKIP:SKIP001094,
SKIP:SKIP004709,
Wikidata:Q54930073
cvcl_y861 CVCL_Y820 2026-08-29 04:54:11 0
ND38554
 
Resource Report
Resource Website
1+ mentions
Discontinued
Coriell Cat# ND38554, RRID:CVCL_Y821 Homo sapiens (Human) Induced pluripotent stem cell Female Coriell ND38554 Coriell:ND38554,
NHCDR:ND38554,
SKIP:SKIP001364,
SKIP:SKIP004710,
Wikidata:Q54930074
cvcl_y882 CVCL_Y821 2026-08-29 04:54:11 1
ND37180
 
Resource Report
Resource Website
Discontinued
Discontinued
RRID:CVCL_EZ18 Homo sapiens (Human) Parkinson disease Population: Caucasian. PMID:22952635 Finite cell line Male Coriell:ND37180,
NHCDR:ND37180,
Wikidata:Q54930026
CVCL_EZ18 2026-08-29 04:54:09 0
ND38136
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ25 Homo sapiens (Human) Parkinson disease 8, autosomal dominant Population: Caucasian. Finite cell line Female Coriell:ND38136,
NHCDR:ND38136,
Wikidata:Q54930053
CVCL_EZ25 2026-08-29 04:54:18 0
ND38262
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_EZ26 Homo sapiens (Human) Parkinson disease 8, autosomal dominant Population: Caucasian. Finite cell line Male Coriell:ND38262,
NHCDR:ND38262,
Wikidata:Q54930060
CVCL_EZ26 2026-08-29 04:54:10 0
ND38530
 
Resource Report
Resource Website
1+ mentions
Discontinued
Coriell Cat# ND38530, RRID:CVCL_EZ28 Homo sapiens (Human) Population: Caucasian. Finite cell line Male Coriell ND38530 Coriell:ND38530,
NHCDR:ND38530,
Wikidata:Q54930065
CVCL_EZ28 2026-08-29 04:54:10 1

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