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95,747 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
GM01718
 
Resource Report
Resource Website
RRID:CVCL_9R63 Homo sapiens (Human) Neuraminidase deficiency PMID:9054950 Finite cell line Female GM-1718, GM01718A, GM1718A CLO:CLO_0030984,
BioSample:SAMN00807105,
Coriell:GM01718,
Wikidata:Q54837032
CVCL_9R63 2026-07-25 04:32:22 0
GM01736
 
Resource Report
Resource Website
Coriell Cat# GM01736, RRID:CVCL_1F09 Homo sapiens (Human) Xeroderma pigmentosum, complementation group C Population: Caucasian. Finite cell line Female GM-1736, GM1736 Coriell GM01736 CLO:CLO_0030994,
BioSample:SAMN00807123,
Coriell:GM01736,
Wikidata:Q54837044
CVCL_1F09 2026-07-25 04:32:22 0
GM01706
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01706, RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 Coriell GM01706 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-07-25 04:32:22 0
GM01742
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_CX27 Homo sapiens (Human) I-cell disease Finite cell line Female GM-1742 Coriell:GM01742,
Wikidata:Q54837054
CVCL_CX27 2026-07-25 04:32:25 0
GM01667
 
Resource Report
Resource Website
Coriell Cat# GM01667, RRID:CVCL_X082 Homo sapiens (Human) Karyotypic information: 46,XX,del(9)(qter>p22) (Coriell=GM01667)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Female GM-1667, GM 1667 Coriell GM01667 CLO:CLO_0030954,
BioSample:SAMN00807055,
Coriell:GM01667,
Wikidata:Q54836999
CVCL_X082 2026-07-25 04:32:21 0
GM01667
 
Resource Report
Resource Website
RRID:CVCL_X082 Homo sapiens (Human) Karyotypic information: 46,XX,del(9)(qter>p22) (Coriell=GM01667)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Female GM-1667, GM 1667 CLO:CLO_0030954,
BioSample:SAMN00807055,
Coriell:GM01667,
Wikidata:Q54836999
CVCL_X082 2026-07-25 04:32:23 0
GM01739
 
Resource Report
Resource Website
RRID:CVCL_0M02 Homo sapiens (Human) Mucopolysaccharidosis type IIIA Population: Caucasian. Finite cell line Female GM-1739 CLO:CLO_0030992,
BioSample:SAMN00807127,
Coriell:GM01739,
Wikidata:Q54837050
CVCL_0M02 2026-07-25 04:32:22 0
GM01706
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00237, RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 Coriell GM00237 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-07-25 04:32:22 0
GM01724
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01724, RRID:CVCL_X254 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1724 Coriell GM01724 Coriell:GM01724,
Wikidata:Q54837038
CVCL_X254 2026-07-25 04:32:22 0
GM01726
 
Resource Report
Resource Website
Coriell Cat# GM01726, RRID:CVCL_2Z71 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Transformed cell line Female GM-1726, GM01726A Coriell GM01726 CLO:CLO_0030982,
BioSample:SAMN00807117,
Coriell:GM01726,
Wikidata:Q54837040
CVCL_2Z71 2026-07-25 04:32:24 0
GM01730
 
Resource Report
Resource Website
Coriell Cat# GM01730, RRID:CVCL_1R61 Homo sapiens (Human) Karyotypic information: 46,XX,der(21)(21qter->21p11::Xq11->Xqter)mat (Coriell=GM01730)., Population: African American. Finite cell line Female GM-1730, GM01730C Coriell GM01730 CLO:CLO_0030997,
BioSample:SAMN00807121,
Coriell:GM01730,
Wikidata:Q54837042
CVCL_1R61 2026-07-25 04:32:22 0
GM01736
 
Resource Report
Resource Website
RRID:CVCL_1F09 Homo sapiens (Human) Xeroderma pigmentosum, complementation group C Population: Caucasian. Finite cell line Female GM-1736, GM1736 CLO:CLO_0030994,
BioSample:SAMN00807123,
Coriell:GM01736,
Wikidata:Q54837044
CVCL_1F09 2026-07-25 04:32:22 0
GM01744
 
Resource Report
Resource Website
RRID:CVCL_AD63 Homo sapiens (Human) Maple syrup urine disease Population: Caucasian. Finite cell line Female GM1744, GM-1744 CLO:CLO_0030991,
BioSample:SAMN00807135,
Coriell:GM01744,
Wikidata:Q54837057
CVCL_AD63 2026-07-25 04:32:25 0
GM01725
 
Resource Report
Resource Website
RRID:CVCL_2Z70 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Finite cell line Female GM-1725 CLO:CLO_0030981,
BioSample:SAMN00807115,
Coriell:GM01725,
Wikidata:Q54837039
CVCL_2Z70 2026-07-25 04:32:24 0
GM01661
 
Resource Report
Resource Website
RRID:CVCL_R905 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1661, GM1661 CLO:CLO_0030941,
BioSample:SAMN00807045,
Coriell:GM01661,
Wikidata:Q54836993
CVCL_R905 2026-07-25 04:32:23 0
GM01660
 
Resource Report
Resource Website
RRID:CVCL_V426 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1660 CLO:CLO_0030942,
BioSample:SAMN00807043,
Coriell:GM01660,
Wikidata:Q54836992
CVCL_V426 2026-07-25 04:32:21 0
GM01683
 
Resource Report
Resource Website
Coriell Cat# GM01683, RRID:CVCL_0Q03 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;10)(2qter->2p23::10q26->10qter;10pter->10q26::2p23->2pter) (Coriell=GM01683)., Population: Caucasian. Finite cell line Female GM-1683 Coriell GM01683 CLO:CLO_0030965,
BioSample:SAMN00807073,
Coriell:GM01683,
Wikidata:Q54837014
CVCL_0Q03 2026-07-25 04:32:21 0
GM01669
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB62 Homo sapiens (Human) Niemann-Pick disease, type B Finite cell line Female GM-1669 Coriell:GM01669,
Wikidata:Q54837000
CVCL_JB62 2026-07-25 04:32:21 0
GM01669
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01669, RRID:CVCL_JB62 Homo sapiens (Human) Niemann-Pick disease, type B Finite cell line Female GM-1669 Coriell GM01669 Coriell:GM01669,
Wikidata:Q54837000
CVCL_JB62 2026-07-25 04:32:23 0
GM01695
 
Resource Report
Resource Website
RRID:CVCL_V811 Homo sapiens (Human) Duchenne muscular dystrophy Karyotypic information: 46,X,t(X;11)(p21;q13) (PubMed=10377420)., Population: Caucasian. PMID:2498246
PMID:7438786
PMID:10377420
Finite cell line Female GM-1695, GM1695, GM01695A, GM1695A CLO:CLO_0030959,
BioSample:SAMN00807081,
Coriell:GM01695,
Wikidata:Q54837018
CVCL_V811 2026-07-25 04:32:23 0

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