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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
GM04616
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04616, RRID:CVCL_V475 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:17668376
Finite cell line Female GM 4616, GM04616A Coriell GM04616 CLO:CLO_0018955,
Coriell:GM04616,
Wikidata:Q54838601
CVCL_V475 2026-07-25 04:33:00 3
GM04628
 
Resource Report
Resource Website
Coriell Cat# GM04628, RRID:CVCL_2T06 Homo sapiens (Human) Karyotypic information: 46,X,t(X;22)(q12;p11) (PubMed=10377420)., Population: Caucasian; Swiss. PMID:10377420 Finite cell line Female GM4628 Coriell GM04628 CLO:CLO_0018936,
Coriell:GM04628,
Wikidata:Q54838610
CVCL_2T06 2026-07-25 04:33:00 0
GM04663
 
Resource Report
Resource Website
RRID:CVCL_7415 Homo sapiens (Human) Familial dysautonomia Population: Caucasian. PMID:29762696
PMID:30905397
Finite cell line Female CLO:CLO_0018968,
Coriell:GM04663,
GEO:GSM3592407,
GEO:GSM3592413,
Wikidata:Q54838620
CVCL_7415 2026-07-25 04:33:00 0
GM04627
 
Resource Report
Resource Website
RRID:CVCL_X311 Homo sapiens (Human) PMID:6661932 Finite cell line Male GM-4627, GM 4627 CLO:CLO_0018935,
Coriell:GM04627,
Wikidata:Q54838609
CVCL_X311 2026-07-25 04:33:00 0
GM04723
 
Resource Report
Resource Website
Coriell Cat# GM04723, RRID:CVCL_Y871 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female Coriell GM04723 CLO:CLO_0019072,
Coriell:GM04723,
Wikidata:Q54838655
CVCL_Y871 2026-07-25 04:33:01 0
GM04734
 
Resource Report
Resource Website
RRID:CVCL_1I28 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04734A CLO:CLO_0019069,
Coriell:GM04734,
Wikidata:Q54838661
CVCL_1I28 2026-07-25 04:33:01 0
GM04610
 
Resource Report
Resource Website
Coriell Cat# GM04610, RRID:CVCL_X309 Homo sapiens (Human) Trisomy 8 Karyotypic information: 47,XX,+8 [75]; 46,XX,+8,dic(14;21)(14qter->14p13::21p13->21qter) [25] (Coriell=GM04610). PMID:6661932 Finite cell line Female GM 4610 Coriell GM04610 CLO:CLO_0018902,
Coriell:GM04610,
Wikidata:Q54838597
CVCL_X309 2026-07-25 04:33:00 0
GM04718
 
Resource Report
Resource Website
RRID:CVCL_V569 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04718A CLO:CLO_0019022,
Coriell:GM04718,
Wikidata:Q54838650
CVCL_V569 2026-07-25 04:33:01 0
GM04608
 
Resource Report
Resource Website
Coriell Cat# GM04608, RRID:CVCL_Y797 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Female Coriell GM04608 CLO:CLO_0018912,
Coriell:GM04608,
Wikidata:Q54838596
CVCL_Y797 2026-07-25 04:32:59 0
GM04708
 
Resource Report
Resource Website
Coriell Cat# GM04708, RRID:CVCL_1I26 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04708A Coriell GM04708 CLO:CLO_0019025,
Coriell:GM04708,
Wikidata:Q54838642
CVCL_1I26 2026-07-25 04:33:00 0
GM04614
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_V474 Homo sapiens (Human) Down syndrome PMID:6661932 Finite cell line Female GM 4614 CLO:CLO_0018905,
Coriell:GM04614,
Wikidata:Q54838600
CVCL_V474 2026-07-25 04:33:00 0
GM04720
 
Resource Report
Resource Website
Coriell Cat# GM04720, RRID:CVCL_0I33 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04720A Coriell GM04720 CLO:CLO_0019077,
Coriell:GM04720,
Wikidata:Q54838652
CVCL_0I33 2026-07-25 04:33:01 0
GM04681
 
Resource Report
Resource Website
Coriell Cat# GM04681, RRID:CVCL_AT05 Homo sapiens (Human) Multiple sulfatase deficiency disease Population: Caucasian. PMID:6132606 Finite cell line Male GM 4681 Coriell GM04681 CLO:CLO_0019037,
Coriell:GM04681,
Wikidata:Q54838627
CVCL_AT05 2026-07-25 04:33:00 0
GM04709
 
Resource Report
Resource Website
Coriell Cat# GM04709, RRID:CVCL_Y863 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female Coriell GM04709 CLO:CLO_0019026,
Coriell:GM04709,
Wikidata:Q54838643
CVCL_Y863 2026-07-25 04:33:01 0
GM04674
 
Resource Report
Resource Website
RRID:CVCL_9R22 Homo sapiens (Human) Population: Caucasian. PMID:19127062 Transformed cell line Female GM04674A CLO:CLO_0019012,
Coriell:GM04674,
Wikidata:Q54838626
CVCL_9R22 2026-07-25 04:33:00 0
GM04715
 
Resource Report
Resource Website
Coriell Cat# GM04715, RRID:CVCL_Y865 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male Coriell GM04715 CLO:CLO_0019019,
Coriell:GM04715,
Wikidata:Q54838646
CVCL_Y865 2026-07-25 04:33:01 0
GM04688
 
Resource Report
Resource Website
RRID:CVCL_Y862 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04688A CLO:CLO_0019035,
Coriell:GM04688,
Wikidata:Q54838630
CVCL_Y862 2026-07-25 04:33:00 0
GM04716
 
Resource Report
Resource Website
RRID:CVCL_Y866 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04716A CLO:CLO_0019020,
Coriell:GM04716,
Wikidata:Q54838647
CVCL_Y866 2026-07-25 04:33:01 0
GM04726
 
Resource Report
Resource Website
RRID:CVCL_HJ75 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female Coriell:GM04726,
Wikidata:Q54838657
CVCL_HJ75 2026-07-25 04:33:01 0
GM04726
 
Resource Report
Resource Website
Coriell Cat# GM04726, RRID:CVCL_HJ75 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female Coriell GM04726 Coriell:GM04726,
Wikidata:Q54838657
CVCL_HJ75 2026-07-25 04:33:01 0

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