Type Race
Original Tissue Vector
Disease Status Feeder
Age Grade
Sex Database
ICD10

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Pubmed ID/Title


Search Result (6 records)

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Accession Cell Line Name Species Type Original Tissue Disease
Status
Disease Name Mutated Gene Age Sex Race Vector Database
Summary
SKIP000007 iPS-TIG114-4f1 Human iPS Cell Skin Normal 30-39 Male Asian Retrovirus
SKIP000007 iPS-TIG114-4f1 JCRB1437 Human iPS Cell Normal Skin Established Cell Human iPS cell line
SKIP000823 418C-1 Human iPS Cell Skin Normal 30-39 Male Asian : Japanese Plasmid
fibloblast(JCRB TIG114). human ES-like -- Plasmid Episomal vector pCXLE, Oct3/4, Sox2, Klf4, L-Myc, Lin28
SKIP001135 iPS-TIG114-4f1 Human iPS Cell Skin Normal 30-39 Male Asian Retrovirus
SKIP001135 iPS-TIG114-4f1 JCRB1437.01 Human iPS Cell Normal Skin Established Cell Human iPS cell
SKIP003039 iPS-SPG5-Y275X Human iPS Cell Skin fibroblast Diseased hereditary spastic paraplegia 40-49 Female Unknown episomal plasmid
-MYC, hLIN28 -- hereditary spastic paraplegia G114 270800 47 40-49 Female Unknown Yes
SKIP003112 PG1-iPSC_HGPS Human iPS Cell Skin Diseased Hutchinson-Gillford progeria syndrome (HGPS) 10-19 Male African-American Retrovirus
. Parent Fibroblast : AG11498 Mother Fibroblast : AG03512 human ES-like Research Grade Retrovirus OCT4
SKIP003114 N1-iPSC_HGPS Human iPS Cell Skin Gene carrier Hutchinson-Gillford progeria syndrome (HGPS) 40-49 Female Caucasian Retrovirus
of HGPS patient. Parent Fibroblast : AG03512 Patient's Fibroblast : AG11498 human ES-like Research Grade