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Search Result (3 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
SKIP003113 PG2-iPSC_HGPS Human iPS Cell Skin Diseased Hutchinson-Gillford progeria syndrome (HGPS) 0-9 Male Caucasian Retrovirus
. Parent cell : AG06297 Mother Fibroblast : AG06299 human ES-like Research Grade Retrovirus OCT4, SOX2
SKIP003115 N2-iPSC_HGPS Human iPS Cell Skin Gene carrier Hutchinson-Gillford progeria syndrome (HGPS) 30-39 Female Caucasian Retrovirus
of HGPS patient. Parent Fibroblast : AG06299 Patient's Fibroblast : AG06297 human ES-like Research Grade
SKIP005462 HGPS-iPS_lamin A/C mutated-iPSCs Human iPS Cell Skin fibroblasts Diseased Hutchinson-Gillford progeria syndrome (HGPS) 0-9 Male Caucasian Retrovirus
patient-derived human iPS cells. Parent cell : AG06917 3YR(At Sampling) Mother Fibroblast : AG06299