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

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Pubmed ID/Title


Search Result (139 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
SKIP000194 PARK4-4 Human Fibroblast Skin Diseased familial parkinson's disease PARK2 -- -- Caucasian Retrovirus
parkinson's disease PARK2 G20 600116 -1 -- -- Caucasian Yes Establishment of induced pluripotent stem
SKIP000195 PARK4-14 Human Fibroblast Skin Diseased familial parkinson's disease PARK2 -- -- Caucasian Retrovirus
parkinson's disease PARK2 G20 600116 -1 -- -- Caucasian Yes Establishment of induced pluripotent stem
SKIP000202 PB1 Human iPS Cell Skin Diseased Parkinson disease 50-59 Male Asian Retrovirus
G20 600116 -1 50-59 Male Asian Yes Mitochondrial dysfunction associated with increased
SKIP000203 PB2 Human iPS Cell Skin Diseased Parkinson disease 50-59 Male Asian Retrovirus
G20 600116 -1 50-59 Male Asian Yes Mitochondrial dysfunction associated with increased
SKIP000204 PB18 Human iPS Cell Skin Diseased Parkinson disease 50-59 Male Asian Retrovirus
G20 600116 -1 50-59 Male Asian Yes Mitochondrial dysfunction associated with increased
SKIP000205 PB20 Human iPS Cell Skin Diseased Parkinson disease 50-59 Male Asian Retrovirus
G20 600116 -1 50-59 Male Asian Yes Mitochondrial dysfunction associated with increased
SKIP000206 PA9 Human iPS Cell Skin Diseased familial parkinson's disease PARK2 parkin 70-79 Female Asian Retrovirus
disease PARK2 G20 600116 71 70-79 Female Asian Yes parkin a homozygous deletion of parkin exons 2-4
SKIP000207 PA22 Human iPS Cell Skin Diseased familial parkinson's disease PARK2 parkin 70-79 Female Asian Retrovirus
disease PARK2 G20 600116 71 70-79 Female Asian Yes parkin a homozygous deletion of parkin exons 2-4
SKIP000265 HPS0264 Human iPS Cell Skin Diseased Parkinson disease 40-49 Male Asian Retrovirus
human basic FGF Parkinson disease G20 -1 40-49 Male Asian Yes cellips@brc.riken.jp Riken
SKIP000290 L1-1Mut Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
with LRRK2 G2019S mutation. -- -- Retrovirus OKSM Yes MEF Parkinson's disease G20 607060 -1
SKIP000291 C4 Human iPS Cell Skin Normal -- Female Unknown Retrovirus
#2. Isogenic parent line of C4+G2019S, Subclone of C4 with inserted G2019S mutation. -- Research
SKIP000292 L1-2Mut Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
with LRRK2 G2019S mutation. -- Research Grade Retrovirus OSK Yes MEF Parkinson's disease G20 607060
SKIP000293 L1-1GC2 Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
-1Mut (LRRK2 mutation) -- Research Grade Retrovirus OSKM -- G2019S - Wt correction ZFN Parkinson's
SKIP000294 C1-1 Human iPS Cell Skin Normal -- Female Unknown Lentivirus
mutation G2019S is the most common genetic cause of Parkinson's disease (PD). To better understand the link
SKIP000295 C4+G2019S Human iPS Cell Skin Normal -- Female Unknown Retrovirus
SKIP000295 C4+G2019S Human iPS Cell Normal Skin Established Cell Subclone of C4 (healthy control
SKIP000296 C2 Human iPS Cell Skin Normal -- Female Unknown --
/pubmed/23472874 23472874 10.1016/j.stem.2013.01.008 The LRRK2 mutation G2019S is the most common genetic
SKIP000297 L2-1Mut Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
with LRRK2 mutation Born in 1931 -- Research Grade Retrovirus OSKM Yes MEF Parkinson's disease G20 607060
SKIP000298 L2-2Mut Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
with LRRK2 mutation Born in 1931 -- Research Grade Retrovirus OSKM Yes MEF Parkinson's disease G20 607060
SKIP000299 L2-3Mut Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
with LRRK2 mutation Born in 1931 -- Research Grade Retrovirus OSKM Yes MEF Parkinson's disease G20 607060
SKIP000300 L2-1GC Human iPS Cell Skin Diseased Parkinson's disease LRRK2 -- Female Unknown Retrovirus
-1Mut (iPSC with LRRK2 mutation) -- Research Grade Retrovirus OSKM -- LRRK2 G2019S\WT correction ZFN