|
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 |