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Search results 401 to 500 out of 1772 for Parkinson

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Type Details Score
Publication
34465795 | J:313885
First Author: Li Y
Year: 2021
Journal: Sci Rep
Title: Quantitative X-ray tomographic analysis reveals calcium precipitation in cataractogenesis.
Volume: 11
Issue: 1
Pages: 17401
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Publication
33347679 | J:309563
First Author: Rafipay A
Year: 2021
Journal: Dev Dyn
Title: Knockdown of slit signaling during limb development leads to a reduction in humerus length.
Volume: 250
Issue: 9
Pages: 1340-1357
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Publication
19332122 | J:150474
First Author: Turner BJ
Year: 2009
Journal: Neurobiol Dis
Title: Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.
Volume: 34
Issue: 3
Pages: 511-7
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Publication
31509576 | J:279439
First Author: Rahimi-Balaei M
Year: 2019
Journal: PLoS One
Title: Loss of prostatic acid phosphatase and α-synuclein cause motor circuit degeneration without altering cerebellar patterning.
Volume: 14
Issue: 9
Pages: e0222234
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Publication
1286213 | J:26641
First Author: Baumrind NL
Year: 1992
Journal: Dev Dyn
Title: EMA: a developmentally regulated cell-surface glycoprotein of CNS neurons that is concentrated at the leading edge of growth cones.
Volume: 194
Issue: 4
Pages: 311-25
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Publication
8624249 | J:33777
First Author: Forkert PG
Year: 1996
Journal: Am J Respir Cell Mol Biol
Title: Diminished expression of CYP1A1 in urethane-induced lung tumors in strain A/J mice: analysis by in situ hybridization and immunohistochemical methods.
Volume: 14
Issue: 5
Pages: 444-53
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Publication
15051735 | J:89272
First Author: Halet G
Year: 2004
Journal: J Cell Biol
Title: Conventional PKCs regulate the temporal pattern of Ca2+ oscillations at fertilization in mouse eggs.
Volume: 164
Issue: 7
Pages: 1033-44
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Publication
32457148 | J:289322
First Author: Chen B
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: Forward genetic analysis using OCT screening identifies Sfxn3 mutations leading to progressive outer retinal degeneration in mice.
Volume: 117
Issue: 23
Pages: 12931-12942
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Protein Coding Gene
MGI:1355296 | Prkn
Type: protein_coding_gene
Organism: mouse, laboratory
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Publication
23786406 | J:200778
First Author: Goldstein DS
Year: 2013
Journal: J Neurochem
Title: Determinants of buildup of the toxic dopamine metabolite DOPAL in Parkinson's disease.
Volume: 126
Issue: 5
Pages: 591-603
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Publication
19553450 | J:150414
First Author: Taylor TN
Year: 2009
Journal: J Neurosci
Title: Nonmotor symptoms of Parkinson's disease revealed in an animal model with reduced monoamine storage capacity.
Volume: 29
Issue: 25
Pages: 8103-13
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Publication
24025942 | J:214496
 
First Author: Taylor TN
Year: 2014
Journal: Neuropharmacology
Title: Reduced vesicular storage of catecholamines causes progressive degeneration in the locus ceruleus.
Volume: 76 Pt A
Pages: 97-105
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Publication
17100850 | J:117157
First Author: Colebrooke RE
Year: 2006
Journal: Eur J Neurosci
Title: Age-related decline in striatal dopamine content and motor performance occurs in the absence of nigral cell loss in a genetic mouse model of Parkinson's disease.
Volume: 24
Issue: 9
Pages: 2622-30
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Publication
17652604 | J:123245
First Author: Caudle WM
Year: 2007
Journal: J Neurosci
Title: Reduced vesicular storage of dopamine causes progressive nigrostriatal neurodegeneration.
Volume: 27
Issue: 30
Pages: 8138-48
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Publication
12716422 | J:83388
First Author: Patel J
Year: 2003
Journal: J Neurochem
Title: Presynaptic control of striatal dopamine neurotransmission in adult vesicular monoamine transporter 2 (VMAT2) mutant mice.
Volume: 85
Issue: 4
Pages: 898-910
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Publication
26428905 | J:229557
 
First Author: Alter SP
Year: 2016
Journal: Exp Neurol
Title: Reduced vesicular monoamine transport disrupts serotonin signaling but does not cause serotonergic degeneration.
Volume: 275 Pt 1
Pages: 17-24
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Publication
27287315 | J:254134
First Author: Lohr KM
Year: 2016
Journal: Toxicol Sci
Title: Vesicular Monoamine Transporter 2 (VMAT2) Level Regulates MPTP Vulnerability and Clearance of Excess Dopamine in Mouse Striatal Terminals.
Volume: 153
Issue: 1
Pages: 79-88
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Publication
22768297 | J:189524
First Author: Dean ED
Year: 2012
Journal: PLoS One
Title: 25-Hydroxyvitamin D depletion does not exacerbate MPTP-induced dopamine neuron damage in mice.
Volume: 7
Issue: 7
Pages: e39227
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Publication
27917116 | J:290172
 
First Author: Baumann A
Year: 2016
Journal: Front Hum Neurosci
Title: Preliminary Evidence of Apathetic-Like Behavior in Aged Vesicular Monoamine Transporter 2 Deficient Mice.
Volume: 10
Pages: 587
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Publication
31898856 | J:322114
First Author: Branco RC
Year: 2020
Journal: Genes Brain Behav
Title: Vesicular monoamine transporter 2 mediates fear behavior in mice.
Volume: 19
Issue: 5
Pages: e12634
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Genotype
Genotype
Symbol: Slc18a2/Slc18a2
Background: involves: 129P2/OlaHsd * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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DO Term
DOID:0060369 | Parkinson's disease 6
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DO Term
DOID:0060368 | Parkinson's disease 2
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DO Term
DOID:0060556 | Kufor-Rakeb syndrome
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DO Term
DOID:0060372 | Parkinson's disease 15
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DO Term
DOID:0111250 | Parkinson's disease 3
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Publication
31758049 | J:287103
First Author: Kilpeläinen T
Year: 2019
Journal: Sci Rep
Title: Behavioural and dopaminergic changes in double mutated human A30P*A53T alpha-synuclein transgenic mouse model of Parkinson´s disease.
Volume: 9
Issue: 1
Pages: 17382
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Gene
116442 | RAB39B
Type: gene
Organism: human
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Allele
Park7<tm1Tmd> | MGI:3514165
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1, Ted Dawson
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Park7<tm1Cai> | MGI:3522482
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1, Hubaibin Cai
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Park7<tm1Dsp> | MGI:3576227
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1, David S Park
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Park7<tm1Shn> | MGI:3579140
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1, Jie Shen
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Park7<tm1Xz> | MGI:3586448
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1, Xiaoxi Zhuang
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Park7<Gt(XE726)Byg> | MGI:3587946
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap XE726, BayGenomics
Allele Type: Gene trapped
Attribute String: Null/knockout, Reporter
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Allele
Park7<Gt(AV0722)Wtsi> | MGI:3853092
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap AV0722, Wellcome Trust Sanger Institute
Allele Type: Gene trapped
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Allele
Park7<Gt(PST12175)Mfgc> | MGI:3862169
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap PST12175, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
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Allele
Park7<Gt(RHA035)Byg> | MGI:3867531
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap RHA035, BayGenomics
Allele Type: Gene trapped
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Allele
Park7<Gt(DC0485)Wtsi> | MGI:3871123
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap DC0485, Wellcome Trust Sanger Institute
Allele Type: Gene trapped
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Allele
Park7<Gt(CSH784)Byg> | MGI:3879022
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap CSH784, BayGenomics
Allele Type: Gene trapped
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Allele
Park7<Gt(E198C04)Wrst> | MGI:3917795
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap E198C04, German Gene Trap Consortium
Allele Type: Gene trapped
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Allele
Park7<Gt(E199B04)Wrst> | MGI:3918187
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap E199B04, German Gene Trap Consortium
Allele Type: Gene trapped
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Allele
Park7<Gt(PST1223)Mfgc> | MGI:4122385
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap PST1223, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
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Allele
Park7<Gt(A037A06)Wrst> | MGI:4122677
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap A037A06, German Gene Trap Consortium
Allele Type: Gene trapped
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Allele
Park7<Gt(OST54527)Lex> | MGI:4163564
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST54527, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST87709)Lex> | MGI:4178923
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST87709, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST102541)Lex> | MGI:4184127
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST102541, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST118339)Lex> | MGI:4191169
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST118339, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST131455)Lex> | MGI:4197861
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST131455, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST158621)Lex> | MGI:4209401
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST158621, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST171287)Lex> | MGI:4213935
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST171287, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST172246)Lex> | MGI:4214402
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST172246, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST177257)Lex> | MGI:4216897
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST177257, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST186477)Lex> | MGI:4221131
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST186477, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST193742)Lex> | MGI:4225233
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST193742, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST194226)Lex> | MGI:4225522
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST194226, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST211320)Lex> | MGI:4234279
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST211320, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST214299)Lex> | MGI:4235539
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST214299, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST216332)Lex> | MGI:4236532
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST216332, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST236300)Lex> | MGI:4244810
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST236300, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST249505)Lex> | MGI:4250633
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST249505, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST252079)Lex> | MGI:4251919
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST252079, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST260594)Lex> | MGI:4255008
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST260594, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST264822)Lex> | MGI:4256620
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST264822, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST271095)Lex> | MGI:4258494
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST271095, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST285090)Lex> | MGI:4264498
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST285090, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST285898)Lex> | MGI:4264883
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST285898, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST286190)Lex> | MGI:4265044
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST286190, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST289857)Lex> | MGI:4266723
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST289857, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST323056)Lex> | MGI:4280314
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST323056, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST325065)Lex> | MGI:4281008
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST325065, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST325715)Lex> | MGI:4281194
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST325715, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST329098)Lex> | MGI:4282372
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST329098, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST333886)Lex> | MGI:4283844
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST333886, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST334127)Lex> | MGI:4283960
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST334127, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST350833)Lex> | MGI:4290132
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST350833, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST353720)Lex> | MGI:4291359
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST353720, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST376213)Lex> | MGI:4298997
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST376213, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST379264)Lex> | MGI:4300277
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST379264, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST412704)Lex> | MGI:4309070
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST412704, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST437108)Lex> | MGI:4316831
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST437108, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST450567)Lex> | MGI:4321630
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST450567, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(OST465110)Lex> | MGI:4326312
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap OST465110, Lexicon Genetics
Allele Type: Gene trapped
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Allele
Park7<Gt(F063A04)Wrst> | MGI:4333349
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap F063A04, German Gene Trap Consortium
Allele Type: Gene trapped
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Allele
Park7<Gt(PST6428)Mfgc> | MGI:4342668
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap PST6428, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
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Allele
Park7<Gt(Q001D04)Wrst> | MGI:4348423
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap Q001D04, German Gene Trap Consortium
Allele Type: Gene trapped
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Allele
Park7<Gt(EUCE0051b11)Hmgu> | MGI:4383093
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap EUCE0051b11, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
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Allele
Park7<tm1(NCOM)Mfgc> | MGI:4880456
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1, Mammalian Functional Genomics Centre
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
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Allele
Park7<Gt(S23-1H1)Sor> | MGI:4973583
 
Name: Parkinson disease (autosomal recessive, early onset) 7; gene trap S23-1H1, Philippe Soriano
Allele Type: Gene trapped
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Allele
Smg6<Tg(SMN1*delta5)1Pks> | MGI:5493450
Name: SMG6 nonsense mediated mRNA decay factor; transgene insertion 1, Nick Parkinson
Allele Type: Transgenic
Attribute String: Inserted expressed sequence
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Allele
Park7<em1(IMPC)H> | MGI:6336217
Name: Parkinson disease (autosomal recessive, early onset) 7; endonuclease-mediated mutation 1, Harwell
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Park7<em2(IMPC)H> | MGI:6336218
Name: Parkinson disease (autosomal recessive, early onset) 7; endonuclease-mediated mutation 2, Harwell
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Park7<em1Smoc> | MGI:6430689
Name: Parkinson disease (autosomal recessive, early onset) 7; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Park7<em17Gpt> | MGI:7303870
Name: Parkinson disease (autosomal recessive, early onset) 7; endonuclease-mediated mutation 17, GemPharmatech Co., Ltd
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Allele
Park7<em1Gpt> | MGI:7303871
Name: Parkinson disease (autosomal recessive, early onset) 7; endonuclease-mediated mutation 1, GemPharmatech Co., Ltd
Allele Type: Endonuclease-mediated
Attribute String: Conditional ready, No functional change
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Allele
Park7<tm1.1Xko> | MGI:7356317
Name: Parkinson disease (autosomal recessive, early onset) 7; targeted mutation 1.1, Xiaoni Kong
Allele Type: Targeted
Attribute String: Conditional ready
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Allele
Park7<em1Cya> | MGI:7585609
Name: Parkinson disease (autosomal recessive, early onset) 7; endonuclease-mediated mutation 1, Cyagen Biosciences
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Publication
24386432 | J:211120
First Author: Hennis MR
Year: 2013
Journal: PLoS One
Title: Behavioral and neurotransmitter abnormalities in mice deficient for Parkin, DJ-1 and superoxide dismutase.
Volume: 8
Issue: 12
Pages: e84894
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Publication
30908580 | J:273695
First Author: Chen B
Year: 2019
Journal: Invest Ophthalmol Vis Sci
Title: A Mouse Model of Retinal Recovery From Photo-Oxidative/Photo-Inflammatory Injury: Nrf2, SOD1, DJ-1, and Parkin Are Not Essential to Recovery.
Volume: 60
Issue: 4
Pages: 1165-1174
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Publication
22215708 | J:330095
First Author: Cuevas S
Year: 2012
Journal: Hypertension
Title: Role of renal DJ-1 in the pathogenesis of hypertension associated with increased reactive oxygen species production.
Volume: 59
Issue: 2
Pages: 446-52
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Publication
27975168 | J:330089
First Author: Tahir W
Year: 2018
Journal: Mol Neurobiol
Title: Molecular Alterations in the Cerebellum of Sporadic Creutzfeldt-Jakob Disease Subtypes with DJ-1 as a Key Regulator of Oxidative Stress.
Volume: 55
Issue: 1
Pages: 517-537
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