BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 11784370)

  • 1. A putative polymorphic Val44Ala variation in the synphilin-1 gene is undetectable in Japanese sporadic Parkinson's disease patients.
    Satoh JI; Kuroda Y
    Eur J Neurol; 2002 Jan; 9(1):15-8. PubMed ID: 11784370
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic association study of synphilin-1 in idiopathic Parkinson's disease.
    Myhre R; Klungland H; Farrer MJ; Aasly JO
    BMC Med Genet; 2008 Mar; 9():19. PubMed ID: 18366718
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.
    Marx FP; Holzmann C; Strauss KM; Li L; Eberhardt O; Gerhardt E; Cookson MR; Hernandez D; Farrer MJ; Kachergus J; Engelender S; Ross CA; Berger K; Schöls L; Schulz JB; Riess O; Krüger R
    Hum Mol Genet; 2003 Jun; 12(11):1223-31. PubMed ID: 12761037
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Organization of the human synphilin-1 gene, a candidate for Parkinson's disease.
    Engelender S; Wanner T; Kleiderlein JJ; Wakabayashi K; Tsuji S; Takahashi H; Ashworth R; Margolis RL; Ross CA
    Mamm Genome; 2000 Sep; 11(9):763-6. PubMed ID: 10967135
    [TBL] [Abstract][Full Text] [Related]  

  • 5. No pathogenic mutations in the synphilin-1 gene in Parkinson's disease.
    Bandopadhyay R; de Silva R; Khan N; Graham E; Vaughan J; Engelender S; Ross C; Morris H; Morris C; Wood NW; Daniel S; Lees A
    Neurosci Lett; 2001 Jul; 307(2):125-7. PubMed ID: 11427316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
    Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
    Mov Disord; 2006 Dec; 21(12):2157-64. PubMed ID: 17078049
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The role of synphilin-1 in synaptic function and protein degradation.
    Krüger R
    Cell Tissue Res; 2004 Oct; 318(1):195-9. PubMed ID: 15322916
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population.
    Satoh J; Kuroda Y
    J Neurol Sci; 2001 Aug; 189(1-2):113-7. PubMed ID: 11535241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synphilin-1 is present in Lewy bodies in Parkinson's disease.
    Wakabayashi K; Engelender S; Yoshimoto M; Tsuji S; Ross CA; Takahashi H
    Ann Neurol; 2000 Apr; 47(4):521-3. PubMed ID: 10762166
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synphilin-1A: an aggregation-prone isoform of synphilin-1 that causes neuronal death and is present in aggregates from alpha-synucleinopathy patients.
    Eyal A; Szargel R; Avraham E; Liani E; Haskin J; Rott R; Engelender S
    Proc Natl Acad Sci U S A; 2006 Apr; 103(15):5917-22. PubMed ID: 16595633
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interaction of alpha-synuclein and synphilin-1: effect of Parkinson's disease-associated mutations.
    Kawamata H; McLean PJ; Sharma N; Hyman BT
    J Neurochem; 2001 May; 77(3):929-34. PubMed ID: 11331421
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Parkin and synphilin-1 isoform expression changes in Lewy body diseases.
    Humbert J; Beyer K; Carrato C; Mate JL; Ferrer I; Ariza A
    Neurobiol Dis; 2007 Jun; 26(3):681-7. PubMed ID: 17467279
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease.
    Soehn AS; Franck T; Biskup S; Giaime E; Melle C; Rott R; Cebo D; Kalbacher H; Ott E; Pahnke J; Meitinger T; Krüger R; Gasser T; Berg D; von Eggeling F; Engelender S; da Costa CA; Riess O
    Neurogenetics; 2010 May; 11(2):203-15. PubMed ID: 19730898
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation screening in exons 3 and 4 of alpha-synuclein in sporadic Parkinson's and sporadic and familial dementia with Lewy bodies cases.
    El-Agnaf OM; Curran MD; Wallace A; Middleton D; Murgatroyd C; Curtis A; Perry R; Jaros E
    Neuroreport; 1998 Dec; 9(17):3925-7. PubMed ID: 9875730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered α-synuclein, parkin, and synphilin isoform levels in multiple system atrophy brains.
    Brudek T; Winge K; Rasmussen NB; Bahl JM; Tanassi J; Agander TK; Hyde TM; Pakkenberg B
    J Neurochem; 2016 Jan; 136(1):172-85. PubMed ID: 26465922
    [TBL] [Abstract][Full Text] [Related]  

  • 16. alpha-Synuclein is colocalized with 14-3-3 and synphilin-1 in A53T transgenic mice.
    Shirakashi Y; Kawamoto Y; Tomimoto H; Takahashi R; Ihara M
    Acta Neuropathol; 2006 Dec; 112(6):681-9. PubMed ID: 16957925
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease.
    Liani E; Eyal A; Avraham E; Shemer R; Szargel R; Berg D; Bornemann A; Riess O; Ross CA; Rott R; Engelender S
    Proc Natl Acad Sci U S A; 2004 Apr; 101(15):5500-5. PubMed ID: 15064394
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic analysis of synphilin-1 in familial Parkinson's disease.
    Farrer M; Destée A; Levecque C; Singleton A; Engelender S; Becquet E; Mouroux V; Richard F; Defebvre L; Crook R; Hernandez D; Ross CA; Hardy J; Amouyel P; Chartier-Harlin MC
    Neurobiol Dis; 2001 Apr; 8(2):317-23. PubMed ID: 11300726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of the coding and the 5' flanking regions of the alpha-synuclein gene in patients with Parkinson's disease.
    Pastor P; Muñoz E; Ezquerra M; Obach V; Martí MJ; Valldeoriola F; Tolosa E; Oliva R
    Mov Disord; 2001 Nov; 16(6):1115-9. PubMed ID: 11748744
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aggregate formation and toxicity by wild-type and R621C synphilin-1 in the nigrostriatal system of mice using adenoviral vectors.
    Krenz A; Falkenburger BH; Gerhardt E; Drinkut A; Schulz JB
    J Neurochem; 2009 Jan; 108(1):139-46. PubMed ID: 19094062
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.