These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

77 related articles for article (PubMed ID: 18300012)

  • 1. HD phenocopies--possible role of Saitohin gene.
    Janković N; Kecmanović M; Dimitrijević R; Keckarević Marković M; Dobricić V; Keckarević D; Savić Pavicević D; Romac S
    Int J Neurosci; 2008 Mar; 118(3):391-7. PubMed ID: 18300012
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular evolution and genetics of the Saitohin gene and tau haplotype in Alzheimer's disease and argyrophilic grain disease.
    Conrad C; Vianna C; Schultz C; Thal DR; Ghebremedhin E; Lenz J; Braak H; Davies P
    J Neurochem; 2004 Apr; 89(1):179-88. PubMed ID: 15030402
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Is the saitohin gene involved in neurodegenerative diseases?
    Verpillat P; Ricard S; Hannequin D; Dubois B; Bou J; Camuzat A; Pradier L; Frebourg T; Brice A; Clerget-Darpoux F; Deleuze JF; Campion D;
    Ann Neurol; 2002 Dec; 52(6):829-32. PubMed ID: 12447938
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease.
    Wang B; Zhou S; Yang Z; Xie YC; Wang J; Zhang P; Lv Z; Zheng C; Ma X
    J Neurol Sci; 2008 Jul; 270(1-2):148-51. PubMed ID: 18396294
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease.
    Conrad C; Vianna C; Freeman M; Davies P
    Proc Natl Acad Sci U S A; 2002 May; 99(11):7751-6. PubMed ID: 12032355
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin, and Jp-3 genes.
    Keckarević M; Savić D; Svetel M; Kostić V; Vukosavić S; Romac S
    Int J Neurosci; 2005 Feb; 115(2):299-301. PubMed ID: 15764008
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference.
    Lombardi MS; Jaspers L; Spronkmans C; Gellera C; Taroni F; Di Maria E; Donato SD; Kaemmerer WF
    Exp Neurol; 2009 Jun; 217(2):312-9. PubMed ID: 19289118
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.
    Schneider SA; Walker RH; Bhatia KP
    Nat Clin Pract Neurol; 2007 Sep; 3(9):517-25. PubMed ID: 17805246
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sequence analysis of tau 3'untranslated region and saitohin gene in sporadic progressive supranuclear palsy.
    Ezquerra M; Campdelacreu J; Muñoz E; Oliva R; Tolosa E
    J Neurol Neurosurg Psychiatry; 2004 Jan; 75(1):155-7. PubMed ID: 14707330
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Saitohin, which is nested within the tau gene, interacts with tau and Abl and its human-specific allele influences Abl phosphorylation.
    Wang Y; Gao L; Conrad CG; Andreadis A
    J Cell Biochem; 2011 Nov; 112(11):3482-8. PubMed ID: 21769920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype.
    Mancuso M; Kiferle L; Petrozzi L; Nesti C; Rocchi A; Ceravolo R; Orsucci D; Maluccio MR; Bonuccelli U; Filosto M; Siciliano G; Murri L
    Neurosci Lett; 2008 Oct; 444(1):83-6. PubMed ID: 18706972
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population.
    Pepłońska B; Zekanowski C; Religa D; Czyzewski K; Styczyńska M; Pfeffer A; Gabryelewicz T; Gołebiowski M; Luczywek E; Wasiak B; Barczak A; Chodakowska M; Barcikowska M; Kuźnicki J
    Neurosci Lett; 2003 Sep; 348(3):163-6. PubMed ID: 12932819
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Homozygotes for Huntington's disease.
    Wexler NS; Young AB; Tanzi RE; Travers H; Starosta-Rubinstein S; Penney JB; Snodgrass SR; Shoulson I; Gomez F; Ramos Arroyo MA
    Nature; 1987 Mar 12-18; 326(6109):194-7. PubMed ID: 2881213
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians.
    Das G; Misra AK; Das SK; Ray K; Ray J
    Neurosci Lett; 2009 Aug; 460(1):16-20. PubMed ID: 19450659
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular diagnosis of Huntington's disease in Mexican patients by polymerase chain reaction.
    Cisneros Vega B; Alonso Vilatela ME; Yescas Gomez P; Silva Arreola G; Montañez Ojeda C
    Arch Med Res; 1996; 27(1):87-92. PubMed ID: 8867374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic variation in D7S1875 repeat polymorphism of leptin gene is associated with increased risk for depression: a case-control study from India.
    Kapoor M; Kapur S; Mehra S; Dube U; Sharad S; Sidhu S
    Depress Anxiety; 2009; 26(9):791-5. PubMed ID: 19382181
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Association of single nucleotide polymorphisms of Axis inhibitor-2 gene rs224030, rs8081536, rs9913621 with Hirschsprung disease].
    Gao H; Zhang J; Wang W; Zhang Z; Huang Y; Zhang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):697-700. PubMed ID: 19065536
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genetic variation in the ADORA2A gene modifies age at onset in Huntington's disease.
    Dhaenens CM; Burnouf S; Simonin C; Van Brussel E; Duhamel A; Defebvre L; Duru C; Vuillaume I; Cazeneuve C; Charles P; Maison P; Debruxelles S; Verny C; Gervais H; Azulay JP; Tranchant C; Bachoud-Levi AC; Dürr A; Buée L; Krystkowiak P; Sablonnière B; Blum D;
    Neurobiol Dis; 2009 Sep; 35(3):474-6. PubMed ID: 19591938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of tissue inhibitor of metalloproteinase-2 gene polymorphisms in a caucasian population with abdominal aortic aneurysms].
    Hinterseher I; Krex D; Kuhlisch E; Pilarsky C; Schneiders W; Saeger HD; Bergert H
    Zentralbl Chir; 2008 Aug; 133(4):332-7. PubMed ID: 18702016
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Saitohin Q7R polymorphism is associated with late-onset Alzheimer's disease susceptibility among caucasian populations: a meta-analysis.
    Huang R; Tian S; Cai R; Sun J; Xia W; Dong X; Shen Y; Wang S
    J Cell Mol Med; 2017 Aug; 21(8):1448-1456. PubMed ID: 28211174
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.