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 *

83 related articles for article (PubMed ID: 9113500)

  • 1. Mitochondrial tRNA(Gln) and tRNA(Thr) gene variants in Parkinson's disease.
    Mayr-Wohlfart U; Rödel G; Henneberg A
    Eur J Med Res; 1997 Mar; 2(3):111-3. PubMed ID: 9113500
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer's and Parkinson's diseases.
    Egensperger R; Kösel S; Schnopp NM; Mehraein P; Graeber MB
    Neuropathol Appl Neurobiol; 1997 Aug; 23(4):315-21. PubMed ID: 9292870
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients.
    Brown MD; Shoffner JM; Kim YL; Jun AS; Graham BH; Cabell MF; Gurley DS; Wallace DC
    Am J Med Genet; 1996 Jan; 61(3):283-9. PubMed ID: 8741876
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.
    Huerta C; Castro MG; Coto E; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; Martínez C; Lahoz CH; Alvarez V
    J Neurol Sci; 2005 Sep; 236(1-2):49-54. PubMed ID: 15975594
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial polymporphisms in Parkinson's Disease.
    Otaegui D; Paisán C; Sáenz A; Martí I; Ribate M; Martí-Massó JF; Pérez-Tur J; López de Munain A
    Neurosci Lett; 2004 Nov; 370(2-3):171-4. PubMed ID: 15488317
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.
    Pyle A; Foltynie T; Tiangyou W; Lambert C; Keers SM; Allcock LM; Davison J; Lewis SJ; Perry RH; Barker R; Burn DJ; Chinnery PF
    Ann Neurol; 2005 Apr; 57(4):564-7. PubMed ID: 15786469
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High frequency of mitochondrial complex I mutations in Parkinson's disease and aging.
    Smigrodzki R; Parks J; Parker WD
    Neurobiol Aging; 2004; 25(10):1273-81. PubMed ID: 15465623
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Study of mitochondrial DNA mutations in patients with migraine with prolonged aura.
    Rozen TD; Shanske S; Otaegui D; Lu J; Young WB; Bradley K; DiMauro S; Silberstein SD
    Headache; 2004; 44(7):674-7. PubMed ID: 15209689
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assessment of tRNA
    Venkatesan D; Iyer M; Raj N; Gopalakrishnan AV; Narayanasamy A; Kumar NS; Vellingiri B
    J Mol Neurosci; 2023 Dec; 73(11-12):912-920. PubMed ID: 37845428
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease.
    Grasbon-Frodl EM; Kösel S; Sprinzl M; von Eitzen U; Mehraein P; Graeber MB
    Neurogenetics; 1999 Apr; 2(2):121-7. PubMed ID: 10369889
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Association between cytochrome P-450 enzyme gene polymorphisms and Parkinson's disease].
    Wang J; Liu Z; Chen B
    Zhonghua Yi Xue Za Zhi; 2000 Aug; 80(8):585-7. PubMed ID: 11798822
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
    Nichols WC; Uniacke SK; Pankratz N; Reed T; Simon DK; Halter C; Rudolph A; Shults CW; Conneally PM; Foroud T;
    Mov Disord; 2004 Jun; 19(6):649-55. PubMed ID: 15197702
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Association between the debrisoquine hydroxylase gene polymorphism and the genetic susceptibility of Parkinson's disease].
    Tao E; Liu Z; Chen B; Pan X; Shao M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):281-3. PubMed ID: 9758873
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sequence analysis of the entire mitochondrial genome in Parkinson's disease.
    Vives-Bauza C; Andreu AL; Manfredi G; Beal MF; Janetzky B; Gruenewald TH; Lin MT
    Biochem Biophys Res Commun; 2002 Feb; 290(5):1593-601. PubMed ID: 11820805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular implications of the human glutathione transferase A-4 gene (hGSTA4) polymorphisms in neurodegenerative diseases.
    Coppedè F; Armani C; Bidia DD; Petrozzi L; Bonuccelli U; Migliore L
    Mutat Res; 2005 Nov; 579(1-2):107-14. PubMed ID: 16054170
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease.
    Belin AC; Björk BF; Westerlund M; Galter D; Sydow O; Lind C; Pernold K; Rosvall L; Håkansson A; Winblad B; Nissbrandt H; Graff C; Olson L
    Neurosci Lett; 2007 Jun; 420(3):257-62. PubMed ID: 17537576
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Significant association between the tau gene A0/A0 genotype and Parkinson's disease.
    Pastor P; Ezquerra M; Muñoz E; Martí MJ; Blesa R; Tolosa E; Oliva R
    Ann Neurol; 2000 Feb; 47(2):242-5. PubMed ID: 10665497
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease.
    Luoma PT; Eerola J; Ahola S; Hakonen AH; Hellström O; Kivistö KT; Tienari PJ; Suomalainen A
    Neurology; 2007 Sep; 69(11):1152-9. PubMed ID: 17846414
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
    Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE
    Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.