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 *

129 related articles for article (PubMed ID: 18191917)

  • 21. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
    Marcon G; Indaco A; Di Fede G; Suardi S; Finato N; Moretti V; Micoli S; Fociani P; Zerbi P; Pincherle A; Redaelli V; Tagliavini F; Giaccone G
    Brain Pathol; 2014 Mar; 24(2):148-51. PubMed ID: 24118545
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The association between the methionine/valine (M/V) polymorphism (rs1799990) in the PRNP gene and the risk of Alzheimer disease: an update by meta-analysis.
    He J; Li X; Yang J; Huang J; Fu X; Zhang Y; Fan H
    J Neurol Sci; 2013 Mar; 326(1-2):89-95. PubMed ID: 23399523
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prion protein gene M129V polymorphism and variability in age at migraine onset.
    Palmirotta R; Ludovici G; Egeo G; Ialongo C; Aurilia C; Fofi L; De Marchis ML; Della-Morte D; Barbanti P; Guadagni F
    Headache; 2013 Mar; 53(3):540-5. PubMed ID: 23405858
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases.
    Kosami K; Ae R; Hamaguchi T; Sanjo N; Tsukamoto T; Kitamoto T; Yamada M; Mizusawa H; Nakamura Y
    J Neurol Neurosurg Psychiatry; 2022 Jul; 93(7):779-784. PubMed ID: 35387866
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular genetics of human prion diseases in Germany.
    Windl O; Giese A; Schulz-Schaeffer W; Zerr I; Skworc K; Arendt S; Oberdieck C; Bodemer M; Poser S; Kretzschmar HA
    Hum Genet; 1999 Sep; 105(3):244-52. PubMed ID: 10987652
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Polymorphism of PRNP codons in the normal Icelandic population.
    Georgsson G; Tryggvason T; Jonasdottir AD; Gudmundsson S; Thorgeirsdottir S
    Acta Neurol Scand; 2006 Jun; 113(6):419-25. PubMed ID: 16674609
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.
    Rodríguez-Martínez AB; Garrido JM; Zarranz JJ; Arteagoitia JM; de Pancorbo MM; Atarés B; Bilbao MJ; Ferrer I; Juste RA
    BMC Neurol; 2010 Oct; 10():99. PubMed ID: 20973975
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.
    Labate A; Manna I; Gambardella A; Le Piane E; La Russa A; Condino F; Cittadella R; Aguglia U; Quattrone A
    Neurosci Lett; 2007 Jun; 421(1):1-4. PubMed ID: 17092648
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Jeong BH; Lee KH; Kim NH; Jin JK; Kim JI; Carp RI; Kim YS
    Neurogenetics; 2005 Dec; 6(4):229-32. PubMed ID: 16217673
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay.
    Jones M; Peden AH; Wight D; Prowse C; Macgregor I; Manson J; Turner M; Ironside JW; Head MW
    Neuroreport; 2008 Dec; 19(18):1783-6. PubMed ID: 18955905
    [TBL] [Abstract][Full Text] [Related]  

  • 31. PRNP M129V homozygosity in multiple system atrophy vs. Parkinson's disease.
    Shibao C; Garland EM; Gamboa A; Vnencak-Jones CL; Van Woeltz M; Haines JL; Yu C; Biaggioni I
    Clin Auton Res; 2008 Feb; 18(1):13-9. PubMed ID: 18236005
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD.
    Combarros O; Sánchez-Guerra M; Llorca J; Alvarez-Arcaya A; Berciano J; Peña N; Fernández-Viadero C
    Neurology; 2000 Aug; 55(4):593-5. PubMed ID: 10953203
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genotype patterns and characteristics of PRNP in the Korean population.
    Moe Lee S; Ran Ju Y; Choi BY; Wook Hyeon J; Sun Park J; Kyeong Kim C; Yeon Kim S
    Prion; 2012; 6(4):375-82. PubMed ID: 22561193
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The presence of valine at residue 129 in human prion protein accelerates amyloid formation.
    Baskakov I; Disterer P; Breydo L; Shaw M; Gill A; James W; Tahiri-Alaoui A
    FEBS Lett; 2005 May; 579(12):2589-96. PubMed ID: 15862295
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan.
    Ohkubo T; Sakasegawa Y; Asada T; Kinoshita T; Goto Y; Kimura H; Mizusawa H; Hachiya NS; Kaneko K
    Ann Neurol; 2003 Oct; 54(4):553-4; author reply 555. PubMed ID: 14520676
    [No Abstract]   [Full Text] [Related]  

  • 36. Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.
    Diack AB; Ritchie DL; Peden AH; Brown D; Boyle A; Morabito L; Maclennan D; Burgoyne P; Jansen C; Knight RS; Piccardo P; Ironside JW; Manson JC
    Emerg Infect Dis; 2014 Dec; 20(12):1969-79. PubMed ID: 25418327
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
    Hainfellner JA; Parchi P; Kitamoto T; Jarius C; Gambetti P; Budka H
    Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The codon for the methionine at position 129 (M129) in the human prion protein provides an alternative initiation site for translation and renders individuals homozygous for M129 more susceptible to prion disease.
    Concepcion GP; Padlan EA
    Med Hypotheses; 2005; 65(5):865-7. PubMed ID: 16081222
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Analysis of the prion protein in primates reveals a new polymorphism in codon 226 (Y226F).
    Glatzel M; Pekarik V; Lührs T; Dittami J; Aguzzi A
    Biol Chem; 2002 Jun; 383(6):1021-5. PubMed ID: 12222676
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Polymorphisms of the prion protein gene (PRNP) in a Serbian population.
    Dimitrijević R; Cadez I; Keckarević-Marković M; Keckarević D; Kecmanović M; Dobricić V; Savić-Pavićević D; Brajusković G; Romac S
    Int J Neurosci; 2010 Jul; 120(7):496-501. PubMed ID: 20583902
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.