203 related articles for article (PubMed ID: 15739202)
1. One gene, two diseases and three conformations: molecular dynamics simulations of mutants of human prion protein at room temperature and elevated temperatures.
Shamsir MS; Dalby AR
Proteins; 2005 May; 59(2):275-90. PubMed ID: 15739202
[TBL] [Abstract][Full Text] [Related]
2. [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129].
Colombier C; Géraud G; Delisle MB; Laplanche JL; Pavy le Traon A; Alizé P; Delpla PA
Rev Neurol (Paris); 1997 May; 153(4):239-43. PubMed ID: 9296141
[TBL] [Abstract][Full Text] [Related]
3. Polymorphism at residue 129 modulates the conformational conversion of the D178N variant of human prion protein 90-231.
Apetri AC; Vanik DL; Surewicz WK
Biochemistry; 2005 Dec; 44(48):15880-8. PubMed ID: 16313190
[TBL] [Abstract][Full Text] [Related]
4. Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.
Liemann S; Glockshuber R
Biochemistry; 1999 Mar; 38(11):3258-67. PubMed ID: 10079068
[TBL] [Abstract][Full Text] [Related]
5. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
[TBL] [Abstract][Full Text] [Related]
6. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
Mitrová E; Belay G
Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
[TBL] [Abstract][Full Text] [Related]
7. One genetic mutation, two diseases: fatal familial insomnia and Creutzfeldt-Jakob disease.
Bellows JG
Compr Ther; 1993; 19(1):3. PubMed ID: 8334858
[No Abstract] [Full Text] [Related]
8. [The spectrum of prion pathology broadens: fatal familial insomnia].
Delgado-Reyes S; Feito-Ibarz N; Ruiz-Aláez A; García de la Rocha ML; Martín-Araguz A; Moreno-Martínez JM
Rev Neurol; 1997 Dec; 25(148):2006-14. PubMed ID: 9528048
[TBL] [Abstract][Full Text] [Related]
9. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
Monari L; Chen SG; Brown P; Parchi P; Petersen RB; Mikol J; Gray F; Cortelli P; Montagna P; Ghetti B
Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2839-42. PubMed ID: 7908444
[TBL] [Abstract][Full Text] [Related]
10. [Prion diseases, update].
Kitamoto T
Rinsho Shinkeigaku; 2001 Dec; 41(12):1223-5. PubMed ID: 12235843
[TBL] [Abstract][Full Text] [Related]
11. Prion disease genetics.
Mead S
Eur J Hum Genet; 2006 Mar; 14(3):273-81. PubMed ID: 16391566
[TBL] [Abstract][Full Text] [Related]
12. [Spongiform encephalitis].
Domínguez Carmona M; Domínguez de la Calle M
An R Acad Nac Med (Madr); 2001; 118(3):633-52. PubMed ID: 11783043
[TBL] [Abstract][Full Text] [Related]
13. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.
Goldfarb LG; Petersen RB; Tabaton M; Brown P; LeBlanc AC; Montagna P; Cortelli P; Julien J; Vital C; Pendelbury WW
Science; 1992 Oct; 258(5083):806-8. PubMed ID: 1439789
[TBL] [Abstract][Full Text] [Related]
14. [Molecular bases of prion diseases].
Rać M; Rać M
Ann Acad Med Stetin; 2006; 52(3):5-13. PubMed ID: 17385343
[TBL] [Abstract][Full Text] [Related]
15. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
Gambetti P; Parchi P; Petersen RB; Chen SG; Lugaresi E
Brain Pathol; 1995 Jan; 5(1):43-51. PubMed ID: 7767490
[TBL] [Abstract][Full Text] [Related]
16. The unfolded state of the murine prion protein and properties of single-point mutants related to human prion diseases.
Gerum C; Schlepckow K; Schwalbe H
J Mol Biol; 2010 Aug; 401(1):7-12. PubMed ID: 20541558
[TBL] [Abstract][Full Text] [Related]
17. Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.
Tsuboi Y; Baba Y; Doh-ura K; Imamura A; Fujioka S; Yamada T
J Neurol Sci; 2005 May; 232(1-2):45-9. PubMed ID: 15850581
[TBL] [Abstract][Full Text] [Related]
18. Computational studies on prion proteins: effect of Ala(117)-->Val mutation.
Okimoto N; Yamanaka K; Suenaga A; Hata M; Hoshino T
Biophys J; 2002 May; 82(5):2746-57. PubMed ID: 11964260
[TBL] [Abstract][Full Text] [Related]
19. Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease.
Erginel-Unaltuna N; Peoc'h K; Komurcu E; Acuner TT; Issever H; Laplanche JL
Eur J Hum Genet; 2001 Dec; 9(12):965-8. PubMed ID: 11840201
[TBL] [Abstract][Full Text] [Related]
20. Human prion diseases: molecular and clinical aspects.
Glatzel M; Stoeck K; Seeger H; Lührs T; Aguzzi A
Arch Neurol; 2005 Apr; 62(4):545-52. PubMed ID: 15824251
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
