131 related articles for article (PubMed ID: 25027605)
1. Molecular dynamics study of the dominant-negative E219K polymorphism in human prion protein.
Jahandideh S; Jamalan M; Faridounnia M
J Biomol Struct Dyn; 2015; 33(6):1315-25. PubMed ID: 25027605
[TBL] [Abstract][Full Text] [Related]
2. Structural facets of disease-linked human prion protein mutants: a molecular dynamic study.
Rossetti G; Giachin G; Legname G; Carloni P
Proteins; 2010 Dec; 78(16):3270-80. PubMed ID: 20806222
[TBL] [Abstract][Full Text] [Related]
3. Structural basis for the protective effect of the human prion protein carrying the dominant-negative E219K polymorphism.
Biljan I; Giachin G; Ilc G; Zhukov I; Plavec J; Legname G
Biochem J; 2012 Sep; 446(2):243-51. PubMed ID: 22676969
[TBL] [Abstract][Full Text] [Related]
4. Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation.
Biljan I; Ilc G; Giachin G; Raspadori A; Zhukov I; Plavec J; Legname G
J Mol Biol; 2011 Sep; 412(4):660-73. PubMed ID: 21839748
[TBL] [Abstract][Full Text] [Related]
5. NMR structural studies of human cellular prion proteins.
Biljan I; Ilc G; Giachin G; Legname G; Plavec J
Curr Top Med Chem; 2013; 13(19):2407-18. PubMed ID: 24059340
[TBL] [Abstract][Full Text] [Related]
6. Prevalent mutations of human prion protein: a molecular modeling and molecular dynamics study.
Behmard E; Abdolmaleki P; Asadabadi EB; Jahandideh S
J Biomol Struct Dyn; 2011 Oct; 29(2):379-89. PubMed ID: 21875156
[TBL] [Abstract][Full Text] [Related]
7. Systematic investigation of predicted effect of nonsynonymous SNPs in human prion protein gene: a molecular modeling and molecular dynamics study.
Jahandideh S; Zhi D
J Biomol Struct Dyn; 2014; 32(2):289-300. PubMed ID: 23527686
[TBL] [Abstract][Full Text] [Related]
8. Common structural traits across pathogenic mutants of the human prion protein and their implications for familial prion diseases.
Rossetti G; Cong X; Caliandro R; Legname G; Carloni P
J Mol Biol; 2011 Aug; 411(3):700-12. PubMed ID: 21689662
[TBL] [Abstract][Full Text] [Related]
9. In silico analysis of prion protein mutants: a comparative study by molecular dynamics approach.
Doss CG; Rajith B; Rajasekaran R; Srajan J; Nagasundaram N; Debajyoti C
Cell Biochem Biophys; 2013; 67(3):1307-18. PubMed ID: 23723004
[TBL] [Abstract][Full Text] [Related]
10. Effects of the A117V mutation on the folding and aggregation of palindromic sequences (PrP113-120) in prion: insights from replica exchange molecular dynamics simulations.
Ning L; Wang Q; Zheng Y; Liu H; Yao X
Mol Biosyst; 2015 Feb; 11(2):647-55. PubMed ID: 25483828
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular dynamics studies on the NMR and X-ray structures of rabbit prion proteins.
Zhang J; Zhang Y
J Theor Biol; 2014 Feb; 342():70-82. PubMed ID: 24184221
[TBL] [Abstract][Full Text] [Related]
13. Dominant-negative effects in prion diseases: insights from molecular dynamics simulations on mouse prion protein chimeras.
Cong X; Bongarzone S; Giachin G; Rossetti G; Carloni P; Legname G
J Biomol Struct Dyn; 2013; 31(8):829-40. PubMed ID: 22934595
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Flexibility of the murine prion protein and its Asp178Asn mutant investigated by molecular dynamics simulations.
Gsponer J; Ferrara P; Caflisch A
J Mol Graph Model; 2001; 20(2):169-82. PubMed ID: 11775003
[TBL] [Abstract][Full Text] [Related]
16. Molecular dynamics simulations of human prion protein: importance of correct treatment of electrostatic interactions.
Zuegg J; Gready JE
Biochemistry; 1999 Oct; 38(42):13862-76. PubMed ID: 10529232
[TBL] [Abstract][Full Text] [Related]
17. Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.
Peoc'h K; Levavasseur E; Delmont E; De Simone A; Laffont-Proust I; Privat N; Chebaro Y; Chapuis C; Bedoucha P; Brandel JP; Laquerriere A; Kemeny JL; Hauw JJ; Borg M; Rezaei H; Derreumaux P; Laplanche JL; Haïk S
Hum Mol Genet; 2012 Dec; 21(26):5417-28. PubMed ID: 22965875
[TBL] [Abstract][Full Text] [Related]
18. Recognition Mechanisms between a Nanobody and Disordered Epitopes of the Human Prion Protein: An Integrative Molecular Dynamics Study.
Mollica L; Giachin G
J Chem Inf Model; 2023 Jan; 63(2):531-545. PubMed ID: 36580661
[TBL] [Abstract][Full Text] [Related]
19. Pathogenic mutations in the hydrophobic core of the human prion protein can promote structural instability and misfolding.
van der Kamp MW; Daggett V
J Mol Biol; 2010 Dec; 404(4):732-48. PubMed ID: 20932979
[TBL] [Abstract][Full Text] [Related]
20. Structural rearrangements at physiological pH: nuclear magnetic resonance insights from the V210I human prion protein mutant.
Biljan I; Ilc G; Giachin G; Plavec J; Legname G
Biochemistry; 2012 Sep; 51(38):7465-74. PubMed ID: 22947063
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
