Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation

I Biljan, G Ilc, G Giachin, A Raspadori, I Zhukov… - Journal of molecular …, 2011 - Elsevier
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrPC) into a misfolded, pathogenic isoform …
被引用次数：89 相关文章

Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation

I Biljan, G Ilc, G Giachin, A Raspadori, I Zhukov… - Journal of Molecular …, 2011 - infona.pl
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrP C) into a misfolded, pathogenic isoform (PrP …

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation

I Biljan, G Ilc, G Giachin, A Raspadori, I Zhukov… - 2011 - ricerca.unityfvg.it
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrP (C)) into a misfolded, pathogenic isoform …

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation.

I Biljan, G Ilc, G Giachin, A Raspadori… - Journal of Molecular …, 2011 - europepmc.org
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrP (C)) into a misfolded, pathogenic isoform …

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation

I Biljan, G Ilc, G Giachin, A Raspadori… - Journal of …, 2011 - pubmed.ncbi.nlm.nih.gov
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrP (C)) into a misfolded, pathogenic isoform …

[引用][C] Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation

I Biljan, G Ilc, G Giachin, A Raspadori, I Zhukov… - Journal of Molecular …, 2011 - cir.nii.ac.jp
Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion
Protein with V210I Mutation | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation

I Biljan, G Ilc, G Giachin, A Raspadori, I Zhukov… - Journal of molecular …, 2011 - croris.hr
Sažetak The development of transmissible spongiphorm encephalopathies (TSE) is
associated with the conversion of the cellular prion protein (PrPC) into the misfolded …

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with v210i mutation

I Biljan, G Ilc, G Giachin, A Raspadori… - JOURNAL OF …, 2011 - research.unipd.it
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrPC) into a misfolded, pathogenic isoform …

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation

I Biljan, G Ilc, G Giachin, A Raspadori, I Zhukov… - JOURNAL OF …, 2011 - iris.sissa.it
The development of transmissible spongiform encephalopathies (TSEs) is associated with
the conversion of the cellular prion protein (PrP (C)) into a misfolded, pathogenic isoform …
[PDF] academia.edu

[PDF][PDF] Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation

A Raspadori, I Zhukov, J Plavec, G Legname - J. Mol. Biol, 2011 - academia.edu
The cellular form of the prion protein (PrP), PrPC, is a cell-surface
glycosylphosphatidylinositol-anchored glycoprotein localized in cholesterolrich domains. 1 It …