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Hot spots in prion protein for pathogenic conversion
scientific article
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instance of
scholarly article
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title
Hot spots in prion protein for pathogenic conversion
(English)
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main subject
prion protein family
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author name string
Kazuo Kuwata
series ordinal
1
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Noriyuki Nishida
series ordinal
2
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Tomoharu Matsumoto
series ordinal
3
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Yuji O Kamatari
series ordinal
4
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Junji Hosokawa-Muto
series ordinal
5
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Kota Kodama
series ordinal
6
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Hironori K Nakamura
series ordinal
7
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Kiminori Kimura
series ordinal
8
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Makoto Kawasaki
series ordinal
9
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Yuka Takakura
series ordinal
10
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Susumu Shirabe
series ordinal
11
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Jiro Takata
series ordinal
12
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Yasufumi Kataoka
series ordinal
13
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Shigeru Katamine
series ordinal
14
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language of work or name
English
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publication date
17 July 2007
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published in
Proceedings of the National Academy of Sciences of the United States of America
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volume
104
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issue
29
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page(s)
11921-6
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cites work
Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal
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Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulation
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Prions
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Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
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7 April 2017
NMR structure of the mouse prion protein domain PrP(121-231)
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VMD: visual molecular dynamics
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7 April 2017
Mice devoid of PrP are resistant to scrapie
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A hot spot of binding energy in a hormone-receptor interface
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Novel proteinaceous infectious particles cause scrapie
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7 April 2017
Structure-activity relationship study of prion inhibition by 2-aminopyridine-3,5-dicarbonitrile-based compounds: parallel synthesis, bioactivity, and in vitro pharmacokinetics
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A chimeric ligand approach leading to potent antiprion active acridine derivatives: design, synthesis, and biological investigations
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28 September 2017
Styrylbenzoazole derivatives for imaging of prion plaques and treatment of transmissible spongiform encephalopathies
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28 September 2017
Prions and transmissible spongiform encephalopathy (TSE) chemotherapeutics: A common mechanism for anti-TSE compounds?
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28 September 2017
Amyloids, prions and the inherent infectious nature of misfolded protein aggregates
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28 September 2017
Screening a library of potential prion therapeutics against cellular prion proteins and insights into their mode of biological activities by surface plasmon resonance
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28 September 2017
Prion protein NMR structures of cats, dogs, pigs, and sheep
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28 September 2017
Prion protein NMR structures of elk and of mouse/elk hybrids
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28 September 2017
Synthesis of analogues of Congo red and evaluation of their anti-prion activity
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Low-populated folding intermediates of Fyn SH3 characterized by relaxation dispersion NMR.
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Evidence for assembly of prions with left-handed beta-helices into trimers
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Chemical chaperone therapy for brain pathology in G(M1)-gangliosidosis
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28 September 2017
New inhibitors of scrapie-associated prion protein formation in a library of 2000 drugs and natural products
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Specific inhibition of pathological prion protein accumulation by small interfering RNAs
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28 September 2017
Potent inhibition of scrapie prion replication in cultured cells by bis-acridines
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PubMed Central
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28 September 2017
Mapping protein-protein interactions in solution by NMR spectroscopy
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28 September 2017
Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease
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28 September 2017
Prion infection impairs the cellular response to oxidative stress
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28 September 2017
Mimicking dominant negative inhibition of prion replication through structure-based drug design
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28 September 2017
Rational discovery of novel nuclear hormone receptor antagonists
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28 September 2017
Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein
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28 September 2017
Inhibition of protease-resistant prion protein formation by porphyrins and phthalocyanines
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28 September 2017
The anti-prion activity of Congo red. Putative mechanism
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28 September 2017
Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible
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PubMed Central
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28 September 2017
Structural clues to prion replication
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PubMed Central
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28 September 2017
Molecular biology and transgenetics of prion diseases
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28 September 2017
Porphyrin and phthalocyanine antiscrapie compounds.
1 reference
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PubMed Central
reference URL
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30 May 2018
A mouse prion protein transgene rescues mice deficient for the prion protein gene from purkinje cell degeneration and demyelination.
1 reference
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30 May 2018
Sulphated glycosaminoglycans prevent the neurotoxicity of a human prion protein fragment
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924567
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30 May 2018
In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).
1 reference
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28 November 2018
Slow conformational dynamics in the hamster prion protein
1 reference
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PubMed Central
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28 November 2018
A novel generation of heparan sulfate mimetics for the treatment of prion diseases.
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PubMed Central
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28 November 2018
Locally disordered conformer of the hamster prion protein: a crucial intermediate to PrPSc?
1 reference
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28 November 2018
A change in the conformation of prions accompanies the emergence of a new prion strain.
1 reference
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PubMed Central
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28 November 2018
Oxidative folding of murine prion mPrP(23-231).
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924567
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28 November 2018
No propagation of prions in mice devoid of PrP.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924567
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28 November 2018
Effect of Congo red on wild-type and mutated prion proteins in cultured cells
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17616582
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17616582
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.0702671104
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
511264
ADS bibcode
2007PNAS..10411921K
0 references
OpenCitations bibliographic resource ID
511264
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
511264
PMC publication ID
1924567
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
511264
PubMed publication ID
17616582
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
511264
ResearchGate publication ID
6220488
0 references
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