Results
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241.
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Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. [electronic resource] by
- Colucci, Monica
- Moleres, Francisco J
- Xie, Zhi-Liang
- Ray-Chaudhury, Abhik
- Gutti, Sujata
- Butefisch, Cathrin M
- Cervenakova, Larisa
- Wang, Wen
- Goldfarb, Lev G
- Kong, Qingzhong
- Ghetti, Bernardino
- Chen, Shu G
- Gambetti, Pierluigi
Producer: 20060829
In:
Journal of neuropathology and experimental neurology vol. 65
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242.
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Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. [electronic resource] by
- Peoc'h, Katell
- Levavasseur, Etienne
- Delmont, Emilien
- De Simone, Alfonso
- Laffont-Proust, Isabelle
- Privat, Nicolas
- Chebaro, Yassmine
- Chapuis, Céline
- Bedoucha, Pierre
- Brandel, Jean-Philippe
- Laquerriere, Annie
- Kemeny, Jean-Louis
- Hauw, Jean-Jacques
- Borg, Michel
- Rezaei, Human
- Derreumaux, Philippe
- Laplanche, Jean-Louis
- Haïk, Stéphane
Producer: 20130515
In:
Human molecular genetics vol. 21
Availability: No items available.
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243.
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253.
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A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature. [electronic resource] by
- Jansen, Casper
- Voet, Willem
- Head, Mark W
- Parchi, Piero
- Yull, Helen
- Verrips, Aad
- Wesseling, Pieter
- Meulstee, Jan
- Baas, Frank
- van Gool, Willem A
- Ironside, James W
- Rozemuller, Annemieke J M
Producer: 20111114
In:
Acta neuropathologica vol. 121
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254.
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Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP. [electronic resource] by
- Jansen, Casper
- Parchi, Piero
- Capellari, Sabina
- Vermeij, Ad J
- Corrado, Patrizia
- Baas, Frank
- Strammiello, Rosaria
- van Gool, Willem A
- van Swieten, John C
- Rozemuller, Annemieke J M
Producer: 20100302
In:
Acta neuropathologica vol. 119
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255.
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256.
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Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred). [electronic resource] by
- Piccardo, P
- Seiler, C
- Dlouhy, S R
- Young, K
- Farlow, M R
- Prelli, F
- Frangione, B
- Bugiani, O
- Tagliavini, F
- Ghetti, B
Producer: 19970107
In:
Journal of neuropathology and experimental neurology vol. 55
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257.
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258.
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A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred. [electronic resource] by
- Tagliavini, F
- Giaccone, G
- Prelli, F
- Verga, L
- Porro, M
- Trojanowski, J Q
- Farlow, M R
- Frangione, B
- Ghetti, B
- Bugiani, O
Producer: 19930930
In:
Brain research vol. 616
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259.
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260.
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A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles. [electronic resource] by
- Mercer, Robert C C
- Daude, Nathalie
- Dorosh, Lyudmyla
- Fu, Ze-Lin
- Mays, Charles E
- Gapeshina, Hristina
- Wohlgemuth, Serene L
- Acevedo-Morantes, Claudia Y
- Yang, Jing
- Cashman, Neil R
- Coulthart, Michael B
- Pearson, Dawn M
- Joseph, Jeffrey T
- Wille, Holger
- Safar, Jiri G
- Jansen, Gerard H
- Stepanova, Maria
- Sykes, Brian D
- Westaway, David
Producer: 20180706
In:
PLoS pathogens vol. 14
Availability: No items available.
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