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Results: 1-8 |
Results: 8
A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease
Authors: Panegyres, PK Toufexis, K Kakulas, BA Cernevakova, L Brown, P Ghetti, B Piccardo, P Dlouhy, SR
Citation: Pk. Panegyres et al., A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease, ARCH NEUROL, 58(11), 2001, pp. 1899-1902
Prion proteins with different conformations accumulate in Geustmann-Straussler-Scheinker disease caused by A117V and F198S mutations
Authors: Piccardo, P Liepnieks, JJ William, A Dlouhy, SR Farlow, MR Young, K Nochlin, D Bird, TD Nixon, RR Ball, MJ DeCarli, C Bugiani, O Tagliavini, F Benson, MD Ghetti, B
Citation: P. Piccardo et al., Prion proteins with different conformations accumulate in Geustmann-Straussler-Scheinker disease caused by A117V and F198S mutations, AM J PATH, 158(6), 2001, pp. 2201-2207
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome
Authors: Hodes, ME Woodward, K Spinner, NB Emanuel, BS Enrico-Simon, A Kamholz, J Stambolian, D Zackai, EH Pratt, VM Thomas, IT Crandall, K Dlouhy, SR Malcolm, S
Citation: Me. Hodes et al., Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome, AM J HU GEN, 67(1), 2000, pp. 14-22
Detecting point mutations by denaturing-gradient gel electrophoresis
Authors: Dlouhy, SR Wheeler, P Trofatter, JA Stambrook, PJ Tischfield, JA
Citation: Sr. Dlouhy et al., Detecting point mutations by denaturing-gradient gel electrophoresis, NUCLEIC ACID PROTOCOLS HANDBOOK, 2000, pp. 705-716
Different mutations in the same codon of the proteolipid protein gene, PLP, way help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2)
Authors: Hodes, ME Zimmerman, AW Aydanian, A Naidu, S Miller, NR Oller, JLG Barker, B Aleck, KA Hurley, TD Dlouhy, SR
Citation: Me. Hodes et al., Different mutations in the same codon of the proteolipid protein gene, PLP, way help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2), AM J MED G, 82(2), 1999, pp. 132-139
A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum
Authors: Migheli, A Piva, R Casolino, S Atzori, C Dlouhy, SR Ghetti, B
Citation: A. Migheli et al., A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum, AM J PATH, 155(2), 1999, pp. 365-373
Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse
Authors: Schwartz, NB Szabo, M Verina, T Wei, JJ Dlouhy, SR Won, L Heller, A Hodes, ME Ghetti, R
Citation: Nb. Schwartz et al., Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse, NEUROENDOCR, 68(6), 1998, pp. 374-385
Prion diseases: PrP peptides, pathogenesis and treatment perspectives
Authors: Tagliavini, F Salmona, M Forloni, G Malesani, P Giaccone, G Canciani, B McArthur, R Lansen, J Piccardo, P Dlouhy, SR Ghetti, B Frangione, B Prelli, F Bugiani, O
Citation: F. Tagliavini et al., Prion diseases: PrP peptides, pathogenesis and treatment perspectives, PRIONS: MOLECULAR AND CELLULAR BIOLOGY, 1997, pp. 125-138
Risultati: 1-8 |