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La maladie de Parkinson en France (serveur d'exploration) - Curation (Ncbi)

Index « Keywords » - entrée « Amino Acid Substitution (genetics) »
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Amino Acid Substitution (drug effects) < Amino Acid Substitution (genetics) < Amino Acid Transport System X-AG (physiology)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000040 (1999) M B Delisle [France] ; J R Murrell ; R. Richardson ; J A Trofatter ; O. Rascol ; X. Soulages ; M. Mohr ; P. Calvas ; B. GhettiA mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.
000111 (2000) K. Ancolio [France] ; C. Alves Da Costa ; K. Uéda ; F. CheclerAlpha-synuclein and the Parkinson's disease-related mutant Ala53Thr-alpha-synuclein do not undergo proteasomal degradation in HEK293 and neuronal cells.
000611 (2006) Cornelia Hampe [France] ; Hector Ardila-Osorio ; Margot Fournier ; Alexis Brice ; Olga CortiBiochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity.
000B14 (2010) Eric Di Pasquale [France] ; Jacques Fantini ; Henri Chahinian ; Marc Maresca ; Nadira Taïeb ; Nouara YahiAltered ion channel formation by the Parkinson's-disease-linked E46K mutant of alpha-synuclein is corrected by GM3 but not by GM1 gangliosides.
000B28 (2010) Suzanne Lesage [France] ; Etienne Patin ; Christel Condroyer ; Anne-Louise Leutenegger ; Ebba Lohmann ; Nir Giladi ; Anat Bar-Shira ; Soraya Belarbi ; Nassima Hecham ; Pierre Pollak ; Anne-Marie Ouvrard-Hernandez ; Soraya Bardien ; Jonathan Carr ; Traki Benhassine ; Hiroyuki Tomiyama ; Caroline Pirkevi ; Tarik Hamadouche ; Cécile Cazeneuve ; A Nazli Basak ; Nobutaka Hattori ; Alexandra Dürr ; Meriem Tazir ; Avi Orr-Urtreger ; Lluis Quintana-Murci ; Alexis BriceParkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.

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