MTMT-ben szereplő publikációk tallózása szerző szerint "Estivill X"

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  • Rare variants in beta-Amyloid precursor protein (APP) and Parkinson's disease. 
    Schulte EC; Fukumori A; Mollenhauer B; Hor H; Arzberger T; Perneczky R; Kurz A; Diehl-Schmid J; Hull M; Lichtner P; Eckstein G; Zimprich A; Haubenberger D; Pirker W; Brucke T; Bereznai Benjamin; Molnar Mária Judit; Lorenzo-Betancor O; Pastor P; Peters A; Gieger C; Estivill X; Meitinger T; Kretzschmar HA; Trenkwalder C; Haass C; Winkelmann J (2015)
    Many individuals with Parkinson's disease (PD) develop cognitive deficits, and a phenotypic and molecular overlap between neurodegenerative diseases exists. We investigated the contribution of rare variants in seven genes ...
  • Variation in a repeat sequence determines wheter a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign 
    Groman JD; Hefferon TW; Casals T; Bassas L; Estivill X; Des Georges M; Koudova M; Fallin MD; Németh, Krisztina; Fekete, György; Kádasi, Lajos; Friedman K; Schwarz M; Bombieri C; Pignatti GF; Kanavakis E; Tzetis M; Schwartz M; Novelli G; D Apice MR; Sobczynska-Tomaszewska A; Bal J; Stuhrmann M; Macek M Jr; Claustres M; Cutting GR (2004)