Zobrazeno 1 - 10 of 787 pro vyhledávání: '"Ga. Rouleau"'
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Molecular genetic analysis of chromosome 22 in 81 cases of meningioma
Autor: Jp, Dumanski, Ga, Rouleau, Magnus Nordenskjöld, Vp, Collins
Publikováno v: Europe PubMed Central
Constitutional and tumor tissue genotypes from 81 unrelated patients with meningioma were compared at 25 polymorphic loci (restriction fragments length alleles) on chromosome 22. Thirty tumors (37%) retained the constitutional genotype along chromoso
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ea782c251dfdf278c7018847660b483c
https://pubmed.ncbi.nlm.nih.gov/2393856
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7
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
Autor: Andrea Fuhs, Juliane Winkelmann, H.-Erich Wichmann, Werner Poewe, Emmanuel Mignot, Christopher J. Earley, Claire Fontenille, Matthew J. Farrer, Wolfgang H. Oertel, David Kemlink, Olli Polo, Darina Czamara, William G. Ondo, Viola Gschliesser, Marcella Francavilla, Barbara Schormair, Walter Paulus, Franziska Knauf, Birgit Högl, Karel Sonka, Klaus Berger, Bertram Müller-Myhsok, Maria Kaffe, Siong Chi Lin, Ingo Fietze, Wei Dong Le, Nadine Gross, Kaisa Silander, Juliette Faraco, Zbigniew K. Wszolek, Thomas Meitinger, Birgit Frauscher, Pavel Vodicka, Paul E. Peppard, Claudia Trenkwalder, Lan Xiong, Jana Vavrova, Markus Perola, Cornelius G. Bachmann, Thomas Illig, Guy A. Rouleau, Christian Gieger, Sona Nevsimalova, Richard P. Allen, Holger Prokisch, Carles Vilariño-Güell, Karin Stiasny-Kolster, Yves Dauvilliers, Derek Spieler, Johannes Kettunen, Tina Falkenstetter, Isabelle Cournu-Rebeix, Eva C. Schulte, Peter Lichtner, Jacques Montplaisir, Bertrand Fontaine, Alexander Zimprich
Publikováno v: PLoS Genetics
PLoS Genetics, Vol 7, Iss 7, p e1002171 (2011)
PLoS Genetics, Public Library of Science, 2011, 7 (7), pp.e1002171. ⟨10.1371/journal.pgen.1002171⟩
PLoS Genetics, 2011, 7 (7), pp.e1002171. ⟨10.1371/journal.pgen.1002171⟩
PLoS Genet. 7:e1002171 (2011)
Restless legs syndrome (RLS) is a sensorimotor disorder with an age-dependent prevalence of up to 10% in the general population above 65 years of age. Affected individuals suffer from uncomfortable sensations and an urge to move in the lower limbs th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d40590c29234b719bd96ebc654f44ceb
http://hdl.handle.net/10138/162555
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8
Akademický článek
Gold nanoclusters Au 25 AcCys 18 normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neurons.
Autor: Zhang I; Department of Pharmacology and Therapeutics, McGill University, 3655 Promenade Sir-William-Osler, H3G 1Y6 Montreal, Canada. dusica.maysinger@mcgill.ca., Maysinger D; Department of Pharmacology and Therapeutics, McGill University, 3655 Promenade Sir-William-Osler, H3G 1Y6 Montreal, Canada. dusica.maysinger@mcgill.ca., Beus M; Department of Pharmacology and Therapeutics, McGill University, 3655 Promenade Sir-William-Osler, H3G 1Y6 Montreal, Canada. dusica.maysinger@mcgill.ca., Mravak A; Faculty of Science, University of Split, Ruđera Boškovića 33, 21000 Split, Croatia. zsm@pmfst.hr., Yu Z; Division of Experimental Medicine, Faculty of Medicine, McGill University, Montreal, QC, Canada.; Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada., Perić Bakulić M; Faculty of Chemistry and Technology, University of Split, Ruđera Boškovića 35, 21000 Split, Croatia.; Center of Excellence for Science and Technology, Integration of Mediterranean Region (STIM), Faculty of Science, University of Split, Ruđera Boškovića 33, 21000 Split, Croatia., Dion PA; Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada., Rouleau GA; Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada., Bonačić-Koutecký V; Center of Excellence for Science and Technology, Integration of Mediterranean Region (STIM), Faculty of Science, University of Split, Ruđera Boškovića 33, 21000 Split, Croatia.; Chemistry Department, Humboldt University of Berlin, Brook-Taylor-Strasse 2, 12489 Berlin, Germany., Antoine R; Institut Lumière Matière, CNRS UMR 5306, Université Claude Bernard Lyon 1, Univ. Lyon, 69622 Villeurbanne Cedex, France., Sanader Maršić Ž; Faculty of Science, University of Split, Ruđera Boškovića 33, 21000 Split, Croatia. zsm@pmfst.hr.; Center of Excellence for Science and Technology, Integration of Mediterranean Region (STIM), Faculty of Science, University of Split, Ruđera Boškovića 33, 21000 Split, Croatia.
Publikováno v: Nanoscale [Nanoscale] 2024 Nov 28. Date of Electronic Publication: 2024 Nov 28.
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9
Akademický článek
Enhancing variant of uncertain significance (VUS) interpretation in neurogenetics: collaborative experiences from a tertiary care centre.
Autor: Horowitz K; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada., Fotopoulos NH; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada., Mistry AJ; Department of Human Genetics, McGill University, Montreal, Quebec, Canada., Simo J; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada., Medeiros M; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada.; Department of Human Genetics, McGill University, Montreal, Quebec, Canada., Bucco ID; Department of Genetics, Federal University of Parana, Curitiba, Paraná, Brazil., Ginsberg M; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada.; Department of Cognitive Sciences, McGill University, Montreal, Quebec, Canada., Dwosh E; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada.; University of British Columbia Hospital Clinic for Alzheimer Disease and Related Disorders, Vancouver Coastal Health Authority, Vancouver, British Columbia, Canada., La Piana R; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada., Rouleau GA; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada.; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada., Dilliott AA; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada sali.farhan@mcgill.ca allison.dilliott@mcgill.ca.; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada., Farhan SMK; Montreal Neurological Institute-Hospital, Montreal, Quebec, Canada sali.farhan@mcgill.ca allison.dilliott@mcgill.ca.; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
Publikováno v: Journal of medical genetics [J Med Genet] 2024 Nov 15. Date of Electronic Publication: 2024 Nov 15.
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10
Akademický článek
Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome.
Autor: Akçimen F; Neuromuscular Diseases Research Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Chia R; Neuromuscular Diseases Research Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Saez-Atienzar S; Neuromuscular Diseases Research Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Ruffo P; Neuromuscular Diseases Research Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Medical Genetics Laboratory, Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy., Rasheed M; Neuromuscular Diseases Research Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Ross JP; Department of Human Genetics, McGill University, Montréal, Quebec, Canada.; Montreal Neurological Institute-Hospital, McGill University, Montréal, Quebec, Canada., Liao C; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA., Ray A; Neurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA., Dion PA; Montreal Neurological Institute-Hospital, McGill University, Montréal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada., Scholz SW; Neurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.; Department of Neurology, Johns Hopkins University Medical Center, Baltimore, Maryland, USA., Rouleau GA; Department of Human Genetics, McGill University, Montréal, Quebec, Canada.; Montreal Neurological Institute-Hospital, McGill University, Montréal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada., Traynor BJ; Neuromuscular Diseases Research Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Department of Neurology, Johns Hopkins University Medical Center, Baltimore, Maryland, USA.
Publikováno v: Annals of neurology [Ann Neurol] 2024 Nov; Vol. 96 (5), pp. 994-1005. Date of Electronic Publication: 2024 Jul 30.
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