Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""M van Duijn C"" wg kryterium: Autor


Wyświetlanie 1-4 z 4
Tytuł :
Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness.
Autorzy :
Abdellaoui A; Department of Psychiatry, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Sanchez-Roige S; Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.
Sealock J; Vanderbilt Genetics Institute, Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, TN, USA.
Treur JL; Department of Psychiatry, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.; School of Experimental Psychology, University of Bristol, Bristol, UK.; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Dennis J; Vanderbilt Genetics Institute, Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, TN, USA.
Fontanillas P; 23andMe, Inc., Mountain View, CA, USA.
Elson S; 23andMe, Inc., Mountain View, CA, USA.
Nivard MG; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Ip HF; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
van der Zee M; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Baselmans BML; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Hottenga JJ; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Willemsen G; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Mosing M; Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Lu Y; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Pedersen NL; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Denys D; Department of Psychiatry, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Amin N; Genetic Epidemiology Unit, Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
M van Duijn C; Genetic Epidemiology Unit, Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Translational Epidemiology, Faculty Science, Leiden University, Leiden, The Netherlands.
Szilagyi I; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Tiemeier H; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Psychiatry, Erasmus Medical Center, Rotterdam, The Netherlands.
Neumann A; Department of Child and Adolescent Psychiatry/Psychology, Erasmus Medical Center, Rotterdam, The Netherlands.
Verweij KJH; Department of Psychiatry, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Cacioppo S; Center for Cognitive and Social Neuroscience, Department of Psychology, The University of Chicago, Chicago, Illinois, USA.
Cacioppo JT; Center for Cognitive and Social Neuroscience, Department of Psychology, The University of Chicago, Chicago, Illinois, USA.
Davis LK; Vanderbilt Genetics Institute, Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, TN, USA.
Palmer AA; Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.
Boomsma DI; Department of Biological Psychology, Vrije Universiteit, Amsterdam, The Netherlands.
Pokaż więcej
Corporate Authors :
23andme Research Team
Źródło :
Human molecular genetics [Hum Mol Genet] 2019 Nov 15; Vol. 28 (22), pp. 3853-3865.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Genetic Predisposition to Disease/*genetics
Loneliness/*psychology
Phenomics/*methods
Female ; Genome-Wide Association Study/methods ; Genotype ; Health ; Humans ; Male ; Mendelian Randomization Analysis/methods ; Mental Disorders/genetics ; Mental Health ; Multifactorial Inheritance/genetics ; Phenotype ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Tytuł :
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
Autorzy :
Cacace R; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Heeman B; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Van Mossevelde S; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.; Department of Neurology, Antwerp University Hospital, Edegem, Belgium.; Department of Neurology and Memory Clinic, Hospital Network Antwerp (ZNA), Middelheim and Hoge Beuken, Antwerp, Belgium.
De Roeck A; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Hoogmartens J; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
De Rijk P; Center for Molecular Neurology, VIB, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Gossye H; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.; Department of Neurology, Antwerp University Hospital, Edegem, Belgium.; Department of Neurology and Memory Clinic, Hospital Network Antwerp (ZNA), Middelheim and Hoge Beuken, Antwerp, Belgium.
De Vos K; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
De Coster W; Center for Molecular Neurology, VIB, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Strazisar M; Center for Molecular Neurology, VIB, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
De Baets G; Switch Laboratory, VIB-KU Leuven Centre for Brain and Disease Research, Louvain, Belgium.; Switch Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Schymkowitz J; Switch Laboratory, VIB-KU Leuven Centre for Brain and Disease Research, Louvain, Belgium.; Switch Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Rousseau F; Switch Laboratory, VIB-KU Leuven Centre for Brain and Disease Research, Louvain, Belgium.; Switch Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Louvain, Belgium.
Geerts N; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
De Pooter T; Center for Molecular Neurology, VIB, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Peeters K; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Sieben A; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; Department of Neurology, University Hospital Ghent and University of Ghent, Ghent, Belgium.
Martin JJ; Institute Born-Bunge, Antwerp, Belgium.
Engelborghs S; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.; Department of Neurology and Memory Clinic, Hospital Network Antwerp (ZNA), Middelheim and Hoge Beuken, Antwerp, Belgium.
Salmon E; Department of Neurology, Centre Hospitalier Universitaire de Liège and University of Liège, Liège, Belgium.
Santens P; Department of Neurology, University Hospital Ghent and University of Ghent, Ghent, Belgium.
Vandenberghe R; Department of Neurosciences, Faculty of Medicine, KU Leuven, Louvain, Belgium.; Laboratory of Cognitive Neurology, Department of Neurology, University Hospitals Leuven, Louvain, Belgium.
Cras P; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.; Department of Neurology, Antwerp University Hospital, Edegem, Belgium.
P De Deyn P; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.; Department of Neurology and Memory Clinic, Hospital Network Antwerp (ZNA), Middelheim and Hoge Beuken, Antwerp, Belgium.
C van Swieten J; Department of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
M van Duijn C; Department of Epidemiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
van der Zee J; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Sleegers K; Center for Molecular Neurology, VIB, Antwerp, Belgium.; Institute Born-Bunge, Antwerp, Belgium.; University of Antwerp, Antwerp, Belgium.
Van Broeckhoven C; Center for Molecular Neurology, VIB, Antwerp, Belgium. .; Institute Born-Bunge, Antwerp, Belgium. .; University of Antwerp, Antwerp, Belgium. .; Neurodegenerative Brain Diseases Group, VIB Center for Molecular Neurology, University of Antwerp, CDE, Universiteitsplein 1, 2610, Antwerp, Belgium. .
Pokaż więcej
Corporate Authors :
BELNEU Consortium
Źródło :
Acta neuropathologica [Acta Neuropathol] 2019 Jun; Vol. 137 (6), pp. 901-918. Date of Electronic Publication: 2019 Mar 14.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Inversion*
Mutation*
Dementia/*genetics
Dipeptidyl-Peptidases and Tripeptidyl-Peptidases/*deficiency
Nerve Tissue Proteins/*deficiency
Neurodegenerative Diseases/*genetics
Neurons/*physiology
Potassium Channels/*deficiency
Action Potentials/physiology ; Adult ; Aged ; Chromosomes, Human, Pair 7/genetics ; Dementia/physiopathology ; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases/genetics ; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases/physiology ; Female ; Genes, Dominant ; Homeostasis ; Humans ; Male ; Middle Aged ; Nerve Tissue Proteins/genetics ; Nerve Tissue Proteins/physiology ; Neurodegenerative Diseases/physiopathology ; Pedigree ; Penetrance ; Polymorphism, Single Nucleotide ; Potassium Channels/genetics ; Potassium Channels/physiology ; Protein Stability ; Protein Transport ; Synaptic Transmission ; Whole Genome Sequencing
Czasopismo naukowe
    Wyświetlanie 1-4 z 4

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies