Informacja

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

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""CRUTS, M"" wg kryterium: Autor


Wyświetlanie 1-17 z 17
Tytuł :
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval
Autorzy :
RADEMAKERS, R
CRUTS, M
DERMAUT, B
SLEEGERS, K
ROSSO, S. M
VAN DEN BROECK, M
BACKHOVENS, H
VAN SWIETEN, J
VAN DUIJN, C. M
VAN BROECKHOVEN, C
Pokaż więcej
Temat :
Encéphale pathologie
Cerebral disorder
Encéfalo patología
Homme
Human
Hombre
Maladie dégénérative
Degenerative disease
Enfermedad degenerativa
Système nerveux central pathologie
Central nervous system disease
Sistema nervosio central patología
Système nerveux pathologie
Nervous system diseases
Sistema nervioso patología
Adulte
Adult
Adulto
Bras long
Long arm
Brazo largo
Chromosome E17
Cromosoma E17
Dégénérescence
Degeneration
Degeneración
Démence Alzheimer
Alzheimer disease
Demencia Alzheimer
Etude familiale
Family study
Estudio familiar
Généalogie
Genealogy
Genealogía
Génétique
Genetics
Genética
Liaison génétique
Linkage
Ligamiento genético
Lobe frontal
Frontal lobe
Lóbulo frontal
Lobe temporal
Temporal lobe
Lóbulo temporal
Maladie familiale
Familial disease
Enfermedad familiar
Mutation
Mutación
Sciences biologiques et medicales
Biological and medical sciences
Sciences medicales
Medical sciences
Psychopathologie. Psychiatrie
Psychopathology. Psychiatry
Etude clinique de l'enfant
Child clinical studies
Troubles du développement
Developmental disorders
Déficience intellectuelle
Intellectual deficiency
Genetique medicale
Medical genetics
Maladies mentales et troubles du comportement
Mental and behavioral disorders
Psychologie. Psychanalyse. Psychiatrie
Psychology. Psychoanalysis. Psychiatry
PSYCHOPATHOLOGIE. PSYCHIATRIE
Biochemistry, molecular biology, biophysics
Biochimie, biologie moléculaire, biophysique
Psychology, psychopathology, psychiatry
Psychologie, psychopathologie, psychiatrie
Źródło :
Molecular psychiatry. 7(10):1064-1074
Materiał oryginalny :
INIST-CNRS
Opis pliku :
text
Dostęp URL :
http://pascal-francis.inist.fr/vibad/index.php?action=search&terms=14386073
Czasopismo naukowe
Tytuł :
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD.
Autorzy :
Boeynaems S; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.
Bogaert E; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.
Michiels E; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.
Gijselinck I; Department of Molecular Genetics, VIB, B-2610 Antwerp, Belgium.; Institute Born-Bunge, University of Antwerp, B-2610 Antwerp, Belgium.
Sieben A; Department of Molecular Genetics, VIB, B-2610 Antwerp, Belgium.; Institute Born-Bunge, University of Antwerp, B-2610 Antwerp, Belgium.; Department of Neurology, University Hospital Ghent and University of Ghent, B-9000 Ghent, Belgium.
Jovičić A; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305 USA.
De Baets G; Switch Laboratory, VIB, B-3000 Leuven, Belgium.; Switch Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.
Scheveneels W; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.
Steyaert J; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.
Cuijt I; Department of Molecular Genetics, VIB, B-2610 Antwerp, Belgium.; Institute Born-Bunge, University of Antwerp, B-2610 Antwerp, Belgium.
Verstrepen KJ; VIB Laboratory of Systems Biology, Gaston Geenslaan 1, B-3001 Leuven, Belgium.; KU Leuven - University of Leuven, Department of Microbial and Molecular Systems, Laboratory for Genetics and Genomics, Gaston Geenslaan 1, B-3001 Leuven, Belgium.
Callaerts P; KU Leuven - University of Leuven, Department of Human Genetics, Laboratory of Behavioral and Developmental Genetics, B-3000 Leuven, Belgium.; VIB Center for the Biology of Disease, B-3000 Leuven, Belgium.
Rousseau F; Switch Laboratory, VIB, B-3000 Leuven, Belgium.; Switch Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.
Schymkowitz J; Switch Laboratory, VIB, B-3000 Leuven, Belgium.; Switch Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, B-3000 Leuven, Belgium.
Cruts M; Department of Molecular Genetics, VIB, B-2610 Antwerp, Belgium.; Institute Born-Bunge, University of Antwerp, B-2610 Antwerp, Belgium.
Van Broeckhoven C; Department of Molecular Genetics, VIB, B-2610 Antwerp, Belgium.; Institute Born-Bunge, University of Antwerp, B-2610 Antwerp, Belgium.
Van Damme P; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.; University Hospitals Leuven, Department of Neurology, B-3000 Leuven, Belgium.
Gitler AD; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305 USA.
Robberecht W; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.; University Hospitals Leuven, Department of Neurology, B-3000 Leuven, Belgium.
Van Den Bosch L; KU Leuven - University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), B-3000 Leuven, Belgium.; VIB, Vesalius Research Center, Laboratory of Neurobiology, B-3000 Leuven, Belgium.
Pokaż więcej
Źródło :
Scientific reports [Sci Rep] 2016 Feb 12; Vol. 6, pp. 20877. Date of Electronic Publication: 2016 Feb 12.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Genes, Insect*
Genetic Testing*
Repetitive Sequences, Amino Acid*
Amyotrophic Lateral Sclerosis/*genetics
Cell Nucleus/*metabolism
Dipeptides/*chemistry
Drosophila melanogaster/*genetics
Frontotemporal Dementia/*genetics
Active Transport, Cell Nucleus/genetics ; Animals ; Arginine/metabolism ; Disease Models, Animal ; Eye/pathology ; HeLa Cells ; Humans ; Methylation ; RNA Interference
Czasopismo naukowe
Tytuł :
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Autorzy :
Cruts M; Neurodegenerative Brain Diseases Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, Universiteitsplein 1, BE-2610 Antwerpen, Belgium.
Gijselinck I
van der Zee J
Engelborghs S
Wils H
Pirici D
Rademakers R
Vandenberghe R
Dermaut B
Martin JJ
van Duijn C
Peeters K
Sciot R
Santens P
De Pooter T
Mattheijssens M
Van den Broeck M
Cuijt I
Vennekens K
De Deyn PP
Kumar-Singh S
Van Broeckhoven C
Pokaż więcej
Źródło :
Nature [Nature] 2006 Aug 24; Vol. 442 (7105), pp. 920-4. Date of Electronic Publication: 2006 Jul 16.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 17/*genetics
Dementia/*genetics
Frontal Lobe/*physiopathology
Intercellular Signaling Peptides and Proteins/*deficiency
Mutation/*genetics
Temporal Lobe/*physiopathology
Ubiquitin/*metabolism
Belgium ; DNA Mutational Analysis ; Dementia/physiopathology ; Frontal Lobe/metabolism ; Genetic Linkage/genetics ; Humans ; Intercellular Signaling Peptides and Proteins/genetics ; Physical Chromosome Mapping ; Progranulins ; RNA Splice Sites/genetics ; Temporal Lobe/metabolism
Czasopismo naukowe
Tytuł :
Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample.
Autorzy :
van Duijn CM; Department of Epidemiology & Biostatistics, Erasmus University Medical School, Rotterdam, The Netherlands.
Cruts M
Theuns J
Van Gassen G
Backhovens H
van den Broeck M
Wehnert A
Serneels S
Hofman A
Van Broeckhoven C
Pokaż więcej
Źródło :
European journal of human genetics : EJHG [Eur J Hum Genet] 1999 Oct-Nov; Vol. 7 (7), pp. 801-6.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Age of Onset*
Alzheimer Disease/*genetics
Membrane Proteins/*genetics
Polymorphism, Genetic/*genetics
Promoter Regions, Genetic/*genetics
Aged ; Case-Control Studies ; Genes, Regulator/genetics ; Humans ; Introns/genetics ; Linkage Disequilibrium ; Middle Aged ; Mutation ; Presenilin-1 ; Tandem Repeat Sequences/genetics
Czasopismo naukowe
    Wyświetlanie 1-17 z 17

    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