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Wyszukujesz frazę ""RADEMAKERS, R"" wg kryterium: Autor


Wyświetlanie 1-5 z 5
Tytuł:
Partial Tmem106b reduction does not correct abnormalities due to progranulin haploinsufficiency.
Autorzy:
Arrant AE; Center for Neurodegeneration and Experimental Therapeutics, Alzheimer's Disease Center, Evelyn F. McKnight Brain Institute, Departments of Neurology and Neurobiology, University of Alabama at Birmingham, 1825 University Blvd., SHEL, Birmingham, AL, 1110, USA.
Nicholson AM; Department of Neuroscience, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL, USA.
Zhou X; Department of Neuroscience, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL, USA.
Rademakers R; Department of Neuroscience, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL, USA. rademakers..
Roberson ED; Center for Neurodegeneration and Experimental Therapeutics, Alzheimer's Disease Center, Evelyn F. McKnight Brain Institute, Departments of Neurology and Neurobiology, University of Alabama at Birmingham, 1825 University Blvd., SHEL, Birmingham, AL, 1110, USA. .
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Źródło:
Molecular neurodegeneration [Mol Neurodegener] 2018 Jun 22; Vol. 13 (1), pp. 32. Date of Electronic Publication: 2018 Jun 22.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Frontotemporal Dementia/*genetics
Intercellular Signaling Peptides and Proteins/*genetics
Membrane Proteins/*genetics
Nerve Tissue Proteins/*genetics
Animals ; Frontotemporal Dementia/pathology ; Granulins ; Haploinsufficiency ; Heterozygote ; Mice ; Mice, Mutant Strains ; Mutation ; Polymorphism, Single Nucleotide ; Progranulins
Czasopismo naukowe
Tytuł:
Progranulin regulates neuronal outgrowth independent of sortilin.
Autorzy:
Gass J; Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, FL, USA.
Lee WC
Cook C
Finch N
Stetler C
Jansen-West K
Lewis J
Link CD
Rademakers R
Nykjær A
Petrucelli L
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Źródło:
Molecular neurodegeneration [Mol Neurodegener] 2012 Jul 10; Vol. 7, pp. 33. Date of Electronic Publication: 2012 Jul 10.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Cell Proliferation*
Adaptor Proteins, Vesicular Transport/*metabolism
Hippocampus/*metabolism
Intercellular Signaling Peptides and Proteins/*metabolism
Neurites/*metabolism
Adaptor Proteins, Vesicular Transport/genetics ; Animals ; Blotting, Western ; Enzyme-Linked Immunosorbent Assay ; Frontotemporal Lobar Degeneration/genetics ; Frontotemporal Lobar Degeneration/metabolism ; Granulins ; Hippocampus/cytology ; Immunohistochemistry ; Intercellular Signaling Peptides and Proteins/genetics ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Microscopy, Confocal ; Neurons/cytology ; Neurons/metabolism ; Organ Culture Techniques ; Progranulins
Czasopismo naukowe
Tytuł:
Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations.
Autorzy:
Kocerha J; Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA.
Kouri N
Baker M
Finch N
DeJesus-Hernandez M
Gonzalez J
Chidamparam K
Josephs KA
Boeve BF
Graff-Radford NR
Crook J
Dickson DW
Rademakers R
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Źródło:
BMC genomics [BMC Genomics] 2011 Oct 27; Vol. 12, pp. 527. Date of Electronic Publication: 2011 Oct 27.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
DNA-Binding Proteins/*metabolism
Frontotemporal Lobar Degeneration/*genetics
Intercellular Signaling Peptides and Proteins/*genetics
MicroRNAs/*metabolism
Aged ; Aged, 80 and over ; Cerebellum/metabolism ; Cerebellum/pathology ; Female ; Frontal Lobe/metabolism ; Frontal Lobe/pathology ; Frontotemporal Lobar Degeneration/pathology ; Gene Expression Profiling ; Humans ; Male ; MicroRNAs/genetics ; Middle Aged ; Mutation ; Oligonucleotide Array Sequence Analysis ; Progranulins ; Protein Precursors/genetics
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
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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
    Wyświetlanie 1-5 z 5

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