Results 21 to 30 of about 81,114 (212)
Characterisation of an aperture-stacked patch antenna for ultra-wideband wearable radio systems [PDF]
This paper presents, for the first time, the time-domain characteristics of an aperture-stacked patch antenna (ASPA) for ultra-wideband (UWB) wearable devices. The methodology of antennas characterization for UWB radio systems is also outlined.
Klemm, M, Troster, G
core +2 more sources
Aspartoacylase suppresses prostate cancer progression by blocking LYN activation
Background Globally, despite prostate cancer (PCa) representing second most prevalent malignancy in male, the precise molecular mechanisms implicated in its pathogenesis remain unclear.
Hong Weng +13 more
doaj +1 more source
Mass transfer in a membrane aerated biofilm [PDF]
We present experimental results of mass transfer of a non reactive tracer gas (neon)measured in aerobic heterotrophic biofilm developed from activated sludge.
Aimar, Pierre +4 more
core +4 more sources
Genus Aspa H. Adams & A. Adams, 1853 Type species. Ranella laevigata Lamarck, 1822 (= Buccinum marginatum Gmelin, 1791) (H. Adams & A. Adams 1853: 106), by monotypy. Pliocene, Italy.
Sacchetti, Claudia +2 more
openaire +2 more sources
Combining Double Fluorescence In Situ Hybridization with Immunolabelling for Detection of the Expression of Three Genes in Mouse Brain Sections [PDF]
Detection of gene expression in different types of brain cells e.g., neurons, astrocytes, oligodendrocytes, oligodendrocyte precursors and microglia, can be hampered by the lack of specific primary or secondary antibodies for immunostaining.
Fudge, A +4 more
core +1 more source
Gene replacement therapy is a rational therapeutic strategy and clinical intervention for neurodegenerative disorders like Canavan disease, a leukodystrophy caused by biallelic mutations in the aspartoacylase (ASPA) gene.
Manuela Corti +17 more
doaj +1 more source
Loss of central auditory processing in a mouse model of Canavan disease.
Canavan Disease (CD) is a leukodystrophy caused by homozygous null mutations in the gene encoding aspartoacylase (ASPA). ASPA-deficiency is characterized by severe psychomotor retardation, and excessive levels of the ASPA substrate N-acetylaspartate (NAA)
Georg von Jonquieres +5 more
doaj +1 more source
Evidence of global-scale aeolian dispersal and endemism in isolated geothermal microbial communities of Antarctica [PDF]
New evidence in aerobiology challenges the assumption that geographical isolation is an effective barrier to microbial transport. However, given the uncertainty with which aerobiological organisms are recruited into existing communities, the ultimate ...
Cary, S. Craig +3 more
core +2 more sources
Aspartoacylase deficiency affects early postnatal development of oligodendrocytes and myelination
Canavan disease (CD) is a neurodegenerative disease, caused by a deficiency in the enzyme aspartoacylase (ASPA). This enzyme has been localized to oligodendrocytes; however, it is still undefined how ASPA deficiency affects oligodendrocyte development ...
Natalia S. Mattan +6 more
doaj +1 more source
BVLOS UAV missions for vegetation mapping in maritime Antarctic
Polar areas are among the regions where climate change occurs faster than on most of the other areas on Earth. To study the effects of climate change on vegetation, there is a need for knowledge on its current status and properties.
Anna Zmarz +6 more
doaj +1 more source

