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Clues to galaxy evolution from spectroscopic observations of Galactic centre stars

In this work we present results from spectroscopic observations of Galactic centre stars. High resolution stellar spectroscopy can be used to determine accurate stellar metallicities and abundances. Observing stars in the Galactic centre is challenging due to extreme extinction. However, observing bright M giants in the K band is viable with 10 m telescopes, which is what has been carried out in t

Making decision on repointing of clay brick facades on the basis of moisture content and water absorption tests results – a review of assessment methods

Use of clay brick masonry in façades is often motivated by its aesthetic values and durability. Yet, mortar joints exposed to climate agents erode over time, expected to cause elevated moisture content and water absorption. Thus, it is often recommended that 40- to 50-year-old facades should be repointed – a measure which is intrusive and costly. Decision is in many cases taken without a clear evi

Post-transcriptional control of stem and cancer cell fate. New roles for an old RNA modification.

Recent advances in high-throughput sequencing technologies uncovered widespread RNA modifications on coding and non-coding RNAs collectively refer to as the epitranscriptome. However, we are only now starting to appreciate the impact of the epitranscriptome in regulating cell biology. Among more than 150 RNA modifications, I focused on pseudouridine (Ψ) the most abundant single-nucleoside RNA modi

Parkinson's Disease among Immigrant Groups and Swedish-Born Individuals : A Cohort Study of All Adults 50 Years of Age and Older in Sweden

Background: There is a lack of studies of Parkinson's disease (PD) in immigrants. Objective: To study the association between country of birth and incident PD in immigrants in Sweden versus Swedish-born individuals. Methods: Study population included all adults aged 50 years and older in Sweden (n=2775736). PD was defined as having at least one registered diagnosis of PD in the National Patient Re

Defining parameters of quality in municipal fire and rescue services - a case study in Denmark

The Emergency Management sector in Denmark consists of 24 Municipal Fire and Rescue Services (MFRSs) responsible for providing a justifiable response to prevent, limit, and redress personal injury and damage to property and the environment arising from accidents and disasters. This research investigates how the MFRSs throughout Denmark define and direct the prevention and response parameters of qu

Associations between Self-Disorders and First-Rank Symptoms : An Empirical Study

BACKGROUND: The diagnostic weight of the first-rank symptoms was deemphasized in DSM-5 and a similar change is expected in ICD-11. This change was motivated by a lack of solid, empirical evidence of the diagnostic significance of first-rank symptoms for schizophrenia. Yet, it seems that Schneider's original concept of first-rank symptoms was overly simplified when it was introduced in DSM-III. Spe

Direct measurement of lipid membrane disruption connects kinetics and toxicity of Aβ42 aggregation

The formation of amyloid deposits in human tissues is a defining feature of more than 50 medical disorders, including Alzheimer’s disease. Strong genetic and histological evidence links these conditions to the process of protein aggregation, yet it has remained challenging to identify a definitive connection between aggregation and pathogenicity. Using time-resolved fluorescence microscopy of indi

Operando high-temperature near-ambient pressure X-ray photoelectron spectroscopy and impedance spectroscopy study of Ni−Ce0.9Gd0.1O2−δ solid oxide fuel cell anode

In this study we present the results of operando high temperature near-ambient-pressure x-ray photoelectron spectroscopy (HT-NAP-XPS) measurements of a pulsed laser deposited thin film Ni−Ce0.9Gd0.1O2−δ model electrode. In our measurements, we have used the novel three electrode dual-chamber electrochemical cell developed in our previous work at different H2 pressures and at different electrochemi

Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents

BACKGROUND: Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by early-onset cerebellar ataxia, oculomotor apraxia and severe axonal polyneuropathy. The aim of this study was to detect the disease-causing variants in two unrelated consanguineous Jordanian families with cerebellar ataxia u