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Institution

University of Bergen

EducationBergen, Hordaland, Norway
About: University of Bergen is a education organization based out in Bergen, Hordaland, Norway. It is known for research contribution in the topics: Population & Large Hadron Collider. The organization has 17106 authors who have published 52492 publications receiving 2009844 citations. The organization is also known as: Universitetet i Bergen & Universitas Bergensis.


Papers
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Journal ArticleDOI
TL;DR: Results indicate that compounds with a selective PPARα activation profile reduce insulin resistance without having adverse effects on body weight and adipose tissue mass in animal models of IR.

619 citations

Journal ArticleDOI
TL;DR: Practical advice for the application of exercise in heart failure and how to overcome traditional barriers is provided, based on the current scientific and clinical knowledge supporting the beneficial effect of this intervention.
Abstract: The European Society of Cardiology heart failure guidelines firmly recommend regular physical activity and structured exercise training (ET), but this recommendation is still poorly implemented in daily clinical practice outside specialized centres and in the real world of heart failure clinics. In reality, exercise intolerance can be successfully tackled by applying ET. We need to encourage the mindset that breathlessness may be evidence of signalling between the periphery and central haemodynamic performance and regular physical activity may ultimately bring about favourable changes in myocardial function, symptoms, functional capacity, and increased hospitalization-free life span and probably survival. In this position paper, we provide practical advice for the application of exercise in heart failure and how to overcome traditional barriers, based on the current scientific and clinical knowledge supporting the beneficial effect of this intervention.

618 citations

Journal ArticleDOI
TL;DR: A genome-wide analysis of unrelated adults with data on single nucleotide polymorphisms and detailed phenotypes on cognitive traits unequivocally confirms that a substantial proportion of individual differences in human intelligence is due to genetic variation, and is consistent with many genes of small effects underlying the additive genetic influences on intelligence.
Abstract: General intelligence is an important human quantitative trait that accounts for much of the variation in diverse cognitive abilities. Individual differences in intelligence are strongly associated with many important life outcomes, including educational and occupational attainments, income, health and lifespan. Data from twin and family studies are consistent with a high heritability of intelligence, but this inference has been controversial. We conducted a genome-wide analysis of 3511 unrelated adults with data on 549692 single nucleotide polymorphisms (SNPs) and detailed phenotypes on cognitive traits. We estimate that 40% of the variation in crystallized-type intelligence and 51% of the variation in fluid-type intelligence between individuals is accounted for by linkage disequilibrium between genotyped common SNP markers and unknown causal variants. These estimates provide lower bounds for the narrow-sense heritability of the traits. We partitioned genetic variation on individual chromosomes and found that, on average, longer chromosomes explain more variation. Finally, using just SNP data we predicted B1% of the variance of crystallized and fluid cognitive phenotypes in an independent sample (P=0.009 and 0.028, respectively). Our results unequivocally confirm that a substantial proportion of individual differences in human intelligence is due to genetic variation, and are consistent with many genes of small effects underlying the additive genetic influences on intelligence. Molecular Psychiatry advance online publication, 9 August 2011; doi:10.1038/mp.2011.85

618 citations

Journal ArticleDOI
TL;DR: A multicentre randomised controlled trial that compared the standard model of antenatal care with a new model that emphasises actions known to be effective in improving maternal or neonatal outcomes and has fewer clinic visits is presented in this paper.

617 citations

Journal ArticleDOI
TL;DR: Recent advances in the understanding of the biosynthesis and signalling functions of NAD(P) are summarized and new insights into the molecular mechanisms of NADPH generation and their roles in cell physiology are highlighted.
Abstract: The pyridine nucleotides NAD and NADP play vital roles in metabolic conversions as signal transducers and in cellular defence systems. Both coenzymes participate as electron carriers in energy transduction and biosynthetic processes. Their oxidized forms, NAD + and NADP + , have been identified as important elements of regulatory pathways. In particular, NAD + serves as a substrate for ADP-ribosylation reactions and for the Sir2 family of NAD + -dependent protein deacetylases as well as a precursor of the calcium mobilizing molecule cADPr (cyclic ADP-ribose). The conversions of NADP + into the 2′-phosphorylated form of cADPr or to its nicotinic acid derivative, NAADP, also result in the formation of potent intracellular calcium-signalling agents. Perhaps, the most critical function of NADP is in the maintenance of a pool of reducing equivalents which is essential to counteract oxidative damage and for other detoxifying reactions. It is well known that the NADPH/NADP + ratio is usually kept high, in favour of the reduced form. Research within the past few years has revealed important insights into how the NADPH pool is generated and maintained in different subcellular compartments. Moreover, tremendous progress in the molecular characterization of NAD kinases has established these enzymes as vital factors for cell survival. In the present review, we summarize recent advances in the understanding of the biosynthesis and signalling functions of NAD(P) and highlight the new insights into the molecular mechanisms of NADPH generation and their roles in cell physiology.

615 citations


Authors

Showing all 17370 results

NameH-indexPapersCitations
Stephen V. Faraone1881427140298
Patrick O. Brown183755200985
Anil K. Jain1831016192151
Marc Weber1672716153502
Johan Auwerx15865395779
Leif Groop158919136056
Charles M. Perou156573202951
Bart Staels15282486638
Zhenwei Yang150956109344
G. Eigen1482188117450
Thomas Lohse1481237101631
Marco Costa1461458105096
Timothy P. Hughes14583191357
Hermann Kolanoski145127996152
Kjell Fuxe142147989846
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023149
2022448
20213,229
20203,149
20192,800
20182,648