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Advanced Search Results For "Konrad RA"

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 "Konrad RA"
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Comparative transcriptome in large-scale human and cattle populations

Publication Type: Academic Journal

Source(s): Genome Biology, Vol 23, Iss 1, Pp 1-24 (2022)

Abstract: Abstract Background Cross-species comparison of transcriptomes is important for elucidating evolutionary molecular mechanisms underpinning phenotypic variation between and within species, yet to date it has been essentially limited to model organisms w...

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Determinants of hyperglucagonemia in pediatric non-alcoholic fatty liver disease

Publication Type: Academic Journal

Source(s): Frontiers in Endocrinology, Vol 13 (2022)

Abstract: ObjectiveOver the years, non-alcoholic fatty liver (NAFLD) disease has progressed to become the most frequent chronic liver disease in children and adolescents. The full pathology is not yet known, but disease progression leads to cirrhosis and hepatoc...

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Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

Publication Type: Academic Journal

Source(s): Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)

Abstract: Genetic studies of eczema to date have mostly explored common genetic variation. Here, the authors perform a large meta-analysis for common and rare variants and discover 8 loci associated with eczema. Over 20% of the heritability of the condition is a...

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Physician-Confirmed and Administrative Definitions of Stroke in UK Biobank Reflect the Same Underlying Genetic Trait

Publication Type: Academic Journal

Source(s): Frontiers in Neurology, Vol 12 (2022)

Abstract: BackgroundStroke in UK Biobank (UKB) is ascertained via linkages to coded administrative datasets and self-report. We studied the accuracy of these codes using genetic validation.MethodsWe compiled stroke-specific and broad cerebrovascular disease (CVD...

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Cardiovascular Risk Assessment by SCORE2 Predicts Risk for Colorectal Neoplasia and Tumor-Related Mortality

Publication Type: Academic Journal

Source(s): Journal of Personalized Medicine, Vol 12, Iss 848, p 848 (2022)

Abstract: Objectives: The European Society of Cardiology endorsed SCORE2 to assess cardiovascular risk. The aim of this observational, retrospective study was to assess whether SCORE2 is associated with colorectal neoplasia in an asymptomatic screening populatio...

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Identification of epigenome-wide DNA methylation differences between carriers of APOE ε4 and APOE ε2 alleles

Publication Type: Academic Journal

Source(s): Genome Medicine, Vol 13, Iss 1, Pp 1-14 (2021)

Abstract: Abstract Background The apolipoprotein E (APOE) ε4 allele is the strongest genetic risk factor for late onset Alzheimer’s disease, whilst the ε2 allele confers protection. Previous studies report differential DNA methylation of APOE between ε4 and ε2 c...

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