6 research outputs found
How Childcare Services contribute to the Reconciliation of Family and Work. Supporting Disadvantaged Families : European Expert Meeting on 17 and 18 May 2018 Berlin
Leave and financial support for family caregivers in EU member states
This report shows which forms of long-term leave exist in several EU member states for family caregivers who care for a dependent relative at home. It also shows, whether there is some form of financial benefit available for the caregiver during the leave. The support arrangements of 14 member states of the European Union (EU) are presented in brief descriptions and overview tables
Auf dem Weg zu mehr Partnerschaftlichkeit : So wird die Beteiligung von VÀtern an Familienarbeit in Europa gefördert
Der Beitrag der Kindertagesbetreuung zur Vereinbarkeit von Familie und Beruf. UnterstĂŒtzung benachteiligter Familien : EuropĂ€isches FachgesprĂ€ch am 17. und 18. Mai 2018 Berlin
Freistellungen und finanzielle Leistungen zur hÀuslichen Pflege in europÀischen Mitgliedstaaten
Die vorliegende Ăbersicht stellt dar, welche Formen einer lĂ€ngerfristigen Freistellung fĂŒr die hĂ€usliche Pflege von Angehörigen in ausgewĂ€hlten EU-Mitgliedstaaten bestehen und ob es fĂŒr die Phase der Pflege eine finanzielle Leistung fĂŒr die pflegende Person gibt. Es werden die gesetzlichen Regelungen aus 14 EU-Mitgliedstaaten in Form von Kurzbeschreibungen und Ăbersichtstabellen vorgestellt
Longitudinal Multi-omics Analyses Identify Responses of Megakaryocytes, Erythroid Cells, and Plasmablasts as Hallmarks of Severe COVID-19.
Temporal resolution of cellular features associated with a severe COVID-19 disease trajectory is needed for understanding skewed immune responses and defining predictors of outcome. Here, we performed a longitudinal multi-omics study using a two-center cohort of 14 patients. We analyzed the bulk transcriptome, bulk DNA methylome, and single-cell transcriptome (>358,000 cells, including BCR profiles) of peripheral blood samples harvested from up to 5 time points. Validation was performed in two independent cohorts of COVID-19 patients. Severe COVID-19 was characterized by an increase of proliferating, metabolically hyperactive plasmablasts. Coinciding with critical illness, we also identified an expansion of interferon-activated circulating megakaryocytes and increased erythropoiesis with features of hypoxic signaling. Megakaryocyte- and erythroid-cell-derived co-expression modules were predictive of fatal disease outcome. The study demonstrates broad cellular effects of SARS-CoV-2 infection beyond adaptive immune cells and provides an entry point toward developing biomarkers and targeted treatments of patients with COVID-19