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Språk- och litteraturcentrum Ryska 2 RYSA02 Litteraturlista Litteraturlista för RYSA02, RYSKA, FORTSÄTTNINGSKURS, 30 högskolepoäng fastställd av Lärarkollegium 5 2013-01-14, reviderad 2015-06-03 Litteratur Delkurs 1. Grammatik och skriftlig språkfärdighet Wade, Terence (2010). A Comprehensive Russian Grammar , Blackwell: Oxford 3. uppl. (NB Går bra med äldre/nyare upplagor). ISBN: 0631158154 (inb.

https://www.sol.lu.se/media/utbildning/dokument/kurser/RYSA02/20162/RYSA02_HT16_.docx - 2026-05-14

314490_nr1_OMSL_RRSW_2021_5.indd RESEARCH REPORTS IN SOCIAL WORK 2021:5 School of Social Work | Lund University Hur har andrahandslägenheter i Malmö kommun fördelats till hemlösa över tid? En studie av prioriteringar och exkluderingar WEDDIG RUNQUIST SOCIALHÖGSKOLAN | LUNDS UNIVERSITET LUNDS UNIVERSITET Socialhögskolan ISBN 978-91-7895-539-8 www.soch.lu.se 9 7 8 9 1 7 8 9 5 5 3 9 8 Sv an en m är k

https://www.soch.lu.se/sites/soch.lu.se/files/2021-10/Web%20RRSW%202021_5-X.pdf - 2026-05-15

FÖRSLAG TILL DISPOSITION 1 (15) UPPHOVSRÄTT – En översikt I denna översikt görs en genomgång av svensk upphovsrätt i allmänhet; vad och vem som skyddas av upphovsrätt, vilka rättigheter som omfattas och vilka inskränkningar som upphovsmannen får tåla, övergång av upphovsrätt och slutligen intrång i upphovsrätt. Endast den egentliga upphovsrätten, som ger skydd åt alster som kommer av ett andligt s

https://www.ub.lu.se/sites/ub.lu.se/files/upphovsraett_-_en_oeversikt.pdf - 2026-05-15

Nationella forskarskolan om åldrande och hälsa Verksamhetsberättelse 2021 CASE - Centre for Ageing and Supportive Environments Centre for Ageing and Supportive Environments Verksamhetsberättelse 2021 2 Omslagsfoto: K. Ruona. Omslagsbilden visar AnnMari Storm, medlem i CASE Brukarråd, som tillsammans med Susanne Iwarsson är i färd med att registrera data i appen för massexperimentet Bostadsförsöket

https://www.case.lu.se/sites/case.lu.se/files/2022-03/Verksamhetsbera%CC%88ttelse%20CASE%202021.pdf - 2026-05-15

Nationella forskarskolan om åldrande och hälsa Verksamhetsberättelse 2021 CASE - Centre for Ageing and Supportive Environments Centre for Ageing and Supportive Environments Verksamhetsberättelse 2021 2 Omslagsfoto: K. Ruona. Omslagsbilden visar AnnMari Storm, medlem i CASE Brukarråd, som tillsammans med Susanne Iwarsson är i färd med att registrera data i appen för massexperimentet Bostadsförsöket

https://www.case.lu.se/sites/case.lu.se/files/2022-09/Verksamhetsbera%CC%88ttelse%20CASE%202021.pdf - 2026-05-15

With the advent of multimodality therapy, the overall five-year survival rate from childhood cancer has improved considerably now exceeding 80% in developed European countries. This growing cohort of survivors, with many years of life ahead of them, has raised the necessity for knowledge concerning the risks of adverse long-term sequelae of the life-saving treatments in order to provide optimal sc

Ferritin heavy chain (FTH1) is a 21-kDa subunit of the ferritin complex, known for its role in iron metabolism, and which has recently been identified as a favorable prognostic protein for triple negative breast cancer (TNBC) patients. Currently, it is not well understood how FTH1 contributes to an anti-tumor response. Here, we explored whether expression and cellular compartmentalization of FTH1

Recent studies have uncovered thousands of long non-coding RNAs (lncRNAs) in human pancreatic β cells. β cell lncRNAs are often cell type specific and exhibit dynamic regulation during differentiation or upon changing glucose concentrations. Although these features hint at a role of lncRNAs in β cell gene regulation and diabetes, the function of β cell lncRNAs remains largely unknown. In this stud

We explored the role of the Krebs cycle enzyme fumarate hydratase (FH) in glucose-stimulated insulin secretion (GSIS). Mice lacking Fh1 in pancreatic β cells (Fh1βKO mice) appear normal for 6–8 weeks but then develop progressive glucose intolerance and diabetes. Glucose tolerance is rescued by expression of mitochondrial or cytosolic FH but not by deletion of Hif1α or Nrf2. Progressive hyperglycem

Genome-wide association studies (GWASs) have shown that common genetic variation contributes to the heritable risk of childhood acute lymphoblastic leukemia (ALL). To identify new susceptibility loci for the largest subtype of ALL, B-cell precursor ALL (BCP-ALL), we conducted a meta-analysis of two GWASs with imputation using 1000 Genomes and UK10K Project data as reference (totaling 1658 cases an

Trabecular bone score (TBS) is a grey-level textural index of bone microarchitecture derived from lumbar spine dual-energy X-ray absorptiometry (DXA) images. TBS is a BMD-independent predictor of fracture risk. The objective of this meta-analysis was to determine whether TBS predicted fracture risk independently of FRAX probability and to examine their combined performance by adjusting the FRAX pr

We conducted pooled and meta-analyses of the association of the calpain-10 gene (CAPN10) polymorphisms SNP-43, Indel-19 and SNP-63 individually and as haplotypes with type 2 diabetes (T2D) in 3237 patients and 2935 controls of European ancestry. In the pooled analyses, the common SNP-43*G allele was associated with modest but statistically significant increased risk of T2D (odds ratio (OR) = 1.11

We assessed the association between 1,414 single nucleotide polymorphisms (SNPs) in genes involved in synthesis and metabolism of steroid hormones and insulin-like growth factor 1, and risk of breast cancer in situ (BCIS), with the aim of determining whether any of these were disease specific. This was carried out using 1,062 BCIS cases and 10,126 controls as well as 6,113 invasive breast cancer c

Three metabolite patterns have previously shown prospective inverse associations with the risk of aggressive prostate cancer within the European Prospective Investigation into Cancer and Nutrition (EPIC). Here, we investigated dietary and lifestyle correlates of these three prostate cancer-related metabolite patterns, which included: 64 phosphatidylcholines and three hydroxysphingomyelins (Pattern

AIMS: Cellular communication network factor 2 (CCN2) is a matricellular protein implicated in fibrotic diseases, with ongoing clinical trials evaluating anti-CCN2-based therapies. By uncovering CCN2 as abundantly expressed in non-diseased artery tissue, this study aimed to investigate the hypothesis that CCN2 plays a pivotal role in maintaining smooth muscle cell (SMC) phenotype and protection aga

Background. Primary glomerular disease (PGD) is a major cause of end-stage kidney disease (ESKD) leading to kidney replacement therapy (KRT). We aimed to describe incidence (trends) in individuals starting KRT for ESKD due to PGD and to examine their survival and causes of death. Methods. We used data from the European Renal Association (ERA) Registry on 69 854 patients who started KRT for ESKD du

INTRODUCTION: The Alzheimer's Association and the Society of Nuclear Medicine and Molecular Imaging convened a multidisciplinary workgroup to update appropriate use criteria (AUC) for amyloid positron emission tomography (PET) and to develop AUC for tau PET. METHODS: The workgroup identified key research questions that guided a systematic literature review on clinical amyloid/tau PET. Building on

The Alzheimer's Association's Research Roundtable met in November 2017 to explore the new National Institute on Aging and the Alzheimer's Association Research Framework for Alzheimer's disease. The meeting allowed experts in the field from academia, industry, and government to provide perspectives on the new National Institute on Aging and the Alzheimer's Association Research Framework. This revie

Numerous biological mechanisms contribute to outcome after stroke, including brain injury, inflammation, and repair mechanisms. Clinical genetic studies have the potential to discover biological mechanisms affecting stroke recovery in humans and identify intervention targets. Large sample sizes are needed to detect commonly occurring genetic variations related to stroke brain injury and recovery.

Researchers from diverse disciplines, including organismal and cellular physiology, sports science, human nutrition, evolution and ecology, have sought to understand the causes and consequences of the surprising variation in metabolic rate found among and within individual animals of the same species. Research in this area has been hampered by differences in approach, terminology and methodology,