About: Kurt Højlund

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	Forscher (de) forskare (sv) researcher (en) investigador (es) chercheur (fr) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) 研究員 (ja) onderzoeker (nl)
rdfs:label	Kurt Højlund (da) Kurt Højlund (en) Kurt Højlund (es) Kurt Højlund (nl) Kurt Højlund (ast)
skos:prefLabel	Kurt Højlund (da) Kurt Højlund (en) Kurt Højlund (es) Kurt Højlund (nl) Kurt Højlund (ast)
name	Kurt Højlund (da) Kurt Højlund (en) Kurt Højlund (es) Kurt Højlund (nl) Kurt Højlund (ast)
Scopus author ID	wds:Q42591296-8701cc15-4b9b-629c-de5a-153ac16f7f35
Scopus author ID	6603935402
given name	wds:Q42591296-B92266C9-5AA3-46E0-9663-E5E0FED7C84D
given name	Kurt
instance of	wds:Q42591296-2CFBA3D0-824A-4813-9329-A0EC0EE102EB
instance of	Homo sapiens
occupation	wds:Q42591296-ACF6BBED-2532-431B-8B3A-7ED2356F8C2D
sex or gender	wds:Q42591296-4D3B46A3-F57C-40EE-A571-70535EDE1D72
educated at	wds:Q42591296-EC0F2B81-A81F-4FF3-9A03-E89EA1DA88F8
family name	wds:Q42591296-bc1bfff1-41b4-5e86-7106-3a78dcfce5fe
occupation	researcher
sex or gender	male
educated at	Odense University Hospital
family name	Højlund
ORCID iD	wds:Q42591296-f521991c-417a-fba6-3526-4c4401a6ac29
ORCID iD	https://orcid.org/0000-0002-0891-4224
ORCID iD	0000-0002-0891-4224
is owl:sameAs of	Kurt Højlund
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42591296
is author of	Phosphoproteome analysis of functional mitochondria isolated from resting human muscle reveals extensive phosphorylation of inner membrane protein complexes and enzymes Glucose tolerance is associated with differential expression of microRNAs in skeletal muscle: results from studies of twins with and without type 2 diabetes Soluble CD36 and risk markers of insulin resistance and atherosclerosis are elevated in polycystic ovary syndrome and significantly reduced during pioglitazone treatment. Reduced insulin-mediated citrate synthase activity in cultured skeletal muscle cells from patients with type 2 diabetes: evidence for an intrinsic oxidative enzyme defect A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis Genome-wide analysis of DNA methylation differences in muscle and fat from monozygotic twins discordant for type 2 diabetes Insulin increases phosphorylation of mitochondrial proteins in human skeletal muscle in vivo Increased serum concentrations of persistent organic pollutants among prediabetic individuals: potential role of altered substrate oxidation patterns Proteomics analysis of human skeletal muscle reveals novel abnormalities in obesity and type 2 diabetes Increased reactive oxygen species production and lower abundance of complex I subunits and carnitine palmitoyltransferase 1B protein despite normal mitochondrial respiration in insulin-resistant human skeletal muscle Rac1 signaling is required for insulin-stimulated glucose uptake and is dysregulated in insulin-resistant murine and human skeletal muscle AMPK activity and isoform protein expression are similar in muscle of obese subjects with and without type 2 diabetes Characterization of the human skeletal muscle proteome by one-dimensional gel electrophoresis and HPLC-ESI-MS/MS. The primary defect in glycogen synthase activity is not based on increased glycogen synthase kinase-3alpha activity in diabetic myotubes The diabetic phenotype is conserved in myotubes established from diabetic subjects: evidence for primary defects in glucose transport and glycogen synthase activity A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene The proteomic signature of insulin-resistant human skeletal muscle reveals increased glycolytic and decreased mitochondrial enzymes. Mitochondrial dysfunction in type 2 diabetes and obesity RETRACTED: The SNARE protein SNAP23 and the SNARE-interacting protein Munc18c in human skeletal muscle are implicated in insulin resistance/type 2 diabetes The assembly of lipid droplets and its relation to cellular insulin sensitivity Statement of Retraction. The SNARE Protein SNAP23 and the SNARE-Interacting Protein Munc18c in Human Skeletal Muscle Are Implicated in Insulin Resistance/Type 2 Diabetes. Diabetes 2010;59:1870-1878. DOI: 10.2337/db09-1503. PMID: 20460426 Markers of autophagy are adapted to hyperglycaemia in skeletal muscle in type 2 diabetes Total and high molecular weight (HMW) adiponectin levels and measures of glucose and lipid metabolism following pioglitazone treatment in a randomized placebo-controlled study in polycystic ovary syndrome Increased metabolic risk in adolescent offspring of mothers with type 1 diabetes: the EPICOM study Testosterone therapy increased muscle mass and lipid oxidation in aging men. Mitochondrial phosphoproteomics of mammalian tissues Novel tyrosine phosphorylation sites in rat skeletal muscle revealed by phosphopeptide enrichment and HPLC-ESI-MS/MS. Intake of St John's wort improves the glucose tolerance in healthy subjects who ingest metformin compared with metformin alone Microvesicles Correlated with Components of Metabolic Syndrome in Men with Type 2 Diabetes Mellitus and Lowered Testosterone Levels But Were Unaltered by Testosterone Therapy Impaired glycogen synthase activity and mitochondrial dysfunction in skeletal muscle: markers or mediators of insulin resistance in type 2 diabetes? Pioglitazone enhances mitochondrial biogenesis and ribosomal protein biosynthesis in skeletal muscle in polycystic ovary syndrome Effect of testosterone on insulin sensitivity, oxidative metabolism and body composition in aging men with type 2 diabetes on metformin monotherapy. Metabolism and insulin signaling in common metabolic disorders and inherited insulin resistance Hypoglycemia-associated electroencephalogram and electrocardiogram changes appear simultaneously Beta-cell function is associated with carotid intima-media thickness independently of insulin resistance in healthy individuals Follow-up duration influences the relative importance of OGTT and optimal timing of glucose measurements for predicting future type 2 diabetes The Human Skeletal Muscle Proteome Project: a reappraisal of the current literature Adrenal activity and metabolic risk during randomized escitalopram or placebo treatment in PCOS. Studies of association of AGPAT6 variants with type 2 diabetes and related metabolic phenotypes in 12,068 Danes The Mitochondrial Proteomic Signatures of Human Skeletal Muscle Linked to Insulin Resistance Erratum to: The proteomic signature of insulin-resistant human skeletal muscle reveals increased glycolytic and decreased mitochondrial enzymes
is author of	wds:Q34516412-2AF3372D-9BF5-437B-A788-8DEE821B36E0 wds:Q34268235-72C2DF8E-FD28-4111-943C-0B9B2DBEF7C2 wds:Q33556644-C9BD8113-54BE-415B-B79A-64D03F424460 wds:Q42290865-C3AC02BF-DA33-4DC9-9CB3-B68875EF1293 wds:Q38926937-6E36BAB6-DCB2-423C-8390-6CBEE713DCF8 wds:Q42519279-055EB82F-7CEE-4D33-8C13-2DBC79D0D9E5 wds:Q42455953-E8D3EC73-69FC-4DC8-8AA0-49F3FBB3B5A7 wds:Q37332538-41A90F26-F6A5-4986-8C33-24BF7C51C138 wds:Q30495722-CA3D0485-A424-47D1-9B62-AC9497CE272C wds:Q35757202-0B0789BC-2C47-4FFA-AEED-A70F3661C87A wds:Q40939812-77AFC00F-3139-4278-B7D7-4816C09E35D0 wds:Q42133190-3E9F2894-6E64-47B2-8A01-240C6BB52A1D wds:Q40997411-80106DE8-64F2-43D4-87F9-D0EA4E5C23BD

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