about
Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1)--distinct characteristics in neuronsEffect of apolipoprotein M on high density lipoprotein metabolism and atherosclerosis in low density lipoprotein receptor knock-out miceThe role of ANGPTL3 in controlling lipoprotein metabolismAngiopoietin-like 4 mediates PPAR delta effect on lipoprotein lipase-dependent fatty acid uptake but not on beta-oxidation in myotubesProlonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses.USF1 deficiency activates brown adipose tissue and improves cardiometabolic healthAntigenic differences between AS03 adjuvanted influenza A (H1N1) pandemic vaccines: implications for pandemrix-associated narcolepsy risk.Increased apolipoprotein E level and reduced high-density lipoprotein mean particle size associate with low high-density lipoprotein cholesterol and features of metabolic syndrome.The effect of proatherogenic pathogens on adipose tissue transcriptome and fatty acid distribution in apolipoprotein E-deficient mice.Mutations in the ANGPTL3 gene and familial combined hypolipidemia: a clinical and biochemical characterization.Interaction of phospholipid transfer protein with human tear fluid mucins.Quantitation of serum angiopoietin-like proteins 3 and 4 in a Finnish population sampleAnalysis of lipid transfer activity between model nascent HDL particles and plasma lipoproteins: implications for current concepts of nascent HDL maturation and genesis.Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.Patients with type 1 diabetes show signs of vascular dysfunction in response to multiple high-fat meals.Human tear fluid lipidome: from composition to function.Human apoA-I increases macrophage foam cell derived PLTP activity without affecting the PLTP massEffect of simvastatin, an established lipid-lowering drug, on pulmonary Chlamydia pneumoniae infection in mice.The orientation and dynamics of estradiol and estradiol oleate in lipid membranes and HDL disc models.Composition and lipid spatial distribution of HDL particles in subjects with low and high HDL-cholesterol.Specific collagen XVIII isoforms promote adipose tissue accrual via mechanisms determining adipocyte number and affect fat deposition.Isolation and partial characterization of the inactive and active forms of human plasma phospholipid transfer protein (PLTP).Effect of HDL composition and particle size on the resistance of HDL to the oxidation.Adipose tissue gene expression analysis reveals changes in inflammatory, mitochondrial respiratory and lipid metabolic pathways in obese insulin-resistant subjects.Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL.Osbpl8 deficiency in mouse causes an elevation of high-density lipoproteins and gender-specific alterations of lipid metabolismPlasma phospholipid transfer activity is essential for increased atherogenesis in PLTP transgenic mice: a mutation-inactivation study.Silencing of ANGPTL 3 (angiopoietin-like protein 3) in human hepatocytes results in decreased expression of gluconeogenic genes and reduced triacylglycerol-rich VLDL secretion upon insulin stimulation.Atomistic MD simulation reveals the mechanism by which CETP penetrates into HDL enabling lipid transfer from HDL to CETPDry eye symptoms are increased in mice deficient in phospholipid transfer protein (PLTP).Lipoprotein-associated estrogens.Partial sleep restriction activates immune response-related gene expression pathways: experimental and epidemiological studies in humansSerum angiopoietin-like 4 protein levels and expression in adipose tissue are inversely correlated with obesity in monozygotic twins.Effects of whole grain, fish and bilberries on serum metabolic profile and lipid transfer protein activities: a randomized trial (Sysdimet).Apolipoprotein A-I exerts bactericidal activity against Yersinia enterocolitica serotype O:3Matrix metalloproteinase 8 degrades apolipoprotein A-I and reduces its cholesterol efflux capacity.Identification and analysis of anti-HDL scFv-antibodies obtained from phage display based synthetic antibody library.The relationship between plasma angiopoietin-like protein 4 levels, angiopoietin-like protein 4 genotype, and coronary heart disease risk.A Novel Positron Emission Tomography (PET) Approach to Monitor Cardiac Metabolic Pathway Remodeling in Response to Sunitinib Malate.Impaired HDL2-mediated cholesterol efflux is associated with metabolic syndrome in families with early onset coronary heart disease and low HDL-cholesterol level
P50
Q21284156-149CF5DD-94AA-4A79-8B55-C2D66149E208Q24300591-BC1EED68-6986-4BA7-9598-31ECF5CA0AD8Q26769679-4C9C158C-B8B1-422E-BEB0-C8F6D1CF3D03Q27316586-2EB4F376-7D1C-4E6B-A66E-1128DA82950EQ27319844-AD465477-85DC-4EAC-A367-FFC2F595688DQ28272648-BC9C4FE6-C6A3-45AA-87A3-AE678E86D1E6Q30369654-BA9D347E-9437-4FEA-A074-1B77FC773D8FQ30386366-20B9D735-35F8-48A1-9027-A180A06CF5EDQ33558862-030422FE-268F-49B9-B8FC-188D50B792C8Q33569939-E685B534-14C6-4238-94A5-35788635E940Q33666024-8C1FDE4A-4E63-4007-9571-237FDDBA47D0Q33741200-F2885121-2764-40FB-B96F-317581448929Q33741256-9E5029AC-8C0A-4991-890F-F733D25B8EDCQ33772642-A63AEACF-0F0E-4431-9AC3-E2ECC113FA08Q33792579-51056ED4-2894-4209-9698-B55E306F5471Q33900724-BD1B00DA-951A-4599-A89E-36698331EF7AQ33933958-005CA159-8C07-4800-A759-DFCC72D53EE5Q33935447-88B3C56F-0B5A-4AB0-B76D-679EB6BFF738Q33990957-21BE8C02-EB70-4477-961F-B9AF756C144AQ33993200-9C215C27-DD48-4E5A-8A75-A42E7E4A77BEQ34002255-5421F3B0-4850-487E-9CD8-C262B8D93991Q34114968-FD3F02DC-788D-455B-862C-A9D526AF3AEAQ34198872-1ADC1C06-744B-4E1F-A07E-BFDA29029EBBQ34218786-88A297CB-ECD8-4F3A-BB31-0192E4DBB03DQ34610302-DD43CC5A-A2FF-40B6-8DE7-C196CCEF818AQ34648407-E8B5E777-E660-4A1B-B460-11A01C31BF0AQ34656954-5F04717A-2CAB-4414-8293-33636D40F5EEQ34706796-9A556554-AD2C-49BA-9B7E-5A776DAF78ECQ34757508-90F508ED-EFF5-4980-8ECE-371FC693F3C3Q34838652-E4FBAAC7-3B3F-4233-9988-67BF924767EDQ34977195-E8CF86E4-E44B-4E9B-86DC-71A41E473993Q35032380-310D21D8-E053-4110-BF78-6EE913CB7132Q35107317-57B47FED-41BA-4156-8649-084EDEA1CC68Q35108988-DDFED1D4-F4D9-4C6D-B5AE-7F4282B364ABQ35515462-841CE57E-7412-4895-8379-386D12292A1BQ35536038-A5CB420B-EE63-43DE-B437-7AC902A32144Q35866180-230F7706-27B0-4C3C-886A-1AA34EEA05F1Q35869973-735689B6-7772-4397-8AF5-FE90C1B76096Q36262416-C59C2A03-1BD1-45B6-8559-8A52708CFFB7Q36282932-305228D9-7BE9-47AB-81BE-F603AF4FC80E
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Matti Jauhiainen
@ast
Matti Jauhiainen
@en
Matti Jauhiainen
@es
Matti Jauhiainen
@nl
type
label
Matti Jauhiainen
@ast
Matti Jauhiainen
@en
Matti Jauhiainen
@es
Matti Jauhiainen
@nl
prefLabel
Matti Jauhiainen
@ast
Matti Jauhiainen
@en
Matti Jauhiainen
@es
Matti Jauhiainen
@nl
P106
P31
P496
0000-0002-3836-3785