Association between added sugar intake and mortality is

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The text in a 2014 report suggested that APOA1 mRNA is regulated by endogenously expressed antisense RNA. Apolipoprotein A-I induces tubulin phosphorylation in association with cholesterol release in fetal rat astrocytes. ApoA-I may be a protective blood-borne factor involved in the remote ischemic preconditioning mechanism. It maintains cholesterol homeostasis. As the major protein component of plasma HDL, apolipoprotein A-I (ApoA-I) synthesized in the liver and small intestine has been reported to be associated with clinical survival in multiple human cancers, including gastric cancer, nasopharyngeal carcinoma, and breast cancer [14-17]. En forskargrupp vid Lunds universitets Diabetescentrum har visat att proteinet apoA-I har liknande effekt på upptaget av glukos i blodet som insulin. Gruppen har även lyckats identifiera den aktiva delen av apoA-I, vilket på sikt kan leda till nya läkemedel. ApoA-I har antiinflammatoriska och antioxidativa egenskaper, som troligen till stor del bidrar till att förklarara varför apoA-I i HDL-partiklarna kan motverka kärlkomplikationer.

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Thus, our newly generated anti‐apoA‐I fibril mAbs may be utilized for not only diagnosis of apoA‐I‐related amyloidosis but also structural analysis of amyloid fibrils as novel conformation‐selective antibodies. The incidence of CHD is still increasing, which underscores the need for new preventive and therapeutic approaches to decrease CHD risk. In this respect, increasing apoA-I concentrations may be a promising approach, especially through increasing apoA-I synthesis. This review first provides insight into current knowledge on apoA-I production, clearance, and degradation, followed by a systematic Product filter. ApoA-I. molecule 4-1BB Ligand 4-1BB Receptor 6-Phosphogluconate dehydrogenase, decarboxylating ACE-2 Activin A Activin B Adipocyte Fatty Acid Binding Protein Adiponectin Adipophilin Aeromonas Aminopeptidase Agouti-Related Protein AITRL Allograft Inflammatory Factor 1 Alpha-1-Acidic Glycoprotein Alpha-Dystroglycan N-Terminal Domain Aminoacylase-1 Amphiregulin ANG-1 ANG-2 11808 Ensembl ENSG00000110244 ENSMUSG00000032080 UniProt n a P06728 RefSeq (mRNA) NM_000482 NM_007468 RefSeq (protein) n/a NP_031494 Location (UCSC) Chr 11: 116.82 – 116.82 Mb Chr 9: 46.24 – 46.24 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Apolipoprotein A-IV (also known as apoA-IV, apoAIV, or apoA4) is plasma protein that is the product of the human gene APOA4.

from publication:  We study the associations between apoA-II fractional catabolic rate (FCR) and the kinetics of VLDL subspecies and apoA-I and show that, in abdominally obese  Walldius G, Jungner I. ApoB/apoA-I-kvoten – ett enkelt sammanfattande riskvärde för hjärtinfarkt. 2006:1-65.

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This ApoA-I ability enables HDL to remove excess peripheral cholesterol, and return it to the liver for recycling and excretion. This process, called reverse cholesterol transport, is thought to inhibit atherogenesis. ATP binding cassette transporter G1 (ABCG1) mediates the cholesterol transport from cells to high-density lipoprotein (HDL), but the role of apolipoprotein A-I (apoA-I), the main protein constituent of HDL, in this process is not clear.

Apo kvot ApoB/A1-kvot - Vad är Apo kvot? - Blodfetter

Niacin inhibits vascular inflammation via downregulating nuclear transcription factor-[kappa]B signaling pathway Background and Purpose. Apolipoprotein A‐I (apoA‐I) mimetic peptides (AAMPs) are short peptides that can mimic the physiological effects of apoA‐I, including the suppression of atherosclerosis by reversely transporting peripheral cholesterol to the liver. ApoA-I mutations, L202P and K131del, in HDL from heterozygotes with low HDL-C Ljunggren, Stefan (author) Linköpings universitet,Avdelningen för inflammationsmedicin,Hälsouniversitetet Levels, Johannes H M (author) Department of Vascular Medicine, Academic Medical Centre, Amsterdam, The Netherlands Turkina, Maria V (author) Apolipoprotein A-I (apoA-I) is the major protein component of HDL, where it plays an important role in cholesterol transport. The deposition of apoA-I derived amyloid is associated with various hereditary systemic amyloidoses and atherosclerosis; however, very little is known about the mechanism of apoA-I amyloid formation.

molecule 4-1BB Ligand 4-1BB Receptor 6-Phosphogluconate dehydrogenase, decarboxylating ACE-2 Activin A Activin B Adipocyte Fatty Acid Binding Protein Adiponectin Adipophilin Aeromonas Aminopeptidase Agouti-Related Protein AITRL Allograft Inflammatory Factor 1 Alpha-1-Acidic Glycoprotein Alpha-Dystroglycan N-Terminal Domain Aminoacylase-1 Amphiregulin ANG-1 ANG-2 11808 Ensembl ENSG00000110244 ENSMUSG00000032080 UniProt n a P06728 RefSeq (mRNA) NM_000482 NM_007468 RefSeq (protein) n/a NP_031494 Location (UCSC) Chr 11: 116.82 – 116.82 Mb Chr 9: 46.24 – 46.24 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Apolipoprotein A-IV (also known as apoA-IV, apoAIV, or apoA4) is plasma protein that is the product of the human gene APOA4. Contents 1 However, apoA-I infusions did not induce plaque regression (Miyazaki et al. 1995). 3.3 ApoA-I Milano Infusions. Carriers of the apoA-I Milano mutation are characterized by reduced levels of HDL-C without the anticipated increased risk of CVD (Franceschini et al. 1980). Apolipoprotein A-I (ApoA-I), the major protein component of high-density lipoproteins (HDL) is a multifunctional protein, involved in cholesterol traffic and inflammatory and immune response regulation.
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T1 - Structural properties of amyloidogenic apoA-I mutant L178H. AU - Axelsson, A. AU - Cochran, M. AU - Duong, T. AU - Chokshi, M. AU - Voss, J. C. Abstract.
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KEMI-NYTT Nummer 2 , 2010-03-31 ApoB och ApoA-I - Studylib

arbetstagare inom AM och svetsare år 2016 hade en högre kvot för apoB/apoA-I jämfört med kontrollerna.