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Book
Marine Natural Products and Obesity
Authors: ---
ISBN: 3039211927 3039211919 Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Obesity and related co-morbidities are increasing worldwide and pose a serious health problem. Changes in lifestyle and diet would be the best remedies to fight obesity; however, many people will still rely on medical aid. Marine organisms have been prolific in the production of bioactive compounds for many diseases, e.g., cancer, and promise to be an excellent source for natural-derived molecules and novel nutraceuticals. Bioactive compounds with beneficial activities towards obesity have been described from diverse marine organism including marine algae, bacteria, sponges, fungi, crustaceans or fish. This Special Issue will highlight the progress in the following topics: Bioactive compounds for the treatment of obesity and obesity-related co-morbidities (diabetes, fatty liver, hyperlipidemia) from marine organisms; the isolation of novel compounds, the bioactivity screening of marine organisms and the elucidation of molecular mode of action of marine bioactive compounds.


Book
PPARs as Key Mediators of Metabolic and Inflammatory Regulation
Authors: ---
Year: 2022 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Mounting evidence suggests a bidirectional relationship between metabolism and inflammation. Molecular crosstalk between these processes occurs at different levels with the participation of nuclear receptors, including peroxisome proliferator-activated receptors (PPARs). There are three PPAR isotypes, α, β/δ, and γ, which modulate metabolic and inflammatory pathways, making them key for the control of cellular, organ, and systemic processes. PPAR activity is governed by fatty acids and fatty acid derivatives, and by drugs used in clinics (glitazones and fibrates). The study of PPAR action, also modulated by post-translational modifications, has enabled extraordinary advances in the understanding of the multifaceted roles of these receptors in metabolism, energy homeostasis, and inflammation both in health and disease. This Special Issue of IJMS includes a broad range of basic and translational article, both original research and reviews, focused on the latest developments in the regulation of metabolic and/or inflammatory processes by PPARs in all organs and the microbiomes of different vertebrate species.

Keywords

Research & information: general --- Biology, life sciences --- Biochemistry --- nuclear receptor --- gene transcription --- inflammation --- molecular docking --- PPARβ/δ --- lung --- pulmonary artery --- GW0742 --- GSK3787 --- docking --- lipopolysaccharide (LPS) --- PPARγ ligand --- coumarin --- fluorescent ligand --- screening --- crystal structure --- PPAR --- atopic dermatitis --- psoriasis --- metabolic reprograming --- glucose --- fatty acids --- mycobacteria --- M. tuberculosis --- M. leprae --- PPARs --- lipid droplets --- metabolic alterations --- hepatic damage --- nuclear factors --- pharmacological targets --- AMPK --- GDF15 --- insulin resistance --- type 2 diabetes mellitus --- peroxisome proliferator-activated receptor gamma (PPARγ) --- real-time PCR --- ELISA --- immunohistochemistry --- signaling pathway --- PPAR gamma --- brain --- neural stem cells --- infection --- neuroinflammation --- HIV --- Zika --- cytomegalovirus --- neurogenesis --- microglia --- liver damage --- toll-like receptor 4 --- P2Y2 receptor --- metabolic syndrome --- resveratrol --- quercetin --- PPARα --- peroxisome --- β-oxidation --- PPRE --- ligand --- coregulator --- micronutrients --- PPARα knockout --- adipose tissue --- browning --- lipid metabolism --- depression --- PPARg --- neuropathology --- corticotropin releasing hormone --- norepinephrine --- subgenual prefrontal cortex --- amygdala --- nucleus accumbens --- common carotid artery occlusion --- electroretinography --- fibroblast growth factor 21 --- pemafibrate --- peroxisome proliferator-activated receptor alpha --- retinal ischemia --- skeletal muscle --- substrate metabolism --- nonalcoholic fatty liver disease (NAFLD) --- sex dimorphism --- lipidomics --- hepatic sex-biased gene expression --- PPARγ --- pulmonary arterial hypertension --- TGFβ --- vascular injury --- proliferation --- kidney fibrosis --- pattern-recognition receptors --- phagocytosis --- nitric oxide synthase --- fenofibrate --- oleoylethanolamide --- palmitoylethanolamide --- cancer --- immunity --- obesity --- diabetes --- miRNA --- DNA methylation --- histone modification --- peroxisome-proliferator-activated receptor --- fatty acid oxidation --- doping control --- regulatory T cells --- exercise --- nuclear receptors --- nutrigenomics --- energy homeostasis --- dairy animals --- non-alcoholic fatty liver disease (NAFLD) --- non-alcoholic steatohepatitis (NASH) --- peroxisome proliferator-activated receptors (PPAR) --- bezafibrate --- fenofibric acid --- peroxisome proliferator-activated receptor --- dual/pan agonist --- X-ray crystallography --- n/a


Book
AMP-Activated Protein Kinase Signalling
Authors: ---
Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Starting from a kinase of interest, AMP-activated protein kinase (AMPK) has gone far beyond an average biomolecule. Being expressed in all mammalian cell types and probably having a counterpart in every eukaryotic cell, AMPK has attracted interest in virtually all areas of biological research. Structural and biophysical insights have greatly contributed to a molecular understanding of this kinase. From good old protein biochemistry to modern approaches, such as systems biology and advanced microscopy, all disciplines have provided important information. Thus, multiple links to cellular events and subcellular localizations have been established. Moreover, the crucial involvement of AMPK in human health and disease has been evidenced. AMPK accordingly has moved from an interesting enzyme to a pharmacological target. However, despite our extensive current knowledge about AMPK, the growing community is busier than ever. This book provides a snapshot of recent and current AMPK research with an emphasis on work providing molecular insight, including but not limited to novel physiological and pathological functions, or regulatory mechanisms. Up-to-date reviews and research articles are included.

Keywords

n/a --- HDACs --- transcription --- epigenetics --- spermatozoa --- par complex --- A769662 --- MDCK --- skeletal muscle --- AID --- phosphorylation --- energy metabolism --- monocytes --- autophagy --- CML --- liver --- hindlimb suspension --- pregnancy --- preeclampsia --- gestational diabetes mellitus --- CaMKK2 --- assisted reproduction techniques --- nutrient-sensing signals --- sonic hedgehog --- protein acetylation --- glycogen storage disease --- AMPK --- adenosine monophosphate-activated protein kinase --- AICAR --- indirect calorimetry --- IL-1? --- MyHC I(?) --- HDAC4/5 --- endothelial cells --- infection --- hepatocyte --- p70S6K --- lipid metabolism --- host defense --- exercise --- kidney disease --- heat shock protein --- ?RIM --- mycobacteria --- activation loop --- developmental origins of health and disease (DOHaD) --- CREB --- TAK1 --- metabolic-inflammation --- phenylephrine --- AMP-activated protein kinase (AMPK) --- KATs --- 2-methoxyestradiol --- DNA methylation --- NLRP3 --- pump --- ?-linker --- steatosis --- AMPK kinase --- stress --- endothelial nitric-oxide synthase --- vasodilation --- adherent junctions --- epithelial cells --- glycogen --- Akt --- synaptic activation --- cellular energy sensing --- glucose uptake --- transporter --- co-expression --- atrophy --- nutrigenomics --- motility --- vasoconstriction --- fatty acid oxidation --- oxidative stress --- AS160 --- membrane --- histone modification --- sirtuin 1 (SIRT1) --- chromatin remodeling --- insulin signalling --- dietary fatty acids --- ULK --- CMML --- adaptive thermogenesis --- mTOR --- MDS --- mechanical unloading --- AML --- endothelial function --- medulloblastoma --- PKA --- adipose tissue --- NAD+ --- membranes --- nutrition --- ZO-1 --- TBC1D4 --- adipocyte --- soluble Adenylyl cyclase --- metabolism --- renin-angiotensin system --- energy utilization --- proteasome --- differentiation --- signaling --- peroxisome proliferator-activated receptor gamma coactivator 1-? (PGC1?) --- hypertrophy --- AMP-activated protein kinase --- metabolic disease --- LKB1 --- soleus muscle --- macrophages --- Immediate early genes --- CBS --- beiging --- motor endplate remodeling --- ionomycin --- nectin-afadin --- tight junctions --- resveratrol --- protein kinase B --- regrowth --- mitochondria --- protein synthesis --- energy deficiency --- catechol-O-methyltransferase --- fiber-type --- microarrays --- carrier --- acetyl-CoA --- hypertension --- 3T3-L1 --- hypothalamus --- food intake --- benign


Book
PPARs as Key Mediators of Metabolic and Inflammatory Regulation
Authors: ---
Year: 2022 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

Mounting evidence suggests a bidirectional relationship between metabolism and inflammation. Molecular crosstalk between these processes occurs at different levels with the participation of nuclear receptors, including peroxisome proliferator-activated receptors (PPARs). There are three PPAR isotypes, α, β/δ, and γ, which modulate metabolic and inflammatory pathways, making them key for the control of cellular, organ, and systemic processes. PPAR activity is governed by fatty acids and fatty acid derivatives, and by drugs used in clinics (glitazones and fibrates). The study of PPAR action, also modulated by post-translational modifications, has enabled extraordinary advances in the understanding of the multifaceted roles of these receptors in metabolism, energy homeostasis, and inflammation both in health and disease. This Special Issue of IJMS includes a broad range of basic and translational article, both original research and reviews, focused on the latest developments in the regulation of metabolic and/or inflammatory processes by PPARs in all organs and the microbiomes of different vertebrate species.

Keywords

nuclear receptor --- gene transcription --- inflammation --- molecular docking --- PPARβ/δ --- lung --- pulmonary artery --- GW0742 --- GSK3787 --- docking --- lipopolysaccharide (LPS) --- PPARγ ligand --- coumarin --- fluorescent ligand --- screening --- crystal structure --- PPAR --- atopic dermatitis --- psoriasis --- metabolic reprograming --- glucose --- fatty acids --- mycobacteria --- M. tuberculosis --- M. leprae --- PPARs --- lipid droplets --- metabolic alterations --- hepatic damage --- nuclear factors --- pharmacological targets --- AMPK --- GDF15 --- insulin resistance --- type 2 diabetes mellitus --- peroxisome proliferator-activated receptor gamma (PPARγ) --- real-time PCR --- ELISA --- immunohistochemistry --- signaling pathway --- PPAR gamma --- brain --- neural stem cells --- infection --- neuroinflammation --- HIV --- Zika --- cytomegalovirus --- neurogenesis --- microglia --- liver damage --- toll-like receptor 4 --- P2Y2 receptor --- metabolic syndrome --- resveratrol --- quercetin --- PPARα --- peroxisome --- β-oxidation --- PPRE --- ligand --- coregulator --- micronutrients --- PPARα knockout --- adipose tissue --- browning --- lipid metabolism --- depression --- PPARg --- neuropathology --- corticotropin releasing hormone --- norepinephrine --- subgenual prefrontal cortex --- amygdala --- nucleus accumbens --- common carotid artery occlusion --- electroretinography --- fibroblast growth factor 21 --- pemafibrate --- peroxisome proliferator-activated receptor alpha --- retinal ischemia --- skeletal muscle --- substrate metabolism --- nonalcoholic fatty liver disease (NAFLD) --- sex dimorphism --- lipidomics --- hepatic sex-biased gene expression --- PPARγ --- pulmonary arterial hypertension --- TGFβ --- vascular injury --- proliferation --- kidney fibrosis --- pattern-recognition receptors --- phagocytosis --- nitric oxide synthase --- fenofibrate --- oleoylethanolamide --- palmitoylethanolamide --- cancer --- immunity --- obesity --- diabetes --- miRNA --- DNA methylation --- histone modification --- peroxisome-proliferator-activated receptor --- fatty acid oxidation --- doping control --- regulatory T cells --- exercise --- nuclear receptors --- nutrigenomics --- energy homeostasis --- dairy animals --- non-alcoholic fatty liver disease (NAFLD) --- non-alcoholic steatohepatitis (NASH) --- peroxisome proliferator-activated receptors (PPAR) --- bezafibrate --- fenofibric acid --- peroxisome proliferator-activated receptor --- dual/pan agonist --- X-ray crystallography --- n/a


Book
AMP-Activated Protein Kinase Signalling
Authors: ---
Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

Loading...
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Bookmark

Abstract

Starting from a kinase of interest, AMP-activated protein kinase (AMPK) has gone far beyond an average biomolecule. Being expressed in all mammalian cell types and probably having a counterpart in every eukaryotic cell, AMPK has attracted interest in virtually all areas of biological research. Structural and biophysical insights have greatly contributed to a molecular understanding of this kinase. From good old protein biochemistry to modern approaches, such as systems biology and advanced microscopy, all disciplines have provided important information. Thus, multiple links to cellular events and subcellular localizations have been established. Moreover, the crucial involvement of AMPK in human health and disease has been evidenced. AMPK accordingly has moved from an interesting enzyme to a pharmacological target. However, despite our extensive current knowledge about AMPK, the growing community is busier than ever. This book provides a snapshot of recent and current AMPK research with an emphasis on work providing molecular insight, including but not limited to novel physiological and pathological functions, or regulatory mechanisms. Up-to-date reviews and research articles are included.

Keywords

n/a --- HDACs --- transcription --- epigenetics --- spermatozoa --- par complex --- A769662 --- MDCK --- skeletal muscle --- AID --- phosphorylation --- energy metabolism --- monocytes --- autophagy --- CML --- liver --- hindlimb suspension --- pregnancy --- preeclampsia --- gestational diabetes mellitus --- CaMKK2 --- assisted reproduction techniques --- nutrient-sensing signals --- sonic hedgehog --- protein acetylation --- glycogen storage disease --- AMPK --- adenosine monophosphate-activated protein kinase --- AICAR --- indirect calorimetry --- IL-1? --- MyHC I(?) --- HDAC4/5 --- endothelial cells --- infection --- hepatocyte --- p70S6K --- lipid metabolism --- host defense --- exercise --- kidney disease --- heat shock protein --- ?RIM --- mycobacteria --- activation loop --- developmental origins of health and disease (DOHaD) --- CREB --- TAK1 --- metabolic-inflammation --- phenylephrine --- AMP-activated protein kinase (AMPK) --- KATs --- 2-methoxyestradiol --- DNA methylation --- NLRP3 --- pump --- ?-linker --- steatosis --- AMPK kinase --- stress --- endothelial nitric-oxide synthase --- vasodilation --- adherent junctions --- epithelial cells --- glycogen --- Akt --- synaptic activation --- cellular energy sensing --- glucose uptake --- transporter --- co-expression --- atrophy --- nutrigenomics --- motility --- vasoconstriction --- fatty acid oxidation --- oxidative stress --- AS160 --- membrane --- histone modification --- sirtuin 1 (SIRT1) --- chromatin remodeling --- insulin signalling --- dietary fatty acids --- ULK --- CMML --- adaptive thermogenesis --- mTOR --- MDS --- mechanical unloading --- AML --- endothelial function --- medulloblastoma --- PKA --- adipose tissue --- NAD+ --- membranes --- nutrition --- ZO-1 --- TBC1D4 --- adipocyte --- soluble Adenylyl cyclase --- metabolism --- renin-angiotensin system --- energy utilization --- proteasome --- differentiation --- signaling --- peroxisome proliferator-activated receptor gamma coactivator 1-? (PGC1?) --- hypertrophy --- AMP-activated protein kinase --- metabolic disease --- LKB1 --- soleus muscle --- macrophages --- Immediate early genes --- CBS --- beiging --- motor endplate remodeling --- ionomycin --- nectin-afadin --- tight junctions --- resveratrol --- protein kinase B --- regrowth --- mitochondria --- protein synthesis --- energy deficiency --- catechol-O-methyltransferase --- fiber-type --- microarrays --- carrier --- acetyl-CoA --- hypertension --- 3T3-L1 --- hypothalamus --- food intake --- benign


Book
PPARs as Key Mediators of Metabolic and Inflammatory Regulation
Authors: ---
Year: 2022 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Mounting evidence suggests a bidirectional relationship between metabolism and inflammation. Molecular crosstalk between these processes occurs at different levels with the participation of nuclear receptors, including peroxisome proliferator-activated receptors (PPARs). There are three PPAR isotypes, α, β/δ, and γ, which modulate metabolic and inflammatory pathways, making them key for the control of cellular, organ, and systemic processes. PPAR activity is governed by fatty acids and fatty acid derivatives, and by drugs used in clinics (glitazones and fibrates). The study of PPAR action, also modulated by post-translational modifications, has enabled extraordinary advances in the understanding of the multifaceted roles of these receptors in metabolism, energy homeostasis, and inflammation both in health and disease. This Special Issue of IJMS includes a broad range of basic and translational article, both original research and reviews, focused on the latest developments in the regulation of metabolic and/or inflammatory processes by PPARs in all organs and the microbiomes of different vertebrate species.

Keywords

Research & information: general --- Biology, life sciences --- Biochemistry --- nuclear receptor --- gene transcription --- inflammation --- molecular docking --- PPARβ/δ --- lung --- pulmonary artery --- GW0742 --- GSK3787 --- docking --- lipopolysaccharide (LPS) --- PPARγ ligand --- coumarin --- fluorescent ligand --- screening --- crystal structure --- PPAR --- atopic dermatitis --- psoriasis --- metabolic reprograming --- glucose --- fatty acids --- mycobacteria --- M. tuberculosis --- M. leprae --- PPARs --- lipid droplets --- metabolic alterations --- hepatic damage --- nuclear factors --- pharmacological targets --- AMPK --- GDF15 --- insulin resistance --- type 2 diabetes mellitus --- peroxisome proliferator-activated receptor gamma (PPARγ) --- real-time PCR --- ELISA --- immunohistochemistry --- signaling pathway --- PPAR gamma --- brain --- neural stem cells --- infection --- neuroinflammation --- HIV --- Zika --- cytomegalovirus --- neurogenesis --- microglia --- liver damage --- toll-like receptor 4 --- P2Y2 receptor --- metabolic syndrome --- resveratrol --- quercetin --- PPARα --- peroxisome --- β-oxidation --- PPRE --- ligand --- coregulator --- micronutrients --- PPARα knockout --- adipose tissue --- browning --- lipid metabolism --- depression --- PPARg --- neuropathology --- corticotropin releasing hormone --- norepinephrine --- subgenual prefrontal cortex --- amygdala --- nucleus accumbens --- common carotid artery occlusion --- electroretinography --- fibroblast growth factor 21 --- pemafibrate --- peroxisome proliferator-activated receptor alpha --- retinal ischemia --- skeletal muscle --- substrate metabolism --- nonalcoholic fatty liver disease (NAFLD) --- sex dimorphism --- lipidomics --- hepatic sex-biased gene expression --- PPARγ --- pulmonary arterial hypertension --- TGFβ --- vascular injury --- proliferation --- kidney fibrosis --- pattern-recognition receptors --- phagocytosis --- nitric oxide synthase --- fenofibrate --- oleoylethanolamide --- palmitoylethanolamide --- cancer --- immunity --- obesity --- diabetes --- miRNA --- DNA methylation --- histone modification --- peroxisome-proliferator-activated receptor --- fatty acid oxidation --- doping control --- regulatory T cells --- exercise --- nuclear receptors --- nutrigenomics --- energy homeostasis --- dairy animals --- non-alcoholic fatty liver disease (NAFLD) --- non-alcoholic steatohepatitis (NASH) --- peroxisome proliferator-activated receptors (PPAR) --- bezafibrate --- fenofibric acid --- peroxisome proliferator-activated receptor --- dual/pan agonist --- X-ray crystallography


Book
AMP-Activated Protein Kinase Signalling
Authors: ---
Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Starting from a kinase of interest, AMP-activated protein kinase (AMPK) has gone far beyond an average biomolecule. Being expressed in all mammalian cell types and probably having a counterpart in every eukaryotic cell, AMPK has attracted interest in virtually all areas of biological research. Structural and biophysical insights have greatly contributed to a molecular understanding of this kinase. From good old protein biochemistry to modern approaches, such as systems biology and advanced microscopy, all disciplines have provided important information. Thus, multiple links to cellular events and subcellular localizations have been established. Moreover, the crucial involvement of AMPK in human health and disease has been evidenced. AMPK accordingly has moved from an interesting enzyme to a pharmacological target. However, despite our extensive current knowledge about AMPK, the growing community is busier than ever. This book provides a snapshot of recent and current AMPK research with an emphasis on work providing molecular insight, including but not limited to novel physiological and pathological functions, or regulatory mechanisms. Up-to-date reviews and research articles are included.

Keywords

HDACs --- transcription --- epigenetics --- spermatozoa --- par complex --- A769662 --- MDCK --- skeletal muscle --- AID --- phosphorylation --- energy metabolism --- monocytes --- autophagy --- CML --- liver --- hindlimb suspension --- pregnancy --- preeclampsia --- gestational diabetes mellitus --- CaMKK2 --- assisted reproduction techniques --- nutrient-sensing signals --- sonic hedgehog --- protein acetylation --- glycogen storage disease --- AMPK --- adenosine monophosphate-activated protein kinase --- AICAR --- indirect calorimetry --- IL-1? --- MyHC I(?) --- HDAC4/5 --- endothelial cells --- infection --- hepatocyte --- p70S6K --- lipid metabolism --- host defense --- exercise --- kidney disease --- heat shock protein --- ?RIM --- mycobacteria --- activation loop --- developmental origins of health and disease (DOHaD) --- CREB --- TAK1 --- metabolic-inflammation --- phenylephrine --- AMP-activated protein kinase (AMPK) --- KATs --- 2-methoxyestradiol --- DNA methylation --- NLRP3 --- pump --- ?-linker --- steatosis --- AMPK kinase --- stress --- endothelial nitric-oxide synthase --- vasodilation --- adherent junctions --- epithelial cells --- glycogen --- Akt --- synaptic activation --- cellular energy sensing --- glucose uptake --- transporter --- co-expression --- atrophy --- nutrigenomics --- motility --- vasoconstriction --- fatty acid oxidation --- oxidative stress --- AS160 --- membrane --- histone modification --- sirtuin 1 (SIRT1) --- chromatin remodeling --- insulin signalling --- dietary fatty acids --- ULK --- CMML --- adaptive thermogenesis --- mTOR --- MDS --- mechanical unloading --- AML --- endothelial function --- medulloblastoma --- PKA --- adipose tissue --- NAD+ --- membranes --- nutrition --- ZO-1 --- TBC1D4 --- adipocyte --- soluble Adenylyl cyclase --- metabolism --- renin-angiotensin system --- energy utilization --- proteasome --- differentiation --- signaling --- peroxisome proliferator-activated receptor gamma coactivator 1-? (PGC1?) --- hypertrophy --- AMP-activated protein kinase --- metabolic disease --- LKB1 --- soleus muscle --- macrophages --- Immediate early genes --- CBS --- benign --- motor endplate remodeling --- ionomycin --- nectin-afadin --- tight junctions --- resveratrol --- protein kinase B --- regrowth --- mitochondria --- protein synthesis --- energy deficiency --- catechol-O-methyltransferase --- fiber-type --- microarrays --- carrier --- acetyl-CoA --- hypertension --- 3T3-L1 --- hypothalamus --- food intake

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