Catalogue
Articles
RSS feedX
Search Filters
Format
Subjects
Library Location
Language
Publication DateThe Journal of Physiology, ISSN 0022-3751, 10/2014, Volume 592, Issue 20, pp. 4575 - 4589
Key points Oxidative stress is widely considered a major cause of muscle loss not only in disuse but also in most chronic diseases, triggering carbonylation of...
TIBIALIS ANTERIOR | SKELETAL-MUSCLE | GAMMA COACTIVATOR 1-ALPHA | OXIDATIVE STRESS | PHYSIOLOGY | MITOCHONDRIAL BIOGENESIS | GENE-EXPRESSION | TRANSCRIPTIONAL COACTIVATOR | UBIQUITIN LIGASES | PROTEIN-SYNTHESIS | NEUROSCIENCES | ANTIOXIDANT CAPACITY | Up-Regulation | Dynamins - metabolism | Superoxide Dismutase - genetics | Oxidative Stress | SKP Cullin F-Box Protein Ligases - genetics | Mitochondria, Muscle - metabolism | Male | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | RNA, Messenger - metabolism | Autophagy | Tripartite Motif Proteins | Chromans - pharmacology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Muscle Proteins - metabolism | Apoptosis Regulatory Proteins - genetics | NF-E2-Related Factor 2 - genetics | Muscular Atrophy - prevention & control | Muscle Fibers, Skeletal - physiology | Superoxide Dismutase - metabolism | Beclin-1 | Muscular Atrophy - metabolism | Catalase - genetics | Mice, Inbred C57BL | RNA, Messenger - genetics | Ubiquitin-Protein Ligases - metabolism | Dynamins - genetics | SKP Cullin F-Box Protein Ligases - metabolism | Antioxidants - pharmacology | Transcription Factors - genetics | Apoptosis Regulatory Proteins - metabolism | Catalase - metabolism | Muscle Proteins - genetics | Transcription Factors - metabolism | Antioxidants - therapeutic use | Animals | Chromans - therapeutic use | Hindlimb Suspension - adverse effects | NF-E2-Related Factor 2 - metabolism | Mice | Mitochondria, Muscle - drug effects | Superoxide Dismutase-1 | Ubiquitin-Protein Ligases - genetics | Muscle
TIBIALIS ANTERIOR | SKELETAL-MUSCLE | GAMMA COACTIVATOR 1-ALPHA | OXIDATIVE STRESS | PHYSIOLOGY | MITOCHONDRIAL BIOGENESIS | GENE-EXPRESSION | TRANSCRIPTIONAL COACTIVATOR | UBIQUITIN LIGASES | PROTEIN-SYNTHESIS | NEUROSCIENCES | ANTIOXIDANT CAPACITY | Up-Regulation | Dynamins - metabolism | Superoxide Dismutase - genetics | Oxidative Stress | SKP Cullin F-Box Protein Ligases - genetics | Mitochondria, Muscle - metabolism | Male | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | RNA, Messenger - metabolism | Autophagy | Tripartite Motif Proteins | Chromans - pharmacology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Muscle Proteins - metabolism | Apoptosis Regulatory Proteins - genetics | NF-E2-Related Factor 2 - genetics | Muscular Atrophy - prevention & control | Muscle Fibers, Skeletal - physiology | Superoxide Dismutase - metabolism | Beclin-1 | Muscular Atrophy - metabolism | Catalase - genetics | Mice, Inbred C57BL | RNA, Messenger - genetics | Ubiquitin-Protein Ligases - metabolism | Dynamins - genetics | SKP Cullin F-Box Protein Ligases - metabolism | Antioxidants - pharmacology | Transcription Factors - genetics | Apoptosis Regulatory Proteins - metabolism | Catalase - metabolism | Muscle Proteins - genetics | Transcription Factors - metabolism | Antioxidants - therapeutic use | Animals | Chromans - therapeutic use | Hindlimb Suspension - adverse effects | NF-E2-Related Factor 2 - metabolism | Mice | Mitochondria, Muscle - drug effects | Superoxide Dismutase-1 | Ubiquitin-Protein Ligases - genetics | Muscle
Journal Article
Details 
Digital rights
Loading RightsNutrition Reviews, ISSN 0029-6643, 01/2013, Volume 71, Issue 4, pp. 195 - 208
Situations such as recovery from injury or illness require otherwise healthy humans to undergo periods of disuse, which lead to considerable losses of skeletal...
muscle mass | protein synthesis | immobilization | disuse | bed rest | Immobilization | Bed rest | Protein synthesis | Disuse | Muscle mass | LOWER-LIMB SUSPENSION | ORAL CREATINE SUPPLEMENTATION | HUMAN QUADRICEPS MUSCLE | CHAIN AMINO-ACIDS | RANDOMIZED CONTROLLED-TRIAL | HUMAN SKELETAL-MUSCLE | NUTRITION & DIETETICS | MYOFIBRILLAR PROTEIN-SYNTHESIS | SHORT-TERM IMMOBILIZATION | HEALTHY OLDER-ADULTS | HUMAN TRICEPS SURAE | Muscular Disorders, Atrophic - metabolism | Nutritional Requirements | Dietary Proteins - administration & dosage | Protein Biosynthesis | Muscular Atrophy - metabolism | Humans | Muscular Atrophy - pathology | Muscular Atrophy - therapy | Muscle, Skeletal - metabolism | Muscular Disorders, Atrophic - prevention & control | Nutritional Physiological Phenomena - physiology | Dietary Proteins - metabolism | Muscle Proteins - metabolism | Muscular Atrophy - prevention & control | Muscular Disorders, Atrophic - pathology | Muscle, Skeletal - pathology | Care and treatment | Physical fitness | Management | Atrophy, Muscular | Health aspects | Food habits
muscle mass | protein synthesis | immobilization | disuse | bed rest | Immobilization | Bed rest | Protein synthesis | Disuse | Muscle mass | LOWER-LIMB SUSPENSION | ORAL CREATINE SUPPLEMENTATION | HUMAN QUADRICEPS MUSCLE | CHAIN AMINO-ACIDS | RANDOMIZED CONTROLLED-TRIAL | HUMAN SKELETAL-MUSCLE | NUTRITION & DIETETICS | MYOFIBRILLAR PROTEIN-SYNTHESIS | SHORT-TERM IMMOBILIZATION | HEALTHY OLDER-ADULTS | HUMAN TRICEPS SURAE | Muscular Disorders, Atrophic - metabolism | Nutritional Requirements | Dietary Proteins - administration & dosage | Protein Biosynthesis | Muscular Atrophy - metabolism | Humans | Muscular Atrophy - pathology | Muscular Atrophy - therapy | Muscle, Skeletal - metabolism | Muscular Disorders, Atrophic - prevention & control | Nutritional Physiological Phenomena - physiology | Dietary Proteins - metabolism | Muscle Proteins - metabolism | Muscular Atrophy - prevention & control | Muscular Disorders, Atrophic - pathology | Muscle, Skeletal - pathology | Care and treatment | Physical fitness | Management | Atrophy, Muscular | Health aspects | Food habits
Journal Article
Details
Digital rights
Loading RightsJournal of Clinical Investigation, ISSN 0021-9738, 02/2013, Volume 123, Issue 2, pp. 611 - 622
Cachexia is a wasting syndrome associated with cancer, AIDS, multiple sclerosis, and several other disease states. It is characterized by weight loss, fatigue,...
MAMMALIAN TARGET | MEDICINE, RESEARCH & EXPERIMENTAL | CACHEXIA | METABOLISM | P38 MAPK | GROWTH-HORMONE RELEASE | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | EXPRESSION | GENE-TRANSCRIPTION | TRANSGENIC MICE | TOR Serine-Threonine Kinases - metabolism | Ghrelin - chemistry | Muscle Denervation | Male | Muscle, Skeletal - metabolism | Mechanistic Target of Rapamycin Complex 2 | MAP Kinase Signaling System | Multiprotein Complexes - metabolism | Muscle, Skeletal - drug effects | Receptors, Ghrelin - metabolism | Muscular Atrophy - prevention & control | Proto-Oncogene Proteins c-akt - metabolism | Cachexia - metabolism | Acylation | Cell Line | Muscular Atrophy - metabolism | Signal Transduction | Mice, Inbred C57BL | Muscular Atrophy - pathology | Ghrelin - pharmacology | Mice, Transgenic | Cachexia - prevention & control | Mice, Knockout | Ghrelin - metabolism | Animals | Protein Binding | Mice | Muscle, Skeletal - pathology | Care and treatment | Ghrelin | Physiological aspects | Cachexia | Genetic aspects | Diagnosis | Research | Atrophy, Muscular | Risk factors
MAMMALIAN TARGET | MEDICINE, RESEARCH & EXPERIMENTAL | CACHEXIA | METABOLISM | P38 MAPK | GROWTH-HORMONE RELEASE | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | EXPRESSION | GENE-TRANSCRIPTION | TRANSGENIC MICE | TOR Serine-Threonine Kinases - metabolism | Ghrelin - chemistry | Muscle Denervation | Male | Muscle, Skeletal - metabolism | Mechanistic Target of Rapamycin Complex 2 | MAP Kinase Signaling System | Multiprotein Complexes - metabolism | Muscle, Skeletal - drug effects | Receptors, Ghrelin - metabolism | Muscular Atrophy - prevention & control | Proto-Oncogene Proteins c-akt - metabolism | Cachexia - metabolism | Acylation | Cell Line | Muscular Atrophy - metabolism | Signal Transduction | Mice, Inbred C57BL | Muscular Atrophy - pathology | Ghrelin - pharmacology | Mice, Transgenic | Cachexia - prevention & control | Mice, Knockout | Ghrelin - metabolism | Animals | Protein Binding | Mice | Muscle, Skeletal - pathology | Care and treatment | Ghrelin | Physiological aspects | Cachexia | Genetic aspects | Diagnosis | Research | Atrophy, Muscular | Risk factors
Journal Article
Details
Digital rights
Loading RightsNature Cell Biology, ISSN 1465-7392, 08/2018, Volume 20, Issue 8, pp. 917 - 927
Fibro-adipogenic progenitors (FAPs) are typically activated in response to muscle injury, and establish functional interactions with inflammatory and muscle...
SKELETAL-MUSCLE | SATELLITE CELL NICHE | DYSTROPHIC MUSCLES | REGENERATION | ANTI-INTERLEUKIN-6 MONOCLONAL-ANTIBODY | INJURY | MICE | INTERLEUKIN-6 | CANCER | FIBRO/ADIPOGENIC PROGENITORS | CELL BIOLOGY | Interleukin-6 - antagonists & inhibitors | Adipogenesis - drug effects | Coculture Techniques | Humans | Amyotrophic Lateral Sclerosis - prevention & control | Male | Spinal Cord Injuries - genetics | Cardiotoxins | Muscular Atrophy, Spinal - prevention & control | Spinal Cord Injuries - pathology | Muscular Atrophy, Spinal - genetics | Myoblasts, Skeletal - pathology | Neuromuscular Agents - pharmacology | Quadriceps Muscle - drug effects | Muscular Atrophy - prevention & control | Quadriceps Muscle - innervation | Quadriceps Muscle - pathology | Interleukin-6 - metabolism | STAT3 Transcription Factor - genetics | STAT3 Transcription Factor - metabolism | Disease Models, Animal | Myoblasts, Skeletal - metabolism | Cell Line | Muscular Atrophy, Spinal - metabolism | Denervation - methods | Interleukin-6 - genetics | Muscular Atrophy - metabolism | Signal Transduction | Spinal Cord Injuries - metabolism | Amyotrophic Lateral Sclerosis - genetics | Mice, Inbred C57BL | Muscular Atrophy - pathology | Mice, Transgenic | Muscular Atrophy - genetics | Muscular Atrophy, Spinal - pathology | Spinal Cord Injuries - prevention & control | Amyotrophic Lateral Sclerosis - pathology | Animals | Sciatic Nerve - surgery | Amyotrophic Lateral Sclerosis - metabolism | Fibrosis | Superoxide Dismutase-1 - genetics | Mutation | Myoblasts, Skeletal - drug effects | Quadriceps Muscle - metabolism | STAT3 Transcription Factor - antagonists & inhibitors | Animal models | Spinal cord | Mental disorders | Pathogenesis | Stem cell transplantation | Activation | Spinal cord injury | Macrophages | Inactivation | Spinal muscular atrophy | Interleukin 6 | Atrophy | Cell activation | Rodents | Neuromuscular diseases | Deactivation | Stat3 protein | Muscles | Amyotrophic lateral sclerosis | Inflammation | Regeneration | Signaling | Stem cells | Neuromuscular junctions | Infiltration | Denervation
SKELETAL-MUSCLE | SATELLITE CELL NICHE | DYSTROPHIC MUSCLES | REGENERATION | ANTI-INTERLEUKIN-6 MONOCLONAL-ANTIBODY | INJURY | MICE | INTERLEUKIN-6 | CANCER | FIBRO/ADIPOGENIC PROGENITORS | CELL BIOLOGY | Interleukin-6 - antagonists & inhibitors | Adipogenesis - drug effects | Coculture Techniques | Humans | Amyotrophic Lateral Sclerosis - prevention & control | Male | Spinal Cord Injuries - genetics | Cardiotoxins | Muscular Atrophy, Spinal - prevention & control | Spinal Cord Injuries - pathology | Muscular Atrophy, Spinal - genetics | Myoblasts, Skeletal - pathology | Neuromuscular Agents - pharmacology | Quadriceps Muscle - drug effects | Muscular Atrophy - prevention & control | Quadriceps Muscle - innervation | Quadriceps Muscle - pathology | Interleukin-6 - metabolism | STAT3 Transcription Factor - genetics | STAT3 Transcription Factor - metabolism | Disease Models, Animal | Myoblasts, Skeletal - metabolism | Cell Line | Muscular Atrophy, Spinal - metabolism | Denervation - methods | Interleukin-6 - genetics | Muscular Atrophy - metabolism | Signal Transduction | Spinal Cord Injuries - metabolism | Amyotrophic Lateral Sclerosis - genetics | Mice, Inbred C57BL | Muscular Atrophy - pathology | Mice, Transgenic | Muscular Atrophy - genetics | Muscular Atrophy, Spinal - pathology | Spinal Cord Injuries - prevention & control | Amyotrophic Lateral Sclerosis - pathology | Animals | Sciatic Nerve - surgery | Amyotrophic Lateral Sclerosis - metabolism | Fibrosis | Superoxide Dismutase-1 - genetics | Mutation | Myoblasts, Skeletal - drug effects | Quadriceps Muscle - metabolism | STAT3 Transcription Factor - antagonists & inhibitors | Animal models | Spinal cord | Mental disorders | Pathogenesis | Stem cell transplantation | Activation | Spinal cord injury | Macrophages | Inactivation | Spinal muscular atrophy | Interleukin 6 | Atrophy | Cell activation | Rodents | Neuromuscular diseases | Deactivation | Stat3 protein | Muscles | Amyotrophic lateral sclerosis | Inflammation | Regeneration | Signaling | Stem cells | Neuromuscular junctions | Infiltration | Denervation
Journal Article
Details
Digital rights
Loading RightsCirculation, ISSN 0009-7322, 01/2010, Volume 121, Issue 3, pp. 419 - 425
Background-Cardiac cachexia is characterized by an exaggerated loss of skeletal muscle, weakness, and exercise intolerance, although the cause of these effects...
Atrophy | Heart failure | Myocardium | Muscle, skeletal | Hypertrophy | heart failure | CARDIAC & CARDIOVASCULAR SYSTEMS | hypertrophy | myocardium | MODEL | CARDIOMYOCYTES | BETA SUPERFAMILY MEMBER | METABOLISM | GROWTH | MASS | atrophy | muscle, skeletal | CARDIAC CACHEXIA | PERIPHERAL VASCULAR DISEASE | MICE | HEMATOLOGY | EXPRESSION | Heart Failure - complications | Mice, Inbred C57BL | Muscular Atrophy - pathology | Heart Failure - physiopathology | Muscle, Skeletal - metabolism | Organ Specificity | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Cachexia - prevention & control | Gene Knock-In Techniques | Antibodies - pharmacology | Animals | Mice, Mutant Strains | Cachexia - pathology | Gene Expression - physiology | Cachexia - etiology | Myocytes, Cardiac - metabolism | Myostatin - genetics | Mice | Muscular Atrophy - prevention & control | Muscle, Skeletal - pathology | Myostatin - metabolism | Muscular Atrophy - etiology | Myostatin - immunology | Causes of | Physiological aspects | Myostatin | Cachexia | Research | Atrophy, Muscular | Risk factors | gene-deleted mice | myostatin
Atrophy | Heart failure | Myocardium | Muscle, skeletal | Hypertrophy | heart failure | CARDIAC & CARDIOVASCULAR SYSTEMS | hypertrophy | myocardium | MODEL | CARDIOMYOCYTES | BETA SUPERFAMILY MEMBER | METABOLISM | GROWTH | MASS | atrophy | muscle, skeletal | CARDIAC CACHEXIA | PERIPHERAL VASCULAR DISEASE | MICE | HEMATOLOGY | EXPRESSION | Heart Failure - complications | Mice, Inbred C57BL | Muscular Atrophy - pathology | Heart Failure - physiopathology | Muscle, Skeletal - metabolism | Organ Specificity | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Cachexia - prevention & control | Gene Knock-In Techniques | Antibodies - pharmacology | Animals | Mice, Mutant Strains | Cachexia - pathology | Gene Expression - physiology | Cachexia - etiology | Myocytes, Cardiac - metabolism | Myostatin - genetics | Mice | Muscular Atrophy - prevention & control | Muscle, Skeletal - pathology | Myostatin - metabolism | Muscular Atrophy - etiology | Myostatin - immunology | Causes of | Physiological aspects | Myostatin | Cachexia | Research | Atrophy, Muscular | Risk factors | gene-deleted mice | myostatin
Journal Article
Details
Digital rights
Loading RightsThe Journal of Physiology, ISSN 0022-3751, 11/2007, Volume 585, Issue 1, pp. 203 - 215
Oxidative stress promotes controlled mechanical ventilation (MV)-induced diaphragmatic atrophy. Nonetheless, the signalling pathways responsible for oxidative...
CHAIN MESSENGER-RNA | DISUSE ATROPHY | SKELETAL-MUSCLE | OXIDATIVE STRESS | VITAMIN-E | IN-VITRO | PHYSIOLOGY | SOLEUS MUSCLE | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | EXPRESSION | NEUROSCIENCES | Diaphragm - drug effects | Insulin - physiology | SKP Cullin F-Box Protein Ligases - genetics | Oxidative Stress - physiology | Insulin-Like Growth Factor I - genetics | Proto-Oncogene Proteins c-akt - genetics | Tripartite Motif Proteins | Chromans - pharmacology | Respiration, Artificial - adverse effects | Forkhead Transcription Factors - metabolism | Muscle Proteins - metabolism | Female | Muscular Atrophy - prevention & control | Diaphragm - metabolism | Muscular Atrophy - etiology | Diaphragm - physiopathology | Ubiquitin-Protein Ligases - metabolism | Rats | Proto-Oncogene Proteins c-akt - physiology | SKP Cullin F-Box Protein Ligases - metabolism | Antioxidants - pharmacology | Forkhead Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Rats, Sprague-Dawley | Muscle Proteins - genetics | Nerve Tissue Proteins - metabolism | Phosphatidylinositol 3-Kinases - genetics | Antioxidants - therapeutic use | Animals | Chromans - therapeutic use | Insulin-Like Growth Factor I - physiology | Phosphatidylinositol 3-Kinases - physiology | Signal Transduction - physiology | Oxidative Stress - drug effects | Forkhead Box Protein O3 | Ubiquitin-Protein Ligases - genetics | Antioxidants | Physiological aspects | Protein kinases | Respiratory
CHAIN MESSENGER-RNA | DISUSE ATROPHY | SKELETAL-MUSCLE | OXIDATIVE STRESS | VITAMIN-E | IN-VITRO | PHYSIOLOGY | SOLEUS MUSCLE | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | EXPRESSION | NEUROSCIENCES | Diaphragm - drug effects | Insulin - physiology | SKP Cullin F-Box Protein Ligases - genetics | Oxidative Stress - physiology | Insulin-Like Growth Factor I - genetics | Proto-Oncogene Proteins c-akt - genetics | Tripartite Motif Proteins | Chromans - pharmacology | Respiration, Artificial - adverse effects | Forkhead Transcription Factors - metabolism | Muscle Proteins - metabolism | Female | Muscular Atrophy - prevention & control | Diaphragm - metabolism | Muscular Atrophy - etiology | Diaphragm - physiopathology | Ubiquitin-Protein Ligases - metabolism | Rats | Proto-Oncogene Proteins c-akt - physiology | SKP Cullin F-Box Protein Ligases - metabolism | Antioxidants - pharmacology | Forkhead Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Rats, Sprague-Dawley | Muscle Proteins - genetics | Nerve Tissue Proteins - metabolism | Phosphatidylinositol 3-Kinases - genetics | Antioxidants - therapeutic use | Animals | Chromans - therapeutic use | Insulin-Like Growth Factor I - physiology | Phosphatidylinositol 3-Kinases - physiology | Signal Transduction - physiology | Oxidative Stress - drug effects | Forkhead Box Protein O3 | Ubiquitin-Protein Ligases - genetics | Antioxidants | Physiological aspects | Protein kinases | Respiratory
Journal Article
Details
Digital rights
Loading RightsCurrent Opinion in Clinical Nutrition and Metabolic Care, ISSN 1363-1950, 01/2009, Volume 12, Issue 1, pp. 86 - 90
PURPOSE OF REVIEWTo draw attention to recent work on the role of protein and the amount of protein needed with each meal to preserve skeletal muscle mass in...
Sarcopenia | Leucine | Protein intake | Ageing | Muscle protein synthesis | leucine | muscle protein synthesis | ANABOLIC RESPONSE | ageing | protein intake | NITROGEN-BALANCE | SKELETAL-MUSCLE | OLDER-PEOPLE | NUTRITION & DIETETICS | RESISTANCE EXERCISE | LEAN MASS | ENDOCRINOLOGY & METABOLISM | ELDERLY HUMANS | ESSENTIAL AMINO-ACIDS | BED REST | sarcopenia | Dietary Proteins - administration & dosage | Muscular Atrophy - metabolism | Humans | Protein Deficiency - metabolism | Leucine - therapeutic use | Nutrition Policy | Muscle Proteins - biosynthesis | Aging - physiology | Aged | Exercise - physiology | Muscular Atrophy - prevention & control | Protein Deficiency - prevention & control | Dietary Proteins - therapeutic use | Dietary Supplements
Sarcopenia | Leucine | Protein intake | Ageing | Muscle protein synthesis | leucine | muscle protein synthesis | ANABOLIC RESPONSE | ageing | protein intake | NITROGEN-BALANCE | SKELETAL-MUSCLE | OLDER-PEOPLE | NUTRITION & DIETETICS | RESISTANCE EXERCISE | LEAN MASS | ENDOCRINOLOGY & METABOLISM | ELDERLY HUMANS | ESSENTIAL AMINO-ACIDS | BED REST | sarcopenia | Dietary Proteins - administration & dosage | Muscular Atrophy - metabolism | Humans | Protein Deficiency - metabolism | Leucine - therapeutic use | Nutrition Policy | Muscle Proteins - biosynthesis | Aging - physiology | Aged | Exercise - physiology | Muscular Atrophy - prevention & control | Protein Deficiency - prevention & control | Dietary Proteins - therapeutic use | Dietary Supplements
Journal Article
Details
Digital rights
Loading RightsPLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e45048
Flavonoids have attracted considerable attention in relation to their effects upon health. 8-Prenylnaringenin (8-PN) is found in the common hop (Humulus...
POTENT PHYTOESTROGEN | SKELETAL-MUSCLE | HUMULUS-LUPULUS L | IN-VITRO | MULTIDISCIPLINARY SCIENCES | SOPHORA-FLAVESCENS | PRENYLATED FLAVONOIDS | KAPPA-B | HOPS | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | Water | Cell Line | Phosphorylation | Powders | Flavanones - therapeutic use | Mice, Inbred C57BL | Muscle Denervation | Male | Muscle, Skeletal - innervation | Muscular Disorders, Atrophic - prevention & control | Chromatography, High Pressure Liquid | Muscle Fibers, Skeletal - metabolism | Muscular Atrophy - drug therapy | Flavanones - administration & dosage | Flavanones - pharmacokinetics | Muscular Disorders, Atrophic - drug therapy | Animals | Flavanones - chemistry | Diet | Mice | Muscular Atrophy - prevention & control | Muscle, Skeletal - pathology | Humulus - chemistry | Proto-Oncogene Proteins c-akt - metabolism | Prevention | Flavonoids | Flavones | Bioflavonoids | Analysis | Muscles | Physiological aspects | Hops | Research | Atrophy, Muscular | Denervation | Ubiquitin | Physiological effects | Naringenin | AKT protein | Food science | Beer | Ingestion | Proteins | Atrophy | Metabolites | Bioaccumulation | Physiology | Gastrocnemius muscle | Ubiquitin-protein ligase | Enzymes | Dietary intake | Bioavailability | Metabolism | Skeletal muscle | Laboratory animals | Breweries | Endocrinology
POTENT PHYTOESTROGEN | SKELETAL-MUSCLE | HUMULUS-LUPULUS L | IN-VITRO | MULTIDISCIPLINARY SCIENCES | SOPHORA-FLAVESCENS | PRENYLATED FLAVONOIDS | KAPPA-B | HOPS | FOXO TRANSCRIPTION FACTORS | UBIQUITIN LIGASES | Water | Cell Line | Phosphorylation | Powders | Flavanones - therapeutic use | Mice, Inbred C57BL | Muscle Denervation | Male | Muscle, Skeletal - innervation | Muscular Disorders, Atrophic - prevention & control | Chromatography, High Pressure Liquid | Muscle Fibers, Skeletal - metabolism | Muscular Atrophy - drug therapy | Flavanones - administration & dosage | Flavanones - pharmacokinetics | Muscular Disorders, Atrophic - drug therapy | Animals | Flavanones - chemistry | Diet | Mice | Muscular Atrophy - prevention & control | Muscle, Skeletal - pathology | Humulus - chemistry | Proto-Oncogene Proteins c-akt - metabolism | Prevention | Flavonoids | Flavones | Bioflavonoids | Analysis | Muscles | Physiological aspects | Hops | Research | Atrophy, Muscular | Denervation | Ubiquitin | Physiological effects | Naringenin | AKT protein | Food science | Beer | Ingestion | Proteins | Atrophy | Metabolites | Bioaccumulation | Physiology | Gastrocnemius muscle | Ubiquitin-protein ligase | Enzymes | Dietary intake | Bioavailability | Metabolism | Skeletal muscle | Laboratory animals | Breweries | Endocrinology
Journal Article
Details
Digital rights
Loading RightsNature Reviews Nephrology, ISSN 1759-5061, 2014, Volume 10, Issue 9, pp. 504 - 516
In patients with-chronic kidney disease (CKD), loss of cellular proteins increases the risks of morbidity and mortality. Persistence of muscle protein...
SKELETAL-MUSCLE | INTRADIALYTIC PARENTERAL-NUTRITION | PROTEIN-DEGRADATION | MYOSTATIN GENE-EXPRESSION | CHRONIC METABOLIC-ACIDOSIS | UROLOGY & NEPHROLOGY | MALNOURISHED HEMODIALYSIS-PATIENTS | UREMIA-ASSOCIATED CACHEXIA | UBIQUITIN-PROTEASOME PATHWAY | CHRONIC-RENAL-FAILURE | CATABOLIC CONDITIONS | Renal Insufficiency, Chronic - metabolism | Protein Biosynthesis | Muscular Atrophy - metabolism | Signal Transduction | Proteolysis | Humans | Homeostasis | Muscle, Skeletal - metabolism | Muscular Atrophy - prevention & control | Renal Insufficiency, Chronic - complications | Muscular Atrophy - etiology | Complications and side effects | Development and progression | Care and treatment | Chronic kidney failure | Atrophy, Muscular
SKELETAL-MUSCLE | INTRADIALYTIC PARENTERAL-NUTRITION | PROTEIN-DEGRADATION | MYOSTATIN GENE-EXPRESSION | CHRONIC METABOLIC-ACIDOSIS | UROLOGY & NEPHROLOGY | MALNOURISHED HEMODIALYSIS-PATIENTS | UREMIA-ASSOCIATED CACHEXIA | UBIQUITIN-PROTEASOME PATHWAY | CHRONIC-RENAL-FAILURE | CATABOLIC CONDITIONS | Renal Insufficiency, Chronic - metabolism | Protein Biosynthesis | Muscular Atrophy - metabolism | Signal Transduction | Proteolysis | Humans | Homeostasis | Muscle, Skeletal - metabolism | Muscular Atrophy - prevention & control | Renal Insufficiency, Chronic - complications | Muscular Atrophy - etiology | Complications and side effects | Development and progression | Care and treatment | Chronic kidney failure | Atrophy, Muscular
Journal Article
Details
Digital rights
Loading Rights