نتائج البحث - "Fatty Acid Oxidation"

1

Upregulated PDK4 expression is a sensitive marker of increased fatty acid oxidation

المؤلفون: Linn I. Hodneland, Nils Gunnar Løvsletten, Rolf K. Berge, Kjetil Berge, Nils Halberg, Ina Katrine Nitschke Pettersen, Hege Wergedahl, Bodil Bjørndal, Lena Hansen, Xiao-Zheng Liu, Ove Bruland, Gro V. Røsland, Øystein Fluge, Sissel E. Dyrstad, Arild C. Rustan, Hanan Ashrafi, Deusdedit Tusubira, Karl Johan Tronstad

المصدر: Mitochondrion (Amsterdam. Print)
Mitochondrion

مصطلحات موضوعية: Male, 0301 basic medicine, Mitochondrion, peroxisome proliferator-activated receptor (ppar), metabolic flexibility, chemistry.chemical_compound, 0302 clinical medicine, Metabolic flexibility, cell metabolism, Glycolysis, Beta oxidation, fatty acid oxidation, chemistry.chemical_classification, Fatty Acids, Tetradecylthioacetic acid, Peroxisome, Up-Regulation, Mitochondria, mitochondria, Biochemistry, Organ Specificity, Fatty acid oxidation, Pyruvate dehydrogenase kinase, biomarker, Molecular Medicine, Oxidation-Reduction, VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470::Cellebiologi: 471, PDK4, Sulfides, Gene Expression Regulation, Enzymologic, Mitochondrial Proteins, 03 medical and health sciences, pyruvate dehydrogenase kinase, Metabolic regulation, Animals, Humans, Rats, Wistar, Molecular Biology, Cell metabolism, Pyruvate Dehydrogenase Acetyl-Transferring Kinase, Fatty acid, Cell Biology, Biomarker, Rats, 030104 developmental biology, chemistry, Mitochondrial biogenesis, Peroxisome proliferator-activated receptor (PPAR), metabolic regulation, Biomarkers, 030217 neurology & neurosurgery, HeLa Cells

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4eb42ac0266c96e330b533f9d46c25aTest
https://hdl.handle.net/1956/21104Test

2

Methylene blue decreases mitochondrial lysine acetylation in the diabetic heart

المؤلفون: Sean P. McBrayer, Margaret P. Chandler, Alison B. Austin, Mikayla M. Depuydt, Mariana G. Rosca, Masaru Miyagi, Chia heng Hsiung, Jessica M. Berthiaume

المصدر: Molecular and Cellular Biochemistry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e61478d89b80d42ca732dcdec1aa63dTest
https://doi.org/10.1007/s11010-017-2993-1Test

3

A new leptin-mediated mechanism for stimulating fatty acid oxidation

المؤلفون: Swati S. Jain, Iman Momken, Jan F. C. Glatz, Joost J. F. P. Luiken, Miranda Nabben, Adrian Chabowski, Ellen Dirkx, Jay T. McFarlan, Arend Bonen

المساهمون: RS: CARIM - R2.07 - Gene regulation, Cardiologie, Moleculaire Genetica, RS: CARIM - R2.06 - Intermediate cardiac metabolism, Unité de biologie intégrative des adaptations à l'exercice (UBIAE), Université d'Évry-Val-d'Essonne (UEVE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Medical University of Bialystok, Maastricht University [Maastricht], University of Guelph, Medical University of Białystok (MUB)

المصدر: Biochemical Journal, 474(1), 149-162. Portland Press Ltd.
Biochemical Journal
Biochemical Journal, 2017, 474 (1), pp.149-162. ⟨10.1042/BCJ20160804⟩

مصطلحات موضوعية: 0301 basic medicine, CD36 Antigens, Leptin, [SDV]Life Sciences [q-bio], Glucose uptake, CD36, Oleic Acids, animal cell, AMP-Activated Protein Kinases, Biochemistry, Western blotting, Mice, Sarcolemma, CD36 antigen, Myocyte, rat, animal, genetics, Myocytes, Cardiac, Phosphorylation, Beta oxidation, sulfo-N-succinimidyl oleate, fatty acid oxidation, fatty acid transport, chemistry.chemical_classification, Mice, Knockout, cardiac muscle cell, biology, Chemistry, MEMBRANE-PROTEINS, Fatty Acids, ACTIVATED PROTEIN-KINASE, hydroxymethylglutaryl coenzyme A reductase kinase, Skeletal, succinimide derivative, Protein Transport, medicine.anatomical_structure, priority journal, enzyme active site, Muscle, SKELETAL-MUSCLE, LIPID-ACCUMULATION, Cardiac, Oxidation-Reduction, Vidarabine, medicine.medical_specialty, Knockout, Succinimides, CELLULAR REDISTRIBUTION, RAT CARDIAC MYOCYTES, OB/OB MICE, Article, Fatty acid-binding protein, Cell Line, 03 medical and health sciences, male, Internal medicine, medicine, Animals, controlled study, skeletal muscle, Antigens, Muscle, Skeletal, Molecular Biology, mouse, Myocytes, Cd36 protein, nonhuman, GLUCOSE-UPTAKE, Skeletal muscle, Fatty acid, AMPK, enzyme activation, Cell Biology, TRANSPORT, protein phosphorylation, Rats, 030104 developmental biology, Endocrinology, oleic acid, drug effects, PLASMA-MEMBRANE, biology.protein, fatty acid, knockout mouse, cell membrane, metabolism, oxidation reduction reaction, energy yield

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea71e192503cc2edd157c72263c31070Test
https://doi.org/10.1042/BCJ20160804Test

4

Etomoxir Inhibits Macrophage Polarization by Disrupting CoA Homeostasis

المصدر: Cell metabolism, vol 28, iss 3

مصطلحات موضوعية: 0301 basic medicine, Male, CPT-2, CPT-1, Physiology, Mitochondrion, coenzyme A, Medical Biochemistry and Metabolomics, Inbred C57BL, Oxidative Phosphorylation, Rats, Sprague-Dawley, chemistry.chemical_compound, Mice, Homeostasis, Enzyme Inhibitors, long-chain fatty acid oxidation, Fatty Acids, 3T3 Cells, Hep G2 Cells, Cell biology, Mitochondria, Liver, Intracellular, medicine.drug, Coenzyme A, macrophage polarization, Macrophage polarization, oxidative phosphorylation, Oxidative phosphorylation, Article, interleukin 4, 03 medical and health sciences, Endocrinology & Metabolism, medicine, Animals, Humans, Mitochondrial ADP, Carnitine O-palmitoyltransferase, Carnitine, ATP Translocases, Molecular Biology, Carnitine O-Palmitoyltransferase, Macrophages, Cell Biology, Macrophage Activation, HCT116 Cells, Rats, Mice, Inbred C57BL, 030104 developmental biology, chemistry, A549 Cells, pantothenate, Epoxy Compounds, Sprague-Dawley, Acyl Coenzyme A, Interleukin-4, Biochemistry and Cell Biology, Mitochondrial ADP, ATP Translocases, Etomoxir

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::159495c0d1be78d8c409a5323dfdda36Test
https://escholarship.org/uc/item/7w98t225Test

5

AMP-activated protein kinase and ATP-citrate lyase are two distinct molecular targets for ETC-1002, a novel small molecule regulator of lipid and carbohydrate metabolism

المؤلفون: Mark A. Spahr, Jeffrey C. Hanselman, Roger S. Newton, Rai Ajit K. Srivastava, Mark Naples, Clay T. Cramer, Stephen L. Pinkosky, Timothy R. Hurley, Khosrow Adeli, Jacob L. Houghton, Sergey Filippov, Cheryl D. Bradshaw, Ashley F. Brant, Christopher Baker

المصدر: Journal of Lipid Research, Vol 54, Iss 1, Pp 134-151 (2013)

مصطلحات موضوعية: Male, ATP citrate lyase, AMP-Activated Protein Kinases, Biochemistry, Mice, chemistry.chemical_compound, Endocrinology, AMP-Activated Protein Kinase Kinases, AMP-activated protein kinase, cardiovascular disease, Cricetinae, LDL-cholesterol, Dicarboxylic Acids, Molecular Targeted Therapy, Enzyme Inhibitors, Beta oxidation, Research Articles, fatty acid oxidation, Kinase, Fatty Acids, Hep G2 Cells, Sterols, Liver, Carbohydrate Metabolism, Female, Signal Transduction, Adenylate kinase, QD415-436, Protein Serine-Threonine Kinases, Biology, metabolic syndrome, Animals, Humans, Obesity, Protein kinase A, Fatty acid synthesis, Dyslipidemias, fatty acid synthesis, Lipid metabolism, Cell Biology, Glucagon, Lipid Metabolism, Diet, Rats, Enzyme Activation, Glucose, chemistry, cholesterol synthesis, ATP Citrate (pro-S)-Lyase, biology.protein, Calcium, Energy Metabolism, Biomarkers

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96d7951a1d094c9e3e8454ac8eafbe26Test
https://doi.org/10.1194/jlr.m030528Test

6

Acyl-CoA synthetase 1 deficiency alters cardiolipin species and impairs mitochondrial function

المؤلفون: Sarah A. Martin, Trisha J. Grevengoed, Lalage A. Katunga, Rosalind A. Coleman, Robert C. Murphy, Ethan J. Anderson, Daniel E. Cooper

المصدر: Journal of Lipid Research, Vol 56, Iss 8, Pp 1572-1582 (2015)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5da934ef0275b1cef2c0644b46fa65b0Test
https://europepmc.org/articles/PMC4513998Test/

7

Modulation of the hepatic malonyl-CoA–carnitine palmitoyltransferase 1A partnership creates a metabolic switch allowing oxidation of de novo fatty acids

المؤلفون: Carina Prip-Buus, Jean Girard, Martin Sournac, Catherine Esnous, Isabelle Cohen, Marie Akkaoui, Véronique Lenoir

المساهمون: Peer, Hal, Institut Cochin (UMR_S567 / UMR 8104), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université Paris Descartes - Paris 5 (UPD5) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Centre National de la Recherche Scientifique (CNRS)

المصدر: Biochemical Journal
Biochemical Journal, 2009, 420 (3), pp.429-438. ⟨10.1042/BJ20081932⟩
Biochemical Journal, Portland Press, 2009, 420 (3), pp.429-438. 〈10.1042/BJ20081932〉

مصطلحات موضوعية: Male, medicine.medical_treatment, Fluorescent Antibody Technique, Biochemistry, chemistry.chemical_compound, 0302 clinical medicine, Insulin, Beta oxidation, fatty acid oxidation, Cells, Cultured, 0303 health sciences, Fatty Acids, Mitochondria, Liver, 030220 oncology & carcinogenesis, Lipogenesis, lipids (amino acids, peptides, and proteins), Oxidation-Reduction, medicine.medical_specialty, Genetic Vectors, Immunoblotting, carnitine palmitoyltransferase 1, Biology, Transfection, Models, Biological, Adenoviridae, 03 medical and health sciences, Carnitine palmitoyltransferase 1, Internal medicine, medicine, Animals, triglyceride, Carnitine O-palmitoyltransferase, Rats, Wistar, Glycogen synthase, Molecular Biology, lipogenesis, Triglycerides, 030304 developmental biology, Carnitine O-Palmitoyltransferase, Triglyceride, Cell Biology, Lipid Metabolism, Rats, Glucose, Endocrinology, Malonyl-CoA, chemistry, Mutation, Hepatocytes, biology.protein

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4a879788b9626afd81144d52583a294Test
https://doi.org/10.1042/bj20081932Test

8

Overexpression of PLIN5 in skeletal muscle promotes oxidative gene expression and intramyocellular lipid content without compromising insulin sensitivity

المؤلفون: Madeleen Bosma, Guido J. E. J. Hooiveld, Sander Kersten, Patrick Schrauwen, Johanna Jorgensen, Lauren M. Sparks, Matthijs K. C. Hesselink, Sander M. Houten

المساهمون: Paediatric Metabolic Diseases, Laboratory Genetic Metabolic Diseases, Humane Biologie, Nutrition and Movement Sciences, RS: NUTRIM - R1 - Metabolic Syndrome

المصدر: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1831(4), 844-852. Elsevier
Biochimica et Biophysica Acta. Molecular and Cell Biology of Lipids 1831 (2013) 4
Biochimica et Biophysica Acta. Molecular and Cell Biology of Lipids, 1831(4), 844-852
Biochimica et Biophysica Acta-Molecular and Cell Biology of Lipids, 1831(4), 844-852. Elsevier

مصطلحات موضوعية: Male, Glucose uptake, Peroxisome proliferator-activated receptor, Skeletal muscle, PROTEIN, Muscle Proteins, in-vivo, Voeding, Metabolisme en Genomica, MITOCHONDRIA, Lipid droplet, PPAR-ALPHA, Insulin, PHOSPHORYLATION, IN-VIVO, chemistry.chemical_classification, phosphorylation, Intracellular Signaling Peptides and Proteins, Insulin sensitivity, Metabolism and Genomics, mitochondria, ppar-alpha, medicine.anatomical_structure, Metabolisme en Genomica, Nutrition, Metabolism and Genomics, PPARGC1A, weight-loss, Perilipin, medicine.medical_specialty, FATTY-ACID OXIDATION, perilipin 5, Perilipin 2, PERILIPIN 5, WEIGHT-LOSS, fatty-acid oxidation, Biology, Perilipin-5, Perilipin-2, resistance, Insulin resistance, Voeding, Internal medicine, medicine, Animals, Rats, Wistar, Muscle, Skeletal, Molecular Biology, Triglycerides, VLAG, Nutrition, OXPAT, carnitine, Membrane Proteins, Cell Biology, medicine.disease, Lipid Metabolism, Rats, Endocrinology, chemistry, biology.protein, Oxidative gene expression, Insulin Resistance, protein, RESISTANCE, CARNITINE

وصف الملف: application/pdf; application/octet-stream

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1257279a2dc2cd41f17187929e198c54Test
https://pubmed.ncbi.nlm.nih.gov/23353597Test

9

Malonyl-CoA decarboxylase is present in the cytosolic, mitochondrial and peroxisomal compartments of rat hepatocytes

المؤلفون: Asish K. Saha, Marc Prentki, Raphaël Roduit, Neil B. Ruderman, Moise Bendayan, Erik Joly

المصدر: FEBS Letters. 579:6581-6586

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d87f98a40a76ae16ea7538c2c0db5acfTest
https://doi.org/10.1016/j.febslet.2005.10.050Test

10

Tetradecylthioacetic acid prevents high fat diet induced adiposity and insulin resistance

المؤلفون: Jørgen Jensen, Iwar Klimes, Karl Johan Tronstad, Elena Šeböková, Esben N. Flindt, Elin Bergene, Karsten Kristiansen, Kjetil Berge, Arild C. Rustan, Bart Staels, Michèle Guerre-Millo, Susanne Mandrup, Lise Madsen, Rolf K. Berge

المصدر: Scopus-Elsevier
Madsen, L, Guerre-Millo, M, Flindt, E N, Berge, K, Tronstad, K J, Bergene, E, Sebokova, E, Rustan, A C, Jensen, J, Mandrup, S, Kristiansen, K, Klimes, I, Staels, B & Berge, R K 2002, ' Tetradecylthioacetic acid prevents high fat diet induced adiposity and insulin resistance. ', Journal of Lipid Research, vol. 43, no. 5, pp. 742-750 .
ResearcherID
Europe PubMed Central
Journal of Lipid Research, Vol 43, Iss 5, Pp 742-750 (2002)
University of Southern Denmark

مصطلحات موضوعية: Male, medicine.medical_specialty, medicine.medical_treatment, Receptors, Cytoplasmic and Nuclear, Adipose tissue, Mitochondria, Liver, QD415-436, Sulfides, Biology, PPAR, Biochemistry, Antioxidants, chemistry.chemical_compound, Endocrinology, Insulin resistance, Reference Values, CPT-II, Internal medicine, Ketogenesis, medicine, Animals, Insulin, CPT-I, Obesity, insulin action, Rats, Wistar, Beta oxidation, fatty acid oxidation, Triglycerides, chemistry.chemical_classification, Fatty acid, Tetradecylthioacetic acid, fatty acid analogues, Cell Biology, medicine.disease, Dietary Fats, Rats, Rats, Zucker, Kinetics, Adipose Tissue, chemistry, Fatty acid analog, Insulin Resistance, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75a728d591b427153383d6ccfa11a5d9Test
https://doi.org/10.1016/s0022-2275Test(20)30116-4

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