Artículos de revistas sobre el tema "Long-chain-acyl-CoA dehydrogenase"
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Masterson, C., A. Blackburn y C. Wood. "Acyl-CoA dehydrogenase activity in pea cotyledon tissue during germination and initial growth". Biochemical Society Transactions 28, n.º 6 (1 de diciembre de 2000): 760–62. http://dx.doi.org/10.1042/bst0280760.
Texto completoTreem, William R., Jeffrey S. Hyams, Charles A. Stanley, Daniel E. Hale y Harris B. Leopold. "Hypoglycemia, Hypotonia, and Cardiomyopathy: The Evolving Clinical Picture of Long-Chain Acyl-CoA Dehydrogenase Deficiency". Pediatrics 87, n.º 3 (1 de marzo de 1991): 328–33. http://dx.doi.org/10.1542/peds.87.3.328.
Texto completoCox, Keith B., Jian Liu, Liqun Tian, Stephen Barnes, Qinglin Yang y Philip A. Wood. "Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency". Laboratory Investigation 89, n.º 12 (7 de septiembre de 2009): 1348–54. http://dx.doi.org/10.1038/labinvest.2009.86.
Texto completoYu, Wenfeng, Xiquan Liang, Regina E. Ensenauer, Jerry Vockley, Lawrence Sweetman y Horst Schulz. "Leaky β-Oxidation of atrans-Fatty Acid". Journal of Biological Chemistry 279, n.º 50 (4 de octubre de 2004): 52160–67. http://dx.doi.org/10.1074/jbc.m409640200.
Texto completoWijayabandara, Maheshi, Champika Gamakaranage y Dineshani Hettiarachchi. "Very-Long-Chain Acyl-Co-Enzyme A Dehydrogenase Deficiency Presenting as Rhabdomyolysis: First Case Report from Sri Lanka". Case Reports in Genetics 2020 (13 de octubre de 2020): 1–5. http://dx.doi.org/10.1155/2020/8894518.
Texto completoLiang, X., W. Le, D. Zhang y H. Schulz. "Impact of the intramitochondrial enzyme organization on fatty acid oxidation". Biochemical Society Transactions 29, n.º 2 (1 de mayo de 2001): 279–82. http://dx.doi.org/10.1042/bst0290279.
Texto completoYamaguchi, Seiji, Yasuhiro Indo, Paul M. Coates, Takashi Hashimoto y Kay Tanaka. "Identification of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Three Patients Previously Diagnosed with Long-Chain Acyl-CoA Dehydrogenase Deficiency". Pediatric Research 34, n.º 1 (julio de 1993): 111–13. http://dx.doi.org/10.1203/00006450-199307000-00025.
Texto completoCosta, Catarina G., Lambertus Dorland, Ulbe Holwerda, Isabel Tavares de Almeida, Bwee-Tien Poll-The, Cornelis Jakobs y Marinus Duran. "Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disorders". Clinical Chemistry 44, n.º 3 (1 de marzo de 1998): 463–71. http://dx.doi.org/10.1093/clinchem/44.3.463.
Texto completoNandy, Andreas, Volker Kieweg, Franz-Georg Kräutle, Petra Vock, Burkhard Küchler, Peter Bross, Jung-Ja P. Kim, Ihab Rasched y Sandro Ghisla. "Medium-Long-Chain Chimeric Human Acyl-CoA Dehydrogenase: Medium-Chain Enzyme with the Active Center Base Arrangement of Long-Chain Acyl-CoA Dehydrogenase†". Biochemistry 35, n.º 38 (enero de 1996): 12402–11. http://dx.doi.org/10.1021/bi960785e.
Texto completoParsons, H. G. y V. C. Dias. "Intramitochondrial fatty acid metabolism: riboflavin deficiency and energy production". Biochemistry and Cell Biology 69, n.º 7 (1 de julio de 1991): 490–97. http://dx.doi.org/10.1139/o91-073.
Texto completoTHORPE, Colin, Thomas L. CIARDELLI, Charles J. STEWART y Theodor WIELAND. "Interaction of Long-Chain Acyl-CoA Analogs with Pig Kidney General Acyl-CoA Dehydrogenase". European Journal of Biochemistry 118, n.º 2 (3 de marzo de 2005): 279–82. http://dx.doi.org/10.1111/j.1432-1033.1981.tb06397.x.
Texto completoIndo, Yasuhiro, Paul M. Coates, Daniel E. Hale y Kay Tanaka. "Immunochemical Characterization of Variant Long-Chain Acyl-CoA Dehydrogenase in Cultured Fibroblasts from Nine Patients with Long-Chain Acyl-CoA Dehydrogenase Deficiency". Pediatric Research 30, n.º 3 (septiembre de 1991): 211–15. http://dx.doi.org/10.1203/00006450-199109000-00001.
Texto completoThapa, Dharendra, Manling Zhang, Janet R. Manning, Danielle A. Guimarães, Michael W. Stoner, Robert M. O’Doherty, Sruti Shiva y Iain Scott. "Acetylation of mitochondrial proteins by GCN5L1 promotes enhanced fatty acid oxidation in the heart". American Journal of Physiology-Heart and Circulatory Physiology 313, n.º 2 (1 de agosto de 2017): H265—H274. http://dx.doi.org/10.1152/ajpheart.00752.2016.
Texto completoCox, K. B. "Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse". Human Molecular Genetics 10, n.º 19 (1 de septiembre de 2001): 2069–77. http://dx.doi.org/10.1093/hmg/10.19.2069.
Texto completoRudolf, Jeffrey D., Liao-Bin Dong, Tingting Huang y Ben Shen. "A genetically amenable platensimycin- and platencin-overproducer as a platform for biosynthetic explorations: a showcase of PtmO4, a long-chain acyl-CoA dehydrogenase". Molecular BioSystems 11, n.º 10 (2015): 2717–26. http://dx.doi.org/10.1039/c5mb00303b.
Texto completoFOX, Simon R., Lionel M. HILL, Stephen RAWSTHORNE y Matthew J. HILLS. "Inhibition of the glucose-6-phosphate transporter in oilseed rape (Brassica napus L.) plastids by acyl-CoA thioesters reduces fatty acid synthesis". Biochemical Journal 352, n.º 2 (24 de noviembre de 2000): 525–32. http://dx.doi.org/10.1042/bj3520525.
Texto completoNandy, A., B. Küchler y S. Ghisla. "Molecular evolution and substrate specificity of acyl-CoA dehydrogenases: Chimaeric ‘medium/long’ chain-specific enzyme from medium-chain acyl-CoA dehydrogenase". Biochemical Society Transactions 24, n.º 1 (1 de febrero de 1996): 105–10. http://dx.doi.org/10.1042/bst0240105.
Texto completoTenopoulou, Margarita, Jie Chen, Jean Bastin, Michael J. Bennett, Harry Ischiropoulos y Paschalis-Thomas Doulias. "Strategies for Correcting Very Long Chain Acyl-CoA Dehydrogenase Deficiency". Journal of Biological Chemistry 290, n.º 16 (3 de marzo de 2015): 10486–94. http://dx.doi.org/10.1074/jbc.m114.635102.
Texto completoSenefeld, Carly M. y Jonathon W. Senefeld. "Very long-chain acyl-CoA dehydrogenase deficiency nomenclature: compound heterozygosity". Journal of Human Genetics 65, n.º 4 (27 de enero de 2020): 435–36. http://dx.doi.org/10.1038/s10038-020-0727-9.
Texto completoFatehi, F., A. A. Okhovat, Y. Nilipour, M. Mroczek, V. Straub, A. Töpf, A. Palibrk et al. "Adult‐onset very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD)". European Journal of Neurology 27, n.º 11 (24 de julio de 2020): 2257–66. http://dx.doi.org/10.1111/ene.14402.
Texto completoKakimoto, Pâmela A. H. B., Fábio K. Tamaki, Ariel R. Cardoso, Sandro R. Marana y Alicia J. Kowaltowski. "H2O2 release from the very long chain acyl-CoA dehydrogenase". Redox Biology 4 (abril de 2015): 375–80. http://dx.doi.org/10.1016/j.redox.2015.02.003.
Texto completoVellekoop, P., E. F. Diekman, I. van Tuijl, M. M. C. de Vries, P. M. van Hasselt y G. Visser. "Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency". Molecular Genetics and Metabolism 103, n.º 1 (mayo de 2011): 96–97. http://dx.doi.org/10.1016/j.ymgme.2011.01.010.
Texto completoMurata, Ken-ya, Hideo Sugie, Ichizo Nishino, Tomoyoshi Kondo y Hidefumi Ito. "A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency". Muscle & Nerve 49, n.º 2 (16 de enero de 2014): 295–96. http://dx.doi.org/10.1002/mus.24055.
Texto completoAlatibi, Khaled I., Judith Hagenbuchner, Zeinab Wehbe, Daniela Karall, Michael J. Ausserlechner, Jerry Vockley, Ute Spiekerkoetter, Sarah C. Grünert y Sara Tucci. "Different Lipid Signature in Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders". Cells 10, n.º 5 (18 de mayo de 2021): 1239. http://dx.doi.org/10.3390/cells10051239.
Texto completoOey, N. A., J. P. N. Ruiter, L. IJlst, T. Attie-Bitach, M. Vekemans, R. J. A. Wanders y F. A. Wijburg. "Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain". Biochemical and Biophysical Research Communications 346, n.º 1 (julio de 2006): 33–37. http://dx.doi.org/10.1016/j.bbrc.2006.05.088.
Texto completoCrawford, Sarah, Elizabeth Sablon, Nadia Ali, Ami R. Rosen, Patricia L. Hall y Juanita Neira Fresneda. "Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives". International Journal of Neonatal Screening 9, n.º 4 (6 de octubre de 2023): 53. http://dx.doi.org/10.3390/ijns9040053.
Texto completoMarcì, Marcello y Patrizia Ajovalasit. "Medium-Chain Acyl-CoA Dehydrogenase Deficiency in an Infant with Dilated Cardiomyopathy". Cardiology Research and Practice 2009 (2009): 1–3. http://dx.doi.org/10.4061/2009/281389.
Texto completoAlatibi, Khaled I., Stefan Tholen, Zeinab Wehbe, Judith Hagenbuchner, Daniela Karall, Michael J. Ausserlechner, Oliver Schilling, Sarah C. Grünert, Jerry Vockley y Sara Tucci. "Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders". International Journal of Molecular Sciences 22, n.º 19 (29 de septiembre de 2021): 10556. http://dx.doi.org/10.3390/ijms221910556.
Texto completoOnkenhout, W., V. Venizelos, P. F. van der Poel, M. P. van den Heuvel y B. J. Poorthuis. "Identification and quantification of intermediates of unsaturated fatty acid metabolism in plasma of patients with fatty acid oxidation disorders". Clinical Chemistry 41, n.º 10 (1 de octubre de 1995): 1467–74. http://dx.doi.org/10.1093/clinchem/41.10.1467.
Texto completoEaton, S., T. Bursby, B. Middleton, M. Pourfarzam, K. Mills, A. W. Johnson y K. Bartlecc. "The mitochondrial trifunctional protein: centre of a β-oxidation metabolon?" Biochemical Society Transactions 28, n.º 2 (1 de febrero de 2000): 177–82. http://dx.doi.org/10.1042/bst0280177.
Texto completoSauer, Sven W., Jürgen G. Okun, Marina A. Schwab, Linda R. Crnic, Georg F. Hoffmann, Stephen I. Goodman, David M. Koeller y Stefan Kölker. "Bioenergetics in Glutaryl-Coenzyme A Dehydrogenase Deficiency". Journal of Biological Chemistry 280, n.º 23 (19 de abril de 2005): 21830–36. http://dx.doi.org/10.1074/jbc.m502845200.
Texto completoDiekman, Eugène F., Michel van Weeghel, Mayte Suárez-Fariñas, Carmen Argmann, Pablo Ranea-Robles, Ronald J. A. Wanders, Gepke Visser, Ingeborg van der Made, Esther E. Creemers y Sander M. Houten. "Dietary restriction in the long-chain acyl-CoA dehydrogenase knockout mouse". Molecular Genetics and Metabolism Reports 27 (junio de 2021): 100749. http://dx.doi.org/10.1016/j.ymgmr.2021.100749.
Texto completoDjordjevic, Snezana, Yu Dong, Rosemary Paschke, Frank E. Frerman, Arnold W. Strauss y Jung-Ja P. Kim. "Identification of the Catalytic Base in Long Chain Acyl-CoA Dehydrogenase". Biochemistry 33, n.º 14 (12 de abril de 1994): 4258–64. http://dx.doi.org/10.1021/bi00180a021.
Texto completoSchrijver-Wieling, I., G. H. M. B. van Rens, D. Wittebol-Post, J. A. M. Smeitink, J. P. de Jager, H. B. C. de Klerk y G. H. M. van Lith. "Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency". British Journal of Ophthalmology 81, n.º 4 (1 de abril de 1997): 291–94. http://dx.doi.org/10.1136/bjo.81.4.291.
Texto completoAndresen, B. S., C. Vianey-Saban, P. Bross, P. Divry, C. R. Roe, M. A. Nada, I. Knudsen y N. Gregersen. "The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency". Journal of Inherited Metabolic Disease 19, n.º 2 (marzo de 1996): 169–72. http://dx.doi.org/10.1007/bf01799421.
Texto completoMason, Katherine E., Daniel A. Stofan y Luke I. Szweda. "Inhibition of very long chain acyl-CoA dehydrogenase during cardiac ischemia". Archives of Biochemistry and Biophysics 437, n.º 2 (mayo de 2005): 138–43. http://dx.doi.org/10.1016/j.abb.2005.03.004.
Texto completoWinter, Susan, Neil R. M. Buist, Nicola Longo, Saro H. Armenian, Gary Lopaschuk y Anna Wasilewska. "Round Table Discussion". Annals of Nutrition and Metabolism 68, Suppl. 3 (2016): 21–23. http://dx.doi.org/10.1159/000448323.
Texto completoLetteron, P., N. Brahimi-Bourouina, M. A. Robin, A. Moreau, G. Feldmann y D. Pessayre. "Glucocorticoids inhibit mitochondrial matrix acyl-CoA dehydrogenases and fatty acid beta-oxidation". American Journal of Physiology-Gastrointestinal and Liver Physiology 272, n.º 5 (1 de mayo de 1997): G1141—G1150. http://dx.doi.org/10.1152/ajpgi.1997.272.5.g1141.
Texto completoChen, Xiaobo, Jiayue Chen, Bing Yan, Wei Zhang, Luke W. Guddat, Xiang Liu y Zihe Rao. "Structural basis for the broad substrate specificity of two acyl-CoA dehydrogenases FadE5 from mycobacteria". Proceedings of the National Academy of Sciences 117, n.º 28 (29 de junio de 2020): 16324–32. http://dx.doi.org/10.1073/pnas.2002835117.
Texto completoKatagiri, Hideki, Tomoichiro Asano, Tetsuya Yamada, Toshifumi Aoyama, Yasushi Fukushima, Masatoshi Kikuchi, Tatsuhiko Kodama y Yoshitomo Oka. "Acyl-Coenzyme A Dehydrogenases Are Localized on GLUT4-Containing Vesicles via Association with Insulin-Regulated Aminopeptidase in a Manner Dependent on Its Dileucine Motif". Molecular Endocrinology 16, n.º 5 (1 de mayo de 2002): 1049–59. http://dx.doi.org/10.1210/mend.16.5.0831.
Texto completoZytkovicz, Thomas H., Eileen F. Fitzgerald, Deborah Marsden, Cecilia A. Larson, Vivian E. Shih, Donna M. Johnson, Arnold W. Strauss, Anne Marie Comeau, Roger B. Eaton y George F. Grady. "Tandem Mass Spectrometric Analysis for Amino, Organic, and Fatty Acid Disorders in Newborn Dried Blood Spots". Clinical Chemistry 47, n.º 11 (1 de noviembre de 2001): 1945–55. http://dx.doi.org/10.1093/clinchem/47.11.1945.
Texto completoDamore, Mary Beth, Charles R. Roe, Teresia Goldberg, Mohammed A. Nada, Christine Vlaney-Saban y Alfred E. Slonim. "DIAGNOSIS AND TREATMENT OF VERY-LONG-CHAIN ACYL CoA DEHYDROGENASE DEFICIENCY.846". Pediatric Research 39 (abril de 1996): 143. http://dx.doi.org/10.1203/00006450-199604001-00868.
Texto completoKabuyama, Yukihito, Toshiyuki Suzuki, Naomi Nakazawa, Junko Yamaki, Miwako K. Homma y Yoshimi Homma. "Dysregulation of very long chain acyl-CoA dehydrogenase coupled with lipid peroxidation". American Journal of Physiology-Cell Physiology 298, n.º 1 (enero de 2010): C107—C113. http://dx.doi.org/10.1152/ajpcell.00231.2009.
Texto completoAndresen, B. S., S. Olpin, E. A. Kvittingen, P. Augoustides-Savvopoulou, D. Lindhout, D. J. J. Halley, C. Vianey-Saban et al. "DNA-based prenatal diagnosis for very-long- chain acyl-CoA dehydrogenase deficiency". Journal of Inherited Metabolic Disease 22, n.º 3 (mayo de 1999): 281–85. http://dx.doi.org/10.1023/a:1005558828223.
Texto completoEminoglu, Tuba F., Leyla Tumer, Ilyas Okur, Fatih S. Ezgu, Gursel Biberoglu y Alev Hasanoglu. "Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide". Forensic Science International 210, n.º 1-3 (julio de 2011): e1-e3. http://dx.doi.org/10.1016/j.forsciint.2011.04.003.
Texto completoMaher, Amy C., Al-Walid Mohsen, Jerry Vockley y Mark A. Tarnopolsky. "Low expression of long-chain acyl-CoA dehydrogenase in human skeletal muscle". Molecular Genetics and Metabolism 100, n.º 2 (junio de 2010): 163–67. http://dx.doi.org/10.1016/j.ymgme.2010.03.011.
Texto completoSchiff, Manuel, Al-Walid Mohsen, Anuradha Karunanidhi, Elizabeth McCracken, Renita Yeasted y Jerry Vockley. "Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency". Molecular Genetics and Metabolism 109, n.º 1 (mayo de 2013): 21–27. http://dx.doi.org/10.1016/j.ymgme.2013.02.002.
Texto completoSpiekerkoetter, Ute, Chonan Tokunaga, Udo Wendel, Ertan Mayatepek, Lodewijk Ijlst, Frederic M. Vaz, Naomi Van Vlies et al. "Tissue Carnitine Homeostasis in Very-Long-Chain Acyl-CoA Dehydrogenase–Deficient Mice". Pediatric Research 57, n.º 6 (junio de 2005): 760–64. http://dx.doi.org/10.1203/01.pdr.0000157915.26049.47.
Texto completoOrii, Koji O., Toshifumi Aoyama, Fumiko Saito-Ohara, Tatsuro Ikeuchi, Tadao Orii, Naomi Kondo y Takashi Hashimoto. "Molecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase gene". Mammalian Genome 8, n.º 7 (julio de 1997): 516–18. http://dx.doi.org/10.1007/s003359900488.
Texto completoHesse, Julia, Carina Braun, Sidney Behringer, Uta Matysiak, Ute Spiekerkoetter y Sara Tucci. "The diagnostic challenge in very-long chain acyl-CoA dehydrogenase deficiency (VLCADD)". Journal of Inherited Metabolic Disease 41, n.º 6 (7 de septiembre de 2018): 1169–78. http://dx.doi.org/10.1007/s10545-018-0245-5.
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