Artykuły w czasopismach na temat „Long-chain-acyl-CoA dehydrogenase”
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Masterson, C., A. Blackburn i C. Wood. "Acyl-CoA dehydrogenase activity in pea cotyledon tissue during germination and initial growth". Biochemical Society Transactions 28, nr 6 (1.12.2000): 760–62. http://dx.doi.org/10.1042/bst0280760.
Pełny tekst źródłaTreem, William R., Jeffrey S. Hyams, Charles A. Stanley, Daniel E. Hale i Harris B. Leopold. "Hypoglycemia, Hypotonia, and Cardiomyopathy: The Evolving Clinical Picture of Long-Chain Acyl-CoA Dehydrogenase Deficiency". Pediatrics 87, nr 3 (1.03.1991): 328–33. http://dx.doi.org/10.1542/peds.87.3.328.
Pełny tekst źródłaCox, Keith B., Jian Liu, Liqun Tian, Stephen Barnes, Qinglin Yang i Philip A. Wood. "Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency". Laboratory Investigation 89, nr 12 (7.09.2009): 1348–54. http://dx.doi.org/10.1038/labinvest.2009.86.
Pełny tekst źródłaYu, Wenfeng, Xiquan Liang, Regina E. Ensenauer, Jerry Vockley, Lawrence Sweetman i Horst Schulz. "Leaky β-Oxidation of atrans-Fatty Acid". Journal of Biological Chemistry 279, nr 50 (4.10.2004): 52160–67. http://dx.doi.org/10.1074/jbc.m409640200.
Pełny tekst źródłaWijayabandara, Maheshi, Champika Gamakaranage i 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 (13.10.2020): 1–5. http://dx.doi.org/10.1155/2020/8894518.
Pełny tekst źródłaLiang, X., W. Le, D. Zhang i H. Schulz. "Impact of the intramitochondrial enzyme organization on fatty acid oxidation". Biochemical Society Transactions 29, nr 2 (1.05.2001): 279–82. http://dx.doi.org/10.1042/bst0290279.
Pełny tekst źródłaYamaguchi, Seiji, Yasuhiro Indo, Paul M. Coates, Takashi Hashimoto i 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, nr 1 (lipiec 1993): 111–13. http://dx.doi.org/10.1203/00006450-199307000-00025.
Pełny tekst źródłaCosta, Catarina G., Lambertus Dorland, Ulbe Holwerda, Isabel Tavares de Almeida, Bwee-Tien Poll-The, Cornelis Jakobs i Marinus Duran. "Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disorders". Clinical Chemistry 44, nr 3 (1.03.1998): 463–71. http://dx.doi.org/10.1093/clinchem/44.3.463.
Pełny tekst źródłaNandy, Andreas, Volker Kieweg, Franz-Georg Kräutle, Petra Vock, Burkhard Küchler, Peter Bross, Jung-Ja P. Kim, Ihab Rasched i 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, nr 38 (styczeń 1996): 12402–11. http://dx.doi.org/10.1021/bi960785e.
Pełny tekst źródłaParsons, H. G., i V. C. Dias. "Intramitochondrial fatty acid metabolism: riboflavin deficiency and energy production". Biochemistry and Cell Biology 69, nr 7 (1.07.1991): 490–97. http://dx.doi.org/10.1139/o91-073.
Pełny tekst źródłaTHORPE, Colin, Thomas L. CIARDELLI, Charles J. STEWART i Theodor WIELAND. "Interaction of Long-Chain Acyl-CoA Analogs with Pig Kidney General Acyl-CoA Dehydrogenase". European Journal of Biochemistry 118, nr 2 (3.03.2005): 279–82. http://dx.doi.org/10.1111/j.1432-1033.1981.tb06397.x.
Pełny tekst źródłaIndo, Yasuhiro, Paul M. Coates, Daniel E. Hale i 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, nr 3 (wrzesień 1991): 211–15. http://dx.doi.org/10.1203/00006450-199109000-00001.
Pełny tekst źródłaThapa, Dharendra, Manling Zhang, Janet R. Manning, Danielle A. Guimarães, Michael W. Stoner, Robert M. O’Doherty, Sruti Shiva i 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, nr 2 (1.08.2017): H265—H274. http://dx.doi.org/10.1152/ajpheart.00752.2016.
Pełny tekst źródłaCox, 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, nr 19 (1.09.2001): 2069–77. http://dx.doi.org/10.1093/hmg/10.19.2069.
Pełny tekst źródłaRudolf, Jeffrey D., Liao-Bin Dong, Tingting Huang i 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, nr 10 (2015): 2717–26. http://dx.doi.org/10.1039/c5mb00303b.
Pełny tekst źródłaFOX, Simon R., Lionel M. HILL, Stephen RAWSTHORNE i 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, nr 2 (24.11.2000): 525–32. http://dx.doi.org/10.1042/bj3520525.
Pełny tekst źródłaNandy, A., B. Küchler i 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, nr 1 (1.02.1996): 105–10. http://dx.doi.org/10.1042/bst0240105.
Pełny tekst źródłaTenopoulou, Margarita, Jie Chen, Jean Bastin, Michael J. Bennett, Harry Ischiropoulos i Paschalis-Thomas Doulias. "Strategies for Correcting Very Long Chain Acyl-CoA Dehydrogenase Deficiency". Journal of Biological Chemistry 290, nr 16 (3.03.2015): 10486–94. http://dx.doi.org/10.1074/jbc.m114.635102.
Pełny tekst źródłaSenefeld, Carly M., i Jonathon W. Senefeld. "Very long-chain acyl-CoA dehydrogenase deficiency nomenclature: compound heterozygosity". Journal of Human Genetics 65, nr 4 (27.01.2020): 435–36. http://dx.doi.org/10.1038/s10038-020-0727-9.
Pełny tekst źródłaFatehi, F., A. A. Okhovat, Y. Nilipour, M. Mroczek, V. Straub, A. Töpf, A. Palibrk i in. "Adult‐onset very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD)". European Journal of Neurology 27, nr 11 (24.07.2020): 2257–66. http://dx.doi.org/10.1111/ene.14402.
Pełny tekst źródłaKakimoto, Pâmela A. H. B., Fábio K. Tamaki, Ariel R. Cardoso, Sandro R. Marana i Alicia J. Kowaltowski. "H2O2 release from the very long chain acyl-CoA dehydrogenase". Redox Biology 4 (kwiecień 2015): 375–80. http://dx.doi.org/10.1016/j.redox.2015.02.003.
Pełny tekst źródłaVellekoop, P., E. F. Diekman, I. van Tuijl, M. M. C. de Vries, P. M. van Hasselt i G. Visser. "Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency". Molecular Genetics and Metabolism 103, nr 1 (maj 2011): 96–97. http://dx.doi.org/10.1016/j.ymgme.2011.01.010.
Pełny tekst źródłaMurata, Ken-ya, Hideo Sugie, Ichizo Nishino, Tomoyoshi Kondo i Hidefumi Ito. "A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency". Muscle & Nerve 49, nr 2 (16.01.2014): 295–96. http://dx.doi.org/10.1002/mus.24055.
Pełny tekst źródłaAlatibi, Khaled I., Judith Hagenbuchner, Zeinab Wehbe, Daniela Karall, Michael J. Ausserlechner, Jerry Vockley, Ute Spiekerkoetter, Sarah C. Grünert i Sara Tucci. "Different Lipid Signature in Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders". Cells 10, nr 5 (18.05.2021): 1239. http://dx.doi.org/10.3390/cells10051239.
Pełny tekst źródłaOey, N. A., J. P. N. Ruiter, L. IJlst, T. Attie-Bitach, M. Vekemans, R. J. A. Wanders i 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, nr 1 (lipiec 2006): 33–37. http://dx.doi.org/10.1016/j.bbrc.2006.05.088.
Pełny tekst źródłaCrawford, Sarah, Elizabeth Sablon, Nadia Ali, Ami R. Rosen, Patricia L. Hall i Juanita Neira Fresneda. "Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives". International Journal of Neonatal Screening 9, nr 4 (6.10.2023): 53. http://dx.doi.org/10.3390/ijns9040053.
Pełny tekst źródłaMarcì, Marcello, i 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.
Pełny tekst źródłaAlatibi, Khaled I., Stefan Tholen, Zeinab Wehbe, Judith Hagenbuchner, Daniela Karall, Michael J. Ausserlechner, Oliver Schilling, Sarah C. Grünert, Jerry Vockley i 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, nr 19 (29.09.2021): 10556. http://dx.doi.org/10.3390/ijms221910556.
Pełny tekst źródłaOnkenhout, W., V. Venizelos, P. F. van der Poel, M. P. van den Heuvel i 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, nr 10 (1.10.1995): 1467–74. http://dx.doi.org/10.1093/clinchem/41.10.1467.
Pełny tekst źródłaEaton, S., T. Bursby, B. Middleton, M. Pourfarzam, K. Mills, A. W. Johnson i K. Bartlecc. "The mitochondrial trifunctional protein: centre of a β-oxidation metabolon?" Biochemical Society Transactions 28, nr 2 (1.02.2000): 177–82. http://dx.doi.org/10.1042/bst0280177.
Pełny tekst źródłaSauer, Sven W., Jürgen G. Okun, Marina A. Schwab, Linda R. Crnic, Georg F. Hoffmann, Stephen I. Goodman, David M. Koeller i Stefan Kölker. "Bioenergetics in Glutaryl-Coenzyme A Dehydrogenase Deficiency". Journal of Biological Chemistry 280, nr 23 (19.04.2005): 21830–36. http://dx.doi.org/10.1074/jbc.m502845200.
Pełny tekst źródłaDiekman, 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 i Sander M. Houten. "Dietary restriction in the long-chain acyl-CoA dehydrogenase knockout mouse". Molecular Genetics and Metabolism Reports 27 (czerwiec 2021): 100749. http://dx.doi.org/10.1016/j.ymgmr.2021.100749.
Pełny tekst źródłaDjordjevic, Snezana, Yu Dong, Rosemary Paschke, Frank E. Frerman, Arnold W. Strauss i Jung-Ja P. Kim. "Identification of the Catalytic Base in Long Chain Acyl-CoA Dehydrogenase". Biochemistry 33, nr 14 (12.04.1994): 4258–64. http://dx.doi.org/10.1021/bi00180a021.
Pełny tekst źródłaSchrijver-Wieling, I., G. H. M. B. van Rens, D. Wittebol-Post, J. A. M. Smeitink, J. P. de Jager, H. B. C. de Klerk i G. H. M. van Lith. "Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency". British Journal of Ophthalmology 81, nr 4 (1.04.1997): 291–94. http://dx.doi.org/10.1136/bjo.81.4.291.
Pełny tekst źródłaAndresen, B. S., C. Vianey-Saban, P. Bross, P. Divry, C. R. Roe, M. A. Nada, I. Knudsen i N. Gregersen. "The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency". Journal of Inherited Metabolic Disease 19, nr 2 (marzec 1996): 169–72. http://dx.doi.org/10.1007/bf01799421.
Pełny tekst źródłaMason, Katherine E., Daniel A. Stofan i Luke I. Szweda. "Inhibition of very long chain acyl-CoA dehydrogenase during cardiac ischemia". Archives of Biochemistry and Biophysics 437, nr 2 (maj 2005): 138–43. http://dx.doi.org/10.1016/j.abb.2005.03.004.
Pełny tekst źródłaWinter, Susan, Neil R. M. Buist, Nicola Longo, Saro H. Armenian, Gary Lopaschuk i Anna Wasilewska. "Round Table Discussion". Annals of Nutrition and Metabolism 68, Suppl. 3 (2016): 21–23. http://dx.doi.org/10.1159/000448323.
Pełny tekst źródłaLetteron, P., N. Brahimi-Bourouina, M. A. Robin, A. Moreau, G. Feldmann i D. Pessayre. "Glucocorticoids inhibit mitochondrial matrix acyl-CoA dehydrogenases and fatty acid beta-oxidation". American Journal of Physiology-Gastrointestinal and Liver Physiology 272, nr 5 (1.05.1997): G1141—G1150. http://dx.doi.org/10.1152/ajpgi.1997.272.5.g1141.
Pełny tekst źródłaChen, Xiaobo, Jiayue Chen, Bing Yan, Wei Zhang, Luke W. Guddat, Xiang Liu i 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, nr 28 (29.06.2020): 16324–32. http://dx.doi.org/10.1073/pnas.2002835117.
Pełny tekst źródłaKatagiri, Hideki, Tomoichiro Asano, Tetsuya Yamada, Toshifumi Aoyama, Yasushi Fukushima, Masatoshi Kikuchi, Tatsuhiko Kodama i 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, nr 5 (1.05.2002): 1049–59. http://dx.doi.org/10.1210/mend.16.5.0831.
Pełny tekst źródłaZytkovicz, 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 i George F. Grady. "Tandem Mass Spectrometric Analysis for Amino, Organic, and Fatty Acid Disorders in Newborn Dried Blood Spots". Clinical Chemistry 47, nr 11 (1.11.2001): 1945–55. http://dx.doi.org/10.1093/clinchem/47.11.1945.
Pełny tekst źródłaDamore, Mary Beth, Charles R. Roe, Teresia Goldberg, Mohammed A. Nada, Christine Vlaney-Saban i Alfred E. Slonim. "DIAGNOSIS AND TREATMENT OF VERY-LONG-CHAIN ACYL CoA DEHYDROGENASE DEFICIENCY.846". Pediatric Research 39 (kwiecień 1996): 143. http://dx.doi.org/10.1203/00006450-199604001-00868.
Pełny tekst źródłaKabuyama, Yukihito, Toshiyuki Suzuki, Naomi Nakazawa, Junko Yamaki, Miwako K. Homma i Yoshimi Homma. "Dysregulation of very long chain acyl-CoA dehydrogenase coupled with lipid peroxidation". American Journal of Physiology-Cell Physiology 298, nr 1 (styczeń 2010): C107—C113. http://dx.doi.org/10.1152/ajpcell.00231.2009.
Pełny tekst źródłaAndresen, B. S., S. Olpin, E. A. Kvittingen, P. Augoustides-Savvopoulou, D. Lindhout, D. J. J. Halley, C. Vianey-Saban i in. "DNA-based prenatal diagnosis for very-long- chain acyl-CoA dehydrogenase deficiency". Journal of Inherited Metabolic Disease 22, nr 3 (maj 1999): 281–85. http://dx.doi.org/10.1023/a:1005558828223.
Pełny tekst źródłaEminoglu, Tuba F., Leyla Tumer, Ilyas Okur, Fatih S. Ezgu, Gursel Biberoglu i Alev Hasanoglu. "Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide". Forensic Science International 210, nr 1-3 (lipiec 2011): e1-e3. http://dx.doi.org/10.1016/j.forsciint.2011.04.003.
Pełny tekst źródłaMaher, Amy C., Al-Walid Mohsen, Jerry Vockley i Mark A. Tarnopolsky. "Low expression of long-chain acyl-CoA dehydrogenase in human skeletal muscle". Molecular Genetics and Metabolism 100, nr 2 (czerwiec 2010): 163–67. http://dx.doi.org/10.1016/j.ymgme.2010.03.011.
Pełny tekst źródłaSchiff, Manuel, Al-Walid Mohsen, Anuradha Karunanidhi, Elizabeth McCracken, Renita Yeasted i Jerry Vockley. "Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency". Molecular Genetics and Metabolism 109, nr 1 (maj 2013): 21–27. http://dx.doi.org/10.1016/j.ymgme.2013.02.002.
Pełny tekst źródłaSpiekerkoetter, Ute, Chonan Tokunaga, Udo Wendel, Ertan Mayatepek, Lodewijk Ijlst, Frederic M. Vaz, Naomi Van Vlies i in. "Tissue Carnitine Homeostasis in Very-Long-Chain Acyl-CoA Dehydrogenase–Deficient Mice". Pediatric Research 57, nr 6 (czerwiec 2005): 760–64. http://dx.doi.org/10.1203/01.pdr.0000157915.26049.47.
Pełny tekst źródłaOrii, Koji O., Toshifumi Aoyama, Fumiko Saito-Ohara, Tatsuro Ikeuchi, Tadao Orii, Naomi Kondo i Takashi Hashimoto. "Molecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase gene". Mammalian Genome 8, nr 7 (lipiec 1997): 516–18. http://dx.doi.org/10.1007/s003359900488.
Pełny tekst źródłaHesse, Julia, Carina Braun, Sidney Behringer, Uta Matysiak, Ute Spiekerkoetter i Sara Tucci. "The diagnostic challenge in very-long chain acyl-CoA dehydrogenase deficiency (VLCADD)". Journal of Inherited Metabolic Disease 41, nr 6 (7.09.2018): 1169–78. http://dx.doi.org/10.1007/s10545-018-0245-5.
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