Дисертації з теми "Methylmalonyl coenzyme A mutase"
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Roy, Ipsita. "Studies on methylmalonyl-CoA mutase." Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240978.
Повний текст джерелаFarah, Rita S. "Intragenic complementation in methylmalonyl CoA mutase." Thesis, McGill University, 1994. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=55444.
Повний текст джерелаMcKie, Norman. "Methylmalonyl CoA mutase from Saccharopolyspora erythraea." Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259763.
Повний текст джерелаThomä, Nicolas Holger. "The mechanism of methylmalonyl-CoA mutase." Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624301.
Повний текст джерелаMancia, Filippo. "The crystal structure of methylmalonyl-CoA mutase." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627037.
Повний текст джерелаKannan, Suresh M. "Studies on methylmalonyl-CoA mutase from Escherichia coli." Thesis, University of Westminster, 2008. https://westminsterresearch.westminster.ac.uk/item/91652/studies-on-methylmalonyl-coa-mutase-from-escherichia-coli.
Повний текст джерелаKeep, Nicholas herbert. "Studies on the structure and mechanisms of methylmalonyl-CoA mutase." Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259593.
Повний текст джерелаDarley, Daniel James. "Mechanistic investigations into coenzyme Bâ†1â†2 dependent enzymes." Thesis, University of Newcastle Upon Tyne, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364804.
Повний текст джерелаQureshi, Amber A. (Amber Ateef). "The molecular characterization of mutations at the methylmalonyl CoA mutase locus involved in interallelic complementation /." Thesis, McGill University, 1993. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=69686.
Повний текст джерелаMarsh, Edward Neil. "A structural investigation of a Bâ†1â†2-dependent enzyme : methylmalonyl-CoA mutase from Propionibacterium shermanii." Thesis, University of Cambridge, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303288.
Повний текст джерелаTouraine, Renaud Laurian. "Les acidemies methylmaloniques : revue generale ; etudes sur le gene de la methylmalonyl coa mutase ; rapport d'un cas associe a une diarrhee congenitale chronique." Lyon 1, 1992. http://www.theses.fr/1992LYO1M352.
Повний текст джерелаGradinger, Abigail. "Atypical methylmalonic aciduria : frequency of mutations in the methylmalonyl-CoA epimerase (MCEE) gene." Thesis, McGill University, 2007. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=101848.
Повний текст джерелаGaire, Delphine. "La méthylmalonyl coenzyme A mutase de l'oligodendrocyte de rat en culture : effet de la carence en cobalamines." Nancy 1, 1999. http://www.theses.fr/1999NAN10004.
Повний текст джерелаBenoist, Jean-François. "Profil enzymatique et moléculaire des acidémies méthylmaloniques isolées : aspects de la régulation de la méthylmalonyl-CoA mutase." Paris 11, 2004. http://www.theses.fr/2004PA114838.
Повний текст джерелаLyatuu, Fredrick Edwin [Verfasser], and W. [Akademischer Betreuer] Buckel. "Investigations into the mechanism of the coenzyme B12 dependent reaction catalyzed by glutamate mutase from Clostridium cochlearium / Fredrick Edwin Lyatuu. Betreuer: W. Buckel." Marburg : Philipps-Universität Marburg, 2013. http://d-nb.info/1034420593/34.
Повний текст джерелаWong, Edward Sern Yuen. "Gene therapy for methylmalonic aciduria." Thesis, 2012. http://hdl.handle.net/2440/80601.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Paediatrics and Reproductive Health, 2012
Toeche-Mittler, Caroline. "Konstruktion eines bakteriellen Systems zum Export von Coenzym B12." Doctoral thesis, 2002. http://hdl.handle.net/11858/00-1735-0000-0006-AB97-8.
Повний текст джерелаHsu, Huei-Ju, and 許惠茹. "The interaction between glutamate mutase and coenzyme B12 analogs." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/8cjy8j.
Повний текст джерела國立臺北科技大學
生物科技研究所
96
Glutamate mutase from Clostridium tetanomorphum is one of a group of adenosylcobalamin(AdoCbl)-dependent mutases which catalyzes the interconversion of L-glutamate and threo-β-methyl-L-aspartate. Glutamate mutase is comprised of two weakly-associating subunits: GlmE(Mr 53,700Da) and MutS(Mr 14,700Da). To further characterize the interactions between glutamate mutase and the coenzyme three different coenzyme B12 analogs, methylcobinamide (MeCbi), adenosylcobinamide (AdoCbi), and adeosylcobinamide-GDP (AdoCbi-GDP), were chemoenzymaticlly synthesized. In this study, a HPLC-based method was used to investigate the enzyme’s kinetic properties. In each case, kcat was decreased by about 2000 fold when AdoCbi or AdoCbi-GDP was used as cofactor.
Teng, Yu-Ting, and 鄧友婷. "Molecular Genetic Studies of the MUT Gene in Chinese Methylmalonic Acidemia Caused by Methylmalonyl CoA Mutase Deficiency." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/03556075092127356116.
Повний текст джерела國立陽明大學
遺傳學研究所
91
mut type methylmalonic acidemia (mut MMA, MIM 251000) is an autosomal recessive disorder of organic acid metabolism caused by methylmalonyl CoA mutase (MCM, E.C.5.4.99.2; gene symbol: MUT) deficiency. In this study, 13 exons of the MUT gene were PCR amplified and sequenced subsequently to identify the molecular defects of four unrelated Chinese mut MMA patients. Seven MUT gene mutations, namely c.683G>A (R228Q), c.1050C>G (H350Q), c.1106G>A (R369H), c.1280G>A (G427D), c.1741C>T (R581X), IVS9-1G>A and c.1046_1058del (A349delX368), were identified. Three transitions, c.683G>A, c.1106G>A and c.1280G>A, had been reported in other mut MMA patients. The c.1106G>A and c.1280G>A mutations had been proved to be disease-causing mutations by functional analysis previously. The c.1050C>G, c.1741C>T, IVS9-1G>A substitutions and 1046_1058del are novel mutations found in the MUT gene. None of 100 alleles of unrelated normal Chinese was found to have c.1050C>G, c.1741C>T, IVS9-1G>A and 1046_1058del alterations. The c.683G>A, c.1050C>G and c.1741C>T mutations were found to abolish MCM activity by functional study. These data indicated that these three alterations identified in this study might be the disease-causing mutations in mut MMA patients. The allele frequency of c.1280G>A and c.[1630G>T+1631G>A] mutations identified in Chinese mut MMA patients previously were 17% (3/18) and 17% (3/18), respectively. These two mutations were all linked to the 190bp allele of D6S269 microsatellite marker while the 190bp allele of D6S269 was found to be a rare allele in normal Chinese population. The allele frequency of 190bp allele in Chinese mut MMA patient with c.1280G>A or c.[1630G>T+1631G>A] mutations was statistically different from that in the normal Chinese population. These indicated that c.1280G>A and c.[1630G>T+1631G>A] mutations might have founder effects in Chinese mut type MMA patients.
Duscher, Sonja. "Vergleichende Genomanalyse bei Mensch und Schwein am Beispiel ausgewählter syntenischer Regionen des humanen Chromosoms 6." Doctoral thesis, 2001. http://hdl.handle.net/11858/00-1735-0000-0006-B6F0-5.
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