Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Nadine Romain"'
Autor:
Katja Heinicke, Ivan E Dimitrov, Nadine Romain, Sergey Cheshkov, Jimin Ren, Craig R Malloy, Ronald G Haller
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e108706 (2014)
Carbon-13 magnetic resonance spectroscopy (13C MRS) offers a noninvasive method to assess glycogen levels in skeletal muscle and to identify excess glycogen accumulation in patients with glycogen storage disease (GSD). Despite the clinical potential
Externí odkaz:
https://doaj.org/article/aaf9969504584e73bd0c926b71b7aa87
Autor:
Ronald G. Haller, Manall F. Jaffery, Nadine Romain, Steven A. Romero, Craig G. Crandall, Matthew N. Cramer, Mu Huang, Gilbert Moralez, Ken Kouda
Publikováno v:
Am J Physiol Regul Integr Comp Physiol
Long-term rehabilitative strategies are important for individuals with well-healed burn injuries. Such information is particularly critical because patients are routinely surviving severe burn injuries given medical advances in the acute care setting
Autor:
Nadine Romain, Thomas Meitinger, Claudia Donnini, Patrick F. Chinnery, Christopher A. Powell, Tim M. Strom, Ileana Ferrero, Richard J. Rodenburg, Markus Schuelke, Gudrun Schottmann, Joanna Rorbach, Helen Griffin, Laura S. Kremer, Robert W. Taylor, Angela Pyle, Holger Prokisch, Michal Minczuk, Robert Kopajtich, Charlotte L. Alston, Tobias B. Haack, Cristina Dallabona, Ralf A. Husain, Ronald G. Haller, Aaron R. D’Souza
Publikováno v:
American Journal of Human Genetics, 97, 2, pp. 319-28
American Journal of Human Genetics, 97, 319-28
Am J Hum Genet
American Journal of Human Genetics, 97, 319-28
Am J Hum Genet
Contains fulltext : 154074.pdf (Publisher’s version ) (Open Access) Deficiencies in respiratory-chain complexes lead to a variety of clinical phenotypes resulting from inadequate energy production by the mitochondrial oxidative phosphorylation syst
Autor:
Pedro Mancias, Nadine Romain, Jonathan C. Cohen, Lydia Sharp, Christoffer Rasmus Vissing, Nicolai Preisler, Lauren Phillips, Sun Young Park, Henrik Galbo, Ronald G. Haller, Karen Lindhardt Madsen, Phil Wyrick, John Vissing, Katja Heinicke, Marta Newby
Publikováno v:
Molecular genetics and metabolism. 122(3)
Objective We investigated metabolism and physiological responses to exercise in an 18-year-old woman with multiple congenital abnormalities and exertional muscle fatigue, tightness, and rhabdomyolysis. Methods We studied biochemistry in muscle and fi
Autor:
Katja Heinicke, M. Dean Palmer, Peter G. Snell, Eric Pacini, Benjamin D. Levine, Jeffrey L. Hastings, Nadine Romain, Phil Wyrick, Felix Krainski, Ronald G. Haller
Publikováno v:
Journal of Applied Physiology. 116:1569-1581
Exposure to microgravity causes functional and structural impairment of skeletal muscle. Current exercise regimens are time-consuming and insufficiently effective; an integrated countermeasure is needed that addresses musculoskeletal along with cardi
Autor:
Ronald G. Haller, Nadine Romain, Aaron M. Armando, Natalia Ermolova, Oswald Quehenberger, Stanley F. Nelson, Irina Kramerova, Melissa J. Spencer, Andrea L. Hevener, Ascia Eskin
Publikováno v:
Human molecular genetics, vol 25, iss 11
Limb girdle muscular dystrophy 2A is due to loss-of-function mutations in the Calpain 3 (CAPN3) gene. Our previous data suggest that CAPN3 helps to maintain the integrity of the triad complex in skeletal muscle. In Capn3 knock-out mice (C3KO), Ca2+ r
Autor:
Ronald G. Haller, Scot C. Leary, Jeffrey L. Elliott, Nadine Romain, Marjatta Son, Dennis R. Winge, Fabien Pierrel
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2008, 283 (18), pp.12267-75. ⟨10.1074/jbc.M708523200⟩
Journal of Biological Chemistry, 2008, 283 (18), pp.12267-75. ⟨10.1074/jbc.M708523200⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2008, 283 (18), pp.12267-75. ⟨10.1074/jbc.M708523200⟩
Journal of Biological Chemistry, 2008, 283 (18), pp.12267-75. ⟨10.1074/jbc.M708523200⟩
International audience; G93A SOD1 transgenic mice overexpressing CCS protein develop an accelerated disease course that is associated with enhanced mitochondrial pathology and increased mitochondrial localization of mutant SOD1. Because these results
Autor:
Romero, Steven A., Moralez, Gilbert, Jaffery, Manall F., Mu Huang, Cramer, Matthew N., Nadine Romain, Kouda, Ken, Haller, Ronald G., Crandall, Craig G.
Publikováno v:
American Journal of Physiology: Regulatory, Integrative & Comparative Physiology; Oct2019, Vol. 317 Issue 4, pR563-R570, 8p
Autor:
S. Cheshkov, Ronald G. Haller, Craig R. Malloy, Nadine Romain, Ivan E. Dimitrov, Jimin Ren, Katja Heinicke
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e108706 (2014)
PLoS ONE
PLoS ONE
Carbon-13 magnetic resonance spectroscopy (13C MRS) offers a noninvasive method to assess glycogen levels in skeletal muscle and to identify excess glycogen accumulation in patients with glycogen storage disease (GSD). Despite the clinical potential
Autor:
Ronald G. Haller, Sean Germain, M. Anthony Verity, Krista Vandenborne, Elena Kudryashova, Nadine Romain, Irina Kramerova, Melissa J. Spencer, Benjamin G. Wu
Publikováno v:
Human molecular genetics. 18(17)
Mutations in the non-lysosomal cysteine protease calpain-3 cause autosomal recessive limb girdle muscular dystrophy. Pathological mechanisms occurring in this disease have not yet been elucidated. Here, we report both morphological and biochemical ev