Results 191 to 200 of about 51,297 (232)

Regulation of ornithine transcarbamylase in Rhodotorula glutinis

Archives of Microbiology, 1976
The regulation of ornithine transcarbamylase (OTC) of Rhodotorula glutinis has been studied, by growing the yeasts in different carbon and nitrogen sources and estimating the enzyme level in crude yeasts extracts. The results show a nutritional repression of OTC by arginine, when added to the culture media as carbon, nitrogen or carbon and nitrogen ...
F J, Mataix, J, Fernández, M R, Amil
openaire   +2 more sources

Ornithine Transcarbamylase Deficiency Presenting as Hepatitis

Pediatric Emergency Care, 2011
Ornithine transcarbamylase deficiency is an inborn error of metabolism that commonly presents as hyperammonemia in neonates. We present a case of a 2-year-old girl who was referred to a pediatric emergency department for evaluation of hepatitis, an uncommon presentation of ornithine transcarbamylase deficiency. Recognition of late presentations of this
Paul L, Aronson, Rakesh D, Mistry
openaire   +2 more sources

An autopsy case of ornithine transcarbamylase deficiency

Brain and Development, 2002
We present an autopsy case of ornithine transcarbamylase (OTC) deficiency with grumose degeneration in the dentate nucleus of the cerebellum. The patient had intractable neonatal convulsions and hyperammonemia from the 3rd day after birth. Diagnosis of OTC deficiency was made based on null activity of the enzyme and four-base deletions in exon 9 of the
Hideo, Yamanouchi, Hideaki, Yokoo, Yukihiro, Yuhara, Ken-ichi, Maruyama, Atsushi, Sasaki, Junko, Hirato, Yoichi, Nakazato   +6 more
openaire   +2 more sources

Cell free synthesis of ornithine transcarbamylase

Biochimica et Biophysica Acta, 1960
Abstract Synthesis of ornithine transcarbamylase activity by four different disrupted preparations of lysozyme protoplasts of Escherichia coli W cells was investigated. Whole protoplast contamination was found sufficient to account for all enzyme synthesis observed in water-lysed protoplasts.
P, ROGERS, G D, NOVELLI
openaire   +2 more sources

Ornithine Transcarbamylase

2009
Marc Slawik, Felix Beuschlein, Katrina Light, Roger Mulder, Gordon Dent, Mark G. Buckley, Stephen T. Holgate, Rosalia Misseri, Kirstan K. Meldrum, Massimiliano Mirabella, Gabriella Silvestri, Thomas Frieling, Alexander K. C. Leung, Andrew L. Wong, Marcus Schmitt, Jürgen Kohlhase, Sevan Hopyan, Alexander K. C. Leung, William Lane M. Robson, Andrew L. Wong, Maria Judit Molnar, Andrew J. Saxon, Simone Schimpf, Stefan R. Bornstein, Regina Ensenauer, Arno Fuchshuber, Carlo Nunes, Michael Escudier, Jo Spencer, Miranda Lomer, Stephen Challacombe, Jeremy Sanderson, Manish Suneja, Christie P. Thomas, Donatella Granchi, Nicola Baldini, George E. Ehrlich, Matthew B. Dobbs, Yasuaki Nakagawa, James Hyland, Roland Staud, Rajiv Kumar, Mary H. Hohenhaus, Nananda F. Col, Miep Helfrich, Anna Villa, Jan Hellemans, Geert Mortier, Minrong Ai, Matthew L. Warman, Markus Pfister, Hans-Peter Zenner, Markus Pfister, Hans-Peter Zenner, Stefan K. Plontke, Hans-Peter Zenner   +55 more
openaire   +1 more source

Long-Term Treatment of Girls With Ornithine Transcarbamylase Deficiency

New England Journal of Medicine, 1996
Susan S Bassett, Saul W Brusilow, S W Brusilow   +2 more
exaly  

Reye's Syndrome Due to a Novel Protein-Tolerant Variant of Ornithine-Transcarbamylase Deficiency.

Lancet, The, 1974
M Michael Thaler
exaly  

Ornithine Transcarbamylase

2004
openaire   +1 more source

Cerebral Dysfunction in Asymptomatic Carriers of Ornithine Transcarbamylase Deficiency

New England Journal of Medicine, 1980
Saul W Brusilow, S W Brusilow, A L Jung
exaly  

Prenatal Diagnosis of Ornithine Transcarbamylase Deficiency With Use of DNA Polymorphisms

New England Journal of Medicine, 1986
Wayne A Fenton, Rima Rozen, F Kalousek
exaly