Results 151 to 160 of about 6,069 (180)

A PATIENT WITH HEREDITARY GALACTOKINASE DEFICIENCY

Acta Paediatrica, 1970
SUMMARYA case of hereditary galactokinase deficiency is reported, occurring in a newborn boy and detected through routine screening of newborns for increased blood concentration of galactose. Symptoms were equivocal and consisted only of mild feeding difficulties and a slightly insufficient weight gain.
A, Dahlqvist, I, Gamstorp, H, Madsen
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Galactokinase activity and red blood cell age

AGE, 1980
Human erythrocyte galactokinase has been studied during red cell aging. The decay rate of enzyme activity is slower than glucose-6-phosphate dehydrogenase which is used as red cell age marker. The Michaelis constants for galactose and ATPMg2− of galactokinase of young cells are similar to the Km’s of the enzyme of total cells, while the Km increases in
MAGNANI, MAURO, CUCCHIARINI, LUIGI, DACHÁ M., FORNAINI G.   +3 more
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Galactokinase of Vicia faba seeds

European Journal of Biochemistry, 1983
Galactokinase (EC 2.7.1.6) from the dormant seeds of Vicia faba was purified approximately 1300‐fold with an 18% recovery through an eight‐step procedure. The preparation showed the presence of only minor contaminations as judged by disc‐gel electrophoresis.
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GALACTOKINASE AND CATARACTS

The Lancet, 1978
E, Beutler, F, Matsumoto
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Substrate specificity of Saccharomyces fragilis galactokinase

Biochimica et Biophysica Acta, 1960
Abstract The substrate specificity of Saacharomyces fragilis galactokinase has been investigated using a series of compounds structurally related to galactose. Only those compounds, which, having the α-pyranose configuration, differ from galactose at the level of C2 (2-deoxygalactose, galactosamine, talose) have been found to be phosphorylated ...
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Galactokinase Deficiency and Cataracts

American Journal of Ophthalmology, 1972
N S, Levy, A E, Krill, E, Beutler
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Galactokinase

1997
Dietmar Schomburg, Dörte Stephan
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[74] Galactokinase

1966
M.R. Heinrich, Sally M. Howard
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Galactokinase Deficiency

2009
David J. Timson, Richard J. Reece, James B. Thoden, Hazel M. Holden, Andrea L. Utz, Beverly M. K. Biller, Eugen-Matthias Strehle, Markus Böhm, Thomas A. Luger, Alexander K. C. Leung, Andrew L. Wong, Markus G. Donner, Dieter Häussinger, Nirmal S. Mann, Marcus Schmitt, Alexander K. C. Leung, William Lane M. Robson, Andrew L. Wong, Manisha Balwani, Ainu Prakash-Cheng*, Robert J. Desnick, Holger Lerche, Ingrid E. Scheffer, Samuel F. Berkovic, Brigitte M. Lobnig, Peter L. M. Jansen, Siegfried Waldegger, Florian Lang, Hugo ten Cate, Hagen Thieme, Michael Weller, Bärbel Schütte, Ronnie Fass, Hideki Kato, Masaomi Nangaku, Hideki Kato, Masaomi Nangaku, Anthony Chang, Pradeep V. Kadambi, Jessy J. Alexander, Pierre Ronco, Hanna Debiec, Christian Hugo, Brigitte M. Lobnig, Brigitte M. Lobnig, John-John B. Schnog, Victor E. A. Gerdes, Jean Francis, David S. Geller, Knut Brockmann, Dong Wang, Darryl C. Vivo, Stefan Kölker, Stefan Kölker, Elardus Erasmus, Lodewyk J. Mienie, John Vissing, Arnold Reuser, Catherine E. Correia, David A. Weinstein, Joseph I. Wolfsdorf, Yoon S. Shin, Reinout P. Hesselink, Maarten R. Drost, Anton J. M. Wagenmakers, Ger J. Vusse, Stefan Kiechl, Jonas Denecke, Ute Schepers, Thomas Kolter, Konrad Sandhoff, Dianna C. Martin, Barbara L. Triggs-Raine, Seda Sancak, Ralf Paschke, Dorin-Bogdan Borza, Sonja Ständer, Heiko Traupe, Michael A. Becker, Hanneke M. Straaten, Leo F. Verdonck, Hugo Ten Cate, Martin Mempel, Dietrich Abeck, Ismat Ghanem, Samer El Hage, Johannes G. Bode, Thomas A. Fleisher, Steven M. Holland, Bennett Myers, David Herrmann, Zaki Kraiem, Yaron Tomer, Terry F. Davies, James G. White, Sylvia Stöckler-Ipsiroglu, Guido Stoll, Klaus V. Toyka, Valéria Lamounier-Zepter, Klaus Ruether   +99 more
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Galactokinase Deficiency: A Case Report

Journal of Pediatric Ophthalmology & Strabismus, 2002
Ismail, Kurt, Muhittin, Serdar, Fatih, Mutlu, Atilla, Bayer, J T, Allen, Turker, Kutluay   +5 more
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