Results 321 to 330 of about 352,162 (366)

Glucose 6-Phosphate dehydrogenase deficiency in congenital and senile cataracts

Indian Journal of Ophthalmology, 1979
Behera U, Devdas G
doaj  

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Glucose-6-phosphate dehydrogenase deficiency

The Lancet, 2008
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being present in more than 400 million people worldwide. The global distribution of this disorder is remarkably similar to that of malaria, lending support to the so-called malaria protection hypothesis.
M.D. Cappellini, G. Fiorelli
openaire   +4 more sources

Glucose-6-phosphate dehydrogenase deficiency

Best Practice & Research Clinical Haematology, 2000
Glucose-6-phosphate dehydrogenase (G6PD) is expressed in all tissues, where it catalyses the first step in the pentose phosphate pathway. G6PD deficiency is prevalent throughout tropical and subtropical regions of the world because of the protection it affords during malaria infection.
A, Mehta, P J, Mason, T J, Vulliamy
openaire   +2 more sources

Glucose-6-Phosphate Dehydrogenase Velletri

Acta Haematologica, 1977
A new variant of red cell glucose-6-phosphate dehydrogenase (G6PD) has been found in a Caucasian man with congenital non-spherocytic haemolytic anaemia. This variant has reduced activity, increased thermolability, increased Michaelis constants for glucose-6-phosphate and NADP, slightly increased electrophoretic mobility, and a biphasic pH-activity ...
F, Mandelli, S, Amadori, A, De Laurenzi, A, Kahn, G, Isacchi, G, Papa   +5 more
openaire   +2 more sources

Neuroprotection by glucose‐6‐phosphate dehydrogenase and the pentose phosphate pathway

Journal of Cellular Biochemistry, 2019
Glucose‐6‐phosphate dehydrogenase (G6PD), the rate limiting enzyme that channels glucose catabolism from glycolysis into the pentose phosphate pathway (PPP), is vital for the production of reduced nicotinamide adenine dinucleotide phosphate (NADPH) in ...
B. Tang
semanticscholar   +1 more source

Glucose-6-Phosphate Dehydrogenase

1985
Genetic systems have been of interest to human genetics mainly because they exhibit polymorphism in various populations, and therefore seem to be relevant to human evolution, or because they are associated with pathological manifestations. In addition, whereas frequently biological systems are easier to investigate in microorganisms or in experimental ...
L, Luzzatto, G, Battistuzzi
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Glucose-6-phosphate dehydrogenase deficiency

Baillière's Clinical Haematology, 1992
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy. Because its gene locus is on the X-chromosome it is more common in males than females in all populations. Prevalence rates vary from 62% among Kurdish Jews to the very low rates (0.1% or less in Japan, for example), which are compatible with sporadic cases arising
openaire   +2 more sources

Muscle glucose-6-phosphate dehydrogenase deficiency

Journal of Neurology, 1989
Muscle glucose-6-phosphate dehydrogenase (G6PD) deficiency is described in four clinically heterogeneous patients: an athlete who developed myoglobinuria after physical exercise; a 7-year-old, mildly mentally retarded boy, who had episodes of dark urine and high creatine kinase; and two brothers of Sardinian origin, the elder showing moderate exercise ...
N, Bresolin, L, Bet, M, Moggio, G, Meola, F, Fortunato, G, Comi, L, Adobbati, L, Geremia, S, Pittalis, G, Scarlato   +9 more
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Glucose-6-Phosphate Dehydrogenase Ferrara

Acta Haematologica, 1976
A new variant of glucose-6-phosphate dehydrogenase (G-6-PD) has been discovered in Northern Italy, in the district of Ferrara.
G. Carandina, E. Moretto, G. Zecchi, C. Conighi   +3 more
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