Results 301 to 310 of about 1,229,349 (338)
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Biochemistry in the U.S.S.R.

Annual Review of Biochemistry, 1957
A summary is presented of recent Soviet articles in the field of animal biochemistry. Reports on the effects of ionizing radiations on plants and animals were omitted. (C.H.)
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Biochemistry of Statins

2016
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality worldwide. Elevated blood lipids may be a major risk factor for CVD. Due to consistent and robust association of higher low-density lipoprotein (LDL)-cholesterol levels with CVD across experimental and epidemiologic studies, therapeutic strategies to decrease risk have focused
Emmanuel E. Egom   +2 more
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Biochemistry of Monofluorophosphate

Caries Research, 1983
Monofluorophosphate (MFP) can be synthesized in vitro by the transfer of a phosphoryl group from ATP to F-, catalyzed by pyruvate kinase, or by the autocatalytic transfer of a phosphoryl group from the enzyme phosphoglucomutase. There is, however, no evidence that MFP is a normal intermediate in cell metabolism. MFP can be degraded by both alkaline and
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Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes.

Free Radical Biology & Medicine, 1991
H. Esterbauer, R. Schaur, H. Zollner
semanticscholar   +1 more source

The Biochemistry of Coagulation

Clinics in Laboratory Medicine, 1984
This article describes the hemostatic process following vascular injury, which involves an integrated response of the blood vessel wall, blood platelets, and plasma blood clotting factors, and the way in which these processes relate to one another. A number of diagrams are presented that diagram the component processes.
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Biochemistry of multidrug resistance mediated by the multidrug transporter.

Annual Review of Biochemistry, 1993
M. Gottesman, I. Pastan
semanticscholar   +1 more source

Biochemistry

Annual Reports on the Progress of Chemistry, 1928
A. C. Chibnall, J. Pryde
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Biochemistry of porphyria

International Journal of Biochemistry, 1993
1. The porphyrias are a group of metabolic disorders arising from defects in the haem biosynthetic pathway. Most forms are inherited as Mendelian autosomal dominants, but some types are recessive and others acquired through exposure to porphyrinogenic drugs and chemicals. There is a linked group of diseases, which are not porphyrias, but have in common
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