11 Titel in Klassifikation (DDC) → Naturwissenschaften und Mathematik → Biowissenschaften; Biologie → Biochemie 1
zu den Filteroptionen11 Titel in Klassifikation (DDC) → Naturwissenschaften und Mathematik → Biowissenschaften; Biologie → Biochemie
1
Malate dehydrogenase isolated from extremely halophilic bacteria of the Dead Sea. 1. Purification and molecular characterization
In: Biochemistry, Jg. 16 H. 17, S. 3781-37851977
Malate dehydrogenase isolated from extremely halophilic bacteria of the Dead Sea. 2. Effect of salt on the catalytic activity and structure
In: Biochemistry, Jg. 16 H. 17, S. 3786-37921977
Mechanisms of membrane processes, electric gene transfer and cell fusion Report on the workshop held at the Zentrum für Interdisziplinäre Forschung in Bielefeld on 3–4 April 1986
In: Bioelectrochemistry and Bioenergetics, Jg. 17 H. 1, S. 7-81987
Membrane electroporation and direct gene transfer
In: Bioelectrochemistry and Bioenergetics, Jg. 28 H. 1-2, S. 247-2671992
Miscibility gap of octyl glucoside-phosphatidylcholine micellar solutions. Partition of the nicotinic acetylcholine receptor into the surfactant-rich phase
In: Biochimica et Biophysica Acta (BBA) - Biomembranes, Jg. 986 H. 2, S. 225-2331989
Model of cell electrofusion Membrane electroporation, pore coalescence and percolation
In: Biophysical Chemistry, Jg. 26 H. 2-3, S. 321-3351987
Molecular mechanisms and kinetics between DNA and DNA binding ligands
In: Biophysical Journal, Jg. 88 H. 1, S. 404-4112005
Molecular recognition in enzyme-catalyzed reactions of ionic and dipolar substrates
In: Comments on molecular and cellular biophysics, Jg. 4 H. 2, S. 121-1411987
A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease
In: Disease Models & Mechanisms, Jg. 9 H. 9, S. 1015-10282016
Multiple repressor binding sites in the genome of bacteriophage P1
In: Proceedings of the National Academy of Sciences of the United States of America, Jg. 84 H. 16, S. 5570-55741987
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects
In: JOURNAL OF EXPERIMENTAL MEDICINE, Jg. 214 H. 12, S. 3707-37292017