Titlebook: Biological Signal Transduction; Elliott M. Ross,Karel W. A. Wirtz Conference proceedings 1991 Springer-Verlag Berlin Heidelberg 1991 G-Pro

dragon

CHOKE

Gene Targeting by Homologous Recombination as a Tool to Study the Biophysical Role of the Interferoning to a specific cell surface receptor, which is encoded by a single copy gene. To design novel models for investigating the physiological role of IFN-γ we plan to generate IFN-γ receptor deficient mice using recently established strategies for gene targeting by homologous recombination. In this ch

AUGUR

Expression of Novel Cloned Rat Pituitary Receptors in Mammalian Cellsone concerned with mechanisms of cell signalling. Information about the structure of these receptors has become far more accessible using molecular cloning techniques, especially homology cloning strategies.

Employee

Cellular Localization of Seven Transmembrane Domain Receptor mRNA’S by In-Situ Hybridizationcific cDNA libraries, using molecular cloning techniques. The primary structure of a number of G-protein coupled receptors has previously been analysed and it is generally accepted that the members of this receptor superfamily possess a characteristic structure consisting of seven hydrophobic transm

aristocracy

公豬

G Protein-Coupled Receptors: Structural Basis of Selective Signalingrated to yield appropriate intracellular signals in the form of second messengers, such as cyclic AMP, inositol phosphates, Ca., . Although receptors are responsible for detecting extracellular signals, signal integration and sorting frequently depend on the activities of GTP-binding transducer prot

conservative

Hormone Receptor-Effector Coupling in Prolactin Producing Pituitary Cell Lines (GH Cells)(Gautvik et al. 1988). Recently, we have been interested in the coupling of pituitary peptide hormone receptors to specific GTP-binding regulatory proteins (G proteins) and how these signal proteins initiate intracellular messenger effector systems.

CUR

雪白

The Transducin Cycle in the Phototransduction Cascaden vertebrate retinal rods, was often considered as a special case: It is enormously abondant in the highly specialised rod outer segment (10 to 20% of total protein content of the retinal rod outer segment) and it is soluble: its extraction from ROS membranes does not require any detergent. Indeed,