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Volume 30 examines the prominent role of calcium as an intracellular second messenger. Leading investigators review a wide variety of studies on how calcium enters and moves through cells, how it interacts with its many binding proteins, and how calcium and its intracellular receptor, calmodulin, control vital cellular processes. Coverage includes a detailed analysis of the mechanisms by which calcium bound to calmodulin regulates contractile proteins in smooth muscle cells. Close attention is given to the roles of calcium and calmodulin-dependent protein kinases and phosphatases in synaptic signal transduction, protein synthesis, gene expression, programmed cell death, activation of T-lymphocytes, and control of cell division cycles. Other chapters discuss studies using genetically manipulable nonmammalian organisms to further proble the functions of calcium and calmodulin.
Volume 33 reviews the current understanding of ion channel
regulation by signal transduction pathways. Ion channels are no
longer viewed simply as the voltage-gated resistors of
biophysicists or the ligand-gated receptors of biochemists. They
have been transformed during the past 20 years into signaling
proteins that regulate every aspect of cell physiology. In addition
to the voltage-gated channels, which provide the ionic currents to
generate and spread neuronal activity, and the calcium ions to
trigger synaptic transmission, hormonal secretion, and muscle
contraction, new gene families of ion channel proteins regulate
cell migration, cell cycle progression, apoptosis, and gene
transcription, as well as electrical excitability. Even the genome
of the lowly roundworm Caenorhabditis elegans encodes almost 100
distinct genes for potassium-selective channels alone. Most of
these new channel proteins are insensitive to membrane potential,
yet in humans, mutations in these genes disrupt development and
increase individual susceptibility to debilitating and lethal
diseases.
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