Titlebook: Schmerz in Psychiatrie und Neurologie; Karl Einhäupl,Markus Gastpar Conference proceedings 2003 Springer-Verlag Berlin Heidelberg 2003 Auf

clot-buster

书目名称Schmerz in Psychiatrie und Neurologie影响因子(影响力)




书目名称Schmerz in Psychiatrie und Neurologie影响因子(影响力)学科排名




书目名称Schmerz in Psychiatrie und Neurologie网络公开度




书目名称Schmerz in Psychiatrie und Neurologie网络公开度学科排名




书目名称Schmerz in Psychiatrie und Neurologie被引频次




书目名称Schmerz in Psychiatrie und Neurologie被引频次学科排名




书目名称Schmerz in Psychiatrie und Neurologie年度引用




书目名称Schmerz in Psychiatrie und Neurologie年度引用学科排名




书目名称Schmerz in Psychiatrie und Neurologie读者反馈




书目名称Schmerz in Psychiatrie und Neurologie读者反馈学科排名

follicle

ls.Covers computational methods to evaluate protein stabilit.In the post-genomic era, in vitro mutagenesis has emerged as a critically important tool for establishing the functions of components of the proteome. The third edition of .In Vitro Mutagenesis Protocols. represents a practical toolbox con

支架

该得

Hans-Georg Schaible. The third edition of .In Vitro Mutagenesis Protocols. represents a practical toolbox containing protocols vital to advancing our understanding of the connection between nucleotide sequence and sequence function. Fully updated from the previous editions, this volume contains a variety of specialty

Minatory

MOAN

. The third edition of .In Vitro Mutagenesis Protocols. represents a practical toolbox containing protocols vital to advancing our understanding of the connection between nucleotide sequence and sequence function. Fully updated from the previous editions, this volume contains a variety of specialty

anaerobic

同来核对

M. Banger,V. Reissnerd range of neuroscientific research endeavors including the investigation of spatial-, temporal-, drug-induced-, or activity-dependent-differential gene expression, The actual measure required, however, depends to a large extent upon the experimental paradigm. For example, one of the first questions

BOGUS

Christian Schmahl,Martin Bohusneuroscientific community with neuronal probes containing thousands of recording sites. These next-generation probes are capable of simultaneously recording neuronal signals from a large number of channels. Numerically, a simple 128-channel neuronal data acquisition system equipped with a 16 bits A/

共同确定为确

ubstrate-integrated planar multielectrode arrays (MEA) are limited to recording of extracellular field potentials (FPs) rather than the entire electrophysiological signaling repertoire of the brain, have prompted a number of laboratories to merge the advantages of planar MEA technologies (non-damagi