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Autor:
T. Wurch, P.J. Pauwels
Publikováno v:
Neuroscience Research Communications. 23:45-53
Publikováno v:
Biochemical and Biophysical Research Communications. 214:639-645
The mRNA content of the brain-specific metallothionein-III (MT-III) protein was measured by quantitative reverse transcription-polymerase chain reaction (RT-PCR) in two transformed glial cell lines: rat C6-glial and human U-373 MG cells. Low levels o
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 1993, 90 (4), pp.1470-3
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 1993, 90 (4), pp.1470-3
We cloned in Escherichia coli truncated versions of the protein p15 encoded by open reading frame III of cauliflower mosaic virus. We then compared the ability of the wild-type p15 (129 amino acids) and the deleted p15 to bind viral double-stranded D
Publikováno v:
Virology
Virology, Elsevier, 1991, 180 (2), pp.837-41
Virology, Elsevier, 1991, 180 (2), pp.837-41
The capsid protein and the reverse transcriptase of cauliflower mosaic virus (CaMV) are encoded by two genes (ORF IV and ORF V) that lie in different translation reading frames. A comparison can be drawn between the synthesis of both CaMV proteins an
Publikováno v:
Current pharmaceutical biotechnology. 9(6)
Publikováno v:
Molecular pharmacology. 60(4)
The C-terminal portion of G(alpha) proteins plays a key role in their selective activation by cognate receptors. alpha(2A)-Adrenoceptors (alpha(2A)-ARs) can differentially inhibit or stimulate adenylyl cyclases by the activation of distinct G(i/o) an
Publikováno v:
British journal of pharmacology. 133(6)
Using a combination of RT - PCR and inverse-PCR techniques, we amplified, cloned and sequenced a full-length porcine 5-HT(1B) receptor cDNA derived from porcine cerebral cortex. Sequence analysis revealed 1170 bp encoding an open reading frame of 390
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 297(1)
Antipsychotic drugs comprise a wide range of structurally diverse compounds and are considered to be antagonists at dopamine D2 receptors. High-resolution kinetic analyses of their antagonist properties was performed by monitoring dynamic dopamine (D