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Publikováno v:
FEBS Letters. 378:27-31
The TSH receptor (TSHR) and the LHCG receptor (LHR) are members of the family of G protein-coupled receptors. Recently, point mutations conferring constitutive activity to the TSHR and LHR have been observed as a cause of toxic adenoma and familial/s
Publikováno v:
FEBS Letters. 261:67-70
Adenosine analogs, such as N6-cyclohexyladenosine (CHA) that are selective for A1-adenosine receptors, and analogs, such as 5'-N-ethylcarboxamidoadenosine (NECA) that are active at both A1 and A2 receptors, cause a profound depression of locomotor ac
Publikováno v:
FEBS letters. 422(3)
ADP acts as an agonist of platelet aggregation via specific receptors which are still to be characterised. Amplification by PCR of a human platelet cDNA library confirmed the presence of mRNA of the P2Y1 receptor in platelets. In order to determine i
Autor:
Marc Laburthe, Brigitte Amiranoff, Kazuhiko Tatemoto, Luis Moroder, N. Boige, Christiane Rouyer-Fessard
Publikováno v:
FEBS Letters. 159:89-92
GRF (10(-8) - 10(-5) M) is shown to inhibit competitively the binding of [125I]VIP to human and rat intestinal epithelial membranes. The affinity of GRF for VIP receptor is 700-800-times lower than that of VIP in both species. The order of affinity o
Publikováno v:
FEBS Letters. 190:161-164
Acetylcholine treatment of [3H]inositol pre-labelled cultured chick embryo myotubes results in the stimulation of phosphatidylinositol breakdown, as shown by the measurement of inositol-1-phosphate accumulating in the presence of lithium. The describ