computer-fitting program prism 3.02 (GraphPad Software Inc)
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GraphPad Software Inc
computer-fitting program prism 3.02
Computer Fitting Program Prism 3.02, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/prism+3+software+program/computer+fitting+program+prism+3+02/pm12472900-77-9-13
Average 90 stars, based on 1 article reviews
Computer Fitting Program Prism 3.02, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/prism+3+software+program/computer+fitting+program+prism+3+02/pm12472900-77-9-13
Average 90 stars, based on 1 article reviews
computer-fitting program prism 3.02 - by Bioz Stars,
2026-11
90/100 stars
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other:Article Title: Differential chemokine activation of CC chemokine receptor 1-regulated pathways: ligand selective activation of Galpha 14-coupled pathways. Article Snippet: Chemokines regulate the chemotaxis, development, and differentiation of many cell types enabling the regulation of routine immunosurveillance and immunological adaptation.. CC chemokine receptor 1 (CCR1) is the target of 11 chemokines.. This promiscuity of receptorligand interactions and the potential for functional redundancy has led us to investigate the selective activation of CCR1-coupled pathways by known CCR1 agonists. Article Title: Co-expressions of different opioid receptor types differentially modulate their signaling via G(16). Article Snippet: Combinations of two different types of opioid receptors – ‰-, Î-, Ì-opioid receptors (DOR, KOR, and MOR) and opioid receptor-like receptor 1 (ORL1) – were co-expressed with the · subunit of G16 in COS-7 cells, and the ability of various selective agonists to induce activation of phospholipase Cß was examined.. Nociceptin/orphanin FQ-induced response was enhanced when ORL1 was co-expressed with MOR or KOR but not DOR.. The Î-agonist U50,488H induced a modest inositol phosphate formation when KOR was expressed alone or with MOR, but the response was attenuated when co-expressing with either DOR or ORL1. Article Title: Constitutive activation of the opioid receptor-like (ORL1) receptor by mutation of Asn133 to tryptophan in the third transmembrane region. Article Snippet: Data were analysed by nonlinear least-squares regression using the Article Title: BML-190 and AM251 act as inverse agonists at the human cannabinoid CB2 receptor: signalling via cAMP and inositol phosphates. Article Snippet: The aminoalkylindole BML-190 and diarylpyrazole AM251 ligands have previously been shown to bind to cannabinoid CB2 and CB1 receptors, respectively.. In HEK-293 cells stably expressing the human CB2 receptor, BML-190 and AM251 potentiated the forskolin-stimulated accumulation of cAMP.. Moreover, the CB2 receptor can interact productively with 16z44, a promiscuous GK16=z chimera. Article Title: A transmembrane domain-derived peptide inhibits D1 dopamine receptor function without affecting receptor oligomerization. Article Snippet: Data were analyzed using nonlinear least squares regression equations on the Article Title: Inhibition of cell surface expression by mutant receptors demonstrates that D2 dopamine receptors exist as oligomers in the cell. Article Snippet: Numerous mutant G protein-coupled receptors with diminished or no function have been described that are naturally occurring or that are the product of gene manipulation.. It has largely been assumed that receptor mutants do not affect the function of the wild-type receptor; however, the occurrence of G protein-coupled receptor dimerization suggests the possibility that an intermolecular interaction between mutant and wild-type receptors can occur.. We have shown previously that the D2 dopamine receptor (D2DR) exists as dimers in cell lines and brain tissue. Article Title: The first and third intracellular loops together with the carboxy terminal tail of the delta-opioid receptor contribute toward functional interaction with Galpha16. Article Snippet: Data were analyzed by non-linear leastsquares regression using the |