Zobrazeno 1 - 10
of 68
pro vyhledávání: '"D J Graves"'
Publikováno v:
Advances in experimental medicine and biology. 419
Earlier we demonstrated that meta-iodobenzylguanidine (MIBG), a specific inhibitor of arginine mono-ADP-ribosylation blocks proliferation and differentiation of chick skeletal myogenic cells in culture (Exp. Cell Res., 1992, 201:33-42). Membrane frac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::269e1aa6451a8d64ee6031bb4ecd32c6
https://pubmed.ncbi.nlm.nih.gov/9193670
https://pubmed.ncbi.nlm.nih.gov/9193670
Publikováno v:
The Journal of biological chemistry. 269(39)
A truncated form of the gamma subunit of phosphorylase kinase is inactivated by Cu2+ with the formation of two intra-molecular disulfide bonds. The formation of a disulfide bond between Cys-36 and Cys-172 (semioxidized form) results in approximately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c58325f0766d8f159bc1fd54e0a915ef
https://pubmed.ncbi.nlm.nih.gov/7929096
https://pubmed.ncbi.nlm.nih.gov/7929096
Publikováno v:
The Journal of biological chemistry. 268(24)
Phosphorylase kinase is shown to be a dual specificity kinase. The specificity of phosphorylation is determined by divalent cation. Mg2+ causes seryl phosphorylation of phosphorylase b, but Mn2+ activates tyrosine phosphorylation of angiotensin II. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::80ff0771fa06cdc9fb451dfdaf3488d4
https://pubmed.ncbi.nlm.nih.gov/8349652
https://pubmed.ncbi.nlm.nih.gov/8349652
Publikováno v:
The Journal of biological chemistry. 266(1)
A high performance liquid chromatographic method has been developed for the assay of arginine-specific ADP-ribosyl transferases. The assay utilizes L-arginine methyl ester (LAME) as the acceptor substrate. ADP-ribosylated-LAME is separated from the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7e77a947102475727a8d9f30a6a5bccf
https://pubmed.ncbi.nlm.nih.gov/1898725
https://pubmed.ncbi.nlm.nih.gov/1898725
Publikováno v:
Methods in enzymology. 200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5625ca6c302508097db34f57b8f69da2
https://pubmed.ncbi.nlm.nih.gov/1956330
https://pubmed.ncbi.nlm.nih.gov/1956330
Publikováno v:
The Journal of biological chemistry. 265(28)
Integral membrane-associated arginine-specific mono-ADP-ribosyltransferase was purified from rabbit skeletal muscle microsomes. The ADP-ribosyltransferase was solubilized from the 100,000 x g pellet with 0.3% sodium deoxycholate and purified to great
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0c87ae94dd8a5ebeca1bdb0f863a831
https://pubmed.ncbi.nlm.nih.gov/2120212
https://pubmed.ncbi.nlm.nih.gov/2120212
Publikováno v:
The Journal of biological chemistry. 265(27)
Two gastrin analogs containing a D- and a L-tetrafluorinated tyrosyl residue (Arg-Arg-Leu-Glu-Glu-Glu-Glu-Glu-Ala-(F4)Tyr-Gly) were synthesized and tested as substrates and inhibitors of the insulin receptor kinase. No phosphorylation of these peptid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11493b6621e2159001b5a500d124a899
https://pubmed.ncbi.nlm.nih.gov/2168884
https://pubmed.ncbi.nlm.nih.gov/2168884
Publikováno v:
The Journal of biological chemistry. 265(13)
Biological tyrosine phosphorylation has become an extensively studied reaction. Little, however, is known of the chemistry involved. The acetylation of the tyrosyl phenolic hydroxyl group by N-acetylimidazole was studied as a model acylation reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1db72ae440bf68b561dfc1408f6969ae
https://pubmed.ncbi.nlm.nih.gov/2158985
https://pubmed.ncbi.nlm.nih.gov/2158985
Publikováno v:
Journal of Applied Physiology. 67:1670-1686
We present an analytic method for determining the effects of skin perfusion--vasculature and flow rates--on the flux of inert gases through human skin. We systematically specify the underlying blood flow and examine the resulting fluxes of several ga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31253311902b4fc2f5d485eaa94a5034
https://doi.org/10.1152/jappl.1989.67.4.1670
https://doi.org/10.1152/jappl.1989.67.4.1670
Publikováno v:
Biochemistry. 26:360-367
A new vitamin B/sub 6/ analogue, 6-fluoro-5'-deoxypyridoxal (6-FDPL), was synthesized and characterized. This analogue, as well as 6-fluoropyridoxal (6-FPAL), 6-fluoropyridoxal phosphate (6-FPLP), and 6-fluoropyridoxine, showed positive heteronuclear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23f5d7263a400b9fff302bae7a0fe0d5
https://doi.org/10.1021/bi00376a005
https://doi.org/10.1021/bi00376a005