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cAMP analog antagonists of cAMP action.
Botelho LH, Rothermel JD, Coombs RV, Jastorff B. Botelho LH, et al. Among authors: jastorff b. Methods Enzymol. 1988;159:159-72. doi: 10.1016/0076-6879(88)59017-1. Methods Enzymol. 1988. PMID: 2842582 No abstract available.
Competitive cAMP antagonists for cAMP-receptor proteins.
Van Haastert PJ, Van Driel R, Jastorff B, Baraniak J, Stec WJ, De Wit RJ. Van Haastert PJ, et al. Among authors: jastorff b. J Biol Chem. 1984 Aug 25;259(16):10020-4. J Biol Chem. 1984. PMID: 6088478
Blockade of granulosa cell differentiation by an antagonistic analog of adenosine 3',5'-cyclic monophosphate (cAMP): central but non-exclusive intermediary role of cAMP in follicle-stimulating hormone action.
Adashi EY, Resnick CE, Jastorff B. Adashi EY, et al. Among authors: jastorff b. Mol Cell Endocrinol. 1990 Jul 30;72(1):1-11. doi: 10.1016/0303-7207(90)90234-y. Mol Cell Endocrinol. 1990. PMID: 2177013
Inhibitory action of certain cyclophosphate derivatives of cAMP on cAMP-dependent protein kinases.
de Wit RJ, Hekstra D, Jastorff B, Stec WJ, Baraniak J, Van Driel R, Van Haastert PJ. de Wit RJ, et al. Among authors: jastorff b. Eur J Biochem. 1984 Jul 16;142(2):255-60. doi: 10.1111/j.1432-1033.1984.tb08279.x. Eur J Biochem. 1984. PMID: 6086345
Diastereomers of adenosine 3',5'-monothionophosphate (cAMP[S]) antagonize the activation of cGMP-dependent protein kinase.
Hofmann F, Gensheimer HP, Landgraf W, Hullin R, Jastorff B. Hofmann F, et al. Among authors: jastorff b. Eur J Biochem. 1985 Jul 1;150(1):85-8. doi: 10.1111/j.1432-1033.1985.tb08991.x. Eur J Biochem. 1985. PMID: 2990928
Novel (Rp)-cAMPS analogs as tools for inhibition of cAMP-kinase in cell culture. Basal cAMP-kinase activity modulates interleukin-1 beta action.
Gjertsen BT, Mellgren G, Otten A, Maronde E, Genieser HG, Jastorff B, Vintermyr OK, McKnight GS, Døskeland SO. Gjertsen BT, et al. Among authors: jastorff b. J Biol Chem. 1995 Sep 1;270(35):20599-607. doi: 10.1074/jbc.270.35.20599. J Biol Chem. 1995. PMID: 7657638
Membrane-permeant derivatives of cyclic AMP optimized for high potency, prolonged activity, or rapid reversibility.
Schultz C, Vajanaphanich M, Genieser HG, Jastorff B, Barrett KE, Tsien RY. Schultz C, et al. Among authors: jastorff b. Mol Pharmacol. 1994 Oct;46(4):702-8. Mol Pharmacol. 1994. PMID: 7969049
(Rp)- and (Sp)-8-piperidino-adenosine 3',5'-(cyclic)thiophosphates discriminate completely between site A and B of the regulatory subunits of cAMP-dependent protein kinase type I and II.
Ogreid D, Dostmann W, Genieser HG, Niemann P, Døskeland SO, Jastorff B. Ogreid D, et al. Among authors: jastorff b. Eur J Biochem. 1994 May 1;221(3):1089-94. doi: 10.1111/j.1432-1033.1994.tb18828.x. Eur J Biochem. 1994. PMID: 8181466
Investigations on stimulation of lac transcription in vivo in Escherichia coli by cAMP analogues. Biological activities and structure-activity correlations.
Scholübbers HG, van Knippenberg PH, Baraniak J, Stec WJ, Morr M, Jastorff B. Scholübbers HG, et al. Among authors: jastorff b. Eur J Biochem. 1984 Jan 2;138(1):101-9. doi: 10.1111/j.1432-1033.1984.tb07887.x. Eur J Biochem. 1984. PMID: 6319129
Structural features of the noncatalytic cGMP binding sites of frog photoreceptor phosphodiesterase using cGMP analogs.
Hebert MC, Schwede F, Jastorff B, Cote RH. Hebert MC, et al. Among authors: jastorff b. J Biol Chem. 1998 Mar 6;273(10):5557-65. doi: 10.1074/jbc.273.10.5557. J Biol Chem. 1998. PMID: 9488681
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