Browse By Person: Semmler, Annalese
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Number of items: 6.
Journal Article
Savarimuthu Francis, Santiyagu M, Tan, Maxine E, Fung , Pamela R, Shaw, Janet G, Semmler, Annalese BT, Nataatmadja, Maria, et al. (2012) Peripheral compartment innate immune response to Haemophilus influenzae and Streptococcus pneumoniae in chronic obstructive pulmonary disease patients. Innate Immunity.
Chen, Lu, Meyers, Deborah, Javorsky, George, Burstow, Darryl, Lolekha, Pakorn, Lucas, Margaret, et al. (2007) Arg389Gly-[beta]1-adrenergic receptors determine improvement in left ventricular systolic function in nonischemic cardiomyopathy patients with heart failure after chronic treatment with carvedilol. Pharmacogenetics and Genomics, 17(11), pp. 941-949.
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29Kaumann, Alberto, Semmler, Annalese, & Molenaar, Peter (2007) The effects of both noradrenaline and CGP12177, mediated through human Beta1-adrenoceptors, are reduced by PDE3 in human atrium but PDE4 in CHO cells. Naunyn-Schmiedebergs Archives of Pharmacology, 375(2), pp. 123-131.
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Molenaar, P., Klenowski, P., Semmler, A., Chee, K., Iconomou, M., Tugiono, N., et al. (2010) The highs (B1H) and lows (B1L) of human heart B1-adrenoceptors (AR). In Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists and Carney Symposium, 29-31 August 2010, Christchurch, New Zealand.
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26Klenowski, P., Semmler, A., Chee, K., Iconomou, M., & Molenaar, P. (2010) Contribution of transmembrane domain V amino acids to β1l-adrenoceptor activity and affinity. In Ngo, Suong, Hay, Debbie, & Polasek, Tom (Eds.) Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists 44th Annual Scientific Meeting, 28th November 2010 - 1st December 2010, Melbourne.
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11Klenowski, Paul, Semmler, A., Chee, K., Iconomou, Mary, & Molenaar, Peter (2010) Contribution of transmembrane domain V amino acids to β1l-adrenoceptor activity and affinity. In Drug Discovery Biology, Monash University : Molecular Pharmacology of G Protein-Coupled Receptors meeting 2010, December 2nd - 4th, 2010, Monash Institute of Pharmaceutical Sciences.
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