au.\*:("MALLI, Roland")
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Mitochondrial protein phosphorylation: instigator or target of lipotoxicity?GRAIER, Wolfgang F; MALLI, Roland; KOSTNER, Gerhard M et al.Trends in endocrinology and metabolism. 2009, Vol 20, Num 4, pp 186-193, issn 1043-2760, 8 p.Article
Acyl chain-dependent effect of lysophosphatidylcholine on cyclooxygenase (COX)-2 expression in endothelial cellsBRKIC, Lada; RIEDERER, Monika; GRAIER, Wolfgang F et al.Atherosclerosis. 2012, Vol 224, Num 2, pp 348-354, issn 0021-9150, 7 p.Article
Anandamide initiates Ca2+ signaling via CB2 receptor linked to phospholipase C in calf pulmonary endothelial cellsZORATTI, Cristina; KIPMEN-KORGUN, Dijle; OSIBOW, Karin et al.British journal of pharmacology. 2003, Vol 140, Num 8, pp 1351-1362, issn 0007-1188, 12 p.Article
Oxidized phospholipids stimulate tissue factor expression in human endothelial cells via activation of ERK/EGR-1 and Ca++/NFATBOCHKOV, Valery N; MECHTCHERIAKOVA, Diana; LUCERNA, Marcus et al.Blood. 2002, Vol 99, Num 1, pp 199-206, issn 0006-4971Article
Tissue-specific expression of human lipoprotein lipase in the vascular system affects vascular reactivity in transgenic miceESENABHALU, Victor E; CERIMAGIC, Mirza; MALLI, Roland et al.British journal of pharmacology. 2002, Vol 135, Num 1, pp 143-154, issn 0007-1188Article
GPR55-dependent and -independent ion signalling in response to lysophosphatidylinositol in endothelial cellsBONDARENKO, Alexander; WALDECK-WEIERMAIR, Markus; NAGHDI, Shamim et al.British journal of pharmacology. 2010, Vol 161, Num 2, pp 308-320, issn 0007-1188, 13 p.Article
Nitric oxide inhibits capacitative Ca2+ entry by suppression of mitochondrial Ca2+ handlingTHYAGARAJAN, Baskaran; MALLI, Roland; SCHMIDT, Kurt et al.British journal of pharmacology. 2002, Vol 137, Num 6, pp 821-830, issn 0007-1188, 10 p.Article
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndromeWINDPASSINGER, Christian; AUER-GRUMBACH, Michaela; WARNER, Thomas T et al.Nature genetics. 2004, Vol 36, Num 3, pp 271-276, issn 1061-4036, 6 p.Article
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual DisabilityAHMAD KHAN, Muzammil; RAFIQ, Muhammad Arshad; ISHAK, Gisele E et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 856-863, issn 0002-9297, 8 p.Article
Lysophosphatidic acid receptor activation affects the C13NJ microglia cell line proteome leading to alterations in glycolysis, motility, and cytoskeletal architectureBERNHART, Eva; KOLLROSER, Manfred; ZORN-PAULY, Klaus et al.Proteomics (Weinheim. Print). 2010, Vol 10, Num 1, pp 141-158, issn 1615-9853, 18 p.Article