@article{MTMT:2802051,
	title = {Extracellular cell wall beta(1,3) glucan is required to couple septation to actomyosin ring contraction},
	url = {https://m2.mtmt.hu/api/publication/2802051},
	author = {Munoz, Javier and Cortes, Juan Carlos G and Sipiczki, Mátyás and Ramos, Mariona and Angel, Clemente-Ramos Jose and Belen, Moreno M and Martins, Ivone M and Perez, Pilar and Carlos, Ribas Juan},
	doi = {10.1083/jcb.201304132},
	journal-iso = {J CELL BIOL},
	journal = {JOURNAL OF CELL BIOLOGY},
	volume = {203},
	unique-id = {2802051},
	issn = {0021-9525},
	year = {2013},
	eissn = {1540-8140},
	pages = {265-282},
	orcid-numbers = {Sipiczki, Mátyás/0000-0002-1059-1305}
}

@article{MTMT:114815,
	title = {Analysis of vibrational spectra of some new E- and Z-4-arylidene-3-isochromanones Part 2. Isomers and conformers of the 2 '-pyrrolyl and 2 '-nitrophenyl derivatives},
	url = {https://m2.mtmt.hu/api/publication/114815},
	author = {Keresztury, Gábor and Holly, Sándor and István, Krisztina and Sundius, T and Lóránd, Tamás},
	doi = {10.1016/j.jbbm.2004.04.012},
	journal-iso = {J BIOCHEM BIOPH METH},
	journal = {JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS},
	volume = {61},
	unique-id = {114815},
	issn = {0165-022X},
	year = {2004},
	pages = {107-118}
}

@article{MTMT:1329710,
	title = {Improved solvent-free synthesis and structure elucidation of (E)- and (Z)-4-(arylmethylene)-3-isochromanones},
	url = {https://m2.mtmt.hu/api/publication/1329710},
	author = {Lóránd, Tamás and Forgó, Péter and Foldesi, Andras and Osz, Erzsebet and Prókai, László},
	doi = {10.1002/1099-0690(200209)2002:17<2996::AID-EJOC2996>3.0.CO;2-G},
	journal-iso = {EUR J ORG CHEM},
	journal = {EUROPEAN JOURNAL OF ORGANIC CHEMISTRY},
	volume = {2002},
	unique-id = {1329710},
	issn = {1434-193X},
	year = {2002},
	eissn = {1099-0690},
	pages = {2996-3003},
	orcid-numbers = {Forgó, Péter/0000-0002-0279-6896}
}

@article{MTMT:1486611,
	title = {The in vitro antimycotic activity and acute toxicity of third-generation bezylidenetetralones and heteroarylidenetetralones},
	url = {https://m2.mtmt.hu/api/publication/1486611},
	author = {Al-Nakib, TM and Lóránd, Tamás and Foldesi, A and Varghese, R},
	doi = {10.1159/000050368},
	journal-iso = {MED PRIN PRACT},
	journal = {MEDICAL PRINCIPLES AND PRACTICE},
	volume = {10},
	unique-id = {1486611},
	issn = {1011-7571},
	abstract = {Objectives: A new series of E-2-arylmethylene-1-tetralones and E-2-heteroarylmethylene-1-tetralones (third generation) were designed as potential antimycotic agents against human pathogenic yeasts. Methods: The new compounds were obtained by aldol condensation of 1-tetralone with the appropriately substituted aldehydes in either acid- or base-catalysed conditions. These compounds were tested for their in vitro antimycotic activity against 24 strains of Cryptococcus neoformans, Candida spp. and Trichosporon cutaneum by a microtitre well technique in a liquid casitone medium, using a double dilution method. The toxicity of the new compounds was determined in vitro in cultured HeLa cells, in HeLa growth medium and in vivo in MFI mice. Results: Nineteen new E-2-benzylidine-1-tetralones were prepared, and 16 of the tested compounds showed superior antimycotic activity when compared to the first-generation E-2-benzylidine-1-tetralones synthesised previously. Twelve of these third-generation compounds were more active against different strains of yeasts than 6 commercial antimycotic agents similarly tested. An in vitro toxicity study and an in vivo acute toxicity study in MA mice showed that these compounds were severalfold less toxic than most of the commerical antimycotics, with 4 being comparable to or less toxic than the least toxic of the commercial agents (amphotericin B) tested by the same procedures. Conclusions: Twelve members of this new E-2-benzylidine-1-tetralone class of compounds are promising candidates for antimycotic agents worthy of further investigation. Copyright (C) 2001 S. Karger AG, Basel.},
	year = {2001},
	eissn = {1423-0151},
	pages = {191-196}
}

@article{MTMT:1154229,
	title = {One- and two-dimensional gradient-selected HSQMBC NMR experiments for the efficient analysis of long-range heteronuclear coupling constants},
	url = {https://m2.mtmt.hu/api/publication/1154229},
	author = {Williamson, RT and Marquez, BL and Gerwick, WH and E Kövér, Katalin},
	doi = {10.1002/(SICI)1097-458X(200004)38:4<265::AID-MRC637>3.0.CO;2-#},
	journal-iso = {MAGN RESON CHEM},
	journal = {MAGNETIC RESONANCE IN CHEMISTRY},
	volume = {38},
	unique-id = {1154229},
	issn = {0749-1581},
	abstract = {Three new gradient-selected NMR experiments for the analysis of long-range heteronuclear coupling constants are presented. They are demonstrated on a series of compounds including sucrose, strychnine and a complex macrolide, phormidolide, isolated from a marine cyanobacterium. These 1D and 2D heteronuclear single quantum multiple bond correlation (HSQMBC) experiments provide pure absorption, antiphase lineshapes for precise, direct measurement of (n)J(C,H) coupling constants. The example compounds were chosen to demonstrate the high sensitivity and ease of spectral interpretation provided by these HSQMBC experiments. In addition, suppression of one-bond CH correlations has been introduced into the HSQMBC pulse sequence. Copyright (C) 2000 John Wiley & Sons, Ltd.},
	year = {2000},
	eissn = {1097-458X},
	pages = {265-273}
}