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Allergy|September 13, 2011
Mast cells are critically involved in serum-mediated vascular leakage in chronic urticaria beyond high-affinity IgE receptor stimulationF Bossi, B Frossi, O Radillo, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|September 18, 2020
The Chronic Urticaria Registry: rationale, methods and initial implementationK Weller, A Giménez-Arnau, C Grattan, et al.Journal of Medicinal Chemistry|February 1, 1986
Pyrazolo[4,5-c]quinolines. 2. Synthesis and specific inhibition of benzodiazepine receptor bindingF Melani, L Cecchi, G Palazzino, et al.Journal of Medicinal Chemistry|July 8, 1999
4,5-Dihydro-1,2,4-triazolo[1,5-a]quinoxalin-4-ones: excitatory amino acid antagonists with combined glycine/NMDA and AMPA receptor affinityD Catarzi, V Colotta, F Varano, et al.Archiv Der Pharmazie|December 1, 1996
Structure-activity relationship studies of novel pyrazolo[1,5-c][1,3]benzoxazines: synthesis and benzodiazepine receptor affinityF Varano, D Catarzi, V Colotta, et al.Journal of Medicinal Chemistry|July 19, 1996
Synthesis and binding activity of some pyrazolo[1,5-c]quinazolines as tools to verify an optional binding site of a benzodiazepine receptor ligandV Colotta, D Catarzi, F Varano, et al.European Journal of Medicinal Chemistry|April 20, 2001
Synthesis of a set of ethyl 1-carbamoyl-3-oxoquinoxaline-2-carboxylates and of their constrained analogue imidazoF Varano, D Catarzi, V Colotta, et al.Journal of Medicinal Chemistry|October 1, 1987
1,3-Diarylpyrazolo[4,5-c]- and -[5,4-c]quinolin-4-ones. 4. Synthesis and specific inhibition of benzodiazepine receptor bindingG Palazzino, L Cecchi, F Melani, et al.Archiv Der Pharmazie|February 25, 1998
Tricyclic heteroaromatic systems. 1,2,4-triazolo[4,3-a]quinoxalines and 1,2,4-Triazino[4,3-a]quinoxalines: synthesis and central benzodiazepine receptor activityV Colotta, D Catarzi, F Varano, et al.Il Farmaco; Edizione Scientifica|July 1, 1985
Synthesis and binding studies of 1-arylpyrazolo[4,5-c]- and 2-arylpyrazolo[4,3-c]quinolin-4-ones. IL Cecchi, F Melani, G Palazzino, et al.Pageof 28