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Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|December 27, 2017
Genotyping of Brucella melitensis and Brucella abortus strains in Kazakhstan using MLVA-15Аida Daugaliyeva, Akhmetzhan Sultanov, Bekbolat Usserbayev, et al.
Archives of Virology|October 21, 2016
Evidence of circulation of the novel border disease virus genotype 8 in chamoisClaudio Caruso, Simone Peletto, Francesco Cerutti, et al.
Veterinary Microbiology|March 4, 2020
Yersinia enterocolitica-specific modulation of innate immune responses in jejunal epithelial cellsElisabetta Razzuoli, Walter Vencia, Paola Modesto, et al.
Pharmaceutics|August 10, 2021
Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) TargetingSara Pastorino, Sara Baldassari, Giorgia Ailuno, et al.
Neurochemical Research|October 18, 2007
Protective effects of some creatine derivatives in brain tissue anoxiaLuisa Perasso, Gian Luigi Lunardi, Federica Risso, et al.
Pituitary|November 19, 2010
In vivo and in vitro response to octreotide LAR in a TSH-secreting adenoma: characterization of somatostatin receptor expression and role of subtype 5Federico Gatto, Federica Barbieri, Lara Castelletti, et al.
Annals of the New York Academy of Sciences|April 5, 2007
Amyloid precursor protein and Presenilin 1 interaction studied by FRET in human H4 cellsMario Nizzari, Valentina Venezia, Paolo Bianchini, et al.
BMC Neuroscience|April 28, 2012
In vitro study of uptake and synthesis of creatine and its precursors by cerebellar granule cells and astrocytes suggests some hypotheses on the physiopathology of the inherited disorders of creatine metabolismClaudia Carducci, Carla Carducci, Silvia Santagata, et al.
Genes|October 29, 2025
A New Variant in the NALCN Channel Is Responsible for Cerebellar Ataxia and Cognitive ImpairmentRute Luísa Cabrita Pinto, Roberto Fancellu, Tiziana Benzi Markushi, et al.
Genes|April 28, 2023
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert SyndromeRute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, et al.
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