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International Journal of Food Microbiology|March 12, 2018
The bacterial biota of laboratory-reared edible mealworms (Tenebrio molitor L.): From feed to frassAndrea Osimani, Vesna Milanović, Federica Cardinali, et al.
Meat Science|March 30, 2020
Is there any still undisclosed biodiversity in Ciauscolo salami? A new glance into the microbiota of an artisan production as revealed by high-throughput sequencingLuca Belleggia, Vesna Milanović, Ilario Ferrocino, et al.
Cell Reports|December 16, 2016
Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α AcetylationSarah Pambianco, Matteo Giovarelli, Cristiana Perrotta, et al.
International Journal of Molecular Sciences|April 24, 2015
Undetected toxicity risk in pharmacogenetic testing for dihydropyrimidine dehydrogenaseFelicia Stefania Falvella, Marta Caporale, Stefania Cheli, et al.
Skeletal Muscle|December 23, 2014
Deficient nitric oxide signalling impairs skeletal muscle growth and performance: involvement of mitochondrial dysregulationClara De Palma, Federica Morisi, Sarah Pambianco, et al.
Cell Death and Differentiation|February 12, 2020
Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscleMatteo Giovarelli, Silvia Zecchini, Emanuele Martini, et al.
Journal of Endocrinological Investigation|January 5, 2022
SARS-CoV-2 detection in primary thyroid sarcoma: coincidence or interaction?M L Tanda, S Ippolito, D Gallo, et al.
Food Microbiology|April 28, 2019
Unveiling hákarl: A study of the microbiota of the traditional Icelandic fermented fishAndrea Osimani, Ilario Ferrocino, Monica Agnolucci, et al.
British Journal of Clinical Pharmacology|March 19, 2015
DPD and UGT1A1 deficiency in colorectal cancer patients receiving triplet chemotherapy with fluoropyrimidines, oxaliplatin and irinotecanFelicia Stefania Falvella, Stefania Cheli, Antonia Martinetti, et al.
Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
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