Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Rodolfo C. Garcia"'
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Extracellular vesicles are membrane-bound structures released by living cells and present in body fluids. Their composition includes proteins, lipids, carbohydrates, and nucleic acids and are involved in transfers between cells. Extracellular vesicle
Externí odkaz:
https://doaj.org/article/11b29b32fbb04d7b9ca200a37b5a01e6
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology
Frontiers in Immunology
Extracellular vesicles are membrane-bound structures released by living cells and present in body fluids. Their composition includes proteins, lipids, carbohydrates, and nucleic acids and are involved in transfers between cells. Extracellular vesicle
Autor:
Federica Grilli, Federica Rizzo, Fabian Feiguin, Rodolfo C. Garcia, Giulia Romano, Monica Nizzardo, Corrado Guarnaccia, Nikola Holodkov, Raffaella Klima
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects the motor system, comprised of motoneurons and associated glia. Accordingly, neuronal or glial defects in TDP-43 function provoke paralysis due to the degeneration
Publikováno v:
International Immunopharmacology. 14:54-65
We report the effect of an immunomodulatory and anti-mycobacterial naphthoquinone, lapachol, on the bi-dimensional patterns of protein expression of toll-like receptor 2 (TLR2)-agonised and IFN-γ-treated THP-1 macrophages. This non-hypothesis driven
Autor:
Jens Forsberg, Charlotte Woschnagg, Federico Odreman, Åke Engström, Rodolfo C. Garcia, Per Venge
Publikováno v:
Journal of Proteome Research. 8:2720-2732
Proteins from human eosinophils were separated bidimensionally and identified by mass spectrometry (336 spots/bands, 98 different proteins). Of these, 24.7% belonged to the cytoskeleton/migration group. Highly basic proteins (11.3%) were concentrated
Autor:
Caterina Piva, Federico Odreman, Li-jun Tang, Secondo Guaschino, Per Venge, Rodolfo C. Garcia, Francesco De Seta
Publikováno v:
Journal of Proteome Research. 6:2874-2883
The pathophysiology of vaginal conditions is still ill-defined at a molecular level. Because the proteome of the human cervical-vaginal fluid (CVF) has not been reported to date, we undertook the identification of proteins present in the cell-free fr
Comparative proteomic analysis of spermatozoa isolated by swim-up or density gradient centrifugation
Autor:
Monica Martinelli, Rodolfo C. Garcia, Stefania Luppi, Elisa Giacomini, Gabriella Zito, Giuseppe Ricci, Elena Giolo
Publikováno v:
Reproductive Biology and Endocrinology : RB&E
Background Reports about the morphologic and functional characteristics of spermatozoa prepared by density gradient centrifugation (DC) or swim-up (SU) have produced discordant results. We have performed a proteomic comparison of cells prepared by DC
Publikováno v:
Microbes and infection. 17(9)
MicroRNAs (miRNAs) are evolutionarily conserved and naturally abundant molecules of single-stranded, non-coding RNA from ∼17 to 25 nucleotides long. MiRNAs act at post-transcriptional level either to suppress gene translation or to induce mRNA degr
Autor:
Elisa Giacomini, Giuseppe Ricci, Monica Martinelli, Stefania Luppi, Rodolfo C. Garcia, Blendi Ura, Elena Giolo
A comparative proteomic study of oligoasthenozoospermic and normozoospermic seminal plasmas was conducted to establish differences in protein expression. Oligoasthenozoospermia (when semen presents with a low concentration and reduced motility of spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a9589ec7279e2e186835f532dbb184
http://hdl.handle.net/11368/2871827
http://hdl.handle.net/11368/2871827
Autor:
Rodolfo C. Garcia, Bruno Bembi, Maria Gabriela Pittis, Marta Deganuto, Roberta Cariati, Veronica Guerci, Giovanni Ciana, Anna Lisa E. Montalvo
Publikováno v:
Molecular Genetics and Metabolism. 81:203-208
Glycogenosis type II (GSDII) is an autosomal recessive disorder due to the deficiency of the lysosomal enzyme acid α-glucosidase (GAA). We identified three novel point mutations, C399A, T1064C, and C2104T, in three unrelated Italian patients with th