Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Raffaella Stallone"'
Autor:
Simona De Summa, Debora Traversa, Antonella Daniele, Orazio Palumbo, Massimo Carella, Raffaella Stallone, Antonio Tufaro, Andreina Oliverio, Eleonora Bruno, Maria Digennaro, Katia Danza, Patrizia Pasanisi, Stefania Tommasi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundBreast cancer onset is determined by a genetics-environment interaction. BRCA1/2 gene alterations are often genetically shared in familial context, but also food intake and hormonal assessment seem to influence the lifetime risk of developi
Externí odkaz:
https://doaj.org/article/df766af27fde48da81be1b838199c8e7
Autor:
Marilena P. Etna, Martina Severa, Valerio Licursi, Manuela Pardini, Melania Cruciani, Fabiana Rizzo, Elena Giacomini, Gianfranco Macchia, Orazio Palumbo, Raffaella Stallone, Massimo Carella, Mark Livingstone, Rodolfo Negri, Sandra Pellegrini, Eliana M. Coccia
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
In human primary dendritic cells (DC) rapamycin—an autophagy inducer and protein synthesis inhibitor—overcomes the autophagy block induced by Mycobacterium tuberculosis (Mtb) and promotes a Th1 response via IL-12 secretion. Here, the immunostimul
Externí odkaz:
https://doaj.org/article/eb748d7cd1c049debd23f736020b2119
Autor:
Sandra Pellegrini, Manuela Pardini, Raffaella Stallone, Massimo Carella, Valerio Licursi, Orazio Palumbo, Marilena P. Etna, Eliana M. Coccia, Gianfranco Macchia, Melania Cruciani, Rodolfo Negri, Mark Livingstone, Fabiana Rizzo, Elena Giacomini, Martina Severa
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology
Frontiers in Immunology
In human primary dendritic cells (DC) rapamycin—an autophagy inducer and protein synthesis inhibitor—overcomes the autophagy block induced by Mycobacterium tuberculosis (Mtb) and promotes a Th1 response via IL-12 secretion. Here, the immunostimul
Autor:
Massimo Carella, Antonio Scorrano, Pietro Palumbo, Raffaella Stallone, Maria Pia Leone, Maria Clara Bonaglia, Teresa Palladino, Maria Accadia, Orazio Palumbo
Publikováno v:
European Journal of Medical Genetics. 61:248-252
Non-recurrent microdeletion (≤2 Mb in size) in 7p22.1 is a rarely described cytogenetic aberration, only recently reported in patients with developmental delay/intellectual disability, short stature and microcephaly. The size of the deletions range
Autor:
Maria Pia Leone, Raffaella Stallone, Rocco Pio Ortore, Salvatore Melchionda, Roberto Cocchi, Massimo Carella, Pietro Palumbo, Tommaso Mazza, Teresa Palladino, Stefano Castellana, Orazio Palumbo
Publikováno v:
Molecular and Cellular Probes. 33:24-27
The paper describes a putative digenic form of deafness in two siblings affected by non-syndromic hereditary hearing loss, detected by a Targeted resequencing approach. Given that a previous paper suggested TMPRSS3 and GJB2 genes as responsible for a
Autor:
Orazio Palumbo, Anna Panza, Caterina Fusilli, Gianluigi Mazzoccoli, Stefano Castellana, Annamaria Gentile, Angelo De Cata, Tommaso Mazza, Raffaella Stallone, Ada Piepoli, Massimo Carella, Rosa Rubino, Tommaso Biagini, Daniele Capocefalo
Publikováno v:
Nucleic Acids Research
Alterations in the balance of mRNA and microRNA (miRNA) expression profiles contribute to the onset and development of colorectal cancer. The regulatory functions of individual miRNA-gene pairs are widely acknowledged, but group effects are largely u
Autor:
Francesco Papadia, Stefano Palladino, Raffaella Stallone, Teresa Palladino, Maria Pia Leone, Orazio Palumbo, Rira Fischetto, Marcella Vendemiale, Massimo Carella, Pietro Palumbo
Publikováno v:
Molecular Syndromology. 7:282-286
We report on a patient with psychomotor deficits, language delay, dyspraxia, skeletal anomalies, and facial dysmorphisms (hirsutism, right palpebral ptosis, a bulbous nasal tip with enlarged and anteverted nares, and a mild prominent antihelix stem).
Autor:
Pietro Palumbo, Raffaella Stallone, Massimo Carella, Orazio Palumbo, Leopoldo Zelante, Teresa Palladino, Maria Pia Leone
Publikováno v:
American Journal of Medical Genetics Part A. 167:2219-2222
Correspondence to: Massimo Carella, Ph.D., Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo (FG), Italy. E-mail: m.carella@operapadrepio.it Article first published online in Wiley Online Library (wileyonlinelibr
Autor:
Pietro Palumbo, Orazio Palumbo, Massimo Carella, Maria Pia Leone, Maria Accadia, Teresa Palladino, Raffaella Stallone
Publikováno v:
American journal of medical genetics. Part A. 176(2)
Microdeletion of chromosome 22q13.31 is a very rare condition. Fourteen patients have been annotated in public databases but, to date, a clinical comparison has not been done and, consequently, a specific phenotype has not been delineated yet. We des
Autor:
Raffaella Stallone, Massimo Carella, Teresa Palladino, Adelaide Franca Minenna, Orazio Palumbo, Leopoldo Zelante, Leonardo D'Agruma, Pietro Palumbo
Publikováno v:
Gene. 516:107-113
Interstitial deletion of chromosome region 3p14.1, including FOXP1 gene, is relatively rare and, until recently, there were no strong evidences to support the hypothesis that this microdeletion could play a role in the etiology of genomic disorders.