Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Simona Paladino"'
Autor:
Stéphanie Lebreton, Simona Paladino, Mickaël Lelek, Marc Tramier, Christophe Zimmer, Chiara Zurzolo
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
The spatiotemporal compartmentalization of membrane-associated glycosylphosphatidylinositol-anchored proteins (GPI-APs) on the cell surface regulates their biological activities. These GPI-APs occupy distinct cellular functions such as enzymes, recep
Externí odkaz:
https://doaj.org/article/9fa0b161e643413bbf6e4506620c1af9
Autor:
Serenella Anzilotti, Valeria Valente, Paola Brancaccio, Cristina Franco, Antonella Casamassa, Giovanna Lombardi, Alessandra Palazzi, Andrea Conte, Simona Paladino, Lorella Maria Teresa Canzoniero, Lucio Annunziato, Giovanna Maria Pierantoni, Giuseppe Pignataro
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 167, Iss , Pp 115503- (2023)
Background: Amyotrophic lateral sclerosis (ALS) is a progressive and often fatal neurodegenerative disease characterized by the loss of Motor Neurons (MNs) in spinal cord, motor cortex and brainstem. Despite significant efforts in the field, the exac
Externí odkaz:
https://doaj.org/article/a84cdf8669204766828c056dbe6b5a2a
Autor:
Laura De Rosa, Dominga Fasano, Lucrezia Zerillo, Valeria Valente, Antonella Izzo, Nunzia Mollo, Giuseppina Amodio, Elena Polishchuk, Roman Polishchuk, Mariarosa Anna Beatrice Melone, Chiara Criscuolo, Anna Conti, Lucio Nitsch, Paolo Remondelli, Giovanna Maria Pierantoni, Simona Paladino
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Endosomal trafficking is essential for cellular homeostasis. At the crossroads of distinct intracellular pathways, the endolysosomal system is crucial to maintain critical functions and adapt to the environment. Alterations of endosomal compartments
Externí odkaz:
https://doaj.org/article/bb7c01ded3ef4671ac7aa624d3cba628
Autor:
Nunzia Mollo, Roberta Scognamiglio, Anna Conti, Simona Paladino, Lucio Nitsch, Antonella Izzo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2918 (2023)
Down syndrome (DS), a complex disorder that is caused by the trisomy of chromosome 21 (Hsa21), is a major cause of congenital heart defects (CHD). Interestingly, only about 50% of individuals with Hsa21 trisomy manifest CHD. Here we review the geneti
Externí odkaz:
https://doaj.org/article/27de18e3537c4418974f59a00483c313
Autor:
Federica Liotti, Narender Kumar, Nella Prevete, Maria Marotta, Daniela Sorriento, Caterina Ieranò, Andrea Ronchi, Federica Zito Marino, Sonia Moretti, Renato Colella, Efiso Puxeddu, Simona Paladino, Yoshihito Kano, Michael Ohh, Stefania Scala, Rosa Marina Melillo
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 40, Iss 1, Pp 1-16 (2021)
Abstract Background The programmed cell death-1 (PD-1) receptor and its ligands PD-L1 and PD-L2 are immune checkpoints that suppress anti-cancer immunity. Typically, cancer cells express the PD-Ls that bind PD-1 on immune cells, inhibiting their acti
Externí odkaz:
https://doaj.org/article/2f4f62c217e14f8f9af474f8e752ef34
Autor:
Nunzia Mollo, Miriam Aurilia, Roberta Scognamiglio, Lucrezia Zerillo, Rita Cicatiello, Ferdinando Bonfiglio, Pasqualina Pagano, Simona Paladino, Anna Conti, Lucio Nitsch, Antonella Izzo
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Down syndrome is a neurodevelopmental disorder frequently characterized by other developmental defects, such as congenital heart disease. Analysis of gene expression profiles of hearts from trisomic fetuses have shown upregulation of extracellular ma
Externí odkaz:
https://doaj.org/article/6f3f852b01ea4178816acde55f113e27
Autor:
Luigi Marino, Bruno Charlier, Valentina Giudice, Paolo Remondelli, Simona Paladino, Rosa Vitolo, Fabrizio Dal Piaz, Barbara Izzo, Pio Zeppa, Viviana Izzo, Amelia Filippelli, Carmine Selleri
Publikováno v:
eJHaem, Vol 1, Iss 1, Pp 356-360 (2020)
Externí odkaz:
https://doaj.org/article/b9c5fbbb22784fa28441231d92ac56a5
Autor:
Claudia Riccardi, Federica D’Aria, Dominga Fasano, Filomena Anna Digilio, Maria Rosaria Carillo, Jussara Amato, Laura De Rosa, Simona Paladino, Mariarosa Anna Beatrice Melone, Daniela Montesarchio, Concetta Giancola
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12412 (2022)
Two analogues of the MS3 aptamer, which was previously shown to have an exquisite capability to selectively bind and modulate the activity of mutant huntingtin (mHTT), have been here designed and evaluated in their physicochemical and biological prop
Externí odkaz:
https://doaj.org/article/9ee2118330bc416e9eb9c2c184cb036c
Autor:
Vincenzo Vestuto, Giuseppina Amodio, Giacomo Pepe, Manuela Giovanna Basilicata, Raffaella Belvedere, Enza Napolitano, Daniela Guarnieri, Valentina Pagliara, Simona Paladino, Manuela Rodriquez, Alessia Bertamino, Pietro Campiglia, Paolo Remondelli, Ornella Moltedo
Publikováno v:
Biomedicines, Vol 10, Iss 8, p 2009 (2022)
Parkinson’s disease (PD) represents one of the most common neurodegenerative disorders, characterized by a dopamine (DA) deficiency in striatal synapses and misfolded toxic α-synuclein aggregates with concomitant cytotoxicity. In this regard, the
Externí odkaz:
https://doaj.org/article/8273afd6b2414f98a31c9f0baef5e4d5
Autor:
Filomena Napolitano, Milena Dell’Aquila, Chiara Terracciano, Giuseppina Franzese, Maria Teresa Gentile, Giulio Piluso, Claudia Santoro, Davide Colavito, Anna Patanè, Paolo De Blasiis, Simone Sampaolo, Simona Paladino, Mariarosa Anna Beatrice Melone
Publikováno v:
Genes, Vol 13, Iss 7, p 1130 (2022)
Neurofibromatosis type 1 (NF1) is one of the most common genetic tumor predisposition syndrome, caused by mutations in the NF1. To date, few genotype-phenotype correlations have been discerned in NF1, due to a highly variable clinical presentation. W
Externí odkaz:
https://doaj.org/article/804878effeb94049b30b5816ff1324d8