Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Nunzia Mollo"'
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:
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:
Gaia Maria Anelli, Francesca Parisi, Laura Sarno, Ottavia Fornaciari, Annunziata Carlea, Chiara Coco, Matteo Della Porta, Nunzia Mollo, Paola Maria Villa, Maurizio Guida, Roberta Cazzola, Ersilia Troiano, Monica Pasotti, Graziella Volpi, Laura Vetrani, Manuela Maione, Irene Cetin
Publikováno v:
Nutrients, Vol 14, Iss 17, p 3631 (2022)
Background: Maternal nutrition represents a critical risk factor for adverse health outcomes in both mother and offspring. We aimed to investigate associations between maternal nutritional habits, biomarker status, and pregnancy outcome among Italian
Externí odkaz:
https://doaj.org/article/b26d637e0bdb41699209da18bb7cf52a
Autor:
Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Rossella Accarino, Agnese Secondo, Tiziana Petrozziello, Gaetano Calì, Rita Cicatiello, Ferdinando Bonfiglio, Viviana Sarnataro, Rita Genesio, Antonella Izzo, Paolo Pinton, Giuseppe Matarese, Simona Paladino, Anna Conti, Lucio Nitsch
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/e7a461318e36402eb25ecba9b05896ba
Autor:
Antonella Izzo, Nunzia Mollo, Maria Nitti, Simona Paladino, Gaetano Calì, Rita Genesio, Ferdinando Bonfiglio, Rita Cicatiello, Maria Barbato, Viviana Sarnataro, Anna Conti, Lucio Nitsch
Publikováno v:
Molecular Medicine, Vol 24, Iss 1, Pp 1-8 (2018)
Abstract Trisomy of chromosome 21 (TS21) is the most common autosomal aneuploidy compatible with postnatal survival with a prevalence of 1 in 700 newborns. Its phenotype is highly complex with constant features, such as mental retardation, dysmorphic
Externí odkaz:
https://doaj.org/article/4ee9b0798112484caf1c2a218a487dab
Autor:
Nunzia Mollo, Matteo Esposito, Miriam Aurilia, Roberta Scognamiglio, Rossella Accarino, Ferdinando Bonfiglio, Rita Cicatiello, Maria Charalambous, Claudio Procaccini, Teresa Micillo, Rita Genesio, Gaetano Calì, Agnese Secondo, Simona Paladino, Giuseppe Matarese, Gabriella De Vita, Anna Conti, Lucio Nitsch, Antonella Izzo
Publikováno v:
Biology, Vol 10, Iss 7, p 609 (2021)
Background: The presence of mitochondrial alterations in Down syndrome suggests that it might affect neuronal differentiation. We established a model of trisomic iPSCs, differentiating into neural precursor cells (NPCs) to monitor the occurrence of d
Externí odkaz:
https://doaj.org/article/e283770a81d44bdaa3143288d2f1f94a
Autor:
Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Rossella Accarino, Agnese Secondo, Tiziana Petrozziello, Gaetano Calì, Rita Cicatiello, Ferdinando Bonfiglio, Viviana Sarnataro, Rita Genesio, Antonella Izzo, Paolo Pinton, Giuseppe Matarese, Simona Paladino, Anna Conti, Lucio Nitsch
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Mitochondrial dysfunction plays a primary role in neurodevelopmental anomalies and neurodegeneration of Down syndrome (DS) subjects. For this reason, targeting mitochondrial key genes, such as PGC-1α/PPARGC1A, is emerging as a good therapeutic appro
Externí odkaz:
https://doaj.org/article/8a750e35c731476aaf9c71b295b4d1b3
Autor:
Nunzia Mollo, Rita Cicatiello, Miriam Aurilia, Roberta Scognamiglio, Rita Genesio, Maria Charalambous, Simona Paladino, Anna Conti, Lucio Nitsch, Antonella Izzo
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 9, p 3134 (2020)
Mitochondria are organelles that mainly control energy conversion in the cell. In addition, they also participate in many relevant activities, such as the regulation of apoptosis and calcium levels, and other metabolic tasks, all closely linked to ce
Externí odkaz:
https://doaj.org/article/b2644e2fc8774d4c90b4ccd610b894e1
Autor:
Antonella Izzo, Rosanna Manco, Tiziana de Cristofaro, Ferdinando Bonfiglio, Rita Cicatiello, Nunzia Mollo, Marco De Martino, Rita Genesio, Mariastella Zannini, Anna Conti, Lucio Nitsch
Publikováno v:
International Journal of Genomics, Vol 2017 (2017)
Dosage-dependent upregulation of most of chromosome 21 (Hsa21) genes has been demonstrated in heart tissues of fetuses with Down syndrome (DS). Also miRNAs might play important roles in the cardiac phenotype as they are highly expressed in the heart
Externí odkaz:
https://doaj.org/article/97f028a9da27488e96b539718db24af1