Publications by authors named "Anna Conti"

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Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix Regulation.
Nunzia Mollo, Roberta Scognamiglio, Anna Conti, Simona Paladino, Lucio Nitsch

Int J Mol Sci· February 2023

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Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression.
Laura De Rosa, Dominga Fasano, Lucrezia Zerillo, Valeria Valente, Antonella Izzo, Anna Conti

Front Genet· May 2022

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Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells.
Nunzia Mollo, Miriam Aurilia, Roberta Scognamiglio, Lucrezia Zerillo, Rita Cicatiello, Anna Conti

Front Genet· March 2022

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First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature.
Laura Sarno, Giuseppe Maria Maruotti, Antonella Izzo, Cristina Mazzaccara, Luigi Carbone, Anna Conti

J Matern Fetal Neonatal Med· September 2021

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Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation.
Nunzia Mollo, Matteo Esposito, Miriam Aurilia, Roberta Scognamiglio, Rossella Accarino, Anna Conti

Biology (Basel)· June 2021

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Corrigendum: Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells.
Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Anna Conti

Front Genet· July 2020

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Targeting Mitochondrial Network Architecture in Down Syndrome and Aging.
Nunzia Mollo, Rita Cicatiello, Miriam Aurilia, Roberta Scognamiglio, Rita Genesio, Anna Conti

Int J Mol Sci· April 2020

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Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells.
Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Anna Conti

Front Genet· June 2019

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Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency.
Rita Cicatiello, Piero Pignataro, Antonella Izzo, Nunzia Mollo, Lucia Pezone, Anna Conti

Med Sci (Basel)· February 2019

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Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report.
Rita Genesio, Giuseppe Maria Maruotti, Gabriele Saccone, Angela Mormile, Anna Conti

Clin Case Rep· April 2018

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Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets.
Antonella Izzo, Nunzia Mollo, Maria Nitti, Simona Paladino, Gaetano Calì, Anna Conti

Mol Med· March 2018

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Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses.
Antonella Izzo, Rosanna Manco, Tiziana de Cristofaro, Ferdinando Bonfiglio, Rita Cicatiello, Anna Conti

Int J Genomics· September 2017

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Validation of a method for noninvasive prenatal testing for fetal aneuploidies risk and considerations for its introduction in the Public Health System.
Francesca Gerundino, Claudia Giachini, Elisa Contini, Matteo Benelli, Giuseppina Marseglia, Anna Conti

J Matern Fetal Neonatal Med· March 2017

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Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells.
Antonella Izzo, Maria Nitti, Nunzia Mollo, Simona Paladino, Claudio Procaccini, Anna Conti

Hum Mol Genet· March 2017

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Constitutional chromothripsis involving the critical region of 9q21.13 microdeletion syndrome.
Rita Genesio, Paolo Fontana, Angela Mormile, Alberto Casertano, Mariateresa Falco, Anna Conti

Mol Cytogenet· December 2015

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Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation.
Rita Genesio, Angela Mormile, Maria Rosaria Licenziati, Daniele De Brasi, Graziella Leone, Anna Conti

Mol Cytogenet· July 2015

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NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome.
Antonella Izzo, Rosanna Manco, Ferdinando Bonfiglio, Gaetano Calì, Tiziana De Cristofaro, Anna Conti

Hum Mol Genet· August 2014

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Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event.
Rita Genesio, Valentina Ronga, Pia Castelluccio, Gennaro Fioretti, Angela Mormile, Anna Conti

Mol Cytogenet· August 2013

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Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects.
Claudia Piccoli, Antonella Izzo, Rosella Scrima, Ferdinando Bonfiglio, Rosanna Manco, Anna Conti

Hum Mol Genet· March 2013

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Clinical description of a patient carrying the smallest reported deletion involving 10p14 region.
Daniela Melis, Rita Genesio, Pasquale Boemio, Ennio Del Giudice, Gerarda Cappuccio, Anna Conti

Am J Med Genet A· April 2012

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Identification of novel Pax8 targets in FRTL-5 thyroid cells by gene silencing and expression microarray analysis.
Tina Di Palma, Anna Conti, Tiziana de Cristofaro, Serena Scala, Lucio Nitsch

PLoS One· February 2012

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Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring.
Daniela Melis, Rita Genesio, Ennio Del Giudice, Roberta Taurisano, Angela Mormile, Anna Conti

Clin Dysmorphol· January 2012

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Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region.
Francesca Fusco, Mariateresa Paciolla, Emily Chen, Xu Li, Rita Genesio, Anna Conti

Hum Reprod· November 2011

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Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype.
Rita Genesio, Daniela Melis, Sole Gatto, Antonella Izzo, Valentina Ronga, Anna Conti

Epigenetics· October 2011

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Trisomy 18 caused by isochromosome 18p and 18q formation: Is there a milder phenotype?
Giuseppe Maria Maruotti, Floriana Fabbrini, Raffaele Napolitano, Rita Genesio, Anna Conti

Am J Med Genet A· January 2011

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