Protein oligomerization modulates raft partitioning and apical sorting of GPI-anchored proteins

por Paladino, Simona, Sarnataro, Daniela, Pillich, Rudolf, Tivodar, Simona, Nitsch, Lucio, Zurzolo, Chiara
Publicado 2004

Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix Regulation

por Mollo, Nunzia, Scognamiglio, Roberta, Conti, Anna, Paladino, Simona, Nitsch, Lucio, Izzo, Antonella
Publicado 2023

Identification of Novel Pax8 Targets in FRTL-5 Thyroid Cells by Gene Silencing and Expression Microarray Analysis

por Di Palma, Tina, Conti, Anna, de Cristofaro, Tiziana, Scala, Serena, Nitsch, Lucio, Zannini, Mariastella
Publicado 2011

Caveolin Transfection Results in Caveolae Formation but Not Apical Sorting of Glycosylphosphatidylinositol (GPI)-anchored Proteins in Epithelial Cells

por Lipardi, Concetta, Mora, Rosalia, Colomer, Veronica, Paladino, Simona, Nitsch, Lucio, Rodriguez-Boulan, Enrique, Zurzolo, Chiara
Publicado 1998

Physiology, Pathology and Relatedness of Human Tissues from Gene Expression Meta-Analysis

por Greco, Dario, Somervuo, Panu, Di Lieto, Antonio, Raitila, Tuomas, Nitsch, Lucio, Castrén, Eero, Auvinen, Petri
Publicado 2008

Regulation of sub-compartmental targeting and folding properties of the Prion-like protein Shadoo

por Pepe, Anna, Avolio, Rosario, Matassa, Danilo Swann, Esposito, Franca, Nitsch, Lucio, Zurzolo, Chiara, Paladino, Simona, Sarnataro, Daniela
Publicado 2017

Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event

por Genesio, Rita, Ronga, Valentina, Castelluccio, Pia, Fioretti, Gennaro, Mormile, Angela, Leone, Graziella, Conti, Anna, Cavaliere, Maria Luigia, Nitsch, Lucio
Publicado 2013

The 37/67kDa laminin receptor (LR) inhibitor, NSC47924, affects 37/67kDa LR cell surface localization and interaction with the cellular prion protein

por Sarnataro, Daniela, Pepe, Anna, Altamura, Gennaro, De Simone, Imma, Pesapane, Ada, Nitsch, Lucio, Montuori, Nunzia, Lavecchia, Antonio, Zurzolo, Chiara
Publicado 2016

The microRNA-Processing Enzyme Dicer Is Essential for Thyroid Function

por Frezzetti, Daniela, Reale, Carla, Calì, Gaetano, Nitsch, Lucio, Fagman, Henrik, Nilsson, Ola, Scarfò, Marzia, De Vita, Gabriella, Di Lauro, Roberto
Publicado 2011

Constitutional chromothripsis involving the critical region of 9q21.13 microdeletion syndrome

por Genesio, Rita, Fontana, Paolo, Mormile, Angela, Casertano, Alberto, Falco, Mariateresa, Conti, Anna, Franzese, Adriana, Mozzillo, Enza, Nitsch, Lucio, Melis, Daniela
Publicado 2015

Targeting Mitochondrial Network Architecture in Down Syndrome and Aging

por Mollo, Nunzia, Cicatiello, Rita, Aurilia, Miriam, Scognamiglio, Roberta, Genesio, Rita, Charalambous, Maria, Paladino, Simona, Conti, Anna, Nitsch, Lucio, Izzo, Antonella
Publicado 2020

Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells

por Mollo, Nunzia, Aurilia, Miriam, Scognamiglio, Roberta, Zerillo, Lucrezia, Cicatiello, Rita, Bonfiglio, Ferdinando, Pagano, Pasqualina, Paladino, Simona, Conti, Anna, Nitsch, Lucio, Izzo, Antonella
Publicado 2022

New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants

por Cappuccio, Gerarda, Vitiello, Francesco, Casertano, Alberto, Fontana, Paolo, Genesio, Rita, Bruzzese, Dario, Ginocchio, Virginia Maria, Mormile, Angela, Nitsch, Lucio, Andria, Generoso, Melis, Daniela
Publicado 2016

Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report

por Genesio, Rita, Maruotti, Giuseppe Maria, Saccone, Gabriele, Mormile, Angela, Conti, Anna, Cicatiello, Rita, Sarnataro, Viviana, Sirico, Angelo, Izzo, Antonella, Martinelli, Pasquale, Nitsch, Lucio
Publicado 2018

Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency

por Cicatiello, Rita, Pignataro, Piero, Izzo, Antonella, Mollo, Nunzia, Pezone, Lucia, Maruotti, Giuseppe Maria, Sarno, Laura, Sglavo, Gabriella, Conti, Anna, Genesio, Rita, Nitsch, Lucio
Publicado 2019

Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy

por Conti, Anna, Fabbrini, Floriana, D'Agostino, Paola, Negri, Rosa, Greco, Dario, Genesio, Rita, D'Armiento, Maria, Olla, Carlo, Paladini, Dario, Zannini, Mariastella, Nitsch, Lucio
Publicado 2007

Lithium chloride induces mesenchymal-to-epithelial reverting transition in primary colon cancer cell cultures

por COSTABILE, VALERIA, DURATURO, FRANCESCA, DELRIO, PAOLO, REGA, DANIELA, PACE, UGO, LICCARDO, RAFFAELLA, ROSSI, GIOVANNI BATTISTA, GENESIO, RITA, NITSCH, LUCIO, IZZO, PAOLA, DE ROSA, MARINA
Publicado 2015

Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses

por Izzo, Antonella, Manco, Rosanna, de Cristofaro, Tiziana, Bonfiglio, Ferdinando, Cicatiello, Rita, Mollo, Nunzia, Martino, Marco De, Genesio, Rita, Zannini, Mariastella, Conti, Anna, Nitsch, Lucio
Publicado 2017

Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets

por Izzo, Antonella, Mollo, Nunzia, Nitti, Maria, Paladino, Simona, Calì, Gaetano, Genesio, Rita, Bonfiglio, Ferdinando, Cicatiello, Rita, Barbato, Maria, Sarnataro, Viviana, Conti, Anna, Nitsch, Lucio
Publicado 2018

In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1

por Silberschmidt, Daniel, Rodriguez-Mallon, Alina, Mithboakar, Prathiba, Calì, Gaetano, Amendola, Elena, Sanges, Remo, Zannini, Mariastella, Scarfò, Marzia, De Luca, Pasquale, Nitsch, Lucio, Di Lauro, Roberto, De Felice, Mario
Publicado 2011