Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum

por Selicorni, Angelo, Mariani, Milena, Lettieri, Antonella, Massa, Valentina
Publicado 2021

The Differential Roles for Neurodevelopmental and Neuroendocrine Genes in Shaping GnRH Neuron Physiology and Deficiency

por Oleari, Roberto, Massa, Valentina, Cariboni, Anna, Lettieri, Antonella
Publicado 2021

In Vitro, Ex Vivo and In Vivo Techniques to Study Neuronal Migration in the Developing Cerebral Cortex

por Azzarelli, Roberta, Oleari, Roberto, Lettieri, Antonella, Andre', Valentina, Cariboni, Anna
Publicado 2017

Semaphorin Regulation by the Chromatin Remodeler CHD7: An Emerging Genetic Interaction Shaping Neural Cells and Neural Crest in Development and Cancer

por Lettieri, Antonella, Oleari, Roberto, Paganoni, Alyssa J. J., Gervasini, Cristina, Massa, Valentina, Fantin, Alessandro, Cariboni, Anna
Publicado 2021

Protein Kinase CK2 Subunits Differentially Perturb the Adhesion and Migration of GN11 Cells: A Model of Immature Migrating Neurons

por Lettieri, Antonella, Borgo, Christian, Zanieri, Luca, D’Amore, Claudio, Oleari, Roberto, Paganoni, Alyssa, Pinna, Lorenzo A., Cariboni, Anna, Salvi, Mauro
Publicado 2019

LAM Cells as Potential Drivers of Senescence in Lymphangioleiomyomatosis Microenvironment

por Bernardelli, Clara, Ancona, Silvia, Lazzari, Melania, Lettieri, Antonella, Selvaggio, Piera, Massa, Valentina, Gervasini, Cristina, Di Marco, Fabiano, Chiaramonte, Raffaella, Lesma, Elena
Publicado 2022

Epigenetic disorders: Lessons from the animals–animal models in chromatinopathies

por Di Fede, Elisabetta, Grazioli, Paolo, Lettieri, Antonella, Parodi, Chiara, Castiglioni, Silvia, Taci, Esi, Colombo, Elisa Adele, Ancona, Silvia, Priori, Alberto, Gervasini, Cristina, Massa, Valentina
Publicado 2022

Lack of ApoA-I in ApoEKO Mice Causes Skin Xanthomas, Worsening of Inflammation, and Increased Coronary Atherosclerosis in the Absence of Hyperlipidemia

por Busnelli, Marco, Manzini, Stefano, Colombo, Alice, Franchi, Elsa, Bonacina, Fabrizia, Chiara, Matteo, Arnaboldi, Francesca, Donetti, Elena, Ambrogi, Federico, Oleari, Roberto, Lettieri, Antonella, Horner, David, Scanziani, Eugenio, Norata, Giuseppe Danilo, Chiesa, Giulia
Publicado 2022

KMT2A: Umbrella Gene for Multiple Diseases

por Castiglioni, Silvia, Di Fede, Elisabetta, Bernardelli, Clara, Lettieri, Antonella, Parodi, Chiara, Grazioli, Paolo, Colombo, Elisa Adele, Ancona, Silvia, Milani, Donatella, Ottaviano, Emerenziana, Borghi, Elisa, Massa, Valentina, Ghelma, Filippo, Vignoli, Aglaia, Lesma, Elena, Gervasini, Cristina
Publicado 2022

Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency

por Oleari, Roberto, Lettieri, Antonella, Manzini, Stefano, Paganoni, Alyssa, André, Valentina, Grazioli, Paolo, Busnelli, Marco, Duminuco, Paolo, Vitobello, Antonio, Philippe, Christophe, Bizaoui, Varoona, Storr, Helen L., Amoruso, Federica, Memi, Fani, Vezzoli, Valeria, Massa, Valentina, Scheiffele, Peter, Howard, Sasha R., Cariboni, Anna
Publicado 2023

LGR4 deficiency results in delayed puberty through impaired Wnt/β-catenin signaling

por Mancini, Alessandra, Howard, Sasha R., Marelli, Federica, Cabrera, Claudia P., Barnes, Michael R., Sternberg, Michael J.E., Leprovots, Morgane, Hadjidemetriou, Irene, Monti, Elena, David, Alessia, Wehkalampi, Karoliina, Oleari, Roberto, Lettieri, Antonella, Vezzoli, Valeria, Vassart, Gilbert, Cariboni, Anna, Bonomi, Marco, Garcia, Marie Isabelle, Guasti, Leonardo, Dunkel, Leo
Publicado 2020

A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia

por Whittaker, Danielle E., Oleari, Roberto, Gregory, Louise C., Le Quesne-Stabej, Polona, Williams, Hywel J., Torpiano, John G., Formosa, Nancy, Cachia, Mario J., Field, Daniel, Lettieri, Antonella, Ocaka, Louise A., Paganoni, Alyssa J.J., Rajabali, Sakina H., Riegman, Kimberley L.H., De Martini, Lisa B., Chaya, Taro, Robinson, Iain C.A.F., Furukawa, Takahisa, Cariboni, Anna, Basson, M. Albert, Dattani, Mehul T.
Publicado 2021