LETTIERI, ANTONELLA
LETTIERI, ANTONELLA
Dipartimento di Scienze della Salute
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer Predisposition
2025 L. Rigotti, S. Rebellato, A. Lettieri, S. Castiglioni, M. Mariani, S. Totaro, C. Saitta, C. Gervasini, G. Fazio, V. Massa, G. Cazzaniga, A. Selicorni
p300 inhibition delays premature cellular senescence
2025 E. Di Fede, E. Taci, S. Castiglioni, S. Rebellato, S. Ancona, P. Grazioli, C. Parodi, E.A. Colombo, C. Bernardelli, E. Lesma, I. Daniel Krantz, S. Corti, A. Priori, G. Fazio, C. Gervasini, V. Massa, A. Lettieri
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies
2024 E. Di Fede, A. Lettieri, E. Taci, S. Castiglioni, S. Rebellato, C. Parodi, E.A. Colombo, P. Grazioli, F. Natacci, P. Marchisio, L. Pezzani, G. Fazio, D. Milani, V. Massa, C. Gervasini
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter
2024 S. Castiglioni, L. Pezzoli, L. Pezzani, A. Lettieri, E. Di Fede, A. Cereda, S. Ancona, A. Gallina, E.A. Colombo, C. Parodi, P. Grazioli, E. Taci, D. Milani, M. Iascone, V. Massa, C. Gervasini
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical management
2024 L. Avagliano, S. Castiglioni, A. Lettieri, C. Parodi, E. Di Fede, E. Taci, P. Grazioli, E.A. Colombo, C. Gervasini, V. Massa
Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency
2023 R. Oleari, A. Lettieri, S. Manzini, A. Paganoni, V. André, P. Grazioli, M. Busnelli, P. Duminuco, A. Vitobello, C. Philippe, V. Bizaoui, H.L. Storr, F. Amoruso, F. Memi, V. Vezzoli, V. Massa, P. Scheiffele, S.R. Howard, A. Cariboni
SEMA6A drives GnRH neuron-dependent puberty onset by tuning median eminence vascular permeability
2023 A. Lettieri, R. Oleari, M.H. van den Munkhof, E.Y. van Battum, M.G. Verhagen, C. Tacconi, M. Spreafico, A.J.J. Paganoni, R. Azzarelli, V. Andre', F. Amoruso, L. Palazzolo, I. Eberini, L. Dunkel, S.R. Howard, A. Fantin, R.J. Pasterkamp, A. Cariboni
KMT2A : umbrella gene for multiple diseases
2022 S. Castiglioni, E. Di Fede, C. Bernardelli, A. Lettieri, C. Parodi, P. Grazioli, E.A. Colombo, S. Ancona, D. Milani, E. Ottaviano, E. Borghi, V. Massa, F. Ghelma, A. Vignoli, E. Lesma, C. Gervasini
Gonadotropin-releasing hormone-secreting neuron development and function : an update
2022 A. Passarelli, A. Lettieri, T.N. Demirci, P. Magni
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies
2022 E. Di Fede, P. Grazioli, A. Lettieri, C. Parodi, S. Castiglioni, E. Taci, E.A. Colombo, S. Ancona, A. Priori, C. Gervasini, V. Massa
Lack of ApoA-I in ApoEKO Mice Causes Skin Xanthomas, Worsening of Inflammation, and Increased Coronary Atherosclerosis in the Absence of Hyperlipidemia
2022 M. Busnelli, S. Manzini, A. Colombo, E. Franchi, F. Bonacina, M. Chiara, F. Arnaboldi, E. Donetti, F. Ambrogi, R. Oleari, A. Lettieri, D. Horner, E. Scanziani, G.D. Norata, G. Chiesa
LAM cells as potential drivers of senescence in lymphangioleiomyomatosis microenvironment
2022 C. Bernardelli, S. Ancona, M. Lazzari, A. Lettieri, P. Selvaggio, V. Massa, C.C.G. Gervasini, F. DI MARCO, R. Chiaramonte, E.A. Lesma
A novel SEMA3G mutation in two siblings affected by syndromic GnRH deficiency
2021 R. Oleari, V. Andrè, A. Lettieri, S. Tahir, L. Roth, A. Paganoni, I. Eberini, C. Parravicini, V. Scagliotti, L. Cotellessa, F. Bedogni, L.B. De Martini, M.V. Corridori, S. Gulli, H.G. Augustin, C. Gaston-Massuet, K. Hussain, A. Cariboni
The differential roles for neurodevelopmental and neuroendocrine genes in shaping gnrh neuron physiology and deficiency
2021 R. Oleari, V. Massa, A. Cariboni, A. Lettieri
Coronary atherosclerosis and systemic inflammation in HDL deficient mice
2021 A. Colombo, M. Busnelli, S. Manzini, F. Arnaboldi, E. Donetti, R. Oleari, A. Lettieri, E. Scanziani, G.D. Norata, G. Chiesa
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
2021 D.E. Whittaker, R. Oleari, L.C. Gregory, P. Le Quesne-Stabej, H.J. Williams, J.G. Torpiano, N. Formosa, M.J. Cachia, D. Field, A. Lettieri, L.A. Ocaka, A.J.J. Paganoni, S.H. Rajabali, K.L.H. Riegman, L.B. de Martini, T. Chaya, I.C.A.F. Robinson, T. Furukawa, A. Cariboni, M.A. Basson, M.T. Dattani
Semaphorin Regulation by the Chromatin Remodeler CHD7 : An Emerging Genetic Interaction Shaping Neural Cells and Neural Crest in Development and Cancer
2021 A. Lettieri, R. Oleari, A.J.J. Paganoni, C. Gervasini, V. Massa, A. Fantin, A. Cariboni
Cornelia de Lange Syndrome : from a disease to a broader spectrum
2021 A. Selicorni, M. Mariani, A. Lettieri, V. Massa
LGR4 deficiency results in delayed puberty through impaired Wnt/β-catenin signaling
2020 A. Mancini, S.R. Howard, F. Marelli, C.P. Cabrera, M.R. Barnes, M.J.E. Sternberg, M. Leprovots, I. Hadjidemetriou, E. Monti, A. David, K. Wehkalampi, R. Oleari, A. Lettieri, V. Vezzoli, G. Vassart, A. Cariboni, M. Bonomi, M.I. Garcia, L. Guasti, L. Dunkel
Protein kinase CK2 subunits differentially perturb the adhesion and migration of GN11 cells: A model of immature migrating neurons
2019 A. Lettieri, C. Borgo, L. Zanieri, C. D'Amore, R. Oleari, A. Paganoni, L.A. Pinna, A. Cariboni, M. Salvi