Sfoglia per Autore
From trascriptomic analysis to in vivo functional experiments: zebrafish as a model for studying GnRH system
2016 V. Andrè, R. Oleari, A. Lettieri, F. Cotelli, Y. Gothilf, A. Cariboni
From trascriptomic analysis to in vivo functional experiments: zebrafish as a model for studying GnRH system
2016 V.I. Andre', R. Oleari, A. Lettieri, F. Cotelli, Y. Gothilf, A. Cariboni
The role of semaphorin signaling in the etiology of hypogonadotropic hypogonadism
2016 A. Lettieri, R. Oleari, J. Gimmelli, V. André, A. Cariboni
Iron overload induces hypogonadism in male mice via extrahypothalamic mechanisms
2017 C. Macchi, L. Steffani, R. Oleari, A. Lettieri, L. Valenti, P. Dongiovanni, A. Romero Ruiz, M. Tena Sempere, A. Cariboni, P. Magni, M. Ruscica
In vitro, ex vivo and in vivo techniques to study neuronal migration in the developing cerebral cortex
2017 R. Azzarelli, R. Oleari, A. Lettieri, V. Andre’, A. Cariboni
Semaphorin signalling in GnRH neurons: from development to disease
2019 R. Oleari, A. Lettieri, A.J.J. Paganoni, L. Zanieri, A. Cariboni
PLXNA1 and PLXNA3 cooperate to pattern the nasal axons that guide gonadotropin-releasing hormone neurons
2019 R. Oleari, A. Caramello, S. Campinoti, A. Lettieri, E. Ioannou, A. Paganoni, A. Fantin, A. Cariboni, C. Ruhrberg
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
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
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
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
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
Cornelia de Lange Syndrome : from a disease to a broader spectrum
2021 A. Selicorni, M. Mariani, A. Lettieri, V. Massa
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
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
Gonadotropin-releasing hormone-secreting neuron development and function : an update
2022 A. Passarelli, A. Lettieri, T.N. Demirci, P. Magni
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
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
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
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