Sfoglia per SSD
La capacità di migrazione delle cellule di neuroblastoma umano è direttamente correlata all'espressione della proteina doublecortin, marker dell'aggressività tumorale
2005 E. Messi, M.C. Florian, R. Maggi, M.G. Zanisi
La divisione cellulare
2022 A. Poletti
La genetica delle malattie neurodegenerative : dal nervo periferico al cervello
2007 A. Poletti, E. Cattaneo
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA
2005 G. Soldà, R. Asselta, R. Ghiotto, M. Malcovati, M.L. Tenchini, G. Castaman, S. Duga
La progressione metastatica del cancro prostatico umano: effetto degli analoghi del GnRH sul sistema attivatore del plasminogeno
2005 D. Dondi, M. Piccolella, C. Festuccia, M. Bologna, M. Motta
Label-free mass spectrometry-based quantification of linker histone h1 variants in clinical samples
2020 R. Noberini, C.M. Torres, E.O. Savoia, S. Brandini, M.G. Jodice, G. Bertalot, G. Bonizzi, M. Capra, G. Diaferia, P. Scaffidi, T. Bonaldi
Lack of huntingtin promotes neural stem cells differentiation into glial cells while neurons expressing huntingtin with expanded polyglutamine tracts undergo cell death
2013 P. Conforti, S. Camnasio, C. Mutti, M. Valenza, M. Thompson, E. Fossale, S. Zeitlin, M.E. Macdonald, C. Zuccato, E. Cattaneo
Lack of movement in neurological diseases : effects on neurogenesis and muscle-nerve interaction
2016 D. Bottai, R. Adami, J. Pagano, M. Colombo, N. Platonova, R. Chiaramonte, R. Ghidoni, R.B.A.M.C. Bottinelli, M. Canepari
Lactic acid bacteria as potential probiotics for the pharyngeal mucosa
2011 V. Taverniti, M. Minuzzo, S. Arioli, M. Stuknytė, I. Zanoni, F. Granucci, M. Karp, D. Mora, S. Guglielmetti
Lactobacillus helveticus MIMLh5-Specific Antibodies for Detection of S-Layer Protein in Grana Padano Protected-Designation-of-Origin Cheese
2014 M. Stuknyte, E. Brockmann, T. Huovinen, S. Guglielmetti, D. Mora, V. Taverniti, S. Arioli, I. De Noni, U. Lamminmäki
Lag-time as a plasmatic oxidative stress marker associated with apoe4 carrier status in Alzheimer's disease patients
2019 L. Massaccesi, D. Galimberti, C. Fenoglio, M. Arcaro, A. Barassi, G. Goi, M.M. Corsi Romanelli, E. Galliera
Lag-time in Alzheimer's disease patients: A potential plasmatic oxidative stress marker associated with ApoE4 isoform
2019 L. Massaccesi, E. Galliera, D. Galimberti, C. Fenoglio, M. Arcaro, G. Goi, A. Barassi, M.M. Corsi Romanelli
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
Laminin 211 inhibits protein kinase A in Schwann cells to modulate neuregulin 1 type III-driven myelination
2017 M. Ghidinelli, Y. Poitelon, K. Shin Yoon, D. Ameroso, C. Williamson, C. Ferri, M. Pellegatta, K. Espino, A. Mogha, K. Monk, P. Podini, C. Taveggia, K. Nave, L. Wrabetz, T. Park Hwan, M. Feltri
A Laminin-2, Dystroglycan, Utrophin Axis Is Required for Compartmentalization and Elongation of Myelin Segments
2009 A. Court Felipe, E. Hewitt Jane, K. Davies, L. Patton Bruce, A. Uncini, L. Wrabetz, M. Feltri
Laminins and their receptors in Schwann cells and hereditary neuropathies
2005 M. Feltri, L. Wrabetz
LAMINOPATHIES: PATHOLOGY, CELL MECHANICS ANDENVIRONMENTAL INDUCTION.
2019 M.C. Lionetti
Language impairment in the genetic forms of behavioural variant frontotemporal dementia
2023 K. Samra, A.M. Macdougall, A. Bouzigues, M. Bocchetta, D.M. Cash, C.V. Greaves, R.S. Convery, J.C. van Swieten, H. Seelaar, L. Jiskoot, F. Moreno, R. Sanchez-Valle, R. Laforce, C. Graff, M. Masellis, M.C. Tartaglia, J.B. Rowe, B. Borroni, E. Finger, M. Synofzik, D. Galimberti, R. Vandenberghe, A. de Mendonça, C.R. Butler, A. Gerhard, S. Ducharme, I. Le Ber, P. Tiraboschi, I. Santana, F. Pasquier, J. Levin, M. Otto, S. Sorbi, J.D. Rohrer, L.L. Russell
Large and small extracellular vesicles may contribute to the propagation of ALS and FTD carrying toxic TDP species and potentially harmful miRNAs
2022 E. Casarotto, M. Garofalo, L. Messa, D. Sproviero, S. Carelli, M. Cozzi, M. Chierichetti, R. Cristofani, V. Ferrari, M. Galbiati, M. Piccolella, P. Rusmini, B. Tedesco, P. Pramaggiore, C. Cereda, S. Gagliardi, A. Poletti, V. Crippa
The large phenotypic spectrum of fabry disease requires graduated diagnosis and personalized therapy: A Meta-Analysis can help to differentiate missense mutations
2016 V. Citro, M. Cammisa, L. Liguori, C. Cimmaruta, J. Lukas, M. Vittoria, G. Andreotti
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