Sfoglia per Autore
MARK4 : a tricky balance of L and S isoforms rules glial differentiation and glioma progression
2010 I. Magnani, C. Novielli, S. Tabano, L. Fontana, R.F. Moroni, E.A. Colombo, L. Monti, L. Bello, D. Bauer, S. Mazzoleni, R. Galli, G. Porta, C. Frassoni, L. Larizza
Differential signature of the centrosomal MARK4 isoforms in glioma
2011 I. Magnani, C. Novielli, L. Fontana, S. Tabano, D. Rovina, R.F. Moroni, D. Bauer, S. Mazzoleni, E.A. Colombo, G. Tedeschi, L. Monti, G. Porta, S. Bosari, C. Frassoni, R. Galli, L. Bello, L. Larizza
SINDROME DI ROTHMUND-THOMSON: CARATTERIZZAZIONE CLINICO-MOLECOLARE DI TRE NUOVI PAZIENTI
2012 E.A. Colombo, L. Fontana, G. Roversi, G. Negri, M. Paradisi, D. Castiglia, A. Locatelli, G. Zambruno, L. Larizza
ANALISI SEMIQUANTITATIVA DELL’ESPRESSIONE DELLE ISOFORME DEL GENE C16orf57 IN UN PANNELLO DI LINEE CELLULARI E TESSUTI ED IN PAZIENTI CON POICHILODERMA CON NEUTROPENIA
2012 L. Fontana, G. Negri, E.A. Colombo, L. Larizza
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics
2014 D. Rovina, L. Fontana, L. Monti, C. Novielli, N. Panini, S.M. Sirchia, E. Erba, I. Magnani, L. Larizza
SWITCH TO THE L ISOFORM OF THE MAP/MICROTUBULE AFFINITY-REGULATING KINASE 4 (MARK4) GENE, MAINLY EXPRESSED IN HUMAN GLIOMA, VIA PRE-MRNA ALTERNATIVE SPLICING MODULATED BY POLYPYRIMIDINE TRACT-BINDING PROTEIN (PTB)
2014 L. Fontana
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund-Thomson Syndrome sibs with mild phenotype
2014 E.A. Colombo, L. Fontana, G. Roversi, G. Negri, D. Castiglia, M. Paradisi, G. Zambruno, L. Larizza
Suggestive evidence on the involvement of polypyrimidine-tract binding protein in regulating alternative splicing of MAP/microtubule affinity-regulating kinase 4 in glioma
2015 L. Fontana, D. Rovina, C. Novielli, E. Maffioli, G. Tedeschi, I. Magnani, L. Larizza
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi
2015 L. Paganini, N. Carlessi, L. Fontana, R. Silipigni, S. Motta, S. Fiori, S. Guerneri, F. Lalatta, A. Cereda, S. Sirchia, M. Miozzo, S. Tabano
Expanding the role of the splicing USB1 gene from Poikiloderma with Neutropenia to acquired myeloid neoplasms
2015 G. Negri, B. Crescenzi, E.A. Colombo, L. Fontana, G. Barba, F. Arcioni, C. Gervasini, C. Mecucci, L. Larizza
A zebrafish model of Poikiloderma with Neutropenia recapitulates the human syndrome hallmarks and traces back neutropenia to the myeloid progenitor
2015 E.A. Colombo, S. Carra, L. Fontana, E. Bresciani, F. Cotelli, L. Larizza
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion
2016 L. Fontana, S. Tabano, E. Bonaparte, G. Marfia, C. Pesenti, R. Falcone, C. Augello, N. Carlessi, R. Silipigni, S. Guerneri, R. Campanella, M. Caroli, S.M. Sirchia, S. Bosari, M. Miozzo
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
2016 L. Fontana, B. Gentilin, L. Fedele, C. Gervasini, M. Miozzo
Familial gastrointestinal stromal tumors, lentigines, and café-au-lait macules associated with germline c-kit mutation treated with imatinib
2017 D. Gupta, L. Chandrashekar, L. Larizza, E.A. Colombo, L. Fontana, C. Gervasini, D.M. Thappa, M. Rajappa, K.S. Rajendiran, G.S. Sreenath, V. Kate
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies
2017 J. Azzollini, C. Pesenti, L. Ferrari, L. Fontana, M. Calvello, B. Peissel, G. Portera, S. Tabano, M.L. Carcangiu, P. Riva, M. Miozzo, S. Manoukian
Fragile X syndrome : A review of clinical and molecular diagnoses
2017 C. Ciaccio, L. Fontana, D. Milani, S. Tabano, M. Miozzo, S. Esposito
Mitochondrial DNA content and methylation in fetal cord blood of pregnancies with placental insufficiency
2017 C. Novielli, C. Mandò, S. Tabano, G.M. Anelli, L. Fontana, P. Antonazzo, M. Miozzo, I. Cetin
Mass spectrometry-based assay for the molecular diagnosis of glioma : Concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status
2017 C. Pesenti, L. Paganini, L. Fontana, E. Veniani, R. Letterio, S. Ferrero, S. Bosari, M. Maura, G. Marfia, C. Manuela, R. Silipigni, G. Silvana, S. Tabano, M. Miozzo
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases
2017 B. Maria Francesca, M. Calvello, L. Paganini, L. Pezzani, M. Baccarin, L. Fontana, S.M. Sirchia, G. Silvana, L. Canazza, L. Ernesto, L.L. Colombo, L. Faustina, F. Mosca, S.M. Tabano, M.R. Miozzo
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
2018 L. Fontana, M. Bedeschi, S. Maitz, A. Cereda, C. Faré, S. Motta, A. Seresini, P. D'Ursi, A. Orro, V. Pecile, M. Calvello, A. Selicorni, F. Lalatta, D. Milani, S. Sirchia, M. Miozzo, S. Tabano
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