Laura Fontana
Laura Fontana
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Citata da
Citata da
Genetics of mayer–rokitansky–küster–hauser (MRKH) syndrome
L Fontana, B Gentilin, L Fedele, C Gervasini, M Miozzo
Clinical genetics 91 (2), 233-246, 2017
Fragile X syndrome: a review of clinical and molecular diagnoses
C Ciaccio, L Fontana, D Milani, S Tabano, M Miozzo, S Esposito
Italian journal of pediatrics 43, 1-12, 2017
Decreased serum level of sphingosine‐1‐phosphate: a novel predictor of clinical severity in COVID‐19
G Marfia, S Navone, L Guarnaccia, R Campanella, M Mondoni, ...
EMBO molecular medicine 13 (1), e13424, 2021
Mitochondrial DNA content and methylation in fetal cord blood of pregnancies with placental insufficiency
C Novielli, C Mandò, S Tabano, GM Anelli, L Fontana, P Antonazzo, ...
Placenta 55, 63-70, 2017
The genetic landscape of human glioblastoma and matched primary cancer stem cells reveals intratumour similarity and intertumour heterogeneity
C Pesenti, SE Navone, L Guarnaccia, A Terrasi, J Costanza, R Silipigni, ...
Stem cells international 2019, 2019
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics
D Rovina, L Fontana, L Monti, C Novielli, N Panini, SM Sirchia, E Erba, ...
European journal of cell biology 93 (8-9), 355-365, 2014
Angiogenesis in human brain tumors: Screening of drug response through a patient-specific cell platform for personalized therapy
L Guarnaccia, SE Navone, E Trombetta, C Cordiglieri, A Cherubini, ...
Scientific reports 8 (1), 8748, 2018
Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi
L Paganini, N Carlessi, L Fontana, R Silipigni, S Motta, S Fiori, S Guerneri, ...
Epigenetics 10 (7), 643-649, 2015
Molecular insights into the classification of luminal breast cancers: The genomic heterogeneity of progesterone-negative tumors
G Lopez, J Costanza, M Colleoni, L Fontana, S Ferrero, M Miozzo, ...
International Journal of Molecular Sciences 20 (3), 510, 2019
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15. 5 related imprinting disorders
L Fontana, MF Bedeschi, S Maitz, A Cereda, C Faré, S Motta, A Seresini, ...
Epigenetics 13 (9), 897-909, 2018
Rothmund-Thomson syndrome: insights from new patients on the genetic variability underpinning clinical presentation and cancer outcome
EA Colombo, A Locatelli, L Cubells Sanchez, S Romeo, NH Elcioglu, ...
International Journal of Molecular Sciences 19 (4), 1103, 2018
Differential signature of the centrosomal MARK4 isoforms in glioma
I Magnani, C Novielli, L Fontana, S Tabano, D Rovina, RF Moroni, ...
Analytical Cellular Pathology 34 (6), 319-338, 2011
Clinical and molecular diagnosis of Beckwith-Wiedemann Syndrome with single-or multi-locus imprinting disturbance
L Fontana, S Tabano, S Maitz, P Colapietro, E Garzia, AG Gerli, ...
International journal of molecular sciences 22 (7), 3445, 2021
Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status
C Pesenti, L Paganini, L Fontana, E Veniani, L Runza, S Ferrero, S Bosari, ...
Oncotarget 8 (34), 57134, 2017
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer
J Azzollini, C Pesenti, S Pizzamiglio, L Fontana, C Guarino, B Peissel, ...
Cancers 11 (1), 58, 2019
Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund–Thomson Syndrome sibs with mild phenotype
EA Colombo, L Fontana, G Roversi, G Negri, D Castiglia, M Paradisi, ...
European Journal of Human Genetics 22 (11), 1298-1304, 2014
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion
L Fontana, S Tabano, E Bonaparte, G Marfia, C Pesenti, R Falcone, ...
J Neuropathol Exp Neurol 75 (8), 791-800, 2016
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls
S Tabano, A Caldiroli, A Terrasi, P Colapietro, S Grassi, GS Carnevali, ...
European Archives of Psychiatry and Clinical Neuroscience 270, 893-900, 2020
A HS6ST2 gene variant associated with X‐linked intellectual disability and severe myopia in two male twins
L Paganini, LA Hadi, M Chetta, D Rovina, L Fontana, P Colapietro, ...
Clinical genetics 95 (3), 368-374, 2019
Familial gastrointestinal stromal tumors, lentigines, and café‐au‐lait macules associated with germline c‐kit mutation treated with imatinib
D Gupta, L Chandrashekar, L Larizza, EA Colombo, L Fontana, ...
International Journal of Dermatology 56 (2), 195-201, 2017
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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