Pubblicazioni

Commentary: The histone demethylase Phf2 acts as a molecular checkpoint to prevent NAFLD progression during obesity

2018 - FRONTIERS IN GENETICS

Barbaro, Barbara; Romito, Ilaria; Alisi, Anna

MTHFR, TS and XRCC1 genetic variants may affect survival in patients with myelodysplastic syndromes treated with supportive care or azacitidine

2018 - PHARMACOGENOMICS JOURNAL

Visani, G.; Loscocco, F.; Ruzzo, A.; Galimberti, S.; Graziano, F.; Voso, M. T.; Giacomini, E.; Finelli, C.; Ciabatti, E.; Fabiani, E.; Barulli, S.; Volpe, A.; Magro, D.; Piccaluga, P.; Fuligni, F.; Vignetti, M.; Fazi, P.; Piciocchi, A.; Gabucci, E.; Rocchi, M.; Magnani, M.; Isidori, A.

Clinical and biochemical features of different molecular etiologies of familial chylomicronemia

2018 - JOURNAL OF CLINICAL LIPIDOLOGY

Hegele, Ra; Amanda J., Berberich AJ; Ban, Mr; Wang, J; Digenio, A; Alexander, Vj; DâErasmo, L; Arca, M; Jones, A; Bruckert, E; Stroes, Es; Bergeron, J; Civeira, F; Witztum, Jl; Gaudet, D

Mycobacterium tuberculosis-induced miR-155 subverts autophagy by targeting ATG3 in human dendritic cells

2018 - PLOS PATHOGENS

Etna, Marilena P.; Sinigaglia, Alessandro; Grassi, Angela; Giacomini, Elena; Romagnoli, Alessandra; Pardini, Manuela; Severa, Martina; Cruciani, Melania; Rizzo, Fabiana; Anastasiadou, Eleni; Di Camillo, Barbara; Barzon, Luisa; Fimia, Gian Maria; Manganelli, Riccardo; Coccia, Eliana M.

Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome

2018 - EUROPEAN JOURNAL OF MEDICAL GENETICS

Unolt, Marta; Barry, Jessica; Digilio, Maria Cristina; Marino, Bruno; Bassett, Anne; Oechslin, Erwin; Low, David W.; Belasco, Jean B.; Kallish, Staci; Sullivan, Kathleen; Zackai, Elaine H.; McDonald-McGinn, Donna M.

Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome

2018 - EUROPEAN JOURNAL OF HUMAN GENETICS

Brancati, Francesco; Camerota, Letizia; Colao, Emma; Vega-Warner, Virginia; Zhao, Xiangzhong; Zhang, Ruixiao; Bottillo, Irene; Castori, Marco; Caglioti, Alfredo; Sangiuolo, Federica; Novelli, Giuseppe; Perrotti, Nicola; Otto, Edgar A.; Taruscio, Domenica; Salvatore, Marco; De Stefano, Maria Chiara; Censi, Federica; Floridia, Giovanna; Brancati, Francesco; Daina, Erica; Iatropoulos, Paraskevas; Ferlini, Alessandra; Roccatello, Dario; Baldovino, Simone; Menegatti, Elisa; Bembi, Bruno

Dissecting the Functional Consequences of De Novo DNA Methylation Dynamics in Human Motor Neuron Differentiation and Physiology

2018 - CELL STEM CELL

Ziller, Michael J.; Ortega, Juan A.; Quinlan, Katharina A.; Santos, David P.; Gu, Hongcang; Martin, Eric J.; Galonska, Christina; Pop, Ramona; Maidl, Susanne; Di Pardo, Alba; Huang, Mei; Meltzer, Herbert Y.; Gnirke, Andreas; Heckman, C. J.; Meissner, Alexander; Kiskinis, Evangelos

How to assess drug resistance in cancer stem cells

2018 - Methods in Molecular Biology

De Angelis, Maria Laura; De Maria, Ruggero; Baiocchi, Marta

A multilocus view on Mediterranean aeolid nudibranchs (Mollusca): Systematics and cryptic diversity of Flabellinidae and Piseinotecidae

2018 - MOLECULAR PHYLOGENETICS AND EVOLUTION

Furfaro, Giulia; Salvi, Daniele; Mancini, Emiliano; Mariottini, Paolo

Development of amine-oxidase-based biosensors for spermine and spermidine analysis

2018 - Polyamines. Methods in Molecular Biology

Tortolini, Cristina; Favero, Gabriele; Mazzei, Franco

Genetics of rotator cuff tears: No association of col5a1 gene in a case-control study

2018 - BMC MEDICAL GENETICS

Longo, U. G.; Margiotti, K.; Petrillo, S.; Rizzello, G.; Fusilli, C.; Maffulli, N.; De Luca, A.; Denaro, V.