High-level semi-synthetic production of the potent antimalarial artemisinin von Paddon, C. J., Westfall, P. J., Pitera, D. J., Benjamin, K., Fisher, K., McPhee, D., Leavell, M. D., Tai, A., Main, A., Eng, D., Polichuk, D. R., Teoh, K. H., Reed, D. W., Treynor, T., Lenihan, J., Jiang, H., Fleck, M., Bajad, S., Dang, G., Dengrove, D., Diola, D., Dorin, G., Ellens, K. W., Fickes, S., Galazzo, J., Gaucher, S. P., Geistlinger, T., Henry, R., Hepp, M., Horning, T., Iqbal, T., Kizer, L., Lieu, B., Melis, D., Moss, N., Regentin, R., Secrest, S., Tsuruta, H., Vazquez, R., Westblade, L. F., Xu, L., Yu, M., Zhang, Y., Zhao, L., Lievense, J., Covello, P. S., Keasling, J. D., Reiling, K. K., Renninger, N. S., Newman, J. D.

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CCDC15 localizes to the centriole inner scaffold and controls centriole length and integrity von Arslanhan, Melis D, Cengiz-Emek, Seyma, Odabasi, Ezgi, Steib, Emmanuelle, Hamel, Virginie, Guichard, Paul, Firat-Karalar, Elif Nur

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Aurora Kinase A proximity map reveals centriolar satellites as regulators of its ciliary function von Arslanhan, Melis D, Rauniyar, Navin, Yates, John R, Firat-Karalar, Elif N

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Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity von Siano, M. A., Marchetti, Pagano, S., Di Candia, F., Alessio, M., De Brasi, D., De Luca, A., Pinna, Sestito, S., Concolino, D., Tartaglia, M., Strisciuglio, P., D'Esposito, Cabaro, S., Perruolo, G., Formisano, P., Melis, D.

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CCDC57 Cooperates with Microtubules and Microcephaly Protein CEP63 and Regulates Centriole Duplication and Mitotic Progression von Gurkaslar, H. Kubra, Culfa, Efraim, Arslanhan, Melis D., Lince-Faria, Mariana, Firat-Karalar, Elif Nur

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Endocrine system involvement in patients with RASopathies: A case series von Siano, M A, Pivonello, R, Salerno, M, Falco, M, Mauro, C, De Brasi, D, Klain, A, Sestito, S, De Luca, A, Pinna, V, Simeoli, C, Concolino, D, Mainolfi, Ciro Gabriele, Mannarino, T, Strisciuglio, P, Tartaglia, M, Melis, D

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In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) von Ranieri, C., Di Tommaso, S., Loconte, D. C., Grossi, V., Sanese, P., Bagnulo, R., Susca, F. C., Forte, G., Peserico, A., De Luisi, A., Bartuli, A., Selicorni, A., Melis, D., Lerone, M., Praticò, A. D., Abbadessa, G., Yu, Y., Schwartz, B., Ruggieri, Martino, Simone, Cristiano, Resta, Nicoletta

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Direct interaction between exocyst and Wave complexes promotes cell protrusions and motility von Biondini, Marco, Sadou-Dubourgnoux, Amel, Paul-Gilloteaux, Perrine, Zago, Giulia, Arslanhan, Melis D, Waharte, François, Formstecher, Etienne, Hertzog, Maud, Yu, Jinchao, Guerois, Raphael, Gautreau, Alexis, Scita, Giorgio, Camonis, Jacques, Parrini, Maria Carla

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Estimated glomerular filtration rate, albuminuria and mortality in type 2 diabetes: the Casale Monferrato study von Bruno, G, Merletti, F, Bargero, G, Novelli, G, Melis, D, Soddu, A, Perotto, M, Pagano, G, Cavallo-Perin, P

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Fetal growth patterns in Beckwith-Wiedemann syndrome von Mussa, A., Russo, S., de Crescenzo, A., Freschi, A., Calzari, L., Maitz, S., Macchiaiolo, M., Molinatto, C., Baldassarre, G., Mariani, M., Tarani, L., Bedeschi, M.F., Milani, D., Melis, D., Bartuli, A., Cubellis, M.V., Selicorni, A., Silengo, M.C., Larizza, L., Riccio, A., Ferrero, G.B.

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Aarskog-Scott syndrome: Clinical update and report of nine novel mutations of the FGD1 gene von Orrico, A., Galli, L., Faivre, L., Clayton-Smith, J., Azzarello-Burri, S.M., Hertz, J.M., Jacquemont, S., Taurisano, R., Arroyo Carrera, I., Tarantino, E., Devriendt, K., Melis, D., Thelle, T., Meinhardt, U., Sorrentino, V.

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Impaired Bone Metabolism in Glycogen Storage Disease Type 1 Is Associated with Poor Metabolic Control in Type 1a and with Granulocyte Colony-Stimulating Factor Therapy in Type 1b von Melis, D., Pivonello, R., Cozzolino, M., Della Casa, R., Balivo, F., Del Puente, A., Dionisi-Vici, C., Cotugno, G., Zuppaldi, C., Rigoldi, M., Parini, R., Colao, A., Andria, G., Parenti, G.

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Noonan‐like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations von Capalbo, D., Melis, D., De Martino, L., Palamaro, L., Riccomagno, S., Bona, G., Cordeddu, V., Pignata, C., Salerno, M.

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Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotype von Cappuccio, G., Ginocchio, V.M., Maffè, A., Ungari, S., Andria, G., Melis, D.

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Sensorineural Hearing Loss in a Patient Affected by Congenital Cytomegalovirus Infection: Is It Useful to Identify Comorbid Pathologies? von Fontana, P., Melis, D., D'Amico, A., Cappuccio, G., Auletta, G., Vassallo, P., Genesio, R., Nitsch, L., Buffolano, W.

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Efficacy of ACE-inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study von Melis, D., Parenti, G., Gatti, R., Casa, R. Della, Parini, R., Riva, E., Burlina, A. B., Vici, C. Dionisi, Di Rocco, M., Furlan, F., Torcoletti, M., Papadia, F., Donati, A., Benigno, V., Andria, G.

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Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b von Melis, D., Della Casa, R., Parini, R., Rigoldi, M., Cacciapuoti, C., Marcolongo, P., Benedetti, A., Gaudieri, V., Andria, G., Parenti, G.

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Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL von Lucchiari, S., Pagliarani, S., Salani, S., Filocamo, M., Di Rocco, M., Melis, D., Rodolico, C., Musumeci, O., Toscano, A., Bresolin, N., Comi, G.P.

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Crohn's-like ileo-colitis in patients affected by glycogen storage disease Ib: two years' follow-up of patients with a wide spectrum of gastrointestinal signs von MELIS, D, PARENTI, G, DELLA CASA, R, SIBILIO, M, BERNI CANANI, R, TERRIN, G, CUCCHIARA, S, ANDRIA, G

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Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases von Verloes, Alain, Di Donato, Nataliya, Masliah-Planchon, Julien, Jongmans, Marjolijn, Abdul-Raman, Omar A, Albrecht, Beate, Allanson, Judith, Brunner, Han, Bertola, Debora, Chassaing, Nicolas, David, Albert, Devriendt, Koen, Eftekhari, Pirayeh, Drouin-Garraud, Valérie, Faravelli, Francesca, Faivre, Laurence, Giuliano, Fabienne, Guion Almeida, Leina, Juncos, Jorge, Kempers, Marlies, Eker, Hatice Koçak, Lacombe, Didier, Lin, Angela, Mancini, Grazia, Melis, Daniela, Lourenço, Charles Marques, Siu, Victoria Mok, Morin, Gilles, Nezarati, Marjan, Nowaczyk, Malgorzata J M, Ramer, Jeanette C, Osimani, Sara, Philip, Nicole, Pierpont, Mary Ella, Procaccio, Vincent, Roseli, Zeichi-Seide, Rossi, Massimiliano, Rusu, Cristina, Sznajer, Yves, Templin, Ludivine, Uliana, Vera, Klaus, Mirjam, Van Bon, Bregje, Van Ravenswaaij, Conny, Wainer, Bruce, Fry, Andrew E, Rump, Andreas, Hoischen, Alexander, Drunat, Séverine, Rivière, Jean-Baptiste, Dobyns, William B, Pilz, Daniela T

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