The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells von Palmisano, Ilaria, Bagnato, Paola, Palmigiano, Angela, Innamorati, Giulio, Rotondo, Giuseppe, Altimare, Domenico, Venturi, Consuelo, Sviderskaya, Elena V., Piccirillo, Rosanna, Coppola, Massimiliano, Marigo, Valeria, Incerti, Barbara, Ballabio, Andrea, Surace, Enrico M., Tacchetti, Carlo, Bennett, Dorothy C., Schiaffino, Maria Vittoria

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Identification and Characterization of YME1L1, a Novel Paraplegin-Related Gene von Coppola, Massimiliano, Pizzigoni, Alessandro, Banfi, Sandro, Bassi, Maria Teresa, Casari, Giorgio, Incerti, Barbara

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The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells von Palmisano, Ilaria, Bagnato, Paola, Palmigiano, Angela, Innamorati, Giulio, Rotondo, Giuseppe, Altimare, Domenico, Venturi, Consuelo, Sviderskaya, Elena V, Piccirillo, Rosanna, Coppola, Massimiliano, Marigo, Valeria, Incerti, Barbara, Ballabio, Andrea, Surace, Enrico M, Tacchetti, Carlo, Bennett, Dorothy C, Schiaffino, Maria Vittoria

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Cloning of the Human Interferon-Related Developmental Regulator (IFRD1) Gene Coding for the PC4 Protein, a Member of a Novel Family of Developmentally Regulated Genes von Buanne, Pasquale, Incerti, Barbara, Guardavaccaro, Daniele, Avvantaggiato, Virginia, Simeone, Antonio, Tirone, Felice

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The Gene Encoding a Cationic Amino Acid Transporter (SLC7A4) Maps to the Region Deleted in the Velocardiofacial Syndrome von Sperandeo, Maria Pia, Borsani, Giuseppe, Incerti, Barbara, Zollo, Massimo, Rossi, Elena, Zuffardi, Orsetta, Castaldo, Pasqualina, Taglialatela, Maurizio, Andria, Generoso, Sebastio, Gianfranco

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SLC7A7 , encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance von Borsani, Giuseppe, Sebastio, Gianfranco, Bassi, Maria Teresa, Sperandeo, Maria Pia, Grandi, Alessandro De, Buoninconti, Anna, Riboni, Mirko, Manzoni, Marta, Incerti, Barbara, Pepe, Antonio, Andria, Generoso, Ballabio, Andrea

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Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1 von INCERTI, Barbara, CORTESE, Katia, MARIGO, Valeria, SCHIAFFINO, Maria Vittoria, TACCHETTI, Carlo, BALLABIO, Andrea, PIZZIGNOI, Alessandro, SURACE, Enrico M, VARANI, Simona, COPPOLA, Massimiliano, JEFFERY, Glen, SEELIGER, Mathias, JAISSLE, Gesine, BENNETT, Dorothy C

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules von Franco, Brunella, Guioli, Silvana, Pragliola, Antonella, Incerti, Barbara, Bardoni, Barbara, Tonlorenzi, Rossana, Carrozzo, Romeo, Maestrini, Elena, Pieretti, Maura, Taillon-Miller, Patricia, Brown, Carolyn J, Willard, Huntington F, Lawrence, Charles, Persico, M. Graziella, Camerino, Giovanna, Ballabio, Andrea

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Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1 von D'ADDIO, Marilena, PIZZIGONI, Alessandro, BASSI, Maria Teresa, BASCHIROTTO, Cinzia, VALETTI, Caterina, INCERTI, Barbara, CLEMENTI, Maurizio, DE LUCA, Michele, BALLABIO, Andrea, SCHIAFFINO, Maria Vittoria

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Structure of the SLC7A7 Gene and Mutational Analysis of Patients Affected by Lysinuric Protein Intolerance von Sperandeo, Maria Pia, Bassi, Maria Teresa, Riboni, Mirko, Parenti, Giancarlo, Buoninconti, Anna, Manzoni, Marta, Incerti, Barbara, Larocca, Maria Rosaria, Di Rocco, Maja, Strisciuglio, Pietro, Dianzani, Irma, Parini, Rossella, Candito, Miranda, Endo, Fumio, Ballabio, Andrea, Andria, Generoso, Sebastio, Gianfranco, Borsani, Giuseppe

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Intragenic Deletion of the KALIG-1 Gene in Kallmann's Syndrome von Bick, David, Franco, Brunella, Sherins, Richard J, Heye, Babette, Pike, Lisa, Crawford, John, Maddalena, Anne, Incerti, Barbara, Pragliola, Antonella, Meitinger, Thomas, Ballabio, Andrea

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Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course von Parenti, Giancarlo, Sebastio, Gianfranco, Strisciuglio, Pietro, Incerti, Barbara, Pecoraro, Carmine, Terracciano, Luigi, Andria, Generoso

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SLC7A8, a Gene Mapping within the Lysinuric Protein Intolerance Critical Region, Encodes a New Member of the Glycoprotein-Associated Amino Acid Transporter Family von Bassi, Maria Teresa, Sperandeo, Maria Pia, Incerti, Barbara, Bulfone, Alessandro, Pepe, Antonio, Surace, Enrico Maria, Gattuso, Claudio, De Grandi, Alessandro, Buoninconti, Anna, Riboni, Mirko, Manzoni, Marta, Andria, Generoso, Ballabio, Andrea, Borsani, Giuseppe, Sebastio, Gianfranco

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Structure of the mouse growth/differentiation factor 9 gene von Incerti, Barbara, Dong, Jinwen, Borsani, Giuseppe, Matzuk, Martin M.

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The delta F508 mutation in cystic fibrosis patients of southern Italy von Sebastio, G, Castiglione, O, Incerti, B, Salvatore, D, Santamaria, F

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Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome von Bick, D, Franco, B, Sherins, R J, Heye, B, Pike, L, Crawford, J, Maddalena, A, Incerti, B, Pragliola, A, Meitinger, T, Ballabio, A

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Brief Report: Intragenic Deletion of the Kalig-I Gene in Kallmannʼs Syndrome von BICK, DAVID, FRANCO, BRUNELLA, SHERINS, RICHARD J, HEYE, BABETTE, PIKE, LISA, CRAWFORD, JOHN, MADDALENA, ANNE, INCERTI, BARBARA, PRAGLIOLA, ANTONELLA, MEITINGER, THOMAS, BALLABIO, ANDREA

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Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene von Parenti, Giancarlo, Rizzolo, Maria Grazia, Ghezzi, Monica, Maio, Salvatore Di, Sperandeo, Maria Pia, Incerti, Barbara, Franco, Brunella, Ballabio, Andrea, Andria, Generoso

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Dual-Task Performance in Multiple Sclerosis' Patients: Cerebellum Matters? von Argento, Ornella, Spanò, Barbara, Pisani, Valerio, Incerti, Chiara C, Bozzali, Marco, Foti, Calogero, Caltagirone, Carlo, Nocentini, Ugo

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Dose point kernels in liquid water: An intra-comparison between GEANT4-DNA and a variety of Monte Carlo codes von Champion, C., Incerti, S., Perrot, Y., Delorme, R., Bordage, M.C., Bardiès, M., Mascialino, B., Tran, H.N., Ivanchenko, V., Bernal, M., Francis, Z., Groetz, J.-E., Fromm, M., Campos, L.

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