Search Results - "PIZZIGONI, Alessandro"

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  1. 1

    The primate-specific protein TBC1D3 is required for optimal macropinocytosis in a novel ARF6-dependent pathway by Frittoli, Emanuela, Palamidessi, Andrea, Pizzigoni, Alessandro, Lanzetti, Letizia, Garrè, Massimiliano, Troglio, Flavia, Troilo, Albino, Fukuda, Mitsunori, Di Fiore, Pier Paolo, Scita, Giorgio, Confalonieri, Stefano

    Published in Molecular biology of the cell (01-04-2008)
    “…The generation of novel genes and proteins throughout evolution has been proposed to occur as a result of whole genome and gene duplications, exon shuffling,…”
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    Journal Article
  2. 2

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

    Published in Genomics (San Diego, Calif.) (15-05-2000)
    “…A gene responsible for an autosomal recessive form of hereditary spastic paraplegia (SPG7) was recently identified. This gene encodes paraplegin, a…”
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    Journal Article
  3. 3

    Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1 by 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

    Published in Human molecular genetics (22-11-2000)
    “…Ocular albinism type I (OA1) is an X-linked disorder characterized by severe reduction of visual acuity, strabismus, photophobia and nystagmus. Ophthalmologic…”
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    Journal Article
  4. 4

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

    Published in Human molecular genetics (12-12-2000)
    “…Ocular albinism type 1 (OA1) is an X-linked disorder mainly characterized by a severe reduction of visual acuity, hypopigmentation of the retina and the…”
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    Journal Article
  5. 5

    A New Prenylated Flavone fromArctocarpus champedenInhibits the K+-Dependent Amino Acid Transport inBombyx moriMidgut by Parenti, Paolo, Pizzigoni, Alessandro, Hanozet, Giorgio, Hakim, Euis Holisotan, Makmur, Lukman, Achmad, Sjamsul Arifin, Giordana, Barbara

    “…The effect of some flavonoids on the K+-dependent and K+-independent leucine uptake into brush border membrane vesicles fromBombyx morilarval midgut was…”
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    Journal Article