检索结果 - Paola Fortugno

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    Proteolytic Activation Cascade of the Netherton Syndrome–Defective Protein, LEKTI, in the Epidermis: Implications for Skin Homeostasis

    Proteolytic Activation Cascade of the Netherton Syndrome–Defective Protein, LEKTI, in the Epidermis: Implications for Skin Homeostasis 由 Paola Fortugno, Alberto Bresciani, Chantal Paolini, Chiara Pazzagli, May El Hachem, Marina D’Alessio, Giovanna Zambruno

    出版 2011
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis

    The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis 由 Paola Fortugno, Laetitia Furio, Massimo Teson, M. Berretti, May El Hachem, Giovanna Zambruno, Alain Hovnanian, Marina D’Alessio

    出版 2012
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    Regulation of survivin function by Hsp90

    Regulation of survivin function by Hsp90 由 Paola Fortugno, Elena Beltrami, Janet Plescia, Jason Fontana, Deepti Pradhan, Pier Carlo Marchisio, William C. Sessa, Dario C. Altieri

    出版 2003
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  4. 4
    Full Sequencing of the FLG Gene in Italian Patients with Atopic Eczema: Evidence of New Mutations, but Lack of an Association

    Full Sequencing of the FLG Gene in Italian Patients with Atopic Eczema: Evidence of New Mutations, but Lack of an Association 由 Raffaella Cascella, Valeria Foti Cuzzola, Tiziana Lepre, Elena Galli, Viviana Moschese, L Chini, Chiara Maria Mazzanti, Paola Fortugno, Giuseppe Novelli, Emiliano Giardina

    出版 2011
    获取全文
    Carta
    加到收藏夹
    Saved in:
  5. 5
    Identification of tumor‐associated antigens by screening phage‐displayed human cDNA libraries with sera from tumor patients

    Identification of tumor‐associated antigens by screening phage‐displayed human cDNA libraries with sera from tumor patients 由 Olga Minenkova, Andrea Pucci, Emiliano Pavoni, Amedeo De Tomassi, Paola Fortugno, Nicola Gargano, Maurizio Cianfriglia, Stefano Barca, Sabino De Placido, Angelo Martignetti, Franco Felici, Riccardo Cortese, Paolo Monaci

    出版 2003
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  6. 6
    Rational design of shepherdin, a novel anticancer agent

    Rational design of shepherdin, a novel anticancer agent 由 Janet Plescia, Whitney Salz, Fang Xia, Marzia Pennati, Nadia Zaffaroni, Maria Grazia Daidone, Massimiliano Meli, Takehiko Dohi, Paola Fortugno, Yulia Nefedova, Dmitry I. Gabrilovich, Giorgio Colombo, Dario C. Altieri

    出版 2005
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  7. 7
    Chemerin expression marks early psoriatic skin lesions and correlates with plasmacytoid dendritic cell recruitment

    Chemerin expression marks early psoriatic skin lesions and correlates with plasmacytoid dendritic cell recruitment 由 Cristina Albanesi, Claudia Scarponi, Sabatino Pallotta, Roberta Daniele, Daniela Bosisio, Stefania Madonna, Paola Fortugno, Safiyè Gonzalvo-Feo, Jean‐Denis Franssen, Marc Parmentier, Ornella De Pità, Giampiero Girolomoni, Silvano Sozzani

    出版 2008
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome

    Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome 由 Francesco Brancati, Paola Fortugno, Irene Bottillo, Marc Lopez, Emmanuelle Josselin, O Boudghène-Stambouli, Emanuele Agolini, Laura Bernardini, Emanuele Bellacchio, Miriam Iannicelli, Alfredo Rossi, A. Dib-Lachachi, Liborio Stuppia, Giandomenico Palka, Stefan Mundlos, Sigmar Stricker, Uwe Kornak, Giovanna Zambruno, Bruno Dallapiccola

    出版 2010
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  9. 9
    De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway

    De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway 由 Asif, Maria, Kaygusuz, Emrah, Shinawi, Marwan, Nickelsen, Anna, Hsieh, Tzung-Chien, Wagle, Prerana, Budde, Birgit S., Hochscherf, Jennifer, Abdullah, Uzma, Höning, Stefan, Nienberg, Christian, Lindenblatt, Dirk, Noegel, Angelika A., Altmüller, Janine, Thiele, Holger, Motameny, Susanne, Fleischer, Nicole, Segal, Idan, Pais, Lynn, Tinschert, Sigrid, Samra, Nadra Nasser, Savatt, Juliann M., Rudy, Natasha L., De Luca, Chiara, Paola Fortugno, White, Susan M., Krawitz, Peter, Hurst, Anna C.E., Niefind, Karsten, Jose, Joachim, Brancati, Francesco, Nürnberg, Peter, Hussain, Muhammad Sajid

    出版 2022
    获取全文 获取全文 获取全文
    Text
    加到收藏夹
    Saved in:

检索工具: