نتائج البحث - Paola Fortugno
- يعرض 1 - 9 نتائج من 9
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Proteolytic Activation Cascade of the Netherton Syndrome–Defective Protein, LEKTI, in the Epidermis: Implications for Skin Homeostasis حسب Paola Fortugno, Alberto Bresciani, Chantal Paolini, Chiara Pazzagli, May El Hachem, Marina D’Alessio, Giovanna Zambruno
منشور في 2011Artigo -
2
The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis حسب Paola Fortugno, Laetitia Furio, Massimo Teson, M. Berretti, May El Hachem, Giovanna Zambruno, Alain Hovnanian, Marina D’Alessio
منشور في 2012Artigo -
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4
Full Sequencing of the FLG Gene in Italian Patients with Atopic Eczema: Evidence of New Mutations, but Lack of an Association حسب Raffaella Cascella, Valeria Foti Cuzzola, Tiziana Lepre, Elena Galli, Viviana Moschese, L Chini, Chiara Maria Mazzanti, Paola Fortugno, Giuseppe Novelli, Emiliano Giardina
منشور في 2011Carta -
5
Identification of tumor‐associated antigens by screening phage‐displayed human cDNA libraries with sera from tumor patients حسب 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
منشور في 2003Artigo -
6
Rational design of shepherdin, a novel anticancer agent حسب 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
منشور في 2005Artigo -
7
Chemerin expression marks early psoriatic skin lesions and correlates with plasmacytoid dendritic cell recruitment حسب 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
منشور في 2008Artigo -
8
Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome حسب 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
منشور في 2010Artigo -
9
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway حسب 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
منشور في 2022نص
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Cell biology
Gene
Biochemistry
Immunology
Medicine
Apoptosis
Atopic dermatitis
Cancer
Cancer research
Heat shock protein
Hsp90
Mitosis
Pathology
Programmed cell death
Regulator
Stem cell
Survivin
Adherens junction
Adipokine
Anatomy
Antibody
Antigen
Bacteriophage
Biotechnology
CD15
CD34
Cadherin
Cancer cell