Rezultati pretrage - Vincenzo Nigro

Detaljiziraj rezultate
  1. 1
    Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

    Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein od Vincenzo Nigro

    Izdano 1996
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  2. 2
    Spectrum of muscular dystrophies associated with sarcolemmal-protein genetic defects

    Spectrum of muscular dystrophies associated with sarcolemmal-protein genetic defects od Vincenzo Nigro, Giulio Piluso

    Izdano 2014
    Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  3. 3
    Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations

    Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations od Cristina Peduto, Mariateresa Zanobio, Vincenzo Nigro, Silverio Perrotta, Giulio Piluso, Claudia Santoro

    Izdano 2023
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  4. 4
    Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H

    Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H od Valentina Saccone, Michela Palmieri, Luigia Passamano, Giulio Piluso, Germana Meroni, L. Politano, Vincenzo Nigro

    Izdano 2007
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  5. 5
    A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo.

    A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. od Antonio Simeone, Dario Acampora, Antonello Mallamaci, Anna Stornaiuolo, Maria Rosaria D’Apice, Vincenzo Nigro, E. Boncinelli

    Izdano 1993
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  6. 6
    A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.

    A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycan... od Eloísa S. Moreira, Mariz Vainzof, Suely Kazue Nagahashi Marie, Vincenzo Nigro, Mayana Zatz, Maria Rita Passos‐Bueno

    Izdano 1998
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  7. 7
    Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system

    Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system od Antonio Simeone, Virginia Avantaggiato, Maria Cristina Moroni, Fulvio Mavilio, Claudio Arra, Franco Cotelli, Vincenzo Nigro, Dario Acampora

    Izdano 1995
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  8. 8
    Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy

    Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy od Emanuela Viggiano, Esther Picillo, Luigia Passamano, Maria Elena Onore, Giulio Piluso, Marianna Scutifero, Annalaura Torella, Vincenzo Nigro, Luisa Politano

    Izdano 2023
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  9. 9
    Loss of the Otx2-Binding Site in the Nanog Promoter Affects the Integrity of Embryonic Stem Cell Subtypes and Specification of Inner Cell Mass-Derived Epiblast

    Loss of the Otx2-Binding Site in the Nanog Promoter Affects the Integrity of Embryonic Stem Cell Subtypes and Specification of Inner Cell Mass-Derived Epiblast od Dario Acampora, Daniela Omodei, Giuseppe Petrosino, Arcomaria Garofalo, Marco Savarese, Vincenzo Nigro, Luca Giovanni Di Giovannantonio, Vincenzo Mercadante, Antonio Simeone

    Izdano 2016
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  10. 10
    The human HOX gene family

    The human HOX gene family od Dario Acampora, Maurizio D’Esposito, A. Faiella, Maria Pannese, Enrica Migliaccio, Francesco Morelli, Anna Stornaiuolo, Vincenzo Nigro, Antonio Simeone, Edoardo Boncinelli

    Izdano 1989
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  11. 11
    MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples

    MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples od Marco Savarese, Giuseppina Di Fruscio, Margherita Mutarelli, Annalaura Torella, Francesca Magri, Filippo M. Santorelli, Giacomo P. Comi, Claudio Bruno, Vincenzo Nigro

    Izdano 2014
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  12. 12
    Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathway

    Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathway od Giuseppina Di Fruscio, Angela Schulz, Rossella De Cegli, Marco Savarese, Margherita Mutarelli, Giancarlo Parenti, Sandro Banfi, Thomas Braulke, Vincenzo Nigro, Andrea Ballabio

    Izdano 2015
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  13. 13
    γ1- and γ2-Syntrophins, Two Novel Dystrophin-binding Proteins Localized in Neuronal Cells

    γ1- and γ2-Syntrophins, Two Novel Dystrophin-binding Proteins Localized in Neuronal Cells od Giulio Piluso, Massimiliano Mirabella, Enzo Ricci, Angela Belsito, Ciro Abbondanza, Serenella Servidei, Annibale Alessandro Puca, P. Tonali, Giovanni Alfredo Puca, Vincenzo Nigro

    Izdano 2000
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  14. 14
    The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene

    The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene od Annalaura Torella, Mariateresa Zanobio, Roberta Zeuli, Francesca Del Vecchio Blanco, Marco Savarese, Teresa Giugliano, Arcomaria Garofalo, Giulio Piluso, Luisa Politano, Vincenzo Nigro

    Izdano 2020
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  15. 15
    Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations

    Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations od Mafalda Cacciottolo, G. Numitone, Stefania Aurino, Imma Rosaria Caserta, Francesco Mari, L. Politano, Carlo Minetti, Enzo Ricci, Giulio Piluso, C. Angelini, Vincenzo Nigro

    Izdano 2011
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  16. 16
    Clinical variability in calpainopathy: What makes the difference?

    Clinical variability in calpainopathy: What makes the difference? od Flavia Paula, Mariz Vainzof, Maria Rita Passos‐Bueno, Rita de Cássia M. Pavanello, Sérgio Russo Matioli, Louise V.B. Anderson, Vincenzo Nigro, Mayana Zatz

    Izdano 2002
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  17. 17
    Interaction of Vault Particles with Estrogen Receptor in the MCF-7 Breast Cancer Cell

    Interaction of Vault Particles with Estrogen Receptor in the MCF-7 Breast Cancer Cell od Ciro Abbondanza, Valentina Rossi, Annarita Roscigno, Luigi Gallo, Angela Belsito, Giulio Piluso, Nicola Medici, Vincenzo Nigro, Anna Maria Molinari, Bruno Moncharmont, Giovanni Alfredo Puca

    Izdano 1998
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  18. 18
    A Missense Mutation in CASK Causes FG Syndrome in an Italian Family

    A Missense Mutation in CASK Causes FG Syndrome in an Italian Family od Giulio Piluso, Francesca D'Amico, Valentina Saccone, Ettore Bismuto, Ida Luisa Rotundo, Marina Di Domenico, Stefania Aurino, Charles E. Schwartz, Giovanni Neri, Vincenzo Nigro

    Izdano 2009
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  19. 19
    Restoration of Deficient Membrane Proteins in the Cardiomyopathic Hamster by In Vivo Cardiac Gene Transfer

    Restoration of Deficient Membrane Proteins in the Cardiomyopathic Hamster by In Vivo Cardiac Gene Transfer od Yasuhiro Ikeda, Yusu Gu, Yoshitaka Iwanaga, Masahiko Hoshijima, Sam S. Oh, Frank J. Giordano, Ju Chen, Vincenzo Nigro, Kirk L. Peterson, Kenneth R. Chien, John Ross

    Izdano 2002
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  20. 20
    Molecular diagnosis in LGMD2A: Mutation analysis or protein testing?

    Molecular diagnosis in LGMD2A: Mutation analysis or protein testing? od Francesco Mari, Luigi Fulizio, A. Nascimbeni, Marco Spinazzi, Giulio Piluso, V.M. Ventriglia, G. Ruzza, Gabriele Siciliano, Carlo P. Trevisan, Luisa Politano, Vincenzo Nigro, C. Angelini

    Izdano 2004
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:

Alati za pretragu: