Resultats de la cerca - Behzad Moghadaszadeh

  • Mostrar 1 - 11 resultats de 11
Refinar resultats
  1. 1
    Selenoproteins and Their Impact on Human Health Through Diverse Physiological Pathways

    Selenoproteins and Their Impact on Human Health Through Diverse Physiological Pathways per Behzad Moghadaszadeh, Alan H. Beggs

    Publicat 2006
    Obtenir text complet
    Revisão
    Afegir a favorits
    Guardat en:
  2. 2
    X-Linked Myotubular and Centronuclear Myopathies

    X-Linked Myotubular and Centronuclear Myopathies per Christopher R. Pierson, Kinga K. Tomczak, Pankaj B. Agrawal, Behzad Moghadaszadeh, Alan H. Beggs

    Publicat 2005
    Obtenir text complet
    Revisão
    Afegir a favorits
    Guardat en:
  3. 3
    Mutations of tropomyosin 3 (<i>TPM3</i>) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion

    Mutations of tropomyosin 3 (<i>TPM3</i>) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion per Michael W. Lawlor, Elizabeth T. DeChene, Emily Roumm, Amelia Geggel, Behzad Moghadaszadeh, Alan H. Beggs

    Publicat 2009
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  4. 4
    Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy

    Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy per Ercan Demir, Patrizia Sabatelli, Valérie Allamand, Ana Ferreiro, Behzad Moghadaszadeh, Mohamed Makrelouf, Haluk Topaloğlu, Bernard Échenne, Luciano Merlini, Pascale Guicheney

    Publicat 2002
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  5. 5
    Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes

    Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes per Pamela Barraza‐Flores, Behzad Moghadaszadeh, Won Lee, Biju Isaac, Liang Sun, Emily Hickey, Shira Rockowitz, Piotr Sliz, Alan H. Beggs

    Publicat 2025
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  6. 6
    Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36

    Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36 per Behzad Moghadaszadeh, Isabelle Desguerre, Haluk Topaloğlu, Francesco Muntoni, Sylvana Pavek, Caroline A. Sewry, M. Mayer, Michel Fardeau, F.M.S. Tomé, Pascale Guicheney

    Publicat 1998
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  7. 7
    X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene

    X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene per G. Diane Shelton, Branden E. Rider, Georgina Child, Sophia Tzannes, Ling T. Guo, Behzad Moghadaszadeh, Emily C. Troiano, Bianca Haase, Claire M. Wade, Alan H. Beggs

    Publicat 2015
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  8. 8
    Sarcomeres regulate murine cardiomyocyte maturation through MRTF-SRF signaling

    Sarcomeres regulate murine cardiomyocyte maturation through MRTF-SRF signaling per Yuxuan Guo, Yangpo Cao, Blake D. Jardin, Isha Sethi, Qing Ma, Behzad Moghadaszadeh, Emily C. Troiano, Neil Mazumdar, Michael A. Trembley, Eric M. Small, Guo‐Cheng Yuan, Alan H. Beggs, William T. Pu

    Publicat 2020
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  9. 9
    Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies

    Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Ea... per Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau, Behzad Moghadaszadeh, Nathalie Goemans, Carsten G. Bönnemann, Heinz Jungbluth, Volker Straub, Marcello Villanova, Jean‐Paul Leroy, Norma B. Romero, Jean‐Jacques Martin, Francesco Muntoni, Thomas Voit, B. Estournet, Pascale Richard, Michel Fardeau, Pascale Guicheney

    Publicat 2002
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  10. 10
    SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy

    SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy per Pankaj B. Agrawal, Christopher R. Pierson, Mugdha Joshi, Xiaoli Liu, Gianina Ravenscroft, Behzad Moghadaszadeh, Tiffany Talabere, Marissa G. Viola, Lindsay C. Swanson, Göknur Haliloğlu, Beril Talim, Kyle S. Yau, Richard J.N. Allcock, Nigel G. Laing, Mark A. Perrella, Alan H. Beggs

    Publicat 2014
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  11. 11
    Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species

    Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species per Mohammadsharif Tabebordbar, Kim A. Lagerborg, Alexandra C. Stanton, Emily M. King, Simon Ye, Liana Tellez, Allison Krunnfusz, Sahar Tavakoli, Jeffrey J. Widrick, Kathleen Messemer, Emily C. Troiano, Behzad Moghadaszadeh, Bryan Peacker, Krystynne A Leacock, Naftali Horwitz, Alan H. Beggs, Amy J. Wagers, Pardis C. Sabeti

    Publicat 2021
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:

Eines de cerca: