Cargando…

miRNA Expression in Control and FSHD Fetal Human Muscle Biopsies

BACKGROUND: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal-dominant disorder and is one of the most common forms of muscular dystrophy. We have recently shown that some hallmarks of FSHD are already expressed in fetal FSHD biopsies, thus opening a new field of investigation for mechan...

Descripción completa

Detalles Bibliográficos
Autores principales:	Portilho, Débora Morueco, Alves, Marcelo Ribeiro, Kratassiouk, Gueorgui, Roche, Stéphane, Magdinier, Frédérique, de Santana, Eliane Corrêa, Polesskaya, Anna, Harel-Bellan, Annick, Mouly, Vincent, Savino, Wilson, Butler-Browne, Gillian, Dumonceaux, Julie
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333765/ https://www.ncbi.nlm.nih.gov/pubmed/25692472 http://dx.doi.org/10.1371/journal.pone.0116853

Ejemplares similares

Genome-Wide Exploration of miRNA Function in Mammalian Muscle Cell Differentiation
por: Polesskaya, Anna, et al.
Publicado: (2013)

Does DNA Methylation Matter in FSHD?
por: Salsi, Valentina, et al.
Publicado: (2020)

Therapeutic Strategies Targeting DUX4 in FSHD
por: Le Gall, Laura, et al.
Publicado: (2020)

DUX4c Is Up-Regulated in FSHD. It Induces the MYF5 Protein and Human Myoblast Proliferation
por: Ansseau, Eugénie, et al.
Publicado: (2009)

Differences in the Expression and Distribution of Flotillin-2 in Chick, Mice and Human Muscle Cells
por: Possidonio, Ana Claudia Batista, et al.
Publicado: (2014)

DUX4 Expression in FSHD Muscles: Focus on Its mRNA Regulation
por: Sidlauskaite, Eva, et al.
Publicado: (2020)

Gene Editing Targeting the DUX4 Polyadenylation Signal: A Therapy for FSHD?
por: Joubert, Romains, et al.
Publicado: (2020)

Meeting report: the 2020 FSHD International Research Congress
por: Kyba, Michael, et al.
Publicado: (2020)

Type 1 FSHD with 6–10 Repeated Units: Factors Underlying Severity in Index Cases and Disease Penetrance in Their Relatives Attention
por: Salort-Campana, Emmanuelle, et al.
Publicado: (2020)

Activated dendritic cells modulate proliferation and differentiation of human myoblasts
por: Ladislau, Leandro, et al.
Publicado: (2018)

Correction: Activated dendritic cells modulate proliferation and differentiation of human myoblasts
por: Ladislau, Leandro, et al.
Publicado: (2022)

FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes
por: Tassin, Alexandra, et al.
Publicado: (2012)

Genotype-phenotype correlations in FSHD
por: Zernov, Nikolay, et al.
Publicado: (2019)

Current Therapeutic Approaches in FSHD
por: Wang, Leo H., et al.
Publicado: (2021)

The FSHD Atrophic Myotube Phenotype Is Caused by DUX4 Expression
por: Vanderplanck, Céline, et al.
Publicado: (2011)

Systemic antisense therapeutics inhibiting DUX4 expression ameliorates FSHD-like pathology in an FSHD mouse model
por: Lu-Nguyen, Ngoc, et al.
Publicado: (2021)

Crosstalk Between Innate and T Cell Adaptive Immunity With(in) the Muscle
por: Bonomo, Adriana C., et al.
Publicado: (2020)

MasterPATH: network analysis of functional genomics screening data
por: Rubanova, Natalia, et al.
Publicado: (2020)

Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects
por: Gould, Taylor, et al.
Publicado: (2021)

HGF potentiates extracellular matrix-driven migration of human myoblasts: involvement of matrix metalloproteinases and MAPK/ERK pathway
por: González, Mariela Natacha, et al.
Publicado: (2017)

Gene expression during normal and FSHD myogenesis
por: Tsumagari, Koji, et al.
Publicado: (2011)

Cardiac Involvement in Facioscapulohumeral Muscular Dystrophy (FSHD)
por: Ducharme-Smith, Allison, et al.
Publicado: (2021)

Expression Profiling of FSHD-1 and FSHD-2 Cells during Myogenic Differentiation Evidences Common and Distinctive Gene Dysregulation Patterns
por: Cheli, Stefania, et al.
Publicado: (2011)

Understanding and combating age-related muscle weakness: MYOAGE challenge
por: Butler-Browne, Gillian, et al.
Publicado: (2013)

DUX4 expressing immortalized FSHD lymphoblastoid cells express genes elevated in FSHD muscle biopsies, correlating with the early stages of inflammation
por: Banerji, Christopher R S, et al.
Publicado: (2020)

T cell biology in neuromuscular disorders: a focus on Duchenne Muscular Dystrophy and Amyotrophic Lateral Sclerosis
por: Lemos, Julia Pereira, et al.
Publicado: (2023)

FSHD: copy number variations on the theme of muscular dystrophy
por: Cabianca, Daphne Selvaggia, et al.
Publicado: (2010)

UK Facioscapulohumeral Muscular Dystrophy (FSHD) Patient Registry
por: Wood, Libby, et al.
Publicado: (2014)

Functional domains of the FSHD-associated DUX4 protein
por: Mitsuhashi, Hiroaki, et al.
Publicado: (2018)

Meeting report: the 2021 FSHD International Research Congress
por: Jagannathan, Sujatha, et al.
Publicado: (2022)

FSHD Therapeutic Strategies: What Will It Take to Get to Clinic?
por: Himeda, Charis L., et al.
Publicado: (2022)

The FSHD jigsaw: are we placing the tiles in the right position?
por: Salsi, Valentina, et al.
Publicado: (2023)

RanBP2 regulates the anti-retroviral activity of TRIM5α by SUMOylation at a predicted phosphorylated SUMOylation motif
por: Maarifi, Ghizlane, et al.
Publicado: (2018)

Expression and cellular localization of microRNA-29b and RAX, an activator of the RNA-dependent protein kinase (PKR), in the retina of streptozotocin-induced diabetic rats
por: Silva, Viviane A. O., et al.
Publicado: (2011)

Culture Conditions Affect Expression of DUX4 in FSHD Myoblasts
por: Pandey, Sachchida Nand, et al.
Publicado: (2015)

Are Antioxidants a Potential Therapy for FSHD? A Review of the Literature
por: Denny, Adam Philip, et al.
Publicado: (2017)

Orofacial Muscle Weakening in Facioscapulohumeral Muscular Dystrophy (FSHD) Patients
por: Konstantonis, Dimitrios, et al.
Publicado: (2022)

DUX4 Role in Normal Physiology and in FSHD Muscular Dystrophy
por: Mocciaro, Emanuele, et al.
Publicado: (2021)

Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHD
por: Caputo, Valerio, et al.
Publicado: (2022)

Gastrointestinal cancer occurs as extramuscular manifestation in FSHD1 patients
por: Kurashige, Takashi, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_hsl8k1i583cd8mpt9ddfpagqk5