Related references
Note: Only part of the references are listed.Long-term maintenance of dystrophin expression and resistance to injury of skeletal muscle in gene edited DMD mice
Dileep R. Karri et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2022)
The nuclear envelope protein Net39 is essential for muscle nuclear integrity and chromatin organization
Andres Ramirez-Martinez et al.
NATURE COMMUNICATIONS (2021)
Disrupting the LINC complex by AAV mediated gene transduction prevents progression of Lamin induced cardiomyopathy
Ruth Jinfen Chai et al.
NATURE COMMUNICATIONS (2021)
Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells
Ashley J. Earle et al.
NATURE MATERIALS (2020)
Heterochromatin-Driven Nuclear Softening Protects the Genome against Mechanical Stress-Induced Damage
Michele M. Nava et al.
CELL (2020)
Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular Dystrophy
Anne T. Bertrand et al.
CELLS (2020)
Single-nucleus RNA-seq and FISH identify coordinated transcriptional activity in mammalian myofibers
Matthieu Dos Santos et al.
NATURE COMMUNICATIONS (2020)
Degenerative and regenerative pathways underlying Duchenne muscular dystrophy revealed by single-nucleus RNA sequencing
Francesco Chemello et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
The nucleus acts as a ruler tailoring cell responses to spatial constraints
A. J. Lomakin et al.
SCIENCE (2020)
Improved Multiplex Immunohistochemistry for Immune Microenvironment Evaluation of Mouse Formalin-Fixed, Paraffin-Embedded Tissues
Noah Sorrelle et al.
JOURNAL OF IMMUNOLOGY (2019)
CRISPOR: intuitive guide selection for CRISPR/Cas9 genome editing experiments and screens
Jean-Paul Concordet et al.
NUCLEIC ACIDS RESEARCH (2018)
Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation
Nolwenn Briand et al.
NUCLEUS (2018)
Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation
Nolwenn Briand et al.
NUCLEUS (2018)
Efficient proximity labeling in living cells and organisms with TurboID
Tess C. Branon et al.
NATURE BIOTECHNOLOGY (2018)
CRISPR-Mediated Programmable 3D Genome Positioning and Nuclear Organization
Haifeng Wang et al.
CELL (2018)
The Pathogenesis and Therapies of Striated Muscle Laminopathies
Astrid Brull et al.
FRONTIERS IN PHYSIOLOGY (2018)
Considerations and guidelines for mouse metabolic phenotyping in diabetes research
Thierry Alquier et al.
DIABETOLOGIA (2018)
Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy
Leonela Amoasii et al.
SCIENCE TRANSLATIONAL MEDICINE (2017)
KLHL41 stabilizes skeletal muscle sarcomeres by nonproteolytic ubiquitination
Andres Ramirez-Martinez et al.
ELIFE (2017)
Genome-Nuclear Lamina Interactions Regulate Cardiac Stem Cell Lineage Restriction
Andrey Poleshko et al.
CELL (2017)
Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells
Petra Gimpel et al.
CURRENT BIOLOGY (2017)
Nuclear Pores Regulate Muscle Development and Maintenance by Assembling a Localized Mef2C Complex
Marcela Raices et al.
DEVELOPMENTAL CELL (2017)
Tissue-Specific Gene Repositioning by Muscle Nuclear Membrane Proteins Enhances Repression of Critical Developmental Genes during Myogenesis
Michael I. Robson et al.
MOLECULAR CELL (2016)
MEF2C protects bone marrow B-lymphoid progenitors during stress haematopoiesis
Wenyuan Wang et al.
NATURE COMMUNICATIONS (2016)
Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy
Sherry Dadgar et al.
JOURNAL OF CELL BIOLOGY (2014)
DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death
Anne T. Bertrand et al.
HUMAN MOLECULAR GENETICS (2012)
Fine control of nuclear confinement identifies a threshold deformation leading to lamina rupture and induction of specific genes
Mael Le Berre et al.
INTEGRATIVE BIOLOGY (2012)
Myocyte Enhancer Factor 2 and Class II Histone Deacetylases Control a Gender-Specific Pathway of Cardioprotection Mediated by the Estrogen Receptor
Eva van Rooij et al.
CIRCULATION RESEARCH (2010)
Partial Rescue of Growth Failure in Growth Hormone (GH)-Deficient Mice by a Single Injection of a Double-Stranded Adeno-Associated Viral Vector Expressing the GH Gene Driven by a Muscle-Specific Regulatory Cassette
Marco Martari et al.
HUMAN GENE THERAPY (2009)
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B
Young-Eun Park et al.
NEUROMUSCULAR DISORDERS (2009)
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice
Andrew H. Williams et al.
SCIENCE (2009)
p63 and p73 Transcriptionally Regulate Genes Involved in DNA Repair
Yu-Li Lin et al.
PLOS GENETICS (2009)
A genetic locus targeted to the nuclear periphery in living cells maintains its transcriptional competence
R. Ileng Kumaran et al.
JOURNAL OF CELL BIOLOGY (2008)
Transcriptional repression mediated by repositioning of genes to the nuclear lamina
K. L. Reddy et al.
NATURE (2008)
Histone deacetylase degradation and MEF2 activation promote the formation of slow-twitch myofibers
Matthew J. Potthoff et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration
M Bakay et al.
BRAIN (2006)
Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation
RL Frock et al.
GENES & DEVELOPMENT (2006)
Coupling of the nucleus and cytoplasm: role of the LINC complex
M Crisp et al.
JOURNAL OF CELL BIOLOGY (2006)
Temporally controlled targeted somatic mutagenesis in skeletal muscles of the mouse
M Schuler et al.
GENESIS (2005)
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
T Arimura et al.
HUMAN MOLECULAR GENETICS (2005)
Hematopoietic contribution to skeletal muscle regeneration by myelomonocytic precursors
R Doyonnas et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
DNA damage-induced G2-M checkpoint activation by histone H2AX and 53BP1
O Fernandez-Capetillo et al.
NATURE CELL BIOLOGY (2002)
ATM phosphorylates histone H2AX in response to DNA double-strand breaks
S Burma et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Functional and molecular adaptations in skeletal muscle of myoglobin-mutant mice
RW Grange et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2001)
Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations
CA Sewry et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2001)
MEF2 responds to multiple calcium-regulated signals in the control of skeletal muscle fiber type
H Wu et al.
EMBO JOURNAL (2000)