Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies

Autophagy in skeletal muscle

(2010) Marco Sandri   FEBS LETTERS

Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice

(2010) Virginie Carmignac et al.   HUMAN MOLECULAR GENETICS

Mutations inLama1Disrupt Retinal Vascular Development and Inner Limiting Membrane Formation

(2010) Malia M. Edwards et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Consensus Statement on Standard of Care for Congenital Muscular Dystrophies

(2010) Ching H. Wang et al.   JOURNAL OF CHILD NEUROLOGY

Laminin chain assembly is regulated by specific coiled-coil interactions

(2010) Philip R. Macdonald et al.   JOURNAL OF STRUCTURAL BIOLOGY

Transgenic overexpression of laminin α1 chain in laminin α2 chain-deficient mice rescues the disease throughout the lifespan

(2010) Kinga I. Gawlik et al.   MUSCLE & NERVE

Autophagy is defective in collagen VI muscular dystrophies and its reactivation rescues myofiber degeneration

(2010) Paolo Grumati et al.   NATURE MEDICINE

Distinct Roles for Laminin Globular Domains in Laminin α1 Chain Mediated Rescue of Murine Laminin α2 Chain Deficiency

(2010) Kinga I. Gawlik et al.   PLoS One

O-Mannosyl Phosphorylation of Alpha-Dystroglycan Is Required for Laminin Binding

(2010) T. Yoshida-Moriguchi et al.   SCIENCE

Talin 1 and 2 are required for myoblast fusion, sarcomere assembly and the maintenance of myotendinous junctions

(2009) F. J. Conti et al.   DEVELOPMENT

Sonic hedgehog-dependent synthesis of laminin  1 controls basement membrane assembly in the myotome

(2009) C. Anderson et al.   DEVELOPMENT

Dystrophin glycoprotein complex-associated Gβγ subunits activate phosphatidylinositol-3-kinase/Akt signaling in skeletal muscle in a laminin-dependent manner

(2009) Yongmin Xiong et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Omigapil Ameliorates the Pathology of Muscle Dystrophy Caused by Laminin- 2 Deficiency

(2009) M. Erb et al.   JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of  -dystroglycan

(2009) R. Han et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Pathology is alleviated by doxycycline in a laminin-α2-null model of congenital muscular dystrophy

(2008) Mahasweta Girgenrath et al.   ANNALS OF NEUROLOGY

A Comparative Study of α-Dystroglycan Glycosylation in Dystroglycanopathies Suggests that the Hypoglycosylation of α-Dystroglycan Does Not Consistently Correlate with Clinical Severity

(2008) Cecilia Jimenez-Mallebrera et al.   BRAIN PATHOLOGY

Laminins promote postsynaptic maturation by an autocrine mechanism at the neuromuscular junction

(2008) Hiroshi Nishimune et al.   JOURNAL OF CELL BIOLOGY

Integrin-linked kinase stabilizes myotendinous junctions and protects muscle from stress-induced damage

(2008) Hao-Ven Wang et al.   JOURNAL OF CELL BIOLOGY

A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination

(2008) B. L. Patton et al.   JOURNAL OF CELL SCIENCE

Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy

(2008) Douglas P Millay et al.   NATURE MEDICINE

CD90-positive cells, an additional cell population, produce laminin α2 upon transplantation to dy3k/dy3k mice

(2007) So-ichiro Fukada et al.   EXPERIMENTAL CELL RESEARCH

Bridging structure with function: Structural, regulatory, and developmental role of laminins

(2007) Julia Tzu et al.   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

Inherited diseases of the glomerular basement membrane

(2007) Marie Claire Gubler   Nature clinical practice. Nephrology