Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2Dy-w mice, a model for congenital muscular dystrophy type 1A

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

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

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

Overexpression of IGF-1 in Muscle Attenuates Disease in a Mouse Model of Spinal and Bulbar Muscular Atrophy

(2009) Isabella Palazzolo et al.   NEURON

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

(2008) Mahasweta Girgenrath et al.   ANNALS OF NEUROLOGY

Insulin-like growth factor-I analogue protects muscles of dystrophicmdxmice from contraction-mediated damage

(2008) Stefan M. Gehrig et al.   EXPERIMENTAL PHYSIOLOGY