Gne depletion during zebrafish development impairs skeletal muscle structure and function

Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies

(2013) Elizabeth M. Gibbs et al.   FEBS Journal

Variable Phenotypes of Knockin Mice Carrying the M712T Gne Mutation

(2012) Ilan Sela et al.   NEUROMOLECULAR MEDICINE

A Splice Site Mutation in Laminin-α2 Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish

(2012) Vandana A. Gupta et al.   PLoS One

The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies

(2011) Vandana Gupta et al.   HUMAN MOLECULAR GENETICS

Hereditary Inclusion Body Myopathy: A decade of progress

(2009) Marjan Huizing et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Brain development needs sugar: the role of polysialic acid in controlling NCAM functions

(2009) Martina Mühlenhoff et al.   BIOLOGICAL CHEMISTRY

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment

(2009) A. S. Jacoby et al.   DEVELOPMENT

Lessons from GNE-deficient embryonic stem cells: sialic acid biosynthesis is involved in proliferation and gene expression

(2009) Wenke Weidemann et al.   GLYCOBIOLOGY

Developmental regulation of oligosialylation in zebrafish

(2008) Lan-Yi Chang et al.   GLYCOCONJUGATE JOURNAL

Mitochondrial processes are impaired in hereditary inclusion body myopathy

(2008) Iris Eisenberg et al.   HUMAN MOLECULAR GENETICS

The hereditary inclusion body myopathy enigma and its future therapy

(2008) Zohar Argov et al.   Neurotherapeutics

Heat-shock protein 90 1 is required for organized myofibril assembly in skeletal muscles of zebrafish embryos

(2008) S. J. Du et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA