Variable Phenotypes of Knockin Mice Carrying the M712T Gne Mutation

Deficits in Sialylation Impair Podocyte Maturation

(2012) B. Weinhold et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Glycoprotein Hyposialylation Gives Rise to a Nephrotic-Like Syndrome That Is Prevented by Sialic Acid Administration in GNE V572L Point-Mutant Mice

(2012) Mitutoshi Ito et al.   PLoS One

The Proteomic Profile of Hereditary Inclusion Body Myopathy

(2011) Ilan Sela et al.   PLoS One

Hereditary Inclusion Body Myopathy: A decade of progress

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

Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model

(2009) May Christine V Malicdan et al.   NATURE MEDICINE

Biochemical characterization of human and murine isoforms of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE)

(2008) Stefan O. Reinke et al.   GLYCOCONJUGATE JOURNAL

The hereditary inclusion body myopathy enigma and its future therapy

(2008) Zohar Argov et al.   Neurotherapeutics