Concepedia

A genetic model for muscle–eye–brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1)

Jianmin Liu, Sherry L. Ball, Yuan Yang, Pinchao Mei, Lei Zhang, Haining Shi, Henry J. Kaminski, Vance Lemmon, Huaiyu Hu

Mechanisms of Development · 2006 · 121 citations · 33 references

DOI

Concepts

References

33

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

Oxana Ibraghimov‐Beskrovnaya, James M. Ervasti, Cynthia J. Leveille et al. · Nature · 1992 · 1.4K citations

, , +11

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin

JM Ervasti · The Journal of Cell Biology · 1993 · 1.4K citations · Full text

, , +17

Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies

Daniel E. Michele, Rita Barresi, Motoi Kanagawa et al. · Nature · 2002 · 798 citations

, , +14

Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1

Aruto Yoshida, Kazuhiro Kobayashi, Hiroshi Manya et al. · Developmental Cell · 2001 · 710 citations · Full text

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Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome

Daniel Beltrán-Valero de Bernabé, Sophie Currier, Alice Steinbrecher et al. · The American Journal of Human Genetics · 2002 · 688 citations · Full text

, , +12