Research Summary

We are interested in the role of dystroglycan, a protein associated with several forms of muscular dystrophy, in the central nervous system. We investigate molecular mechanisms underlying the dystroglycan-mediated targeting and polarization of proteins in glial cells.


BSc – University Mohamed V, Rabat, Morocco
MSc – University of Aix Marseille II, France
PhD – University of Aix Marseille II, France
PostDoc – University of Montreal
PostDoc – McGill University


Comprehensive List
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Selected Publications:

  1. Noël G, Belda M, Guadagno E, Micoud J, Klöcker N, Moukhles H. 2005. Dystroglycan and Kir4.1 coclustering in retinal Müller glia is regulated by laminin-1 and requires the PDZ-ligand domain of Kir4.1.J. Neurochem. 94(3):691-702.
  2. Guadagno E and Moukhles H. 2004. Laminin-induced aggregation of the inwardly rectifying potassium channel, Kir4.1, and the water permeable channel, AQP4, via a dystroglycan-containing complex in astrocytes. Glia. 47 (2):138-49.
  3. Côté PD, Moukhles H, Carbonetto S. 2002. Dystroglycan is not required for localization of dystrophin, syntrophin, and neuronal nitric-oxide synthase at the sarcolemma but regulates integrin alpha 7B expression and caveolin-3 distribution. J. Biol. Chem. 277(7):4672-9.
  4. Moukhles H, Carbonetto S. 2001. Dystroglycan contributes to the formation of multiple dystrophin-like complexes in brain. J. Neurochem. 78(4):824-34.
  5. Moukhles H, Roque R, Carbonetto S. 2000. alpha-dystroglycan isoforms are differentially distributed in adult rat retina. J. Comp. Neurol. 420(2):182-94.
  6. Leschziner A, Moukhles H, Lindenbaum M, Gee SH, Butterworth J, Campbell KP, Carbonetto S. 2000. Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle. J. Neurochem. 74(1):70-80.
  7. Côté PD, Moukhles H, Lindenbaum M, Carbonetto S. 1999. Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses. Nat Genet. 23(3):338-42.
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