4 results for author:"Collin H." in Literature citations
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| Protein 4.1R expression in normal and dystrophic skeletal muscle. Delhommeau F., Dalla Venezia N., Moriniere M., Collin H., Maillet P., Guerfali I., Leclerc P., Fardeau M., Delaunay J., Baklouti F. C. R. Biol. 328:43-56(2005) · Mapped (8) |
| Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion island. Fardeau M., Hillaire D., Mignard C., Feingold N., Feingold J., Mignard D., de Ubeda B., Collin H., Tome F.M.S., Richard I. et al. Brain 119:295-308(1996) · UniProtKB (1) |
| Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity. Piccolo F., Roberds S.L., Jeanpierre M., Leturcq F., Azibi K., Beldjord C., Carrie A., Recan D., Chaouch M., Reghis A. et al. Nat. Genet. 10:243-245(1995) · UniProtKB (1) |
| Expression of utrophin and its mRNA in denervated mdx mouse muscle. Jasmin B.J., Alameddine H., Lunde J.A., Stetzkowski-Marden F., Collin H., Tinsley J.M., Davies K.E., Tome F.M., Parry D.J., Cartaud J. FEBS Lett. 374:393-398(1995) · Mapped (8) |