10 results for author:"Gussoni E." in Literature citations
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| Myotubularin-deficient myoblasts display increased apoptosis, delayed proliferation, and poor cell engraftment. Lawlor M.W., Alexander M.S., Viola M.G., Meng H., Joubert R., Gupta V., Motohashi N., Manfready R.A., Hsu C.P., Huang P. et al. Am. J. Pathol. 181:961-968(2012) · Mapped (18) |
| beta4 integrin marks interstitial myogenic progenitor cells in adult murine skeletal muscle. Liadaki K., Casar J.C., Wessen M., Luth E.S., Jun S., Gussoni E., Kunkel L.M. J. Histochem. Cytochem. 60:31-44(2012) · Mapped (6) |
| A role for nephrin, a renal protein, in vertebrate skeletal muscle cell fusion. Sohn R.L., Huang P., Kawahara G., Mitchell M., Guyon J., Kalluri R., Kunkel L.M., Gussoni E. Proc. Natl. Acad. Sci. U.S.A. 106:9274-9279(2009) · UniProtKB (1) · Mapped (8) |
| C6ORF32 is upregulated during muscle cell differentiation and induces the formation of cellular filopodia. Yoon S., Molloy M.J., Wu M.P., Cowan D.B., Gussoni E. |
| Regulation of myogenic progenitor proliferation in human fetal skeletal muscle by BMP4 and its antagonist Gremlin. Frank N.Y., Kho A.T., Schatton T., Murphy G.F., Molloy M.J., Zhan Q., Ramoni M.F., Frank M.H., Kohane I.S., Gussoni E. J. Cell Biol. 175:99-110(2006) · Mapped (5) |
| Melanoma cell adhesion molecule is a novel marker for human fetal myogenic cells and affects myoblast fusion. Cerletti M., Molloy M.J., Tomczak K.K., Yoon S., Ramoni M.F., Kho A.T., Beggs A.H., Gussoni E. J. Cell. Sci. 119:3117-3127(2006) · Mapped (5) |
| Dystrophin expression in the mdx mouse restored by stem cell transplantation. Gussoni E., Soneoka Y., Strickland C.D., Buzney E.A., Khan M.K., Flint A.F., Kunkel L.M., Mulligan R.C. Nature 401:390-394(1999) · Mapped (8) |
| The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives. Ahn A.H., Feener C.A., Gussoni E., Yoshida M., Ozawa E., Kunkel L.M. J. Biol. Chem. 271:2724-2730(1996) · UniProtKB (5) · Mapped (7) |
| Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Boennemann C.G., Modi R., Noguchi S., Mizuno Y., Yoshida M., Gussoni E., McNally E.M., Duggan D.J., Angelini C., Hoffman E.P. et al. Nat. Genet. 11:266-273(1995) · UniProtKB (2) |
| Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Noguchi S., McNally E.M., Othmane K.B., Hagiwara Y., Mizuno Y., Yoshida M., Yamamoto H., Boennemann C.G., Gussoni E., Denton P.H. et al. Science 270:819-822(1995) · UniProtKB (2) |