검색결과 : 5건
| No. | Article |
|---|---|
| 1 |
Dolichol-phosphate mannose synthase depletion in zebrafish leads to dystrophic muscle with hypoglycosylated alpha-dystroglycan Marchese M, Pappalardo A, Baldacci J, Verri T, Doccini S, Cassandrini D, Bruno C, Fiorillo C, Garcia-Gil M, Bertini E, Pitto L, Santorelli FM Biochemical and Biophysical Research Communications, 477(1), 137, 2016 |
| 2 |
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes Biancheri R, Falace A, Tessa A, Pedernonte M, Scapolan S, Cassandrini D, Aiello C, Rossi A, Broda P, Zara F, Santorelli FM, Minetti C, Bruno C Biochemical and Biophysical Research Communications, 363(4), 1033, 2007 |
| 3 |
Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease? Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T Biochemical and Biophysical Research Communications, 342(2), 489, 2006 |
| 4 |
Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan Xiong H, Kobayashi K, Tachikawa M, Manya H, Takeda S, Chiyonobu T, Fujikake N, Wang F, Nishimoto A, Morris GE, Nagai Y, Kanagawa M, Endo T, Toda T Biochemical and Biophysical Research Communications, 350(4), 935, 2006 |
| 5 |
Unusual laminin alpha 2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophy Lattanzi G, Muntoni F, Sabatelli P, Squarzoni S, Maraldi NM, Cenni V, Villanova M, Columbaro M, Merlini L, Marmiroli S Biochemical and Biophysical Research Communications, 277(3), 639, 2000 |