화학공학소재연구정보센터
검색결과 : 4건
No. Article
1 Mutation in dystrophin-encoding gene affects energy metabolism in mouse myoblasts
Onopiuk M, Brutkowski W, Wierzbicka K, Wojciechowska S, Szczepanowska J, Fronk J, Lochmuller H, Gorecki DC, Zablocki K
Biochemical and Biophysical Research Communications, 386(3), 463, 2009
2 No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation
Salama I, Hinderlich S, Shlomai Z, Eisenberg I, Krause S, Yarema K, Argov Z, Lochmuller H, Reutter W, Dabby R, Sadeh M, Ben-Bassat H, Mitrani-Rosenbaum S
Biochemical and Biophysical Research Communications, 328(1), 221, 2005
3 The short MCK1350 promoter/enhancer allows for sufficient dystrophin expression in skeletal muscles of mdx mice
Larochelle N, Oualikene W, Dunant P, Massie B, Karpati G, Nalbantoglu J, Lochmuller H
Biochemical and Biophysical Research Communications, 292(3), 626, 2002
4 Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency
Horvath R, Lochmuller H, Stucka R, Yao JB, Shoubridge EA, Kim SH, Gerbitz KD, Jaksch M
Biochemical and Biophysical Research Communications, 276(2), 530, 2000