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Quoted phrase not found in phrase index: "Abnormal muscle fiber gamma sarcoglycan"
Page 1
Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriers.
Di Blasi C, Morandi L, Barresi R, Blasevich F, Cornelio F, Mora M. Di Blasi C, et al. Acta Neuropathol. 1996 Oct;92(4):369-77. doi: 10.1007/s004010050532. Acta Neuropathol. 1996. PMID: 8891069
We investigated the expression of the DAPs beta-dystroglycan, alpha-sarcoglycan, gamma-sarcoglycan and syntrophin as well as utrophin in the muscles of 13 Duchenne muscular dystrophy (DMD) carriers (with variable percentages of dystrophin-deficient …
We investigated the expression of the DAPs beta-dystroglycan, alpha-sarcoglycan, gamma-sarcoglycan and syntrophin as we …
Laminin abnormality in severe childhood autosomal recessive muscular dystrophy.
Yamada H, Tomé FM, Higuchi I, Kawai H, Azibi K, Chaouch M, Roberds SL, Tanaka T, Fujita S, Mitsui T, et al. Yamada H, et al. Lab Invest. 1995 Jun;72(6):715-22. Lab Invest. 1995. PMID: 7783429
Abnormalities in the expression of laminin were not observed in the three less affected patients. CONCLUSIONS: The expression of laminin is greatly disturbed in severely diseased SCARMD muscle deficient in adhalin. Disturbance of sarcolemma-basal lamina inter …
Abnormalities in the expression of laminin were not observed in the three less affected patients. CONCLUSIONS: The expression …
Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy.
Ishii H, Hayashi YK, Nonaka I, Arahata K. Ishii H, et al. Neuromuscul Disord. 1997 May;7(3):191-7. doi: 10.1016/s0960-8966(97)00462-8. Neuromuscul Disord. 1997. PMID: 9185184
By light microscopy we previously obtained immunocytochemical evidence for basal lamina (BL) abnormality of skeletal muscle in Fukuyama congenital muscular dystrophy (FCMD). ...These features were more prominent in large calibre (> 15 microns) fibres …
By light microscopy we previously obtained immunocytochemical evidence for basal lamina (BL) abnormality of skeletal muscle in …
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion.
Nowak KJ, Walsh P, Jacob RL, Johnsen RD, Peverall J, McNally EM, Wilton SD, Kakulas BA, Laing NG. Nowak KJ, et al. Neuromuscul Disord. 2000 Feb;10(2):100-7. doi: 10.1016/s0960-8966(99)00063-2. Neuromuscul Disord. 2000. PMID: 10714584
Non-inheritance of paternal alleles for D13S232, D13S292 and D13S1243 suggested the inheritance of a deletion, which was confirmed by FISH, using a genomic probe from the gamma-sarcoglycan gene. The gamma-sarcoglycan cDNA was amplified by reverse trans …
Non-inheritance of paternal alleles for D13S232, D13S292 and D13S1243 suggested the inheritance of a deletion, which was confirmed by FISH, …