-
1
-
-
0024490584
-
Total internal reflection fluorescence microscopy
-
Axelrod D. Total internal reflection fluorescence microscopy. Methods Cell Biol 1989;30:245-270.
-
(1989)
Methods Cell Biol
, vol.30
, pp. 245-270
-
-
Axelrod, D.1
-
2
-
-
0028971219
-
Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
-
Bonnemann CG, Modi R, Noguchi S, Mizuno Y, Yoshida M, Gussoni E, et al. Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nat Genet 1995;11:266-273.
-
(1995)
Nat Genet
, vol.11
, pp. 266-273
-
-
Bonnemann, C.G.1
Modi, R.2
Noguchi, S.3
Mizuno, Y.4
Yoshida, M.5
Gussoni, E.6
-
3
-
-
0036166835
-
Primary gamma-sarcoglycanopathy (LGMD 2C): Broadening of the mutational spectrum guided by the immunohistochemical profile
-
Bonnemann CG, Wong J, Jones KJ, Lidov HG, Feener CA, Shapiro F, et al. Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile. Neuromuscul Disord 2002;12:273-280.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 273-280
-
-
Bonnemann, C.G.1
Wong, J.2
Jones, K.J.3
Lidov, H.G.4
Feener, C.A.5
Shapiro, F.6
-
4
-
-
0032882445
-
The limb-girdle muscular dystrophies - Multiple genes, multiple mechanisms
-
Bushby KM. The limb-girdle muscular dystrophies - multiple genes, multiple mechanisms. Hum Mol Genet 1999;8:1875-1882.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1875-1882
-
-
Bushby, K.M.1
-
5
-
-
0032576620
-
Molecular organization of sarcoglycan complex in mouse myotubes in culture
-
Chan YM, Bonnemann CG, Lidov HG, Kunkel LM. Molecular organization of sarcoglycan complex in mouse myotubes in culture. J Cell Biol 1998;143:2033-2044.
-
(1998)
J Cell Biol
, vol.143
, pp. 2033-2044
-
-
Chan, Y.M.1
Bonnemann, C.G.2
Lidov, H.G.3
Kunkel, L.M.4
-
6
-
-
0034641599
-
Molecular and genetic characterization of sarcospan: Insights into sarcoglycan-sarcospan interactions
-
Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, et al. Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions. Hum Mol Genet 2000;9:2019-2027.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2019-2027
-
-
Crosbie, R.H.1
Lim, L.E.2
Moore, S.A.3
Hirano, M.4
Hays, A.P.5
Maybaum, S.W.6
-
7
-
-
0035141941
-
Confocal analysis of the dystrophin protein complex in muscular dystrophy
-
Draviam R, Billington L, Senchak A, Hoffman EP, Watkins SC. Confocal analysis of the dystrophin protein complex in muscular dystrophy. Muscle Nerve 2001;24:262-272.
-
(2001)
Muscle Nerve
, vol.24
, pp. 262-272
-
-
Draviam, R.1
Billington, L.2
Senchak, A.3
Hoffman, E.P.4
Watkins, S.C.5
-
8
-
-
33745033534
-
Alpha-sarcoglycan is recycled from the plasma membrane in the absence of sarcoglycan complex assembly
-
Draviam R, Wang B, Shand S, Xiao X, Watkins SC. Alpha-sarcoglycan is recycled from the plasma membrane in the absence of sarcoglycan complex assembly. Traffic 2006;7:793-810.
-
(2006)
Traffic
, vol.7
, pp. 793-810
-
-
Draviam, R.1
Wang, B.2
Shand, S.3
Xiao, X.4
Watkins, S.C.5
-
9
-
-
33745012208
-
Mini-dystrophin efficiently incorporates into the dystrophin protein complex in living cells
-
Draviam RA, Wang B, Li J, Xiao X, Watkins SC. Mini-dystrophin efficiently incorporates into the dystrophin protein complex in living cells. J Muscle Res Cell Motil 2006;27:53-67.
-
(2006)
J Muscle Res Cell Motil
, vol.27
, pp. 53-67
-
-
Draviam, R.A.1
Wang, B.2
Li, J.3
Xiao, X.4
Watkins, S.C.5
-
10
-
-
0033543647
-
Biochemical characterization of the epithelial dystroglycan complex
-
Durbeej M, Campbell KP. Biochemical characterization of the epithelial dystroglycan complex. J Biol Chem 1999;274:26609-26616.
-
(1999)
J Biol Chem
, vol.274
, pp. 26609-26616
-
-
Durbeej, M.1
Campbell, K.P.2
-
11
-
-
0033997265
-
Truncated N-glycans affect protein folding in the ER of CHO-derived mutant cell lines without preventing calnexin binding
-
Ermonval M, Duvet S, Zonneveld D, Cacan R, Buttin G, Braakman I. Truncated N-glycans affect protein folding in the ER of CHO-derived mutant cell lines without preventing calnexin binding. Glycobiology 2000;10:77-87.
-
(2000)
Glycobiology
, vol.10
, pp. 77-87
-
-
Ermonval, M.1
Duvet, S.2
Zonneveld, D.3
Cacan, R.4
Buttin, G.5
Braakman, I.6
-
12
-
-
0033513456
-
Immunotherapy of NOD mice with bone marrow-derived dendritic cells
-
Feili-Hariri M, Dong X, Alber SM, Watkins SC, Salter RD, Morel PA. Immunotherapy of NOD mice with bone marrow-derived dendritic cells. Diabetes 1999;48:2300-2308.
-
(1999)
Diabetes
, vol.48
, pp. 2300-2308
-
-
Feili-Hariri, M.1
Dong, X.2
Alber, S.M.3
Watkins, S.C.4
Salter, R.D.5
Morel, P.A.6
-
13
-
-
1342302339
-
Conformational changes associated with protein-protein interactions
-
Goh CS, Milburn D, Gerstein M. Conformational changes associated with protein-protein interactions. Curr Opin Struct Biol 2004;14:104-109.
-
(2004)
Curr Opin Struct Biol
, vol.14
, pp. 104-109
-
-
Goh, C.S.1
Milburn, D.2
Gerstein, M.3
-
14
-
-
0032494165
-
Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin
-
Hack AA, Ly CT, Jiang F, Clendenin CJ, Sigrist KS, Wollmann RL, et al. Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. J Cell Biol 1998;142:1279-1287.
-
(1998)
J Cell Biol
, vol.142
, pp. 1279-1287
-
-
Hack, A.A.1
Ly, C.T.2
Jiang, F.3
Clendenin, C.J.4
Sigrist, K.S.5
Wollmann, R.L.6
-
15
-
-
0033885496
-
Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex
-
Hack AA, Lam MY, Cordier L, Shoturma DI, Ly CT, Hadhazy MA, et al. Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex. J Cell Sci 2000;113:2535-2544.
-
(2000)
J Cell Sci
, vol.113
, pp. 2535-2544
-
-
Hack, A.A.1
Lam, M.Y.2
Cordier, L.3
Shoturma, D.I.4
Ly, C.T.5
Hadhazy, M.A.6
-
16
-
-
0031849289
-
Different manners of sarcoglycan expression in genetically proven alpha-sarcoglycan deficiency and gamma-sarcoglycan deficiency
-
(Berl)
-
Higuchi I, Kawai H, Umaki Y, Kawajiri M, Adachi K, Fukunaga H, et al. Different manners of sarcoglycan expression in genetically proven alpha-sarcoglycan deficiency and gamma-sarcoglycan deficiency. Acta Neuropathol (Berl) 1998;96:202-206.
-
(1998)
Acta Neuropathol
, vol.96
, pp. 202-206
-
-
Higuchi, I.1
Kawai, H.2
Umaki, Y.3
Kawajiri, M.4
Adachi, K.5
Fukunaga, H.6
-
17
-
-
0032567420
-
Assembly of the sarcoglycan complex. Insights for muscular dystrophy
-
Holt KH, Campbell KP. Assembly of the sarcoglycan complex. Insights for muscular dystrophy. J Biol Chem 1998;273:34667-34670.
-
(1998)
J Biol Chem
, vol.273
, pp. 34667-34670
-
-
Holt, K.H.1
Campbell, K.P.2
-
18
-
-
0031895132
-
Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies
-
Jones KJ, Kim SS, North KN. Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies. J Med Genet 1998;35:379-386.
-
(1998)
J Med Genet
, vol.35
, pp. 379-386
-
-
Jones, K.J.1
Kim, S.S.2
North, K.N.3
-
19
-
-
0034725650
-
The interaction of beta-arrestin with the AP-2 adaptor is required for the clustering of beta 2-adrenergic receptor into clathrin-coated pits
-
Laporte SA, Oakley RH, Holt JA, Barak LS, Caron MG. The interaction of beta-arrestin with the AP-2 adaptor is required for the clustering of beta 2-adrenergic receptor into clathrin-coated pits. J Biol Chem 2000;275:23120-23126.
-
(2000)
J Biol Chem
, vol.275
, pp. 23120-23126
-
-
Laporte, S.A.1
Oakley, R.H.2
Holt, J.A.3
Barak, L.S.4
Caron, M.G.5
-
20
-
-
3142717832
-
Limb-girdle muscular dystrophies - From genetics to molecular pathology
-
Laval SH, Bushby KM. Limb-girdle muscular dystrophies - from genetics to molecular pathology. Neuropathol Appl Neurobiol 2004;30:91-105.
-
(2004)
Neuropathol Appl Neurobiol
, vol.30
, pp. 91-105
-
-
Laval, S.H.1
Bushby, K.M.2
-
21
-
-
0028971221
-
Beta-sarcoglycan: Characterization and role in limb-girdle muscular dystrophy linked to 4q12
-
Lim LE, Duclos F, Bronx O, Bourg N, Sunada Y, Allamand V, et al. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12. Nat Genet 1995;11:257-265.
-
(1995)
Nat Genet
, vol.11
, pp. 257-265
-
-
Lim, L.E.1
Duclos, F.2
Bronx, O.3
Bourg, N.4
Sunada, Y.5
Allamand, V.6
-
22
-
-
0027959491
-
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
-
McNally EM, Yoshida M, Mizuno Y, Ozawa E, Kunkel LM. Human adhalin is alternatively spliced and the gene is located on chromosome 17q21. Proc Natl Acad Sci USA 1994;91:9690-9694.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 9690-9694
-
-
McNally, E.M.1
Yoshida, M.2
Mizuno, Y.3
Ozawa, E.4
Kunkel, L.M.5
-
23
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
-
Nigro V, de Sa Moreira E, Piluso G, Vainzof M, Belsito A, Politano L, et al. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene. Nat Genet 1996;14:195-198.
-
(1996)
Nat Genet
, vol.14
, pp. 195-198
-
-
Nigro, V.1
De Sa Moreira, E.2
Piluso, G.3
Vainzof, M.4
Belsito, A.5
Politano, L.6
-
24
-
-
0028883973
-
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
-
Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, et al. Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Science 1995;270:819-822.
-
(1995)
Science
, vol.270
, pp. 819-822
-
-
Noguchi, S.1
McNally, E.M.2
Ben Othmane, K.3
Hagiwara, Y.4
Mizuno, Y.5
Yoshida, M.6
-
25
-
-
0033973170
-
Formation of sarcoglycan complex with differentiation in cultured myocytes
-
Noguchi S, Wakabayashi E, Imamura M, Yoshida M, Ozawa E. Formation of sarcoglycan complex with differentiation in cultured myocytes. Eur J Biochem 2000;267:640-648.
-
(2000)
Eur J Biochem
, vol.267
, pp. 640-648
-
-
Noguchi, S.1
Wakabayashi, E.2
Imamura, M.3
Yoshida, M.4
Ozawa, E.5
-
26
-
-
0031943778
-
From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy
-
Ozawa E, Noguchi S, Mizuno Y, Hagiwara Y, Yoshida M. From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy. Muscle Nerve 1998;21:421-438.
-
(1998)
Muscle Nerve
, vol.21
, pp. 421-438
-
-
Ozawa, E.1
Noguchi, S.2
Mizuno, Y.3
Hagiwara, Y.4
Yoshida, M.5
-
27
-
-
27144471385
-
Molecular and cell biology of the sarcoglycan complex
-
Ozawa E, Mizuno Y, Hagiwara Y, Sasaoka T, Yoshida M. Molecular and cell biology of the sarcoglycan complex. Muscle Nerve 2005;32:563-576.
-
(2005)
Muscle Nerve
, vol.32
, pp. 563-576
-
-
Ozawa, E.1
Mizuno, Y.2
Hagiwara, Y.3
Sasaoka, T.4
Yoshida, M.5
-
28
-
-
0033911549
-
Differential expression of dystrophin, utrophin, and dystrophin- associated proteins in human muscle culture
-
Radojevic V, Lin S, Burgunder JM. Differential expression of dystrophin, utrophin, and dystrophin-associated proteins in human muscle culture. Cell Tissue Res 2000;300:447-457.
-
(2000)
Cell Tissue Res
, vol.300
, pp. 447-457
-
-
Radojevic, V.1
Lin, S.2
Burgunder, J.M.3
-
29
-
-
0031471956
-
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex
-
Sakamoto A, Ono K, Abe M, Jasmin G, Eki T, Murakami Y, et al. Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex. Proc Natl Acad Sci USA 1997;94:13873-13878.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13873-13878
-
-
Sakamoto, A.1
Ono, K.2
Abe, M.3
Jasmin, G.4
Eki, T.5
Murakami, Y.6
-
30
-
-
1442279913
-
Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan
-
Shi W, Chen Z, Schottenfeld J, Stahl RC, Kunkel LM, Chan YM. Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan. Muscle Nerve 2004;29:409-419.
-
(2004)
Muscle Nerve
, vol.29
, pp. 409-419
-
-
Shi, W.1
Chen, Z.2
Schottenfeld, J.3
Stahl, R.C.4
Kunkel, L.M.5
Chan, Y.M.6
-
31
-
-
33744934776
-
zeta-Sarcoglycan is a functional homologue of gamma-sarcoglycan in the formation of the sarcoglycan complex
-
Shiga K, Yoshioka H, Matsumiya T, Kimura I, Takeda S, Imamura M. zeta-Sarcoglycan is a functional homologue of gamma-sarcoglycan in the formation of the sarcoglycan complex. Exp Cell Res 2006;312:2083-2092.
-
(2006)
Exp Cell Res
, vol.312
, pp. 2083-2092
-
-
Shiga, K.1
Yoshioka, H.2
Matsumiya, T.3
Kimura, I.4
Takeda, S.5
Imamura, M.6
-
32
-
-
0343183398
-
Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations
-
Takano A, Bonnemann CG, Honda H, Sakai M, Feener CA, Kunkel LM, et al. Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations. Muscle Nerve 2000;23:807-810.
-
(2000)
Muscle Nerve
, vol.23
, pp. 807-810
-
-
Takano, A.1
Bonnemann, C.G.2
Honda, H.3
Sakai, M.4
Feener, C.A.5
Kunkel, L.M.6
-
33
-
-
10544234620
-
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
-
Vainzof M, Passos-Bueno MR, Canovas M, Moreira ES, Pavanello RC, Marie SK, et al. The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies. Hum Mol Genet 1996;5:1963-1969.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1963-1969
-
-
Vainzof, M.1
Passos-Bueno, M.R.2
Canovas, M.3
Moreira, E.S.4
Pavanello, R.C.5
Marie, S.K.6
-
34
-
-
0033559299
-
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population
-
Vainzof M, Passos-Bueno MR, Pavanello RC, Marie SK, Oliveira AS, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. J Neurol Sci 1999;164:44-49.
-
(1999)
J Neurol Sci
, vol.164
, pp. 44-49
-
-
Vainzof, M.1
Passos-Bueno, M.R.2
Pavanello, R.C.3
Marie, S.K.4
Oliveira, A.S.5
Zatz, M.6
-
35
-
-
0035114423
-
Isolated loss of gamma-sarcoglycan: Diagnostic implications in autosomal recessive limb-girdle muscular dystrophies
-
Vorgerd M, Gencik M, Mortier J, Epplen JT, Malin JP, Mortier W. Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies. Muscle Nerve 2001;24:421-424.
-
(2001)
Muscle Nerve
, vol.24
, pp. 421-424
-
-
Vorgerd, M.1
Gencik, M.2
Mortier, J.3
Epplen, J.T.4
Malin, J.P.5
Mortier, W.6
-
36
-
-
0034610364
-
Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model
-
Wang B, Li J, Xiao X. Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model. Proc Natl Acad Sci USA 2000;97:13714-13719.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 13714-13719
-
-
Wang, B.1
Li, J.2
Xiao, X.3
-
37
-
-
0036714792
-
Zeta-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy
-
Wheeler MT, Zarnegar S, McNally EM. Zeta-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy. Hum Mol Genet 2002;11:2147-2154.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2147-2154
-
-
Wheeler, M.T.1
Zarnegar, S.2
McNally, E.M.3
-
38
-
-
0041559837
-
Sarcoglycans in vascular smooth and striated muscle
-
Wheeler MT, McNally EM. Sarcoglycans in vascular smooth and striated muscle. Trends Cardiovasc Med 2003;13:238-243.
-
(2003)
Trends Cardiovasc Med
, vol.13
, pp. 238-243
-
-
Wheeler, M.T.1
McNally, E.M.2
-
39
-
-
0028302369
-
Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside
-
Yoshida M, Suzuki A, Yamamoto H, Noguchi S, Mizuno Y, Ozawa E. Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside. Eur J Biochem 1994;222:1055-1061.
-
(1994)
Eur J Biochem
, vol.222
, pp. 1055-1061
-
-
Yoshida, M.1
Suzuki, A.2
Yamamoto, H.3
Noguchi, S.4
Mizuno, Y.5
Ozawa, E.6
|