-
1
-
-
0033814140
-
The molecular basis of muscular dystrophies
-
Cohn R.D., Campbell K.P. The molecular basis of muscular dystrophies. Muscle Nerve 2000, 23:1456-1471.
-
(2000)
Muscle Nerve
, vol.23
, pp. 1456-1471
-
-
Cohn, R.D.1
Campbell, K.P.2
-
2
-
-
0034106396
-
Diagnostic protein expression in human muscle biopsies
-
Bornemann A., Anderson L.V.B. Diagnostic protein expression in human muscle biopsies. Brain Pathol 2000, 10:193-214.
-
(2000)
Brain Pathol
, vol.10
, pp. 193-214
-
-
Bornemann, A.1
Anderson, L.V.B.2
-
3
-
-
42449109966
-
Sarcoglycan-deficient muscular dystrophy in a Boston terrier
-
Deitz K., Morrison J.A., Kline K., Guo L.T., Shelton G.D. Sarcoglycan-deficient muscular dystrophy in a Boston terrier. J Vet Intern Med 2008, 22:476-480.
-
(2008)
J Vet Intern Med
, vol.22
, pp. 476-480
-
-
Deitz, K.1
Morrison, J.A.2
Kline, K.3
Guo, L.T.4
Shelton, G.D.5
-
4
-
-
33644893355
-
Dystrophin-deficient muscular dystrophy in an old English sheepdog
-
Wieczorek L.A., Garosi L.S., Shelton G.D. Dystrophin-deficient muscular dystrophy in an old English sheepdog. Vet Rec 2006, 25:270-273.
-
(2006)
Vet Rec
, vol.25
, pp. 270-273
-
-
Wieczorek, L.A.1
Garosi, L.S.2
Shelton, G.D.3
-
5
-
-
0346727235
-
Muscular dystrophy with truncated dystrophin in a family of Japanese spitz dogs
-
Jones B.R., Brennan S., Mooney C.T., et al. Muscular dystrophy with truncated dystrophin in a family of Japanese spitz dogs. J Neurol Sci 2004, 217:143-149.
-
(2004)
J Neurol Sci
, vol.217
, pp. 143-149
-
-
Jones, B.R.1
Brennan, S.2
Mooney, C.T.3
-
6
-
-
0036106071
-
Dystrophin-deficient muscular dystrophy in a Labrador retriever
-
Bergman R.L., Inzana K.D., Monroe W.E., et al. Dystrophin-deficient muscular dystrophy in a Labrador retriever. J Am Anim Hosp Assoc 2002, 38:255-261.
-
(2002)
J Am Anim Hosp Assoc
, vol.38
, pp. 255-261
-
-
Bergman, R.L.1
Inzana, K.D.2
Monroe, W.E.3
-
9
-
-
5044243229
-
Laminin alpha2 deficiency-associated muscular dystrophy in a Maine coon cat
-
Poncelet L., Résibois A., Engvall E., Shelton G.D. Laminin alpha2 deficiency-associated muscular dystrophy in a Maine coon cat. J Small Anim Pract 2003, 44:550-552.
-
(2003)
J Small Anim Pract
, vol.44
, pp. 550-552
-
-
Poncelet, L.1
Résibois, A.2
Engvall, E.3
Shelton, G.D.4
-
10
-
-
0035881763
-
Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats
-
O'Brien D.P., Johnson G.C., Liu L.A., et al. Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats. J Neurol Sci 2001, 189:37-43.
-
(2001)
J Neurol Sci
, vol.189
, pp. 37-43
-
-
O'Brien, D.P.1
Johnson, G.C.2
Liu, L.A.3
-
11
-
-
0037738510
-
Defective membrane repair in dysferlin-deficient muscular dystrophy
-
Bansal D., Miyake K., Vogel S.S., et al. Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 2003, 423:168-172.
-
(2003)
Nature
, vol.423
, pp. 168-172
-
-
Bansal, D.1
Miyake, K.2
Vogel, S.S.3
-
12
-
-
17344363640
-
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
-
Bashir R., Britton S., Strachan T., et al. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet 1998, 20:37-42.
-
(1998)
Nat Genet
, vol.20
, pp. 37-42
-
-
Bashir, R.1
Britton, S.2
Strachan, T.3
-
13
-
-
17344365600
-
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
-
Liu J., Aoki M., Illa I., et al. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet 1998, 20:31-36.
-
(1998)
Nat Genet
, vol.20
, pp. 31-36
-
-
Liu, J.1
Aoki, M.2
Illa, I.3
-
14
-
-
66149123674
-
Gene therapy in large animal models of muscular dystrophy
-
Wang Z., Chamberlain J.S., Tapscott S.J., Storb R. Gene therapy in large animal models of muscular dystrophy. ILAR J 2009, 50:187-198.
-
(2009)
ILAR J
, vol.50
, pp. 187-198
-
-
Wang, Z.1
Chamberlain, J.S.2
Tapscott, S.J.3
Storb, R.4
-
15
-
-
33745479703
-
Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD
-
McClorey G., Moulton H.M., Iverson P.L., Fletcher S., Wilton S.D. Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD. Gene Ther 2006, 13:1373-1381.
-
(2006)
Gene Ther
, vol.13
, pp. 1373-1381
-
-
McClorey, G.1
Moulton, H.M.2
Iverson, P.L.3
Fletcher, S.4
Wilton, S.D.5
-
16
-
-
63449141811
-
Efficacy of systemic morpholino exon-skipping in Duchenne dystrophy dogs
-
Yokota T., Lu Q.L., Partridge T., et al. Efficacy of systemic morpholino exon-skipping in Duchenne dystrophy dogs. Ann Neurol 2009, 65:667-676.
-
(2009)
Ann Neurol
, vol.65
, pp. 667-676
-
-
Yokota, T.1
Lu, Q.L.2
Partridge, T.3
-
17
-
-
0033621364
-
Sarcoglycan isoforms in skeletal muscle
-
Liu L.A., Engvall E. Sarcoglycan isoforms in skeletal muscle. J Biol Chem 1999, 274:38171-38176.
-
(1999)
J Biol Chem
, vol.274
, pp. 38171-38176
-
-
Liu, L.A.1
Engvall, E.2
-
18
-
-
0002051540
-
BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT
-
Hall T.A. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser 1999, 41:95-98.
-
(1999)
Nucl Acids Symp Ser
, vol.41
, pp. 95-98
-
-
Hall, T.A.1
-
19
-
-
57449097579
-
Is my antibody-staining specific? How to deal with pitfalls of immunohistochemistry
-
Fritschy J.M. Is my antibody-staining specific? How to deal with pitfalls of immunohistochemistry. Eur J Neurosci 2008, 28:2365-2370.
-
(2008)
Eur J Neurosci
, vol.28
, pp. 2365-2370
-
-
Fritschy, J.M.1
-
20
-
-
22244483775
-
Technical aspects of immunohistochemistry
-
Ramos-Vara J.A. Technical aspects of immunohistochemistry. Vet Pathol 2005, 42:405-426.
-
(2005)
Vet Pathol
, vol.42
, pp. 405-426
-
-
Ramos-Vara, J.A.1
-
21
-
-
0037252413
-
The antigen-antibody reaction in immunohistochemistry
-
Montero C. The antigen-antibody reaction in immunohistochemistry. J Histochem Cytochem 2003, 51:1-4.
-
(2003)
J Histochem Cytochem
, vol.51
, pp. 1-4
-
-
Montero, C.1
-
22
-
-
38749153262
-
Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesis
-
Lo H.P., Cooper S.T., Evesson F.J., et al. Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesis. Neuromuscul Disord 2008, 18:34-44.
-
(2008)
Neuromuscul Disord
, vol.18
, pp. 34-44
-
-
Lo, H.P.1
Cooper, S.T.2
Evesson, F.J.3
-
23
-
-
67349161031
-
Identification and characterization of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms
-
Pramono Z.A., Tan C.L., Seah I.A., et al. Identification and characterization of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms. Hum Genet 2009, 125:413-420.
-
(2009)
Hum Genet
, vol.125
, pp. 413-420
-
-
Pramono, Z.A.1
Tan, C.L.2
Seah, I.A.3
-
24
-
-
0033673056
-
Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies
-
Piccolo F., Moore S.A., Ford G.C., Campbell K.P. Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies. Ann Neurol 2000, 48:902-912.
-
(2000)
Ann Neurol
, vol.48
, pp. 902-912
-
-
Piccolo, F.1
Moore, S.A.2
Ford, G.C.3
Campbell, K.P.4
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