-
2
-
-
0025813402
-
PCR analysis of dystrophin gene mutation and expression
-
Chamberlain JS, Farwell NJ, Ranier JE, Cox GA, Caskey CT: PCR analysis of dystrophin gene mutation and expression. J Cell Biochem 1991;46:334-336.
-
(1991)
J Cell Biochem
, vol.46
, pp. 334-336
-
-
Chamberlain, J.S.1
Farwell, N.J.2
Ranier, J.E.3
Cox, G.A.4
Caskey, C.T.5
-
3
-
-
12644256351
-
-
Genbank accession number M68859
-
Chamberlain JS, Pearlman JA, Muzny DM, Civetello A, Farwell NJ, Malek R, Powaser P, Reeves AA, Lee C, Caskey CT: Mouse dystrophin cDNA Sequence. Genbank accession number M68859.
-
Mouse Dystrophin cDNA Sequence
-
-
Chamberlain, J.S.1
Pearlman, J.A.2
Muzny, D.M.3
Civetello, A.4
Farwell, N.J.5
Malek, R.6
Powaser, P.7
Reeves, A.A.8
Lee, C.9
Caskey, C.T.10
-
4
-
-
0023942674
-
Expression of the murine Duchenne muscular dystrophy gene in muscle and brain
-
Chamberlain JS, Pearlman JA, Muzny DM, Gibbs RA, Ranier JE, Reeves AA, Caskey CT: Expression of the murine Duchenne muscular dystrophy gene in muscle and brain. Science 1988;239:1416-1418.
-
(1988)
Science
, vol.239
, pp. 1416-1418
-
-
Chamberlain, J.S.1
Pearlman, J.A.2
Muzny, D.M.3
Gibbs, R.A.4
Ranier, J.E.5
Reeves, A.A.6
Caskey, C.T.7
-
5
-
-
0027767962
-
PCR Analysis of Muscular Dystrophy in mdx Mice
-
Partridge T (ed): London, Chapman & Hall
-
Chamberlain JS, Phelps SF, Cox GA, Maichele AJ, Greenwood AD: PCR Analysis of Muscular Dystrophy in mdx Mice, in Partridge T (ed): Molecular and Cell Biology of Muscular Dystrophy. London, Chapman & Hall, 1993, pp 167-189.
-
(1993)
Molecular and Cell Biology of Muscular Dystrophy
, pp. 167-189
-
-
Chamberlain, J.S.1
Phelps, S.F.2
Cox, G.A.3
Maichele, A.J.4
Greenwood, A.D.5
-
6
-
-
0027186053
-
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity
-
Cox GA, Cole NM, Matsumura K, Phelps SF, Hauschka SD, Campbell KP, Faulkner JA, Chamberlain JS: Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature 1993;364:725-729.
-
(1993)
Nature
, vol.364
, pp. 725-729
-
-
Cox, G.A.1
Cole, N.M.2
Matsumura, K.3
Phelps, S.F.4
Hauschka, S.D.5
Campbell, K.P.6
Faulkner, J.A.7
Chamberlain, J.S.8
-
7
-
-
0023614188
-
Dystrophin: The protein product of the Duchenne muscular dystrophy locus
-
Hoffman EP, Brown RH Jr, Kunkel LM: Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 1987;51:919-928.
-
(1987)
Cell
, vol.51
, pp. 919-928
-
-
Hoffman, E.P.1
Brown Jr., R.H.2
Kunkel, L.M.3
-
8
-
-
0024605518
-
Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
-
Newton CR, Graham A, Heptinstall LE, Powell SJ, Summers C, Kalsheker N, Smith JC, Markham AF: Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucl Acids Res 1989;17:2503-2516.
-
(1989)
Nucl Acids Res
, vol.17
, pp. 2503-2516
-
-
Newton, C.R.1
Graham, A.2
Heptinstall, L.E.3
Powell, S.J.4
Summers, C.5
Kalsheker, N.6
Smith, J.C.7
Markham, A.F.8
-
9
-
-
0029122523
-
Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice
-
Phelps SF, Hauser MA, Cole NM, Rafael JA, Hinkle RT, Faulkner JA, Chamberlain JS: Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice. Hum Mol Genet 1995;4:1251-1258.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1251-1258
-
-
Phelps, S.F.1
Hauser, M.A.2
Cole, N.M.3
Rafael, J.A.4
Hinkle, R.T.5
Faulkner, J.A.6
Chamberlain, J.S.7
-
10
-
-
0026784665
-
A PCR-based assay for the wild-type dystrophin gene transferred into the mdx mouse
-
Shrager JB, Naji A, Kelly AM, Stedman HH: A PCR-based assay for the wild-type dystrophin gene transferred into the mdx mouse. Muscle Nerve 1992;15:1133-1137.
-
(1992)
Muscle Nerve
, vol.15
, pp. 1133-1137
-
-
Shrager, J.B.1
Naji, A.2
Kelly, A.M.3
Stedman, H.H.4
-
11
-
-
0024353559
-
The molecular basis of muscular dystrophy in the mdx mouse: A point mutation
-
Sicinski P, Geng Y, Ryder-Cook AS, Barnard EA, Darlison MG, Barnard PJ: The molecular basis of muscular dystrophy in the mdx mouse: a point mutation. Science 1989;244:1578-1580.
-
(1989)
Science
, vol.244
, pp. 1578-1580
-
-
Sicinski, P.1
Geng, Y.2
Ryder-Cook, A.S.3
Barnard, E.A.4
Darlison, M.G.5
Barnard, P.J.6
-
12
-
-
0027291449
-
Apolipoprotein E phenotypes and genotypes as determined by polymerase chain reaction using allele-specific oligonucleotide probes and the amplification refractory mutation system in children with insulin-dependent diabetes mellitus
-
Stavljenic-Rukavina A, Sertic J, Salzer B, Dumic M, Radica A, Fumic K, Krajina A: Apolipoprotein E phenotypes and genotypes as determined by polymerase chain reaction using allele-specific oligonucleotide probes and the amplification refractory mutation system in children with insulin-dependent diabetes mellitus. Clin Chim Acta 1993;216:191-198.
-
(1993)
Clin Chim Acta
, vol.216
, pp. 191-198
-
-
Stavljenic-Rukavina, A.1
Sertic, J.2
Salzer, B.3
Dumic, M.4
Radica, A.5
Fumic, K.6
Krajina, A.7
-
13
-
-
0023091942
-
The mutant mdx: Inherited myopathy in the mouse. Morphological studies of nerves, muscles and end-plates
-
Torres LF, Duchen LW: The mutant mdx: inherited myopathy in the mouse. Morphological studies of nerves, muscles and end-plates. Brain 1987;110:269-299.
-
(1987)
Brain
, vol.110
, pp. 269-299
-
-
Torres, L.F.1
Duchen, L.W.2
-
14
-
-
0025869153
-
Analysis of apolipoprotein e genotypes by the amplification refractory mutation system
-
Wenham PR, Newton CR, Price WH: Analysis of apolipoprotein E genotypes by the amplification refractory mutation system. Clin Chem 1991;37:241-244.
-
(1991)
Clin Chem
, vol.37
, pp. 241-244
-
-
Wenham, P.R.1
Newton, C.R.2
Price, W.H.3
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