Restoration of dystrophin expression in mdx muscle cells by chimeraplast-mediated exon skipping (English)
- New search for: Bertoni, Carmen
- New search for: Lau, Catherine
- New search for: Rando, Thomas A.
- New search for: Bertoni, Carmen
- New search for: Lau, Catherine
- New search for: Rando, Thomas A.
In:
Human molecular genetics
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12
, 10
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1087-
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2003
- Article (Journal) / Electronic Resource
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Title:Restoration of dystrophin expression in mdx muscle cells by chimeraplast-mediated exon skipping
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Contributors:
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Published in:Human molecular genetics ; 12, 10 ; 1087-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-05-15
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 12, Issue 10
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1079
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Genetic dissection of anxiety in autoimmune diseaseNakamura, Kazuhiro / Xiu, Yan / Ohtsuji, Mareki / Sugita, Gen / Abe, Masaaki / Ohtsuji, Naomi / Hamano, Yoshitomo / Jiang, Yi / Takahashi, Noriko / Shirai, Toshikazu et al. | 2003
- 1087
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Restoration of dystrophin expression in mdx muscle cells by chimeraplast-mediated exon skippingBertoni, Carmen / Lau, Catherine / Rando, Thomas A. et al. | 2003
- 1101
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Association of a functional 17{beta}-estradiol sensitive IL6-174G/C promoter polymorphism with early-onset type 1 diabetes in femalesKristiansen, Ole P. / Nolsøe, Runa L. / Larsen, Lykke / Gjesing, Anette M.P. / Johannesen, Jesper / Larsen, Zenia M. / Lykkesfeldt, Anne E. / Karlsen, Allan E. / Pociot, Flemming / Mandrup-Poulsen, Thomas et al. | 2003
- 1111
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New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12Pagani, Franco / Stuani, Cristiana / Tzetis, Maria / Kanavakis, Emmanuel / Efthymiadou, Alexandra / Doudounakis, Stavros / Casals, Teresa / Baralle, Francisco E. et al. | 2003
- 1121
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Functional polymorphisms in the paternally expressed XL{alpha}s and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formationFreson, Kathleen / Jaeken, Jaak / Van Helvoirt, Monique / de Zegher, Francis / Wittevrongel, Christine / Thys, Chantal / Hoylaerts, Marc F. / Vermylen, Jos / Van Geet, Chris et al. | 2003
- 1131
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Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humansWen, Xiao-Yan / Hegele, Robert A. / Wang, Jian / Wang, Ding Yan / Cheung, Joseph / Wilson, Michael / Yahyapour, Maryam / Bai, Yahong / Zhuang, Lihua / Skaug, Jennifer et al. | 2003
- 1145
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A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophyHeinzer, Ann K. / Watkins, Paul A. / Lu, Jyh-Feng / Kemp, Stephan / Moser, Ann B. / Li, Yuan Yuan / Mihalik, Stephanie / Powers, James M. / Smith, Kirby D. et al. | 2003
- 1155
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Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossLiu, Xue Zhong / Ouyang, Xiao Mei / Xia, Xia Juan / Zheng, Jing / Pandya, Arti / Li, Fang / Du, Li Lin / Welch, Katherine O. / Petit, Christine / Smith, Richard J.H. et al. | 2003
- 1163
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Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel geneDavy, Brian E. / Robinson, Michael L. et al. | 2003
- 1171
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A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegiaMonnier, Nicole / Ferreiro, Ana / Marty, Isabelle / Labarre-Vila, Annick / Mezin, Paulette / Lunardi, Joel et al. | 2003
- 1179
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FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeKriederman, Benjamin M. / Myloyde, Teressa L. / Witte, Marlys H. / Dagenais, Susan L. / Witte, Charles L. / Rennels, Margaret / Bernas, Michael J. / Lynch, Michelle T. / Erickson, Robert P. / Caulder, Mark S. et al. | 2003
- 1187
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Molecular mechanisms underlying limb anomalies associated with cholesterol deficiency during gestation: implications of Hedgehog signalingGofflot, Françoise / Hars, Carine / Illien, Françoise / Chevy, Françoise / Wolf, Claude / Picard, Jacques J. / Roux, Charles et al. | 2003
- 1199
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Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary diseasePalmer, Lyle J. / Celedón, Juan C. / Chapman, Harold A. / Speizer, Frank E. / Weiss, Scott T. / Silverman, Edwin K. et al. | 2003