<p>(A) Schematic representation of the human dystrophin gene and sequence alignment of two exon 51 regions across the indicated species. Conserved nucleotide sequences are shadowed. (B) Annealing sites of SSOs designed in this study are indicated by boxes. For comparison, the annealing sites of Eteplirsen and Drisapersen are indicated by shaded boxes. Position +1 corresponds to the first nucleotide in exon 51.</p
Dystrophin gene is the largest in the human genome with 79 exons covering greater than 0.1% of the t...
Muscular dystrophy (MD) is a fatal, muscle wasting disease affecting individuals who have acquired a...
<div><p>The alignment of partial sequences of fetidin-lysenins genes.</p> <p>Universal primers (high...
The purpose of this study is to examine the biophysical properties of the rod region of the dystroph...
Antisense oligonucleotides (AOs), directed at amenable splicing motifs across the dystrophin gene tr...
Duchenne muscular dystrophy (DMD) is caused by the lack of functional dystrophin protein, most commo...
<p>(A) Representative gels showing RT-PCR of the native and exon-44-skipped (252 bp) or exon-53-skip...
<p>(A) Schematic representation of the relative sizes of the original plasmid, the full length human...
<p>SNPs used in this study were conserved among species. Arrow heads indicate SNP regions of human D...
<p>(A) Sequence alignment of dystrophin from various mammals. Lysine at the 18<sup>th</sup> position...
International audienceWe have studied the properties of a panel of proteins engineered to be end-pro...
<p><b>Copyright information:</b></p><p>Taken from "Antisense oligonucleotide induced exon skipping a...
<p>α-NE, Dyn A and Dyn B correspond to the α-neoendorphin-, dynorphin A- and dynorphin B-coding sequ...
Duchenne muscular dystrophy (DMD), a fatal X-linked recessive disorder, is caused by mutations in th...
<p>Figure shows relative orientations of the <i>stl</i>, <i>str</i>, and <i>xis</i> genes, and the r...
Dystrophin gene is the largest in the human genome with 79 exons covering greater than 0.1% of the t...
Muscular dystrophy (MD) is a fatal, muscle wasting disease affecting individuals who have acquired a...
<div><p>The alignment of partial sequences of fetidin-lysenins genes.</p> <p>Universal primers (high...
The purpose of this study is to examine the biophysical properties of the rod region of the dystroph...
Antisense oligonucleotides (AOs), directed at amenable splicing motifs across the dystrophin gene tr...
Duchenne muscular dystrophy (DMD) is caused by the lack of functional dystrophin protein, most commo...
<p>(A) Representative gels showing RT-PCR of the native and exon-44-skipped (252 bp) or exon-53-skip...
<p>(A) Schematic representation of the relative sizes of the original plasmid, the full length human...
<p>SNPs used in this study were conserved among species. Arrow heads indicate SNP regions of human D...
<p>(A) Sequence alignment of dystrophin from various mammals. Lysine at the 18<sup>th</sup> position...
International audienceWe have studied the properties of a panel of proteins engineered to be end-pro...
<p><b>Copyright information:</b></p><p>Taken from "Antisense oligonucleotide induced exon skipping a...
<p>α-NE, Dyn A and Dyn B correspond to the α-neoendorphin-, dynorphin A- and dynorphin B-coding sequ...
Duchenne muscular dystrophy (DMD), a fatal X-linked recessive disorder, is caused by mutations in th...
<p>Figure shows relative orientations of the <i>stl</i>, <i>str</i>, and <i>xis</i> genes, and the r...
Dystrophin gene is the largest in the human genome with 79 exons covering greater than 0.1% of the t...
Muscular dystrophy (MD) is a fatal, muscle wasting disease affecting individuals who have acquired a...
<div><p>The alignment of partial sequences of fetidin-lysenins genes.</p> <p>Universal primers (high...