Pages that link to "Q36763352"

The following pages link to Exon structure of the human dystrophin gene (Q36763352):

Displaying 50 items.

• Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene (Q24316279) (← links)
• WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma (Q24322575) (← links)
• Antisense-mediated exon skipping: a versatile tool with therapeutic and research applications (Q24682555) (← links)
• Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients (Q24801630) (← links)
• Dystrophins and dystrobrevins (Q24805434) (← links)
• The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle (Q26770343) (← links)
• Splicing therapy for neuromuscular disease (Q27009581) (← links)
• Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene (Q28285297) (← links)
• Republished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime (Q28385687) (← links)
• Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime (Q28392579) (← links)
• Identification and characterisation of transcript and protein of a new short N-terminal utrophin isoform (Q28580577) (← links)
• The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms. (Q33269611) (← links)
• Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin gene (Q33678153) (← links)
• Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides. (Q33868227) (← links)
• Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter (Q34183444) (← links)
• IRBIS: a systematic search for conserved complementarity (Q34240853) (← links)
• Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations (Q34324968) (← links)
• The influence of antisense oligonucleotide length on dystrophin exon skipping. (Q34590393) (← links)
• Characterization of RNase R-digested cellular RNA source that consists of lariat and circular RNAs from pre-mRNA splicing. (Q34595403) (← links)
• Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy. (Q35239163) (← links)
• Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy (Q35582668) (← links)
• Therapeutics for Duchenne muscular dystrophy: current approaches and future directions. (Q35607136) (← links)
• Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production (Q35643859) (← links)
• The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test (Q35644562) (← links)
• Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy (Q35644576) (← links)
• Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females. (Q35889152) (← links)
• Spectrin, alpha-actinin, and dystrophin (Q36101284) (← links)
• Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus (Q36235194) (← links)
• Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2 , Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. (Q36422465) (← links)
• Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy. (Q37111368) (← links)
• Eteplirsen in the treatment of Duchenne muscular dystrophy (Q37682676) (← links)
• Mammalian cells as biopharmaceutical production hosts in the age of omics (Q37969680) (← links)
• Cardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers. (Q38103213) (← links)
• Exercise and muscular dystrophy: implications and analysis of effects on musculoskeletal and cardiovascular systems (Q38111711) (← links)
• A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs (Q38346817) (← links)
• Viral vector-mediated gene therapies (Q38564564) (← links)
• Analysis of the functional consequences of targeted exon deletion in COL7A1 reveals prospects for dystrophic epidermolysis bullosa therapy (Q38772377) (← links)
• Stability of the human dystrophin transcript in muscle (Q39717109) (← links)
• Hybrid spectrin type repeats produced by exon-skipping in dystrophin (Q40323276) (← links)
• Dystrophin, its gene, and the dystrophinopathies (Q40373239) (← links)
• Dystrophin and its isoforms (Q41160193) (← links)
• 4. Gene Therapy of Duchenne Muscular Dystrophy (Q41625113) (← links)
• An inherited dystrophin deletion without muscle weakness (Q42659012) (← links)
• Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin (Q42951346) (← links)
• The lacZ gene under the control of the 7 kb of human dystrophin muscle specific promoter is expressed in cardiac muscle but not in adult skeletal muscle in transgenic mice (Q43571933) (← links)
• Mutation rates in the dystrophin gene: a hotspot of mutation at a CpG dinucleotide (Q46793620) (← links)
• Molecular characterisation of Duchenne muscular dystrophy and phenotypic correlation (Q47995938) (← links)
• The MurineDNA-PKcsGene Consists of 86 Exons Dispersed in More Than 250 kb (Q48044015) (← links)
• Ataxia-telangiectasia locus: sequence analysis of 184 kb of human genomic DNA containing the entire ATM gene (Q48049185) (← links)
• Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family (Q48086059) (← links)