Molecular Diagnostics in Spinocerebellar ataxia Type 2 Molecular Diagnostics in Spinocerebellar ataxia Type 2 The virus triggered an inherited degenerative disease called Spinocerebellar ataxia Type7 (Photo:... The virus triggered an inherited degenerative disease called Spinocerebellar ataxia Type7 (Photo:... Figure 3. SCA1 neuropathology is improved by shRNAs directed to ataxin-1. ( a ) SCA and wild-type... Figure 3. SCA1 neuropathology is improved by shRNAs directed to ataxin-1. ( a ) SCA and wild-type... Figure 1. Silencing ataxin-1. ( a ) Cartoon of the ataxin-1 cDNA and regions tested for silencing... Figure 1. Silencing ataxin-1. ( a ) Cartoon of the ataxin-1 cDNA and regions tested for silencing... (From left) Dr. Y.Y. Anne CHAN Division of Neurology Department of Medicine and Therapeutics CUHK... (From left) Dr. Y.Y. Anne CHAN, Division of Neurology, Department of Medicine and Therapeutics, CUHK... Figure 5. Sca10 is widely expressed in brain regions that are anatomical substrates for ataxia and... Figure 5. Sca10 is widely expressed in brain regions that are anatomical substrates for ataxia and... There are numerous types of autosomal dominant cerebellar ataxias There are numerous types of autosomal dominant cerebellar ataxias ( Figure 1. Tsuda et al . demonstrate homologous pathways that mediate ataxin-1–induced... ( Figure 1. Tsuda et al . demonstrate homologous pathways that mediate ataxin-1–induced... Figure 1. Expansion mutations in four SCA10 families. a Pedigrees of the four families studied for... Figure 1. Expansion mutations in four SCA10 families. a , Pedigrees of the four families studied for... Figure 1. Clinical findings and haplotype analysis. a b A T1-weighted magnetic resonance imaging... Figure 1. Clinical findings and haplotype analysis. a , b , A T1-weighted magnetic resonance imaging... Figure 4. Correlation between the size of expanded SCA10 ATTCT repeat and the age of onset. A... Figure 4. Correlation between the size of expanded SCA10 ATTCT repeat and the age of onset. A... Figure 3. The physical map of the ATTCT pentanucleotide repeat region. a A schematic presentation... Figure 3. The physical map of the ATTCT pentanucleotide repeat region. a , A schematic presentation... Figure 1. BAC expansion and control constructs. ( a ) Diagram of control BAC (BAC-Ctl) and modified... Figure 1. BAC expansion and control constructs. ( a ) Diagram of control BAC (BAC-Ctl) and modified... Please join Dr. Juan Young in welcoming Dr. Puneet Opal today in Special Seminar Puneet Opal M.D.... Please join Dr. Juan Young in welcoming Dr. Puneet Opal today in Special Seminar Puneet Opal, M.D.,... Ataxia Research Ataxia Research Figure 1 : AFG3L2 mutations cause amino acid substitutions in highly conserved regions of the... Figure 1 : AFG3L2 mutations cause amino acid substitutions in highly conserved regions of the... Figure 4. Model of the resolution of stalled covalent topoisomerase I−DNA complexes that result in... Figure 4. Model of the resolution of stalled covalent topoisomerase I−DNA complexes that result in... Very short stocky and solid build. Very short, stocky and solid build. Next Next Figure 1. RAPID cloning of the SCA8 expanded CTG repeat. a 2D-RED analysis of Eco RI-digested... Figure 1. RAPID cloning of the SCA8 expanded CTG repeat. a , 2D-RED analysis of Eco RI-digested... Figure 2. Physical map of 14q23−q32 and molecular analyses of TDP1 . a Physical map of the... Figure 2. Physical map of 14q23−q32 and molecular analyses of TDP1 . a , Physical map of the... リンク元 「 オリーブ橋小脳萎縮症 」「 線条体黒質変性症 」「 脊髄小脳変性症 」「 多系統萎縮症 」「 SCA 」 リンク元 「 オリーブ橋小脳萎縮症 」「 線条体黒質変性症 」「 脊髄小脳変性症 」「 多系統萎縮症 」「 SCA 」 Figure 2. Large SCA8 kindred. Filled symbols indicate individuals with ataxia symbols with a dot... Figure 2. Large SCA8 kindred. Filled symbols indicate individuals with ataxia, symbols with a dot... ...upon myotonic dystrophy fragile X Spinocerebellar ataxia type 7 and Huntington's disease loci. ...upon myotonic dystrophy, fragile X, Spinocerebellar ataxia type 7, and Huntington's disease loci. ...upon myotonic dystrophy fragile X Spinocerebellar ataxia type 7 and Huntington's disease loci. ...upon myotonic dystrophy, fragile X, Spinocerebellar ataxia type 7, and Huntington's disease loci. ...upon myotonic dystrophy fragile X Spinocerebellar ataxia type 7 and Huntington's disease loci. ...upon myotonic dystrophy, fragile X, Spinocerebellar ataxia type 7, and Huntington's disease loci. ...upon myotonic dystrophy fragile X Spinocerebellar ataxia type 7 and Huntington's disease loci. ...upon myotonic dystrophy, fragile X, Spinocerebellar ataxia type 7, and Huntington's disease loci. ...upon myotonic dystrophy fragile X Spinocerebellar ataxia type 7 and Huntington's disease loci. ...upon myotonic dystrophy, fragile X, Spinocerebellar ataxia type 7, and Huntington's disease loci.
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