RNA structure of trinucleotide repeats associated with human neurological diseases.
暂无分享,去创建一个
Jacek Krol | Krzysztof Sobczak | J. Krol | K. Sobczak | W. Krzyzosiak | Gracjan Michlewski | Wlodzimierz J Krzyzosiak | Mateusz de Mezer | G. Michlewski | M. de Mezer
[1] J. Mandel,et al. Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells. , 2002, Human molecular genetics.
[2] T. Cooper,et al. Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing. , 2002, Molecular cell.
[3] Aaron Klug,et al. Crystallographic and biochemical investigation of the lead(II)-catalyzed hydrolysis of yeast phenylalanine tRNA. , 1985 .
[4] L. Timchenko,et al. Cardiac elav-type RNA-binding protein (ETR-3) binds to RNA CUG repeats expanded in myotonic dystrophy. , 1999, Human molecular genetics.
[5] M. Napierala,et al. CUG Repeats Present in Myotonin Kinase RNA Form Metastable “Slippery” Hairpins* , 1997, The Journal of Biological Chemistry.
[6] W. Krzyzosiak,et al. Patterns of cleavages induced by lead ions in defined RNA secondary structure motifs. , 1998, Journal of molecular biology.
[7] S. Naylor,et al. Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9 , 2001, Science.
[8] R. Sinden,et al. Unexpected formation of parallel duplex in GAA and TTC trinucleotide repeats of Friedreich's ataxia. , 2000, Journal of molecular biology.
[9] Y. Kashi,et al. Simple sequence repeats as a source of quantitative genetic variation. , 1997, Trends in genetics : TIG.
[10] S. Warren,et al. Translational suppression by trinucleotide repeat expansion at FMR1 , 1995, Science.
[11] J. Ebel,et al. Probing the structure of RNAs in solution. , 1987, Nucleic acids research.
[12] M. Hayden,et al. Double-stranded RNA-dependent protein kinase, PKR, binds preferentially to Huntington's disease (HD) transcripts and is activated in HD tissue. , 2001, Human molecular genetics.
[13] M. Tohyama,et al. Human Tra2 Proteins Are Sequence-Specific Activators of Pre-mRNA Splicing , 1998, Cell.
[14] J. Ebel,et al. Characterization of the lead(II)-induced cleavages in tRNAs in solution and effect of the Y-base removal in yeast tRNAPhe. , 1988, Biochemistry.
[15] M. Mahadevan,et al. The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation. , 2001, Human molecular genetics.
[16] J. Eberwine,et al. CAG trinucleotide RNA repeats interact with RNA-binding proteins. , 1996, American journal of human genetics.
[17] Kunio Inoue,et al. Regulation of alternative splicing of α‐actinin transcript by Bruno‐like proteins , 2002 .
[18] Michael Zuker,et al. Algorithms and Thermodynamics for RNA Secondary Structure Prediction: A Practical Guide , 1999 .
[19] H. Zoghbi,et al. Fourteen and counting: unraveling trinucleotide repeat diseases. , 2000, Human molecular genetics.
[20] Brooke L Heidenfelder,et al. Hairpin Formation in Friedreich's Ataxia Triplet Repeat Expansion* , 2003, The Journal of Biological Chemistry.
[21] M. Swanson,et al. Visualization of double-stranded RNAs from the myotonic dystrophy protein kinase gene and interactions with CUG-binding protein. , 1999, Nucleic acids research.
[22] A. Delacourte,et al. Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities. , 2001, Human molecular genetics.
[23] L. Ranum,et al. Dominantly inherited, non-coding microsatellite expansion disorders. , 2002, Current opinion in genetics & development.
[24] M. Napierala,et al. RNA STRUCTURE MODULES WITH TRINUCLEOTIDE REPEAT MOTIFS , 1999 .
[25] A Klug,et al. Crystallographic and biochemical investigation of the lead(II)-catalyzed hydrolysis of yeast phenylalanine tRNA. , 1985, Biochemistry.
[26] S. Tapscott,et al. Biomedicine. Reconstructing myotonic dystrophy. , 2001, Science.
[27] B. McEwen,et al. Structural properties of Friedreich's ataxia d(GAA) repeats. , 1999, Biochimica et biophysica acta.
[28] S. Cannon,et al. Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy. , 2002, Molecular cell.
[29] A. Welm,et al. CUG repeat binding protein (CUGBP1) interacts with the 5'''' region of C/EBPβ β β β mRNA and regulates translation of C/EBPβ , 1999 .
[30] H. Shah,et al. Myotonic syndromes. , 1970, Indian pediatrics.
[31] S. Tapscott,et al. Reconstructing Myotonic Dystrophy , 2001, Science.
[32] P. Patel,et al. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion , 1996, Science.
[33] J. David Brook,et al. In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts , 2001, Nucleic Acids Res..
[34] Marek Napierala,et al. Structures of trinucleotide repeats in human transcripts and their functional implications. , 2003, Nucleic acids research.
[35] Branko Borstnik,et al. Tandem repeats in protein coding regions of primate genes. , 2002, Genome research.
[36] P. Good,et al. A Family of Human RNA-binding Proteins Related to theDrosophila Bruno Translational Regulator* , 2000, The Journal of Biological Chemistry.
[37] C. Caskey,et al. Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy. , 1996, Human molecular genetics.
[38] E. Hoffman,et al. Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation. , 1995, Human molecular genetics.
[39] R I Richards,et al. Dynamic mutation: possible mechanisms and significance in human disease. , 1997, Trends in biochemical sciences.
[40] Richard R. Sinden,et al. Neurodegenerative diseases: Origins of instability , 2001, Nature.
[41] M. Swanson,et al. Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2. , 2001, Human molecular genetics.
[42] T. Cooper,et al. Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy , 2001, Nature Genetics.
[43] P. Patel,et al. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. , 1998, American journal of human genetics.
[44] R. Wells,et al. The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders. , 2001, Progress in nucleic acid research and molecular biology.
[45] T. Cooper,et al. The CELF Family of RNA Binding Proteins Is Implicated in Cell-Specific and Developmentally Regulated Alternative Splicing , 2001, Molecular and Cellular Biology.
[46] L. Timchenko,et al. Myotonic dystrophy: the role of RNA CUG triplet repeats. , 1999, American journal of human genetics.
[47] A. Welm,et al. CUG repeat binding protein (CUGBP1) interacts with the 5' region of C/EBPbeta mRNA and regulates translation of C/EBPbeta isoforms. , 1999, Nucleic acids research.
[48] P. Harper,et al. Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells. , 2002, Human molecular genetics.
[49] D. Turner,et al. Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKR. , 2000, RNA.
[50] M. Mahadevan,et al. Mutant DMPK 3′-UTR transcripts disrupt C2C12 myogenic differentiation by compromising MyoD , 2002, The Journal of cell biology.
[51] T. Cooper,et al. Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy. , 1998, Science.
[52] Kunio Inoue,et al. Regulation of alternative splicing of alpha-actinin transcript by Bruno-like proteins. , 2002, Genes to cells : devoted to molecular & cellular mechanisms.
[53] M. Pandolfo,et al. Sticky DNA, a Self-associated Complex Formed at Long GAA·TTC Repeats in Intron 1 of the Frataxin Gene, Inhibits Transcription* , 2001, The Journal of Biological Chemistry.
[54] J. Jurka,et al. Microsatellites in different eukaryotic genomes: survey and analysis. , 2000, Genome research.
[55] C. Florentz,et al. Chapter 5 – Classical and Novel Chemical Tools for RNA Structure Probing , 2001 .
[56] J. Sabina,et al. Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. , 1999, Journal of molecular biology.
[57] B. Byrne,et al. Recruitment of human muscleblind proteins to (CUG)n expansions associated with myotonic dystrophy , 2000, The EMBO journal.