Repeat instability: mechanisms of dynamic mutations

Cited by (927)

Items 101–200 of 927

1. Coordination between Polymerase β and FEN1 Can Modulate CAG Repeat Expansion
   Yuan Liu, Rajendra Prasad, William A. Beard, Esther W. Hou, Julie K. Horton, Cynthia T. McMurray, Samuel H. Wilson · 2009 · Journal of Biological Chemistry
2. Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry in Genomics Research
   Jiannis Ragoussis, Gareth P. Elvidge, Kulvinder Kaur, Stefano Colella · 2006 · PLoS Genetics
3. Bidirectional transcription stimulates expansion and contraction of expanded (CTG)•(CAG) repeats
   Masayuki Nakamori, Christopher E. Pearson, Charles A. Thornton · 2010 · Human Molecular Genetics
4. Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients
   Irene De Biase, Astrid Rasmussen, Dan Endres, Sahar Al‐Mahdawi, Antonella Monticelli, Sergio Cocozza, Mark A. Pook, Sanjay I. Bidichandani · 2007 · Annals of Neurology
5. Instability and chromatin structure of expanded trinucleotide repeats
   Vincent Dion, John H. Wilson · 2009 · Trends in Genetics
6. AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission
   Carolyn M. Yrigollen, Loreto Martorell, Blythe P Durbin-Johnson, Montserrat Naudó, Jordi Genovès, Alessandra Murgia, Roberta Polli, Lili Zhou, Deborah Barbouth, Abigail Rupchock Deppen et al. · 2014 · Journal of Neurodevelopmental Disorders
7. Processing of double-R-loops in (CAG)·(CTG) and C9orf72 (GGGGCC)·(GGCCCC) repeats causes instability
   Kaalak Reddy, Monika H.M. Schmidt, Jaimie M. Geist, Neha Thakkar, Gagan B. Panigrahi, Yuh‐Hwa Wang, Christopher E. Pearson · 2014 · Nucleic Acids Research
8. Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cells.
   A. Bigot, A. Klein, E. Gasnier, V. Jacquemin, P. Ravassard, G. Butler-Browne, V. Mouly, D. Furling · 2009 · American Journal of Pathology
9. CTG Trinucleotide Repeat “Big Jumps”: Large Expansions, Small Mice
   Mário Gomes-Pereira, Laurent Foiry, Annie Nicole, Aline Huguet-Lachon, Claudine Junien, Arnold Münnich, Geneviève Gourdon · 2007 · PLoS Genetics
10. Epistatic Module Detection for Case-Control Studies: A Bayesian Model with a Gibbs Sampling Strategy
    Wanwan Tang, Xuebing Wu, Rui Jiang, Yanda Li · 2009 · PLoS Genetics
11. DNA base excision repair: a mechanism of trinucleotide repeat expansion
    Yuan Liu, Samuel H. Wilson · 2012 · Trends in Biochemical Sciences
12. De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1
    Sarah A. Cumming, Mark Hamilton, Yvonne Robb, Helen Gregory, Catherine A. McWilliam, Anneli Cooper, Berit Adam, Josephine McGhie, Graham M. Hamilton, Pawel Herzyk et al. · 2018 · European Journal of Human Genetics
13. Hairpin- and cruciform-mediated chromosome breakage: causes and consequences in eukaryotic cells
    S. Lobachev Kirill · 2007 · Frontiers in bioscience
14. A Genomic Portrait of Human Microsatellite Variation
    Bret A. Payseur, Peicheng Jing, Ryan J. Haasl · 2010 · Molecular Biology and Evolution
15. Mechanisms of tandem repeat instability in bacteria
    Marc Bichara, Jérôme E. Wagner, Iain B. Lambert · 2006 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
16. CAG-encoded polyglutamine length polymorphism in the human genome
    S. Butland, R. S. Devon, Yong Huang, Carri-Lyn Mead, A. Meynert, S. J. Neal, Soo-Sen Lee, Anna Wilkinson, George S. Yang, M. M. Yuen et al. · 2007 · BMC Genomics
17. MSH2 ATPase Domain Mutation Affects CTG•CAG Repeat Instability in Transgenic Mice
    Stéphanie Tomé, Ian Holt, Winfried Edelmann, Glenn E. Morris, Arnold Münnich, Christopher E. Pearson, Geneviève Gourdon · 2009 · PLoS Genetics
18. The DNA Replication Program Is Altered at the FMR1 Locus in Fragile X Embryonic Stem Cells
    Jeannine Gerhardt, Mark J. Tomishima, Nikica Zaninović, Dilek Colak, Zi Yan, Qiansheng Zhan, Zev Rosenwaks, Samie R. Jaffrey, Carl L. Schildkraut · 2013 · Molecular Cell
19. Review of tandem repeat search tools: a systematic approach to evaluating algorithmic performance
    K. G. Lim, Chee Keong Kwoh, Li Yang Hsu, Adrianto Wirawan · 2012 · Briefings in Bioinformatics
20. Involvement of long noncoding RNAs in diseases affecting the central nervous system
    Pastori, Chiara, Wahlestedt, Claes · 2012 · RNA Biology
21. PolyQ Repeat Expansions in ATXN2 Associated with ALS Are CAA Interrupted Repeats
    Zhenming Yu, Yongqing Zhu, Alice S. Chen‐Plotkin, Dana Clay-Falcone, Leo F. McCluskey, Lauren B. Elman, Robert Gordon Kalb, John Q. Trojanowski, Virginia M.‐Y. Lee, Vivianna M. Van Deerlin et al. · 2011 · PLoS ONE
22. Spinocerebellar Ataxia Type 2: Clinical Presentation, Molecular Mechanisms, and Therapeutic Perspectives
    Jonathan J. Magaña, Luis Velázquez‐Pérez, Bulmaro Cisneros · 2012 · Molecular Neurobiology
23. Accurate typing of short tandem repeats from genome-wide sequencing data and its applications
    Arkarachai Fungtammasan, Guruprasad Ananda, Suzanne E. Hile, Marcia Shu‐Wei Su, Chen Sun, Robert Harris, Paul Medvedev, Kristin A. Eckert, Kateryna D. Makova · 2015 · Genome Research
24. The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3’-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis
    Arpita Chatterjee, Saikat Saha, Anirban Chakraborty, Anabela Silva‐Fernandes, Santi M. Mandal, Andreia Neves‐Carvalho, Yongping Liu, RAJ KUMAR PANDITA, Muralidhar L. Hegde, Pavana M. Hegde et al. · 2015 · PLoS Genetics
25. Dnmt1 deficiency promotes CAG repeat expansion in the mouse germline
    Vincent Dion, Yunfu Lin, Leroy Hubert, Robert A. Waterland, John H. Wilson · 2008 · Human Molecular Genetics
26. A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
    Ana Westenberger, Charles Jourdan Reyes, Gerard Saranza, Valerija Dobričić, Henrike Hanßen, Aloysius Domingo, Björn‐Hergen Laabs, Susen Schaake, Jelena Pozojevic, Aleksandar Raković et al. · 2019 · Annals of Neurology
27. Local and global functions of Timeless and Tipin in replication fork protection
    Adam R. Leman, Eishi Noguchi · 2012 · Cell Cycle
28. SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination
    A. Kerrest, Ranjith P. Anand, Rangapriya Sundararajan, Rodrigo Bermejo, G. Liberi, B. Dujon, C. Freudenreich, Guy-Franck Richard · 2009 · Nature Structural &Molecular Biology
29. Zinc-finger directed double-strand breaks within CAG repeat tracts promote repeat instability in human cells
    David Mittelman, Christopher Moye, J. Jason Morton, Kristen Sykoudis, Yunfu Lin, Dana Carroll, John H. Wilson · 2009 · Proceedings of the National Academy of Sciences
30. Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSβ, but clustered slip-outs are poorly repaired
    Gagan B. Panigrahi, Meghan M. Slean, Jodie P. Simard, O. Gileadi, Christopher E. Pearson · 2010 · Proceedings of the National Academy of Sciences
31. Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications
    Indhu‐Shree Rajan‐Babu, Egor Dolzhenko, Michael A. Eberle, Jan M. Friedman · 2024 · Nature Reviews Genetics
32. A Genetic Defect Caused by a Triplet Repeat Expansion in Arabidopsis thaliana
    Sridevi Sureshkumar, Marco Todesco, Korbinian Schneeberger, Ramya Harilal, Sureshkumar Balasubramanian, Detlef Weigel · 2009 · Science
33. A FRET-based screening assay for nucleic acid ligands
    Daniel Renčiuk, Jun Zhou, Lionel Beaurepaire, Aurore Guédin, Anne Bourdoncle, Jean‐Louis Mergny · 2012 · Methods
34. Molecular mechanisms underlying polyalanine diseases
    Christiane Messaed, Guy Armand Rouleau · 2009 · Neurobiology of Disease
35. Roles of non-canonical structures of nucleic acids in cancer and neurodegenerative diseases
    Hisae Tateishi‐Karimata, Naoki Sugimoto · 2021 · Nucleic Acids Research
36. CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease
    Alicia Semaka, Chris Kay, Crystal N. Doty, Jennifer A. Collins, Emilia K. Bijlsma, Fiona Richards, Y. Paul Goldberg, Michael R. Hayden · 2013 · Journal of Medical Genetics
37. Common Fragile Sites: Genomic Hotspots of DNA Damage and Carcinogenesis
    Ke Ma, Li Qiu, Kristin Mrasek, Jun Zhang, Thomas Liehr, Luciana Gonçalves Quintana, Zheng Li · 2012 · International Journal of Molecular Sciences
38. Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models
    Vanessa C. Wheeler, Vincent Dion · 2021 · Journal of Huntington s Disease
39. Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation
    Anna Seriola, Claudia Spits, Jodie P. Simard, Pierre Hilven, Patrick Haentjens, Christopher E. Pearson, Karen Sermon · 2010 · Human Molecular Genetics
40. The role of oxidative stress in neurodegenerative diseases and potential antioxidant therapies
    Paula Sienes Bailo, Elena Llorente Martín, Pilar Calmarza, Silvia Montolio Breva, Adrián Bravo Gómez, Adela Pozo Giráldez, Juan J Sánchez-Pascuala Callau, Juana Maria Vaquer Santamaría, Anita Dayaldasani, Concepción Cerdá Micó et al. · 2022 · Advances in Laboratory Medicine / Avances en Medicina de Laboratorio
41. Detection of genomic regions underlying resistance to gastrointestinal parasites in Australian sheep
    Mohammad Al Kalaldeh, John P. Gibson, Sang Lee, Cedric Gondro, Julius H. J. van der Werf · 2019 · Genetics Selection Evolution
42. Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17
    Rui Gao, Tohru Matsuura, Mary I. Coolbaugh-Murphy, Christine Zühlke, Koichiro Nakamura, Astrid Rasmussen, Michael J. Siciliano, Tetsuo Ashizawa, Xi Lin · 2007 · European Journal of Human Genetics
43. Transcription destabilizes triplet repeats
    Yunfu Lin, Leroy Hubert, John H. Wilson · 2008 · Molecular Carcinogenesis
44. Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences
    Terence Gall-Duncan, Nozomu J. Sato, Ryan K. C. Yuen, Christopher E. Pearson · 2021 · Genome Research
45. A Universal Mechanism Ties Genotype to Phenotype in Trinucleotide Diseases
    Shai Kaplan, Shalev Itzkovitz, Ehud Y. Shapiro · 2007 · PLoS Computational Biology
46. Microsatellite Markers in Plants and Insects. Part I: Applications of Biotechnology
    Ming Li Wang, Noelle A. Barkley, Tracie M. Jenkins · 2009
47. Inferring short tandem repeat variation from paired-end short reads
    Minh Duc Cao, Edward Tasker, Kai Willadsen, Michael Imelfort, Sailaja Vishwanathan, Sridevi Sureshkumar, Sureshkumar Balasubramanian, Mikael Bodén A · 2013 · Nucleic Acids Research
48. Abiotic stress leads to somatic and heritable changes in homologous recombination frequency, point mutation frequency and microsatellite stability in Arabidopsis plants
    Youli Yao, Igor Kovalchuk · 2011 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
49. Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation
    Flora Tassone, Dragana D. Protic, Emily Graves Allen, Alison Dalton Archibald, Anna Baud, Ted W. Brown, Dejan B. Budimirovic, Jonathan Cohen, Brett D. Dufour, Rachel Eiges et al. · 2023 · Cells
50. Hijacking of the mismatch repair system to cause CAG expansion and cell death in neurodegenerative disease
    Cynthia T. McMurray · 2008 · DNA repair
51. Myotonic dystrophy types 1 and 2
    Tetsuo Ashizawa, Partha S. Sarkar · 2011 · Handbook of clinical neurology
52. Rad3ATR Decorates Critical Chromosomal Domains with γH2A to Protect Genome Integrity during S-Phase in Fission Yeast
    Sophie Rozenzhak, Eva Mejía-Ramírez, Jessica S. Williams, Lana Schaffer, Jennifer A. Hammond, Steven Robert Head, Paul R. Russell · 2010 · PLoS Genetics
53. The locus of sexual selection: moving sexual selection studies into the post‐genomics era
    Gerald S. Wilkinson, Felix J. Breden, Judith E. Mank, Michael Gordon Ritchie, Andrew D. Higginson, Jacek Radwan, Julie Jaquiéry, Walter Salzburger, Elena Arriero, Seth Michael Barribeau et al. · 2015 · Journal of Evolutionary Biology
54. Semi-automated quantification of C9orf72 expansion size reveals inverse correlation between hexanucleotide repeat number and disease duration in frontotemporal degeneration
    EunRan R. Suh, Edward B. Lee, Donald Neal, Elisabeth McCarty Wood, Jon B. Toledo, Lior Rennert, David John Irwin, Corey T. McMillan, Bryan L. Krock, Lauren B. Elman et al. · 2015 · Acta Neuropathologica
55. Detection of Slipped-DNAs at the Trinucleotide Repeats of the Myotonic Dystrophy Type I Disease Locus in Patient Tissues
    Michelle M. Axford, Yuh‐Hwa Wang, Masayuki Nakamori, Maria Zannis‐Hadjopoulos, Charles A. Thornton, Christopher E. Pearson · 2013 · PLoS Genetics
56. Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1
    Leroy Hubert, Yunfu Lin, Vincent Dion, John H. Wilson · 2011 · Human Molecular Genetics
57. A matter of life or death: How microsatellites emerge in and vanish from the human genome
    Yogeshwar Kelkar, Kristin A. Eckert, Francesca Chiaromonte, Kateryna D. Makova · 2011 · Genome Research
58. FAN1, a DNA Repair Nuclease, as a Modifier of Repeat Expansion Disorders
    Amit Laxmikant Deshmukh, Antônio Porro, Mohiuddin Mohiuddin, Stella Lanni, Gagan B. Panigrahi, Marie‐Christine Caron, Jean‐Yves Masson, Alessandro A. Sartori, Christopher E. Pearson · 2021 · Journal of Huntington s Disease
59. Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus
    Cleary, John D, Tomé, Stéphanie, López Castel, Arturo, Panigrahi, Gagan B, Foiry, Laurent, Hagerman, Katharine A, Sroka, Hana, Chitayat, David, Gourdon, Geneviève, Pearson, Christopher E · 2010 · Nature Structural & Molecular Biology
60. Genome-wide insertion–deletion (InDel) marker discovery and genotyping for genomics-assisted breeding applications in chickpea
    Shouvik Das, Hari Deo Upadhyaya, Rishi Srivastava, Deepak Bajaj, C L L Gowda, Shivali Sharma, Sube Singh, Akhilesh Kumar Tyagi, Swarup Kumar Parida · 2015 · DNA Research
61. RNA toxicity in human disease and animal models: From the uncovering of a new mechanism to the development of promising therapies
    Géraldine Sicot, Mário Gomes-Pereira · 2013 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
62. Low-complexity sequences and single amino acid repeats: not just “junk” peptide sequences
    Wilfried Haerty, G. Brian Golding · 2010 · Genome
63. Myotonic Dystrophy Type 1 Management and Therapeutics
    Cheryl A. S. Smith, Laurie Gutmann · 2016 · Current Treatment Options in Neurology
64. Molecular Genetics and Genetic Testing in Myotonic Dystrophy Type 1
    Dusanka Savic Pavicevic, Jelena Miladinović, Miloš Brkušanin, Saša Šviković, Svetlana Djurica, Goran N. Brajušković, Stanka P. Romac · 2013 · BioMed Research International
65. Quadruplex formation by both G-rich and C-rich DNA strands of theC9orf72(GGGGCC)8•(GGCCCC)8 repeat: effect of CpG methylation
    Bita Zamiri, Mila Mirceta, Karol Bomsztyk, Robert B. Macgregor, Christopher E. Pearson · 2015 · Nucleic Acids Research
66. Type 2 NF1 Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination
    Katharina Steinmann, D.N. Cooper, Lan Kluwe, Nadia A Chuzhanova, Cornelia Senger, Eduard Serra, Conxi Lázaro, Montserrat Gilaberte, Katharina Wimmer, Viktor-Felix Mautner et al. · 2007 · The American Journal of Human Genetics
67. Detecting short tandem repeats from genome data: opening the software black box
    Angelika Merkel, Neil J. Gemmell · 2008 · Briefings in Bioinformatics
68. Risk factors for the onset and progression of Huntington disease
    Ting-Kuang Chao, Jing Ying Hu, Tamara Milka Pringsheim · 2017 · NeuroToxicology
69. Mutation–selection balance and compensatory mechanisms in tumour evolution
    Erez Persi, Yuri I. Wolf, D. Horn, Eytan Ruppin, Francesca Demichelis, Robert A. Gatenby, Robert J. Gillies, Eugene V. Koonin · 2020 · Nature Reviews Genetics
70. Microhomology-mediated DNA strand annealing and elongation by human DNA polymerases λ and β on normal and repetitive DNA sequences
    Emmanuele Crespan, Tibor Czabany, Giovanni Maga, Ulrich Hübscher · 2012 · Nucleic Acids Research
71. Progressive GAA·TTC Repeat Expansion in Human Cell Lines
    Scott Ditch, Mimi C. Sammarco, Ayan Banerjee, Ed Grabczyk · 2009 · PLoS Genetics
72. Unstable familial transmissions of Huntington disease alleles with 27–35 CAG repeats (intermediate alleles)
    Alicia Semaka, Jennifer A. Collins, Michael R. Hayden · 2009 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
73. Dynamic mutations as digital genetic modulators of brain development, function and dysfunction
    Jess Nithianantharajah, Anthony John Hannan · 2007 · BioEssays
74. Double-Strand Break Repair Pathways Protect against CAG/CTG Repeat Expansions, Contractions and Repeat-Mediated Chromosomal Fragility in Saccharomyces cerevisiae
    Rangapriya Sundararajan, Lionel Gellon, Rachel M. Zunder, Catherine H. Freudenreich · 2009 · Genetics
75. Accessing the Inaccessible: The Organization, Transcription, Replication, and Repair of Heterochromatin in Plants
    Wei Feng, Scott D. Michaels · 2015 · Annual Review of Genetics
76. Maternal age and paternal age are associated with distinct childhood behavioural outcomes in a general population birth cohort
    Sukanta Saha, Adrian Gerard Barnett, Stephen L. Buka, John Joseph McGrath · 2009 · Schizophrenia Research
77. Highly Specific Contractions of a Single CAG/CTG Trinucleotide Repeat by TALEN in Yeast
    Guy‐Franck Richard, David Viterbo, Varun Khanna, Valentine Mosbach, Lauriane Castelain, Bernard Dujon · 2014 · PLoS ONE
78. The Genetics of Pulmonary Arterial Hypertension in the Post‐BMPR2 Era
    Joshua P. Fessel, James E. Loyd, Eric D. Austin · 2011 · Pulmonary Circulation
79. Genomic architecture at the Incontinentia Pigmenti locus favours de novo pathological alleles through different mechanisms
    Francesca Fusco, Mariateresa Paciolla, Federico Napolitano, Alessandra Pescatore, Irene D’Addario, Élodie Bal, Maria Brigida Lioi, Asma Smahi, Maria Giuseppina Miano, Matilde Valeria Ursini · 2011 · Human Molecular Genetics
80. DNA slip-outs cause RNA polymerase II arrest in vitro : potential implications for genetic instability
    Viviana Salinas-Rios, Boris P. Belotserkovskii, Philip C. Hanawalt · 2011 · Nucleic Acids Research
81. Small molecule targeting r(UGGAA)n disrupts RNA foci and alleviates disease phenotype in Drosophila model
    T. Shibata, Konami Nagano, Morio Ueyama, Kensuke Ninomiya, Tetsuro Hirose, Yoshitaka Nagai, Kinya Ishikawa, Gota Kawai, Kazuhiko Nakatani · 2021 · Nature Communications
82. Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes
    Francesca Magrinelli, Bettina Balint, Kailash P. Bhatia · 2021 · Movement Disorders Clinical Practice
83. Distinct Mutational Behaviors Differentiate Short Tandem Repeats from Microsatellites in the Human Genome
    Guruprasad Ananda, Erin M. Walsh, Kimberly D. Jacob, Maria M. Krasilnikova, Kristin A. Eckert, Francesca Chiaromonte, Kateryna D. Makova · 2012 · Genome Biology and Evolution
84. Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes
    Fiona Baine, Chris Kay, Maria E. Ketelaar, Jennifer A. Collins, Alicia Semaka, Crystal N. Doty, Amanda Krause, Leslie S. Greenberg, Michael R. Hayden · 2013 · European Journal of Human Genetics
85. APOE ε4-TOMM40 ‘523 haplotypes and the risk of Alzheimer’s disease in older Caucasian and African Americans
    Lei Yu, Michael William Lutz, Robert Smith Wilson, Daniel K. Burns, Allen D. Roses, Ann M. Saunders, Jingyun Yang, Chris Gaiteri, Philip L. De Jager, Lisa Laverne Barnes et al. · 2017 · PLoS ONE
86. Dynamics of strand slippage in DNA hairpins formed by CAG repeats: roles of sequence parity and trinucleotide interrupts
    Pengning Xu, Feng Pan, Christopher Roland, Celeste Sagui, Keith Weninger · 2020 · Nucleic Acids Research
87. Myotonic dystrophy type 1: role of CCG , CTC and CGG interruptions within DMPK alleles in the pathogenesis and molecular diagnosis
    M. Santoro, Marcella Masciullo, Gabriella Silvestri, Giuseppe Novelli, Annalisa Botta · 2016 · Clinical Genetics
88. Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation
    Celine E. F. de Esch, Mehrnaz Ghazvini, Friedemann Loos, Nune Schelling-Kazaryan, W. Widagdo, Shashini T. Munshi, Erik van der Wal, Hannie Douben, Nilhan Gunhanlar, Steven A. Kushner et al. · 2014 · Stem Cell Reports
89. Spinocerebellar ataxias
    Hélio A.G. Teive · 2009 · Arquivos de Neuro-Psiquiatria
90. High levels of somatic DNA diversity at the myotonic dystrophy type 1 locus are driven by ultra-frequent expansion and contraction mutations
    Catherine F. Higham, Fernando Morales, Christina A. Cobbold, Daniel T. Haydon, Darren G. Monckton · 2012 · Human Molecular Genetics
91. Convergent Transcription through a Long CAG Tract Destabilizes Repeats and Induces Apoptosis
    Yunfu Lin, Mei Leng, Ma Wan, John H. Wilson · 2010 · Molecular and Cellular Biology
92. Repeat-associated non-AUG (RAN) translation: insights from pathology
    Mónica Báñez-Coronel, Laura P.W. Ranum · 2019 · Laboratory Investigation
93. Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases
    Giulietta Maria Riboldi, Chiara Zanetta, Michela Ranieri, Monica Nizzardo, Chiara Simone, Francesca Magri, Nereo Bresolin, Giacomo P. Comi, Stefania Paola Corti · 2014 · Molecular Neurobiology
94. Evolution of a Human-Specific Tandem Repeat Associated with ALS
    Meredith M. Course, Kathryn M. Gudsnuk, Samuel N. Smukowski, Kosuke Winston, Nitin Desai, Jay P. Ross, Arvis Sulovari, Cynthia V. Bourassa, Dan Spiegelman, Julien Couthouis et al. · 2020 · The American Journal of Human Genetics
95. Genome-wide characterization of microsatellite DNA in fishes: survey and analysis of their abundance and frequency in genome-specific regions
    Yi Lei, Yu Zhou, Megan Price, Zhaobin Song · 2021 · BMC Genomics
96. RNA–protein interactions in unstable microsatellite diseases
    Apoorva Mohan, Marianne Goodwin, Maurice S. Swanson · 2014 · Brain Research
97. Ontology and diversity of transcript-associated microsatellites mined from a globe artichoke EST database
    Davide Scaglione, Alberto Acquadro, Ezio Portis, Christopher A Taylor, Sergio Lanteri, Steven J. Knapp · 2009 · BMC Genomics
98. A call to arms: on refining Plasmodium vivax microsatellite marker panels for comparing global diversity
    Patrick L Sutton · 2013 · Malaria Journal
99. Sequence determinants of human microsatellite variability
    Trevor J. Pemberton, Conner I. Sandefur, Mattias Jakobsson, Noah A. Rosenberg · 2009 · BMC Genomics
100. TSSV: a tool for characterization of complex allelic variants in pure and mixed genomes
     Seyed Yahya Anvar, Kristiaan J. van der Gaag, Jaap W. F. van der Heijden, Marcel H. A. M. Veltrop, Rolf H. A. M. Vossen, Rick H. de Leeuw, Cor Breukel, Henk P.J. Buermans, J. Sjef Verbeek, Peter de Knijff et al. · 2014 · Bioinformatics