Non-B DNA conformations, mutagenesis and disease von Wells, Robert D.

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DNA Triplet Repeat Expansion and Mismatch Repair von Iyer, Ravi R, Pluciennik, Anna, Napierala, Marek, Wells, Robert D

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Non-B DNA conformations, genomic rearrangements, and human disease von Bacolla, Albino, Wells, Robert D

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Non-B DNA conformations as determinants of mutagenesis and human disease von Bacolla, Albino, Wells, Robert D.

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R Loops Stimulate Genetic Instability of CTG · CAG Repeats von Lin, Yunfu, Dent, Sharon Y. R., Wilson, John H., Wells, Robert D., Napierala, Marek, Hanawalt, Philip C.

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prose: a python framework for modular astronomical images processing von Garcia, Lionel J, Timmermans, Mathilde, Pozuelos, Francisco J, Ducrot, Elsa, Gillon, Michaël, Delrez, Laetitia, Wells, Robert D, Jehin, Emmanuël

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Discovery of the Role of Non-B DNA Structures in Mutagenesis and Human Genomic Disorders von Wells, Robert D.

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DNA triplexes and Friedreich ataxia von Wells, Robert D

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Breakpoints of Gross Deletions Coincide with Non-B DNA Conformations von Bacolla, Albino, Jaworski, Adam, Larson, Jacquelynn E., Jakupciak, John P., Chuzhanova, Nadia, Abeysinghe, Shaun S., O'Connell, Catherine D., Cooper, David N., Wells, Robert D., Modrich, Paul L.

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Gene conversion causing human inherited disease: Evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair von Chuzhanova, Nadia, Chen, Jian-Min, Bacolla, Albino, Patrinos, George P, Férec, Claude, Wells, Robert D, Cooper, David N

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Increased Negative Superhelical Density in Vivo Enhances the Genetic Instability of Triplet Repeat Sequences von Napierala, Marek, Bacolla, Albino, Wells, Robert D.

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The involvement of non-B DNA structures in gross chromosomal rearrangements von Bacolla, Albino, Wojciechowska, Marzena, Kosmider, Beata, Larson, Jacquelynn E., Wells, Robert D.

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Advancements in the pathophysiology of Friedreich’s Ataxia and new prospects for treatments von Babady, Ngolela E., Carelle, Nadege, Wells, Robert D., Rouault, Tracey A., Hirano, Michio, Lynch, David R., Delatycki, Martin B., Wilson, Robert B., Isaya, Grazia, Puccio, Hélène

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Non-B DNA Conformations Formed by Long Repeating Tracts of Myotonic Dystrophy Type 1, Myotonic Dystrophy Type 2, and Friedreich's Ataxia Genes, Not the Sequences per se, Promote Mu... von Wojciechowska, Marzena, Napierala, Marek, Larson, Jacquelynn E., Wells, Robert D.

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Hairpin Structure-forming Propensity of the (CCTG·CAGG) Tetranucleotide Repeats Contributes to the Genetic Instability Associated with Myotonic Dystrophy Type 2 von Dere, Ruhee, Napierala, Marek, Ranum, Laura P W, Wells, Robert D

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Mutation Spectra in Fragile X Syndrome Induced by Deletions of CGG·CCG Repeats von Wells, Robert D.

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The Myotonic Dystrophy Type 1 Triplet Repeat Sequence Induces Gross Deletions and Inversions von Wojciechowska, Marzena, Bacolla, Albino, Larson, Jacquelynn E., Wells, Robert D.

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Advances in mechanisms of genetic instability related to hereditary neurological diseases von Wells, Robert D., Dere, Ruhee, Hebert, Micheal L., Napierala, Marek, Son, Leslie S.

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Preferential Nucleosome Assembly at DNA Triplet Repeats from the Myotonic Dystrophy Gene von Wang, Yuh-Hwa, Amirhaeri, Sorour, Kang, Seongman, Wells, Robert D., Griffith, Jack D.

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Abundance and length of simple repeats in vertebrate genomes are determined by their structural properties von Bacolla, Albino, Larson, Jacquelynn E, Collins, Jack R, Li, Jian, Milosavljevic, Aleksandar, Stenson, Peter D, Cooper, David N, Wells, Robert D

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