Результаты поиска - Reijns, Martin A.M.

Analysis of Lsm1p and Lsm8p domains in the cellular localization of Lsm complexes in budding yeast по Reijns, Martin A M, Auchynnikava, Tatsiana, Beggs, Jean D

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Requirements for nuclear localization of Lsm2-8p and competition between nuclear and cytoplasmic Lsm complexes по Spiller, Michael P., Reijns, Martin A. M., Beggs, Jean D.

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Genome-wide mapping of embedded ribonucleotides and other non-canonical nucleotides using emRiboSeq and EndoSeq по Ding, James, Taylor, Martin S., Jackson, Andrew P., Reijns, Martin A. M.

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The Lsm2-8 complex determines nuclear localization of the spliceosomal U6 snRNA по Spiller, Michael P., Boon, Kum-Loong, Reijns, Martin A. M., Beggs, Jean D.

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A role for Q/N-rich aggregation-prone regions in P-body localization по Reijns, Martin A. M., Alexander, Ross D., Spiller, Michael P., Beggs, Jean D.

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Lagging strand replication shapes the mutational landscape of the genome по Reijns, Martin A. M., Kemp, Harriet, Ding, James, de Procé, Sophie Marion, Jackson, Andrew P., Taylor, Martin S.

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PCNA directs type 2 RNase H activity on DNA replication and repair substrates по Bubeck, Doryen, Reijns, Martin A. M., Graham, Stephen C., Astell, Katy R., Jones, E. Yvonne, Jackson, Andrew P.

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The Structure of the Human RNase H2 Complex Defines Key Interaction Interfaces Relevant to Enzyme Function and Human Disease по Reijns, Martin A. M., Bubeck, Doryen, Gibson, Lucien C. D., Graham, Stephen C., Baillie, George S., Jones, E. Yvonne, Jackson, Andrew P.

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User acceptability of saliva and gargle samples for identifying COVID-19 positive high-risk workers and household contacts по McLennan, Kirsty, Barton, Ellen, Lang, Christie, Adams, Ian R., McAllister, Gina, Reijns, Martin A.M., Templeton, Kate, Johannessen, Ingólfur, Leckie, Alastair, Gilbert, Nick

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Ribonucleotide excision repair is essential to prevent squamous cell carcinoma of the skin. по Hiller, Björn, Hoppe, Anja, Haase, Christa, Hiller, Christina, Schubert, Nadja, Müller, Werner, Reijns, Martin A. M., Jackson, Andrew P., Kunkel, Thomas A., Wenzel, Jörg, Behrendt, Rayk, Roers, Axel

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Novel Escherichia coli active site dnaE alleles with altered base and sugar selectivity по Vaisman, Alexandra, Łazowski, Krystian, Reijns, Martin A. M., Walsh, Erin, McDonald, John P., Moreno, Kristiniana C., Quiros, Dominic R., Schmidt, Marlen, Kranz, Harald, Yang, Wei, Makiela‐Dzbenska, Karolina, Woodgate, Roger

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RNA:DNA hybrids are a novel molecular pattern sensed by TLR9 по Rigby, Rachel E, Webb, Lauren M, Mackenzie, Karen J, Li, Yue, Leitch, Andrea, Reijns, Martin A M, Lundie, Rachel J, Revuelta, Ailsa, Davidson, Donald J, Diebold, Sandra, Modis, Yorgo, MacDonald, Andrew S, Jackson, Andrew P

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Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis по Mill, Pleasantine, Lockhart, Paul J., Fitzpatrick, Elizabeth, Mountford, Hayley S., Hall, Emma A., Reijns, Martin A.M., Keighren, Margaret, Bahlo, Melanie, Bromhead, Catherine J., Budd, Peter, Aftimos, Salim, Delatycki, Martin B., Savarirayan, Ravi, Jackson, Ian J., Amor, David J.

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Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model по Moss, Chloe F., Dalla Rosa, Ilaria, Hunt, Lilian E., Yasukawa, Takehiro, Young, Robert, Jones, Aleck W. E., Reddy, Kaalak, Desai, Radha, Virtue, Sam, Elgar, Greg, Voshol, Peter, Taylor, Martin S., Holt, Ian J., Reijns, Martin A. M., Spinazzola, Antonella

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cGAS surveillance of micronuclei links genome instability to innate immunity по Mackenzie, Karen J., Carroll, Paula, Martin, Carol-Anne, Murina, Olga, Fluteau, Adeline, Simpson, Daniel, Olova, Nelly, Sutcliffe, Hannah, Rainger, Jacqueline, Robertson, Andrea, Osborn, Ruby, Wheeler, Ann, Nowotny, Marcin, Gilbert, Nick, Chandra, Tamir, Reijns, Martin A. M., Jackson, Andrew P.

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Biallelic variants in DNA2 cause microcephalic primordial dwarfism по Tarnauskaitė, Žygimantė, Bicknell, Louise S., Marsh, Joseph A., Murray, Jennie E., Parry, David A., Logan, Clare V., Bober, Michael B., de Silva, Deepthi C., Duker, Angela L., Sillence, David, Wise, Carol, Jackson, Andrew P., Murina, Olga, Reijns, Martin A. M.

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PRIM1 deficiency causes a distinctive primordial dwarfism syndrome по Parry, David A., Tamayo-Orrego, Lukas, Carroll, Paula, Marsh, Joseph A., Greene, Philip, Murina, Olga, Uggenti, Carolina, Leitch, Andrea, Káposzta, Rita, Merő, Gabriella, Nagy, Andrea, Orlik, Brigitta, Kovács-Pászthy, Balázs, Quigley, Alan J., Riszter, Magdolna, Rankin, Julia, Reijns, Martin A.M., Szakszon, Katalin, Jackson, Andrew P.

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Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development по Reijns, Martin A.M., Rabe, Björn, Rigby, Rachel E., Mill, Pleasantine, Astell, Katy R., Lettice, Laura A., Boyle, Shelagh, Leitch, Andrea, Keighren, Margaret, Kilanowski, Fiona, Devenney, Paul S., Sexton, David, Grimes, Graeme, Holt, Ian J., Hill, Robert E., Taylor, Martin S., Lawson, Kirstie A., Dorin, Julia R., Jackson, Andrew P.

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Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndrome по Rice, Gillian I., Reijns, Martin A.M., Coffin, Stephanie R., Forte, Gabriella M.A., Anderson, Beverley H., Szynkiewicz, Marcin, Gornall, Hannah, Gent, David, Leitch, Andrea, Botella, Maria P., Fazzi, Elisa, Gener, Blanca, Lagae, Lieven, Olivieri, Ivana, Orcesi, Simona, Swoboda, Kathryn J., Perrino, Fred W., Jackson, Andrew P., Crow, Yanick J.

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Signatures of TOP1 transcription-associated mutagenesis in cancer and germline по Reijns, Martin A. M., Parry, David A., Williams, Thomas C., Nadeu, Ferran, Hindshaw, Rebecca L., Rios Szwed, Diana O., Nicholson, Michael D., Carroll, Paula, Boyle, Shelagh, Royo, Romina, Cornish, Alex J., Xiang, Hang, Ridout, Kate, Schuh, Anna, Aden, Konrad, Palles, Claire, Campo, Elias, Stankovic, Tatjana, Taylor, Martin S., Jackson, Andrew P.

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