يعرض 1 - 5 نتائج من 5 نتيجة بحث عن '"McNee, Gavin S"', وقت الاستعلام: 0.76s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

    المؤلفون: Grange, Laura J., Reynolds, John J., Ullah, Farid, Isidor, Bertrand, Shearer, Robert F., Latypova, Xenia, Baxley, Ryan M., Oliver, Antony W., Ganesh, Anil, Cooke, Sophie L., Jhujh, Satpal S., McNee, Gavin S., Hollingworth, Robert, Higgs, Martin R., Natsume, Toyoaki, Khan, Tahir, Martos-Moreno, Gabriel Á., Chupp, Sharon, Mathew, Christopher G., Parry, David

    المصدر: Nature Communications; 11/4/2022, Vol. 13 Issue 1, p1-22, 22p

    مصطلحات موضوعية: MOSAICISM, DNA structure, EMBRYOLOGY, CHROMOSOMES, CELL division, DNA replication, SHORT stature, DNA repair

    النص الكامل

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  2. 2
    دورية أكاديمية
    Arginine methylation and ubiquitylation crosstalk controls DNA end-resection and homologous recombination repair.

    المؤلفون: Sanchez-Bailon, Maria Pilar, Choi, Soo-Youn, Dufficy, Elizabeth R., Sharma, Karan, McNee, Gavin S., Gunnell, Emma, Chiang, Kelly, Sahay, Debashish, Maslen, Sarah, Stewart, Grant S., Skehel, J. Mark, Dreveny, Ingrid, Davies, Clare C.

    المصدر: Nature Communications; 11/2/2021, Vol. 12 Issue 1, p1-18, 18p

    مصطلحات موضوعية: DOUBLE-strand DNA breaks, UBIQUITINATION, POST-translational modification, ARGININE, METHYLATION, O6-Methylguanine-DNA Methyltransferase, DNA methyltransferases

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  3. 3
    دورية أكاديمية
    DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain.

    المؤلفون: Zhang, Jing, Bellani, Marina A., James, Ryan C., Pokharel, Durga, Zhang, Yongqing, Reynolds, John J., McNee, Gavin S., Jackson, Andrew P., Stewart, Grant S., Seidman, Michael M.

    المصدر: Nature Communications; 8/7/2020, Vol. 11 Issue 1, p1-15, 15p

    مصطلحات موضوعية: REPLISOMES, CHROMATIN, HETEROCHROMATIN, CARRIER proteins, DNA

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  4. 4
    دورية أكاديمية
    Cross-talk between phospholipase D and MAP kinases activities

    المؤلفون: Wakelam, Michael J.O. michael.wakelam@bbsrc.ac.uk, McNee, Gavin S.1, Rudge, Simon A.1

    المصدر: Advances in Enzyme Regulation. May2010, Vol. 50 Issue 1, p57-61. 5p.


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  5. 5
    دورية أكاديمية
    RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1.

    المؤلفون: Abu-Libdeh, Bassam1, Jhujh, Satpal S.2, Dhar, Srijita3, Sommers, Joshua A.3, Datta, Arindam3, Longo, Gabriel M. C.4, Grange, Laura J.2, Reynolds, John J.2, Cooke, Sophie L.2, McNee, Gavin S.2, Hollingworth, Robert2, Woodward, Beth L.2, Ganesh, Anil N.2, Smerdon, Stephen J.2, Nicolae, Claudia M.5, Durlacher-Betzer, Karina6, Molho-Pessach, Vered7, Abu-Libdeh, Abdulsalam1, Meiner, Vardiella6, Moldovan, George-Lucian5

    المصدر: Journal of Clinical Investigation. Mar2022, Vol. 132 Issue 5, p1-17. 17p.

    مصطلحات موضوعية: *DNA helicases, *GENOMES, *DNA repair, *MUTANT proteins, *DNA replication, *RESEARCH, *DNA, *GENETIC mutation, *EVALUATION research, *HYDROLASES, *COMPARATIVE studies, *DISEASE susceptibility, *MENTAL health surveys, *RESEARCH funding, *BREAST tumors

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