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Prophage-Driven Genomic Structural Changes Promote Bartonella Vertical Evolution.
Gutiérrez R, Markus B, Carstens Marques de Sousa K, Marcos-Hadad E, Mugasimangalam RC, Nachum-Biala Y, Hawlena H, Covo S, Harrus S. Gutiérrez R, et al. Among authors: markus b. Genome Biol Evol. 2018 Nov 1;10(11):3089-3103. doi: 10.1093/gbe/evy236. Genome Biol Evol. 2018. PMID: 30346520 Free PMC article.
Genomic structural plasticity of rodent-associated Bartonella in nature.
de Sousa KCM, Gutiérrez R, Yahalomi D, Shalit T, Markus B, Nachum-Biala Y, Hawlena H, Marcos-Hadad E, Hazkani-Covo E, de Rezende Neves HH, Covo S, Harrus S. de Sousa KCM, et al. Among authors: markus b. Mol Ecol. 2022 Jul;31(14):3784-3797. doi: 10.1111/mec.16547. Epub 2022 Jun 10. Mol Ecol. 2022. PMID: 35620948 Free PMC article.
Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe.
Wormser O, Gradstein L, Kadar E, Yogev Y, Perez Y, Mashkit E, Elbedour K, Drabkin M, Markus B, Kadir R, Halperin D, Khalaila S, Levy J, Lifshitz T, Manor E, Birk OS. Wormser O, et al. Among authors: markus b. Am J Med Genet A. 2018 Dec;176(12):2695-2703. doi: 10.1002/ajmg.a.40668. Epub 2018 Dec 4. Am J Med Genet A. 2018. PMID: 30513137
Divergence of mutational signatures in association with breast cancer subtype.
Perry G, Dadiani M, Kahana-Edwin S, Pavlovski A, Markus B, Hornung G, Balint-Lahat N, Yosepovich A, Hout-Siloni G, Jacob-Hirsch J, Sklair-Levy M, Friedman E, Barshack I, Kaufman B, Gal-Yam EN, Paluch-Shimon S. Perry G, et al. Among authors: markus b. Mol Carcinog. 2022 Nov;61(11):1056-1070. doi: 10.1002/mc.23461. Epub 2022 Sep 16. Mol Carcinog. 2022. PMID: 36111610
Protein recognition by a pattern-generating fluorescent molecular probe.
Pode Z, Peri-Naor R, Georgeson JM, Ilani T, Kiss V, Unger T, Markus B, Barr HM, Motiei L, Margulies D. Pode Z, et al. Among authors: markus b. Nat Nanotechnol. 2017 Dec;12(12):1161-1168. doi: 10.1038/nnano.2017.175. Epub 2017 Oct 16. Nat Nanotechnol. 2017. PMID: 29035400 Review.
VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2).
Feinstein M, Flusser H, Lerman-Sagie T, Ben-Zeev B, Lev D, Agamy O, Cohen I, Kadir R, Sivan S, Leshinsky-Silver E, Markus B, Birk OS. Feinstein M, et al. Among authors: markus b. J Med Genet. 2014 May;51(5):303-8. doi: 10.1136/jmedgenet-2013-101823. Epub 2014 Feb 27. J Med Genet. 2014. PMID: 24577744
268 results