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UV-Protection Timer Controls Linkage between Stress and Pigmentation Skin Protection Systems.
Mol Cell. 2018 Nov 1;72(3):444-456.e7. doi: 10.1016/j.molcel.2018.09.022. Epub 2018 Oct 25.
Mol Cell. 2018.
PMID: 30401431
Free PMC article.
MYORG Mutations: a Major Cause of Recessive Primary Familial Brain Calcification.
Bauer M, Rahat D, Zisman E, Tabach Y, Lossos A, Meiner V, Arkadir D.
Bauer M, et al. Among authors: rahat d.
Curr Neurol Neurosci Rep. 2019 Aug 23;19(10):70. doi: 10.1007/s11910-019-0986-z.
Curr Neurol Neurosci Rep. 2019.
PMID: 31440850
Review.
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Schlafen2 mutation in mice causes an osteopetrotic phenotype due to a decrease in the number of osteoclast progenitors.
Omar I, Guterman-Ram G, Rahat D, Tabach Y, Berger M, Levaot N.
Omar I, et al. Among authors: rahat d.
Sci Rep. 2018 Aug 29;8(1):13005. doi: 10.1038/s41598-018-31428-z.
Sci Rep. 2018.
PMID: 30158544
Free PMC article.
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MYORG is associated with recessive primary familial brain calcification.
Arkadir D, Lossos A, Rahat D, Abu Snineh M, Schueler-Furman O, Nitschke S, Minassian BA, Sadaka Y, Lerer I, Tabach Y, Meiner V.
Arkadir D, et al. Among authors: rahat d.
Ann Clin Transl Neurol. 2018 Nov 15;6(1):106-113. doi: 10.1002/acn3.684. eCollection 2019 Jan.
Ann Clin Transl Neurol. 2018.
PMID: 30656188
Free PMC article.
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Mapping global and local coevolution across 600 species to identify novel homologous recombination repair genes.
Sherill-Rofe D, Rahat D, Findlay S, Mellul A, Guberman I, Braun M, Bloch I, Lalezari A, Samiei A, Sadreyev R, Goldberg M, Orthwein A, Zick A, Tabach Y.
Sherill-Rofe D, et al. Among authors: rahat d.
Genome Res. 2019 Mar;29(3):439-448. doi: 10.1101/gr.241414.118. Epub 2019 Feb 4.
Genome Res. 2019.
PMID: 30718334
Free PMC article.
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Multi-omics data integration analysis identifies the spliceosome as a key regulator of DNA double-strand break repair.
Sherill-Rofe D, Raban O, Findlay S, Rahat D, Unterman I, Samiei A, Yasmeen A, Kaiser Z, Kuasne H, Park M, Foulkes WD, Bloch I, Zick A, Gotlieb WH, Tabach Y, Orthwein A.
Sherill-Rofe D, et al. Among authors: rahat d.
NAR Cancer. 2022 Apr 8;4(2):zcac013. doi: 10.1093/narcan/zcac013. eCollection 2022 Jun.
NAR Cancer. 2022.
PMID: 35399185
Free PMC article.
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SHLD2/FAM35A co-operates with REV7 to coordinate DNA double-strand break repair pathway choice.
Findlay S, Heath J, Luo VM, Malina A, Morin T, Coulombe Y, Djerir B, Li Z, Samiei A, Simo-Cheyou E, Karam M, Bagci H, Rahat D, Grapton D, Lavoie EG, Dove C, Khaled H, Kuasne H, Mann KK, Klein KO, Greenwood CM, Tabach Y, Park M, Côté JF, Masson JY, Maréchal A, Orthwein A.
Findlay S, et al. Among authors: rahat d.
EMBO J. 2018 Sep 14;37(18):e100158. doi: 10.15252/embj.2018100158. Epub 2018 Aug 28.
EMBO J. 2018.
PMID: 30154076
Free PMC article.
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Multi-system neurological disorder associated with a CRYAB variant.
Sadeh M, Rahat D, Meiner V, Fellig Y, Arad M, Schueler-Furman O, Hu Y, Li Y, Bönnemann CG, Lossos A.
Sadeh M, et al. Among authors: rahat d.
Neurogenetics. 2021 May;22(2):117-125. doi: 10.1007/s10048-021-00640-x. Epub 2021 Apr 3.
Neurogenetics. 2021.
PMID: 33811585
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