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manual khatib
(24 results)?
Activation of the cGAS-STING innate immune response in cells with deficient mitochondrial topoisomerase TOP1MT.
Hum Mol Genet. 2023 Jul 20;32(15):2422-2440. doi: 10.1093/hmg/ddad062.
Hum Mol Genet. 2023.
PMID: 37129502
Free PMC article.
Advances Towards Therapeutic Approaches for mtDNA Disease.
Al Khatib I, Shutt TE.
Al Khatib I, et al.
Adv Exp Med Biol. 2019;1158:217-246. doi: 10.1007/978-981-13-8367-0_12.
Adv Exp Med Biol. 2019.
PMID: 31452143
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Functional characterization of two variants of mitochondrial topoisomerase TOP1MT that impact regulation of the mitochondrial genome.
Al Khatib I, Deng J, Symes A, Kerr M, Zhang H, Huang SN, Pommier Y, Khan A, Shutt TE.
Al Khatib I, et al.
J Biol Chem. 2022 Oct;298(10):102420. doi: 10.1016/j.jbc.2022.102420. Epub 2022 Aug 24.
J Biol Chem. 2022.
PMID: 36030054
Free PMC article.
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Loss of Ubiquitin Carboxy-Terminal Hydrolase L1 Impairs Long-Term Differentiation Competence and Metabolic Regulation in Murine Spermatogonial Stem Cells.
Alpaugh WF, Voigt AL, Dardari R, Su L, Al Khatib I, Shin W, Goldsmith TM, Coyle KM, Tang LA, Shutt TE, Klein C, Biernaskie J, Dobrinski I.
Alpaugh WF, et al. Among authors: al khatib i.
Cells. 2021 Aug 31;10(9):2265. doi: 10.3390/cells10092265.
Cells. 2021.
PMID: 34571914
Free PMC article.
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A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects.
Posch MG, Gramlich M, Sunde M, Schmitt KR, Lee SH, Richter S, Kersten A, Perrot A, Panek AN, Al Khatib IH, Nemer G, Mégarbané A, Dietz R, Stiller B, Berger F, Harvey RP, Ozcelik C.
Posch MG, et al. Among authors: al khatib ih.
J Med Genet. 2010 Apr;47(4):230-5. doi: 10.1136/jmg.2009.069997. Epub 2009 Sep 16.
J Med Genet. 2010.
PMID: 19762328
Free PMC article.
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