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Rejection of inappropriate synaptic partners in mouse retina mediated by transcellular FLRT2-UNC5 signaling.
Dev Cell. 2023 Oct 23;58(20):2080-2096.e7. doi: 10.1016/j.devcel.2023.07.011. Epub 2023 Aug 8.
Dev Cell. 2023.
PMID: 37557174
Visual Experience Influences Dendritic Orientation but Is Not Required for Asymmetric Wiring of the Retinal Direction Selective Circuit.
El-Quessny M, Maanum K, Feller MB.
El-Quessny M, et al.
Cell Rep. 2020 Jun 30;31(13):107844. doi: 10.1016/j.celrep.2020.107844.
Cell Rep. 2020.
PMID: 32610144
Free PMC article.
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Dendrite Morphology Minimally Influences the Synaptic Distribution of Excitation and Inhibition in Retinal Direction-Selective Ganglion Cells.
El-Quessny M, Feller MB.
El-Quessny M, et al.
eNeuro. 2021 Sep 7;8(5):ENEURO.0261-21.2021. doi: 10.1523/ENEURO.0261-21.2021. Print 2021 Sep-Oct.
eNeuro. 2021.
PMID: 34380656
Free PMC article.
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Volumetric imaging of fast cellular dynamics with deep learning enhanced bioluminescence microscopy.
Morales-Curiel LF, Gonzalez AC, Castro-Olvera G, Lin LL, El-Quessny M, Porta-de-la-Riva M, Severino J, Morera LB, Venturini V, Ruprecht V, Ramallo D, Loza-Alvarez P, Krieg M.
Morales-Curiel LF, et al. Among authors: el quessny m.
Commun Biol. 2022 Dec 3;5(1):1330. doi: 10.1038/s42003-022-04292-x.
Commun Biol. 2022.
PMID: 36463346
Free PMC article.
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Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathy.
Nakayama T, Wu J, Galvin-Parton P, Weiss J, Andriola MR, Hill RS, Vaughan DJ, El-Quessny M, Barry BJ, Partlow JN, Barkovich AJ, Ling J, Mochida GH.
Nakayama T, et al. Among authors: el quessny m.
Hum Mutat. 2017 Oct;38(10):1348-1354. doi: 10.1002/humu.23250. Epub 2017 Jun 23.
Hum Mutat. 2017.
PMID: 28493438
Free PMC article.
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Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures.
Al-Maawali A, Barry BJ, Rajab A, El-Quessny M, Seman A, Coury SN, Barkovich AJ, Yang E, Walsh CA, Mochida GH, Stoler JM.
Al-Maawali A, et al. Among authors: el quessny m.
Am J Med Genet A. 2016 Feb;170A(2):435-440. doi: 10.1002/ajmg.a.37422. Epub 2015 Oct 13.
Am J Med Genet A. 2016.
PMID: 26463574
Free PMC article.
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Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.
Nakayama T, Al-Maawali A, El-Quessny M, Rajab A, Khalil S, Stoler JM, Tan WH, Nasir R, Schmitz-Abe K, Hill RS, Partlow JN, Al-Saffar M, Servattalab S, LaCoursiere CM, Tambunan DE, Coulter ME, Elhosary PC, Gorski G, Barkovich AJ, Markianos K, Poduri A, Mochida GH.
Nakayama T, et al. Among authors: el quessny m.
Am J Hum Genet. 2015 May 7;96(5):709-19. doi: 10.1016/j.ajhg.2015.03.003. Epub 2015 Apr 9.
Am J Hum Genet. 2015.
PMID: 25865492
Free PMC article.
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