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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

228 related items for PubMed ID: 36396635

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  • 3. Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structures.
    Choo DI, Tawfik KO, Martin DM, Raphael Y.
    Am J Med Genet C Semin Med Genet; 2017 Dec; 175(4):439-449. PubMed ID: 29082607
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  • 4. Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome.
    Hurd EA, Adams ME, Layman WS, Swiderski DL, Beyer LA, Halsey KE, Benson JM, Gong TW, Dolan DF, Raphael Y, Martin DM.
    Hear Res; 2011 Dec; 282(1-2):184-95. PubMed ID: 21875659
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  • 5. CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.
    Micucci JA, Layman WS, Hurd EA, Sperry ED, Frank SF, Durham MA, Swiderski DL, Skidmore JM, Scacheri PC, Raphael Y, Martin DM.
    Hum Mol Genet; 2014 Jan 15; 23(2):434-48. PubMed ID: 24026680
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  • 6. CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.
    Yao H, Hill SF, Skidmore JM, Sperry ED, Swiderski DL, Sanchez GJ, Bartels CF, Raphael Y, Scacheri PC, Iwase S, Martin DM.
    JCI Insight; 2018 Feb 22; 3(4):. PubMed ID: 29467333
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  • 8. Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear.
    Durruthy-Durruthy R, Sperry ED, Bowen ME, Attardi LD, Heller S, Martin DM.
    Front Genet; 2018 Feb 22; 9():473. PubMed ID: 30459807
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  • 13. Directed Differentiation of Human Pluripotent Stem Cells into Inner Ear Organoids.
    Ueda Y, Moore ST, Hashino E.
    Methods Mol Biol; 2022 Feb 22; 2520():135-150. PubMed ID: 34724191
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  • 14. CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellum.
    Reddy NC, Majidi SP, Kong L, Nemera M, Ferguson CJ, Moore M, Goncalves TM, Liu HK, Fitzpatrick JAJ, Zhao G, Yamada T, Bonni A, Gabel HW.
    Nat Commun; 2021 Sep 29; 12(1):5702. PubMed ID: 34588434
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  • 17. A functional assay to study the pathogenicity of CHD7 protein variants encountered in CHARGE syndrome patients.
    Brajadenta GS, Bilan F, Gilbert-Dussardier B, Kitzis A, Thoreau V.
    Eur J Hum Genet; 2019 Nov 29; 27(11):1683-1691. PubMed ID: 31289371
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