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Zohn, Irene

TitleAssociate Professor
InstitutionChildrens National Medical Center
DepartmentCenter for Neuroscience and Behavioral Medicine Research
Address111 Michigan Ave NW
Washington DC 20010
PhoneNA
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    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Sugrue KF, Zohn IE. Mechanism for generation of left isomerism in Ccdc40 mutant embryos. PLoS One. 2017; 12(2):e0171180. PMID: 28182636.
      View in: PubMed
    2. Stokes BA, Sabatino JA, Zohn IE. High levels of iron supplementation prevents neural tube defects in the Fpn1ffe mouse model. Birth Defects Res. 2017 Jan 30; 109(2):81-91. PMID: 28008752.
      View in: PubMed
    3. Sabatino JA, Stokes BA, Zohn IE. Prevention of neural tube defects in Lrp2 mutant mouse embryos by folic acid supplementation. Birth Defects Res. 2017 Jan 20; 109(1):16-26. PMID: 27883261.
      View in: PubMed
    4. Warrier S, Nuwayhid S, Sabatino JA, Sugrue KF, Zohn IE. Supt20 is required for development of the axial skeleton. Dev Biol. 2017 Jan 15; 421(2):245-257. PMID: 27894818.
      View in: PubMed
    5. Sarkar AA, Sabatino JA, Sugrue KF, Zohn IE. Abnormal labyrinthine zone in the Hectd1-null placenta. Placenta. 2016 Feb; 38:16-23. PMID: 26907377; PMCID: PMC4768308 [Available on 02/01/17].
    6. LaMantia AS, Moody SA, Maynard TM, Karpinski BA, Zohn IE, Mendelowitz D, Lee NH, Popratiloff A. Hard to swallow: Developmental biological insights into pediatric dysphagia. Dev Biol. 2016 Jan 15; 409(2):329-42. PMID: 26554723; PMCID: PMC4724484 [Available on 01/15/17].
    7. Sarkar AA, Nuwayhid SJ, Maynard T, Ghandchi F, Hill JT, Lamantia AS, Zohn IE. Hectd1 is required for development of the junctional zone of the placenta. Dev Biol. 2014 Aug 15; 392(2):368-80. PMID: 24855001; PMCID: PMC4578812.
    8. Karpinski BA, Maynard TM, Fralish MS, Nuwayhid S, Zohn IE, Moody SA, LaMantia AS. Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome. Dis Model Mech. 2014 Feb; 7(2):245-57. PMID: 24357327; PMCID: PMC3917245.
    9. Sarkar AA, Zohn IE. An explant assay for assessing cellular behavior of the cranial mesenchyme. J Vis Exp. 2013 Jan 20; (71). PMID: 23381592; PMCID: PMC3582658.
    10. Tran H, Bustos D, Yeh R, Rubinfeld B, Lam C, Shriver S, Zilberleyb I, Lee MW, Phu L, Sarkar AA, Zohn IE, Wertz IE, Kirkpatrick DS, Polakis P. HectD1 E3 ligase modifies adenomatous polyposis coli (APC) with polyubiquitin to promote the APC-axin interaction. J Biol Chem. 2013 Feb 08; 288(6):3753-67. PMID: 23277359; PMCID: PMC3567630.
    11. Zohn IE, Sarkar AA. Does the cranial mesenchyme contribute to neural fold elevation during neurulation? Birth Defects Res A Clin Mol Teratol. 2012 Oct; 94(10):841-8. PMID: 22945385; PMCID: PMC3473154.
    12. Zohn IE. Mouse as a model for multifactorial inheritance of neural tube defects. Birth Defects Res C Embryo Today. 2012 Jun; 96(2):193-205. PMID: 22692891.
      View in: PubMed
    13. Sarkar AA, Zohn IE. Hectd1 regulates intracellular localization and secretion of Hsp90 to control cellular behavior of the cranial mesenchyme. J Cell Biol. 2012 Mar 19; 196(6):789-800. PMID: 22431752; PMCID: PMC3308699.
    14. Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, Sullivan-Brown J, McSheene J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvath J, Reinhardt R, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler R, Niswander L, Omran H, Burdine RD. The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nat Genet. 2011 Jan; 43(1):79-84. PMID: 21131974; PMCID: PMC3132183.
    15. Mao J, McKean DM, Warrier S, Corbin JG, Niswander L, Zohn IE. The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure. Development. 2010 Sep; 137(18):3079-88. PMID: 20702562; PMCID: PMC2926957.
    16. Zohn IE, Sarkar AA. The visceral yolk sac endoderm provides for absorption of nutrients to the embryo during neurulation. Birth Defects Res A Clin Mol Teratol. 2010 Aug; 88(8):593-600. PMID: 20672346.
      View in: PubMed
    17. Singh A, Boyer JL, Der CJ, Zohn IE. Transformation by a nucleotide-activated P2Y receptor is mediated by activation of Galphai, Galphaq and Rho-dependent signaling pathways. J Mol Signal. 2010 Jul 23; 5:11. PMID: 20653955; PMCID: PMC2917412.
    18. Paradkar PN, De Domenico I, Durchfort N, Zohn I, Kaplan J, Ward DM. Iron depletion limits intracellular bacterial growth in macrophages. Blood. 2008 Aug 01; 112(3):866-74. PMID: 18369153; PMCID: PMC2481528.
    19. Zohn IE, Sarkar AA. Modeling neural tube defects in the mouse. Curr Top Dev Biol. 2008; 84:1-35. PMID: 19186242.
      View in: PubMed
    20. Zohn IE, Anderson KV, Niswander L. The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure. Dev Biol. 2007 Jun 01; 306(1):208-21. PMID: 17442300; PMCID: PMC2730518.
    21. Zohn IE, De Domenico I, Pollock A, Ward DM, Goodman JF, Liang X, Sanchez AJ, Niswander L, Kaplan J. The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease. Blood. 2007 May 15; 109(10):4174-80. PMID: 17289807; PMCID: PMC1885502.
    22. Zohn IE, Li Y, Skolnik EY, Anderson KV, Han J, Niswander L. p38 and a p38-interacting protein are critical for downregulation of E-cadherin during mouse gastrulation. Cell. 2006 Jun 02; 125(5):957-69. PMID: 16751104.
      View in: PubMed
    23. Zohn IE, Anderson KV, Niswander L. Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse. Birth Defects Res A Clin Mol Teratol. 2005 Sep; 73(9):583-90. PMID: 15971254.
      View in: PubMed
    24. Zohn IE, Chesnutt CR, Niswander L. Cell polarity pathways converge and extend to regulate neural tube closure. Trends Cell Biol. 2003 Sep; 13(9):451-4. PMID: 12946622.
      View in: PubMed
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