Norann A. Zaghloul, Ph.D. - Publications

Affiliations: 
2006 The George Washington University, Washington, DC, United States 
Area:
Genetics, Neuroscience Biology

27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Khan SY, Vasanth S, Kabir F, Gottsch JD, Khan AO, Chaerkady R, Lee MW, Leitch CC, Ma Z, Laux J, Villasmil R, Khan SN, Riazuddin S, Akram J, Cole RN, ... ... Zaghloul NA, et al. FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1. Nature Communications. 7: 10953. PMID 27218149 DOI: 10.1038/ncomms10953  1
2016 Hostelley TL, Lodh S, Zaghloul NA. Whole organism transcriptome analysis of zebrafish models of Bardet-Biedl Syndrome and Alström Syndrome provides mechanistic insight into shared and divergent phenotypes. Bmc Genomics. 17: 318. PMID 27142762 DOI: 10.1186/s12864-016-2679-1  1
2016 O'Hare EA, Yerges-Armstrong LM, Perry JA, Shuldiner AR, Zaghloul NA. Assignment of functional relevance to genes at type 2 diabetes-associated loci through investigation of β-cell mass deficits. Molecular Endocrinology (Baltimore, Md.). me20151243. PMID 26963759 DOI: 10.1210/me.2015-1243  1
2016 Lodh S, Hostelley TL, Leitch CC, O'Hare EA, Zaghloul NA. Differential effects on β-cell mass by disruption of Bardet-Biedl syndrome or Alstrom syndrome genes. Human Molecular Genetics. 25: 57-68. PMID 26494903 DOI: 10.1093/hmg/ddv447  1
2015 Elkon R, Milon B, Morrison L, Shah M, Vijayakumar S, Racherla M, Leitch CC, Silipino L, Hadi S, Weiss-Gayet M, Barras E, Schmid CD, Ait-Lounis A, Barnes A, Song Y, ... ... Zaghloul NA, et al. RFX transcription factors are essential for hearing in mice. Nature Communications. 6: 8549. PMID 26469318 DOI: 10.1038/ncomms9549  1
2014 O'Hare EA, Wang X, Montasser ME, Chang YP, Mitchell BD, Zaghloul NA. Disruption of ldlr causes increased LDL-c and vascular lipid accumulation in a zebrafish model of hypercholesterolemia. Journal of Lipid Research. 55: 2242-53. PMID 25201834 DOI: 10.1194/jlr.M046540  1
2014 Shah K, Lahiri DK. Cdk5 activity in the brain - multiple paths of regulation. Journal of Cell Science. 127: 2391-400. PMID 24879856 DOI: 10.1242/jcs.147553  1
2014 Leitch CC, Zaghloul NA. BBS4 is necessary for ciliary localization of TrkB receptor and activation by BDNF. Plos One. 9: e98687. PMID 24867303 DOI: 10.1371/journal.pone.0098687  1
2014 Lodh S, O'Hare EA, Zaghloul NA. Primary cilia in pancreatic development and disease. Birth Defects Research. Part C, Embryo Today : Reviews. 102: 139-58. PMID 24864023 DOI: 10.1002/bdrc.21063  1
2014 Liu YP, Tsai IC, Morleo M, Oh EC, Leitch CC, Massa F, Lee BH, Parker DS, Finley D, Zaghloul NA, Franco B, Katsanis N. Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators. The Journal of Clinical Investigation. 124: 2059-70. PMID 24691443 DOI: 10.1172/JCI71898  1
2011 Zaghloul NA, Katsanis N. Zebrafish assays of ciliopathies. Methods in Cell Biology. 105: 257-72. PMID 21951534 DOI: 10.1016/B978-0-12-381320-6.00011-4  1
2011 Dowdle WE, Robinson JF, Kneist A, Sirerol-Piquer MS, Frints SG, Corbit KC, Zaghloul NA, Zaghloul NA, van Lijnschoten G, Mulders L, Verver DE, Zerres K, Reed RR, Attié-Bitach T, Johnson CA, et al. Disruption of a ciliary B9 protein complex causes Meckel syndrome. American Journal of Human Genetics. 89: 94-110. PMID 21763481 DOI: 10.1016/j.ajhg.2011.06.003  1
2011 Kim S, Zaghloul NA, Bubenshchikova E, Oh EC, Rankin S, Katsanis N, Obara T, Tsiokas L. Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry. Nature Cell Biology. 13: 351-60. PMID 21394081 DOI: 10.1038/ncb2183  1
2011 Zaghloul NA, Brugmann SA. The emerging face of primary cilia. Genesis (New York, N.Y. : 2000). 49: 231-46. PMID 21305689 DOI: 10.1002/dvg.20728  1
2010 Zaghloul NA, Liu Y, Gerdes JM, Gascue C, Oh EC, Leitch CC, Bromberg Y, Binkley J, Leibel RL, Sidow A, Badano JL, Katsanis N. Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome. Proceedings of the National Academy of Sciences of the United States of America. 107: 10602-7. PMID 20498079 DOI: 10.1073/pnas.1000219107  1
2010 Zaghloul NA, Katsanis N. Functional modules, mutational load and human genetic disease. Trends in Genetics : Tig. 26: 168-76. PMID 20226561 DOI: 10.1016/j.tig.2010.01.006  1
2010 Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN, Eghrari AO, Minear MA, Li YJ, Klintworth GK, Afshari N, Gregory SG, Gottsch JD, Katsanis N. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. American Journal of Human Genetics. 86: 45-53. PMID 20036349 DOI: 10.1016/j.ajhg.2009.12.001  1
2009 de Pontual L, Zaghloul NA, Thomas S, Davis EE, McGaughey DM, Dollfus H, Baumann C, Bessling SL, Babarit C, Pelet A, Gascue C, Beales P, Munnich A, Lyonnet S, Etchevers H, et al. Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease. Proceedings of the National Academy of Sciences of the United States of America. 106: 13921-6. PMID 19666486 DOI: 10.1073/pnas.0901219106  1
2009 Zaghloul NA, Katsanis N. Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy. The Journal of Clinical Investigation. 119: 428-37. PMID 19252258 DOI: 10.1172/JCI37041  1
2008 Li C, Inglis PN, Leitch CC, Efimenko E, Zaghloul NA, Mok CA, Davis EE, Bialas NJ, Healey MP, Héon E, Zhen M, Swoboda P, Katsanis N, Leroux MR. An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes. Plos Genetics. 4: e1000044. PMID 18369462 DOI: 10.1371/journal.pgen.1000044  1
2008 Leitch CC, Zaghloul NA, Davis EE, Stoetzel C, Diaz-Font A, Rix S, Alfadhel M, Al-Fadhel M, Lewis RA, Eyaid W, Banin E, Dollfus H, Beales PL, Badano JL, Katsanis N. Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nature Genetics. 40: 443-8. PMID 18327255 DOI: 10.1038/ng.97  1
2008 Leitch CC, Zaghloul NA, Davis EE, Stoetzel C, Diaz-Font A, Rix S, Al-Fadhel M, Lewis RA, Eyaid W, Banin E, Dollfus H, Beales PL, Badano JL, Katsanis N. Corrigendum: Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome (Nature Genetics (2008) 40, (443-448)) Nature Genetics. 40: 927. DOI: 10.1038/ng0708-927b  1
2007 Gerdes JM, Liu Y, Zaghloul NA, Leitch CC, Lawson SS, Kato M, Beachy PA, Beales PL, DeMartino GN, Fisher S, Badano JL, Katsanis N. Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response. Nature Genetics. 39: 1350-60. PMID 17906624 DOI: 10.1038/ng.2007.12  1
2007 Zaghloul NA, Moody SA. Alterations of rx1 and pax6 expression levels at neural plate stages differentially affect the production of retinal cell types and maintenance of retinal stem cell qualities. Developmental Biology. 306: 222-40. PMID 17434474 DOI: 10.1016/j.ydbio.2007.03.017  1
2007 Zaghloul NA, Moody SA. Changes in Rx1 and Pax6 activity at eye field stages differentially alter the production of amacrine neurotransmitter subtypes in Xenopus. Molecular Vision. 13: 86-95. PMID 17277735  1
2007 Stoetzel C, Muller J, Laurier V, Davis EE, Zaghloul NA, Vicaire S, Jacquelin C, Plewniak F, Leitch CC, Sarda P, Hamel C, de Ravel TJ, Lewis RA, Friederich E, Thibault C, et al. Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome. American Journal of Human Genetics. 80: 1-11. PMID 17160889 DOI: 10.1086/510256  1
2005 Zaghloul NA, Yan B, Moody SA. Step-wise specification of retinal stem cells during normal embryogenesis. Biology of the Cell / Under the Auspices of the European Cell Biology Organization. 97: 321-37. PMID 15836431 DOI: 10.1042/BC20040521  1
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