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XB-GENEPAGE-877229
Papers associated with chd7
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Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB, Nemes P, Moody SA., iScience. September 15, 2023; 26 (9): 107665.  |
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The CHARGE syndrome ortholog CHD-7 regulates TGF-β pathways in Caenorhabditis elegans., Jofré DM, Hoffman DK, Cervino AS, Hahn GM, Grundy M, Yun S, Amrit FRG, Stolz DB, Godoy LF, Salvatore E, Rossi FA, Ghazi A, Cirio MC, Yanowitz JL, Hochbaum D., Proc Natl Acad Sci U S A. April 12, 2022; 119 (15): e2109508119.  |
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A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB, Willsey HR, Xu Y, Xu Y, Mei Y, Dea J, Wang S, Curtis C, Sempou E, Khokha MK, Chi NC, Willsey AJ, Fisch KM, Ideker T., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.  |
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Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells., Okuno H, Okano H., Regen Ther. August 24, 2021; 18 275-280.  |
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Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J, Pauli S, Borchers A., Genesis. February 1, 2021; 59 (1-2): e23404.  |
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Nucleosome-CHD4 chromatin remodeler structure maps human disease mutations., Farnung L, Ochmann M, Cramer P., Elife. June 16, 2020; 9  |
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The neural border: Induction, specification and maturation of the territory that generates neural crest cells., Pla P, Monsoro-Burq AH., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.  |
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Sema3a plays a role in the pathogenesis of CHARGE syndrome., Ufartes R, Schwenty-Lara J, Freese L, Neuhofer C, Möller J, Wehner P, van Ravenswaaij-Arts CMA, Wong MTY, Schanze I, Tzschach A, Bartsch O, Borchers A, Pauli S., Hum Mol Genet. April 15, 2018; 27 (8): 1343-1352.  |
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HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome., Jenness C, Giunta S, Müller MM, Kimura H, Muir TW, Funabiki H., Proc Natl Acad Sci U S A. January 30, 2018; 115 (5): E876-E885.  |
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Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination., He D, Marie C, Zhao C, Kim B, Wang J, Deng Y, Clavairoly A, Frah M, Wang H, He X, Hmidan H, Jones BV, Witte D, Zalc B, Zhou X, Choo DI, Martin DM, Parras C, Lu QR., Nat Neurosci. May 1, 2016; 19 (5): 678-89.  |
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Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy., Duncan AR, Khokha MK., Semin Cell Dev Biol. March 1, 2016; 51 73-9.  |
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CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance., Schulz Y, Wehner P, Opitz L, Salinas-Riester G, Bongers EM, van Ravenswaaij-Arts CM, Wincent J, Schoumans J, Kohlhase J, Borchers A, Pauli S., Hum Genet. August 1, 2014; 133 (8): 997-1009. |
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sizzled function and secreted factor network dynamics., Shi J, Zhang H, Dowell RD, Klymkowsky MW., Biol Open. March 15, 2012; 1 (3): 286-94.  |
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Snail2 controls mesodermal BMP/Wnt induction of neural crest., Shi J, Severson C, Yang J, Wedlich D, Klymkowsky MW., Development. August 1, 2011; 138 (15): 3135-45.  |
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CHD7 cooperates with PBAF to control multipotent neural crest formation., Bajpai R, Chen DA, Rada-Iglesias A, Zhang J, Xiong Y, Helms J, Chang CP, Zhao Y, Swigut T, Wysocka J., Nature. February 18, 2010; 463 (7283): 958-62.  |
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The SNF2 domain protein family in higher vertebrates displays dynamic expression patterns in Xenopus laevis embryos., Linder B, Cabot RA, Schwickert T, Rupp RA., Gene. February 4, 2004; 326 59-66.  |
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