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Journal Abstract Search

152 related items for PubMed ID: 33772547

  • 1. RERE deficiency contributes to the development of orofacial clefts in humans and mice.
    Kim BJ, Zaveri HP, Kundert PN, Jordan VK, Scott TM, Carmichael J, Scott DA.
    Hum Mol Genet; 2021 May 12; 30(7):595-602. PubMed ID: 33772547
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  • 2. An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
    Kim BJ, Zaveri HP, Shchelochkov OA, Yu Z, Hernández-García A, Seymour ML, Oghalai JS, Pereira FA, Stockton DW, Justice MJ, Lee B, Scott DA.
    PLoS One; 2013 May 12; 8(2):e57460. PubMed ID: 23451234
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  • 4. RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects.
    Kim BJ, Zaveri HP, Jordan VK, Hernandez-Garcia A, Jacob DJ, Zamora DL, Yu W, Schwartz RJ, Scott DA.
    Dis Model Mech; 2018 Aug 28; 11(9):. PubMed ID: 30061196
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  • 5. Patched1 is required in neural crest cells for the prevention of orofacial clefts.
    Metzis V, Courtney AD, Kerr MC, Ferguson C, Rondón Galeano MC, Parton RG, Wainwright BJ, Wicking C.
    Hum Mol Genet; 2013 Dec 15; 22(24):5026-35. PubMed ID: 23900075
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  • 8. De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
    Fregeau B, Kim BJ, Hernández-García A, Jordan VK, Cho MT, Schnur RE, Monaghan KG, Juusola J, Rosenfeld JA, Bhoj E, Zackai EH, Sacharow S, Barañano K, Bosch DGM, de Vries BBA, Lindstrom K, Schroeder A, James P, Kulch P, Lalani SR, van Haelst MM, van Gassen KLI, van Binsbergen E, Barkovich AJ, Scott DA, Sherr EH.
    Am J Hum Genet; 2016 May 05; 98(5):963-970. PubMed ID: 27087320
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  • 10. Shared molecular networks in orofacial and neural tube development.
    Kousa YA, Mansour TA, Seada H, Matoo S, Schutte BC.
    Birth Defects Res; 2017 Jan 30; 109(2):169-179. PubMed ID: 27933721
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  • 14. Mice with Tak1 deficiency in neural crest lineage exhibit cleft palate associated with abnormal tongue development.
    Song Z, Liu C, Iwata J, Gu S, Suzuki A, Sun C, He W, Shu R, Li L, Chai Y, Chen Y.
    J Biol Chem; 2013 Apr 12; 288(15):10440-50. PubMed ID: 23460641
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  • 17. Genotype-phenotype correlations in individuals with pathogenic RERE variants.
    Jordan VK, Fregeau B, Ge X, Giordano J, Wapner RJ, Balci TB, Carter MT, Bernat JA, Moccia AN, Srivastava A, Martin DM, Bielas SL, Pappas J, Svoboda MD, Rio M, Boddaert N, Cantagrel V, Lewis AM, Scaglia F, Undiagnosed Diseases Network, Kohler JN, Bernstein JA, Dries AM, Rosenfeld JA, DeFilippo C, Thorson W, Yang Y, Sherr EH, Bi W, Scott DA.
    Hum Mutat; 2018 May 12; 39(5):666-675. PubMed ID: 29330883
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  • 18. Tissue-specific analysis of Fgf18 gene function in palate development.
    Yue M, Lan Y, Liu H, Wu Z, Imamura T, Jiang R.
    Dev Dyn; 2021 Apr 12; 250(4):562-573. PubMed ID: 33034111
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  • 19. Orofacial clefting: recent insights into a complex trait.
    Jugessur A, Murray JC.
    Curr Opin Genet Dev; 2005 Jun 12; 15(3):270-8. PubMed ID: 15917202
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  • 20. Fibroblast growth factor 9 (FGF9)-pituitary homeobox 2 (PITX2) pathway mediates transforming growth factor β (TGFβ) signaling to regulate cell proliferation in palatal mesenchyme during mouse palatogenesis.
    Iwata J, Tung L, Urata M, Hacia JG, Pelikan R, Suzuki A, Ramenzoni L, Chaudhry O, Parada C, Sanchez-Lara PA, Chai Y.
    J Biol Chem; 2012 Jan 20; 287(4):2353-63. PubMed ID: 22123828
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