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Journal Abstract Search

293 related items for PubMed ID: 28165338

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  • 4. RELN and VLDLR mutations underlie two distinguishable clinico-radiological phenotypes.
    Valence S, Garel C, Barth M, Toutain A, Paris C, Amsallem D, Barthez MA, Mayer M, Rodriguez D, Burglen L.
    Clin Genet; 2016 Dec; 90(6):545-549. PubMed ID: 27000652
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  • 6. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
    Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA.
    Nat Genet; 2000 Sep; 26(1):93-6. PubMed ID: 10973257
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  • 7. Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorder.
    Sánchez-Sánchez SM, Magdalon J, Griesi-Oliveira K, Yamamoto GL, Santacruz-Perez C, Fogo M, Passos-Bueno MR, Sertié AL.
    Hum Mutat; 2018 Oct; 39(10):1372-1383. PubMed ID: 29969175
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  • 9. Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
    Dazzo E, Fanciulli M, Serioli E, Minervini G, Pulitano P, Binelli S, Di Bonaventura C, Luisi C, Pasini E, Striano S, Striano P, Coppola G, Chiavegato A, Radovic S, Spadotto A, Uzzau S, La Neve A, Giallonardo AT, Mecarelli O, Tosatto SC, Ottman R, Michelucci R, Nobile C.
    Am J Hum Genet; 2015 Jun 04; 96(6):992-1000. PubMed ID: 26046367
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  • 10. Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.
    Whittaker DE, Kasah S, Donovan APA, Ellegood J, Riegman KLH, Volk HA, McGonnell I, Lerch JP, Basson MA.
    Am J Med Genet C Semin Med Genet; 2017 Dec 04; 175(4):n/a. PubMed ID: 29168327
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  • 13. A Complex Interaction Between Reduced Reelin Expression and Prenatal Organophosphate Exposure Alters Neuronal Cell Morphology.
    Mullen BR, Ross B, Chou JW, Khankan R, Khialeeva E, Bui K, Carpenter EM.
    ASN Neuro; 2016 Jun 04; 8(3):. PubMed ID: 27364165
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  • 17. Co-cultures of cerebellar slices from mice with different reelin genetic backgrounds as a model to study cortical lamination.
    Merighi A, Lossi L.
    F1000Res; 2022 Jun 04; 11():1183. PubMed ID: 37881513
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  • 18. Epigenetic regulation of RELN and GAD1 in the frontal cortex (FC) of autism spectrum disorder (ASD) subjects.
    Zhubi A, Chen Y, Guidotti A, Grayson DR.
    Int J Dev Neurosci; 2017 Nov 04; 62():63-72. PubMed ID: 28229923
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  • 19. Migration, early axonogenesis, and Reelin-dependent layer-forming behavior of early/posterior-born Purkinje cells in the developing mouse lateral cerebellum.
    Miyata T, Ono Y, Okamoto M, Masaoka M, Sakakibara A, Kawaguchi A, Hashimoto M, Ogawa M.
    Neural Dev; 2010 Sep 01; 5():23. PubMed ID: 20809939
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  • 20. Reelin signaling is impaired in autism.
    Fatemi SH, Snow AV, Stary JM, Araghi-Niknam M, Reutiman TJ, Lee S, Brooks AI, Pearce DA.
    Biol Psychiatry; 2005 Apr 01; 57(7):777-87. PubMed ID: 15820235
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