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PUBMED FOR HANDHELDS

Journal Abstract Search


242 related items for PubMed ID: 33080786

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  • 5. Cerebral ischemic injury is enhanced in a model of oculodentodigital dysplasia.
    Kozoriz MG, Lai S, Vega JL, Sáez JC, Sin WC, Bechberger JF, Naus CC.
    Neuropharmacology; 2013 Dec; 75():549-56. PubMed ID: 23727526
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  • 6. Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia.
    Shao Q, Liu Q, Lorentz R, Gong XQ, Bai D, Shaw GS, Laird DW.
    Mol Biol Cell; 2012 Sep; 23(17):3312-21. PubMed ID: 22809623
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  • 8. Syndromic and non-syndromic disease-linked Cx43 mutations.
    Laird DW.
    FEBS Lett; 2014 Apr 17; 588(8):1339-48. PubMed ID: 24434540
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  • 10. Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review.
    Wang Z, Sun L, Wang P, Chen C, Zhang A, Wang W, Ding X.
    Ophthalmic Genet; 2019 Feb 17; 40(1):54-59. PubMed ID: 30767687
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  • 12. The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice.
    Stewart MK, Gong XQ, Barr KJ, Bai D, Fishman GI, Laird DW.
    Biochem J; 2013 Jan 15; 449(2):401-13. PubMed ID: 23075222
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  • 13. Palmoplantar keratosis in oculodentodigital dysplasia with a GJA1 point mutation out of the C-terminal region of connexin 43.
    Kogame T, Dainichi T, Shimomura Y, Tanioka M, Kabashima K, Miyachi Y.
    J Dermatol; 2014 Dec 15; 41(12):1095-7. PubMed ID: 25388818
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  • 15. A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.
    Hu Y, Chen IP, de Almeida S, Tiziani V, Do Amaral CM, Gowrishankar K, Passos-Bueno MR, Reichenberger EJ.
    PLoS One; 2013 Dec 15; 8(8):e73576. PubMed ID: 23951358
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  • 16. Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.
    Shibayama J, Paznekas W, Seki A, Taffet S, Jabs EW, Delmar M, Musa H.
    Circ Res; 2005 May 27; 96(10):e83-91. PubMed ID: 15879313
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  • 19. Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature.
    Taşdelen E, Durmaz CD, Karabulut HG.
    Cytogenet Genome Res; 2018 May 27; 154(4):181-186. PubMed ID: 29902798
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