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Journal Abstract Search

260 related items for PubMed ID: 11222639

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  • 3. Structural requirements for association of neurofascin with ankyrin.
    Zhang X, Davis JQ, Carpenter S, Bennett V.
    J Biol Chem; 1998 Nov 13; 273(46):30785-94. PubMed ID: 9804856
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  • 4. Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus.
    Sztriha L, Frossard P, Hofstra RM, Verlind E, Nork M.
    J Child Neurol; 2000 Apr 13; 15(4):239-43. PubMed ID: 10805190
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  • 5. Genotype-phenotype correlation in L1 associated diseases.
    Fransen E, Van Camp G, D'Hooge R, Vits L, Willems PJ.
    J Med Genet; 1998 May 13; 35(5):399-404. PubMed ID: 9610803
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  • 8. Clinical mutations in the L1 neural cell adhesion molecule affect cell-surface expression.
    Moulding HD, Martuza RL, Rabkin SD.
    J Neurosci; 2000 Aug 01; 20(15):5696-702. PubMed ID: 10908608
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  • 9. A conserved role for L1 as a transmembrane link between neuronal adhesion and membrane cytoskeleton assembly.
    Hortsch M, O'Shea KS, Zhao G, Kim F, Vallejo Y, Dubreuil RR.
    Cell Adhes Commun; 1998 Jan 01; 5(1):61-73. PubMed ID: 9638342
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  • 12. CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1.
    Fransen E, Lemmon V, Van Camp G, Vits L, Coucke P, Willems PJ.
    Eur J Hum Genet; 1995 Jan 01; 3(5):273-84. PubMed ID: 8556302
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  • 13. Pathological missense mutations of neural cell adhesion molecule L1 affect homophilic and heterophilic binding activities.
    De Angelis E, MacFarlane J, Du JS, Yeo G, Hicks R, Rathjen FG, Kenwrick S, Brümmendorf T.
    EMBO J; 1999 Sep 01; 18(17):4744-53. PubMed ID: 10469653
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  • 15. Cis-activation of L1-mediated ankyrin recruitment by TAG-1 homophilic cell adhesion.
    Malhotra JD, Tsiotra P, Karagogeos D, Hortsch M.
    J Biol Chem; 1998 Dec 11; 273(50):33354-9. PubMed ID: 9837910
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  • 16. Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene.
    Weller S, Gärtner J.
    Hum Mutat; 2001 Dec 11; 18(1):1-12. PubMed ID: 11438988
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  • 19. Identification of a homophilic binding site in immunoglobulin-like domain 2 of the cell adhesion molecule L1.
    Zhao X, Yip PM, Siu CH.
    J Neurochem; 1998 Sep 11; 71(3):960-71. PubMed ID: 9721721
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  • 20. FIGQY phosphorylation defines discrete populations of L1 cell adhesion molecules at sites of cell-cell contact and in migrating neurons.
    Jenkins SM, Kizhatil K, Kramarcy NR, Sen A, Sealock R, Bennett V.
    J Cell Sci; 2001 Nov 11; 114(Pt 21):3823-35. PubMed ID: 11719549
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