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Journal Abstract Search

188 related items for PubMed ID: 16329101

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  • 3. A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene.
    Benson MD, Liepnieks JJ, Yazaki M, Yamashita T, Hamidi Asl K, Guenther B, Kluve-Beckerman B.
    Genomics; 2001 Mar 15; 72(3):272-7. PubMed ID: 11401442
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  • 8. Identification of the core structure of lysozyme amyloid fibrils by proteolysis.
    Frare E, Mossuto MF, Polverino de Laureto P, Dumoulin M, Dobson CM, Fontana A.
    J Mol Biol; 2006 Aug 18; 361(3):551-61. PubMed ID: 16859705
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  • 9. Hereditary lysozyme amyloidosis -- phenotypic heterogeneity and the role of solid organ transplantation.
    Sattianayagam PT, Gibbs SD, Rowczenio D, Pinney JH, Wechalekar AD, Gilbertson JA, Hawkins PN, Lachmann HJ, Gillmore JD.
    J Intern Med; 2012 Jul 18; 272(1):36-44. PubMed ID: 21988333
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  • 10. Lysozyme amyloidogenesis is accelerated by specific nicking and fragmentation but decelerated by intact protein binding and conversion.
    Mishra R, Sörgjerd K, Nyström S, Nordigården A, Yu YC, Hammarström P.
    J Mol Biol; 2007 Feb 23; 366(3):1029-44. PubMed ID: 17196616
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  • 11. Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family.
    Valleix S, Drunat S, Philit JB, Adoue D, Piette JC, Droz D, MacGregor B, Canet D, Delpech M, Grateau G.
    Kidney Int; 2002 Mar 23; 61(3):907-12. PubMed ID: 11849445
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  • 12. Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.
    Maury CP.
    J Clin Invest; 1991 Apr 23; 87(4):1195-9. PubMed ID: 1849145
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  • 15. The workings of the amyloid diseases.
    Bellotti V, Nuvolone M, Giorgetti S, Obici L, Palladini G, Russo P, Lavatelli F, Perfetti V, Merlini G.
    Ann Med; 2007 Apr 23; 39(3):200-7. PubMed ID: 17457717
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  • 16. Insights into the conformational changes of several human lysozyme variants associated with hereditary systemic amyloidosis.
    Liu HL, Wu YC, Zhao JH, Liu YF, Huang CH, Fang HW, Ho Y.
    Biotechnol Prog; 2007 Apr 23; 23(1):246-54. PubMed ID: 17269695
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  • 20. A new family with hereditary lysozyme amyloidosis with gastritis and inflammatory bowel disease as prevailing symptoms.
    Jean E, Ebbo M, Valleix S, Benarous L, Heyries L, Grados A, Bernit E, Grateau G, Papo T, Granel B, Daniel L, Harlé JR, Schleinitz N.
    BMC Gastroenterol; 2014 Sep 13; 14():159. PubMed ID: 25217048
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