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Journal Abstract Search

177 related items for PubMed ID: 10675660

  • 1. A new diagnostic procedure to detect unknown transthyretin (TTR) mutations in familial amyloidotic polyneuropathy (FAP).
    Yamashita T, Ando Y, Bernt Suhr O, Nakamura M, Sakashita N, Ohlsson PI, Terazaki H, Obayashi K, Uchino M, Ando M.
    J Neurol Sci; 2000 Feb 15; 173(2):154-9. PubMed ID: 10675660
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  • 4. A novel compound heterozygote (FAP ATTR Arg104His/ATTR Val30Met) with high serum transthyretin (TTR) and retinol binding protein (RBP) levels.
    Terazaki H, Ando Y, Misumi S, Nakamura M, Ando E, Matsunaga N, Shoji S, Okuyama M, Ideta H, Nakagawa K, Ishizaki T, Ando M, Saraiva MJ.
    Biochem Biophys Res Commun; 1999 Oct 22; 264(2):365-70. PubMed ID: 10529370
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  • 5. Variant transthyretin (TTR) amyloidosis in Argentina. Detection of the trait by electrospray ionization mass spectrometry of lyophilized TTR immunoprecipitate.
    Lendoire JC, Trigo P, Aziz H, Romero MC, Inventarza O, Ando Y, Tashima K, Ohlsson PI, Cederquist K, Holmgren G, Suhr OB.
    Scand J Clin Lab Invest; 1999 Dec 22; 59(8):613-8. PubMed ID: 10691052
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  • 7. A new nonamyloid transthyretin variant, G101S, detected by electrospray ionization/mass spectrometry. Mutations in brief no. 201. Online.
    Kishikawa M, Nakanishi T, Miyazaki A, Hatanaka M, Shimizu A, Tamoto S, Ohsawa N, Hayashi H, Kanai M.
    Hum Mutat; 1998 Dec 22; 12(5):363. PubMed ID: 10671063
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  • 8. Analysis of transthyretin amyloid fibrils from vitreous samples in familial amyloidotic polyneuropathy (Val30Met).
    Ando Y, Ando E, Ohlsson PI, Olofsson A, Sandgren O, Suhr O, Terazaki H, Obayashi K, Lundgren E, Ando M, Negi A.
    Amyloid; 1999 Jun 22; 6(2):119-23. PubMed ID: 10439118
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  • 9. New transthyretin mutation V28M in a Portuguese kindred with amyloid polyneuropathy.
    de Carvalho M, Moreira P, Evangelista T, Ducla-Soares JL, Bento M, Fernandes R, Saraiva MJ.
    Muscle Nerve; 2000 Jul 22; 23(7):1016-21. PubMed ID: 10882995
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  • 10. Unusual self-association properties of transthyretin Y114C related to familial amyloidotic polyneuropathy: effects on detection and quantification.
    Ando Y, Almeida M, Ohlsson PI, Ando E, Negi A, Suhr O, Terazaki H, Obayashi K, Ando M, Saraiva MJ.
    Biochem Biophys Res Commun; 1999 Aug 02; 261(2):264-9. PubMed ID: 10425176
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  • 11. Identification of a new transthyretin variant (Ile49) in familial amyloidotic polyneuropathy using electrospray ionization mass spectrometry and nonisotopic RNase cleavage assay.
    Nakamura M, Yamashita T, Ando Y, Hamidi Asl K, Tashima K, Ohlsson P, Kususe Y, Benson MD.
    Hum Hered; 1999 Jul 02; 49(4):186-9. PubMed ID: 10436378
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  • 12. Analysis of transthyretin in human serum by capillary zone electrophoresis electrospray ionization time-of-flight mass spectrometry. Application to familial amyloidotic polyneuropathy type I.
    Pont L, Benavente F, Barbosa J, Sanz-Nebot V.
    Electrophoresis; 2015 Jun 02; 36(11-12):1265-73. PubMed ID: 25820240
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  • 13. [Protein and DNA sequencing analyses of transthyretin in familial amyloidotic polyneuropathy].
    Nakazato M.
    Rinsho Shinkeigaku; 1995 Dec 02; 35(12):1436-7. PubMed ID: 8752422
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  • 16. [A late onset familial amyloidotic polyneuropathy (FAP) with a novel variant transthyretin characterized by a basic-for-acidic amino acid substitution (Glu61-->Lys)].
    Yamamoto T, Matsunaga K, Ohnishi A, Nakazato M, Murai Y.
    Rinsho Shinkeigaku; 1996 Sep 02; 36(9):1065-8. PubMed ID: 8976129
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  • 18. Antibody recognition of amyloidogenic transthyretin variants in serum of patients with familial amyloidotic polyneuropathy.
    Palha JA, Moreira P, Olofsson A, Lundgren E, Saraiva MJ.
    J Mol Med (Berl); 2001 Sep 02; 78(12):703-7. PubMed ID: 11434723
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  • 20. Identification of S-sulfonation and S-thiolation of a novel transthyretin Phe33Cys variant from a patient diagnosed with familial transthyretin amyloidosis.
    Lim A, Prokaeva T, McComb ME, Connors LH, Skinner M, Costello CE.
    Protein Sci; 2003 Aug 02; 12(8):1775-85. PubMed ID: 12876326
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