BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

220 related articles for article (PubMed ID: 1655325)

  • 1. [Diagnosis of familial amyloid polyneuropathy--gene analysis with primer-directed enzymatic amplification of DNA, isolation of plasma variant prealbumin and immunohistochemical identification of tissue amyloid protein].
    Ikeda S; Nakano T; Yanagisawa N; Hanyu N; Suzuki T; Sakaki Y
    Rinsho Shinkeigaku; 1991 Apr; 31(4):363-71. PubMed ID: 1655325
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy.
    Nakazato M; Sasaki H; Furuya H; Sakaki Y; Kurihara T; Matsukura S; Kangawa K; Matsuo H
    Ann Neurol; 1987 Jun; 21(6):596-8. PubMed ID: 3037992
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cloning of human prealbumin complementary DNA. Localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy.
    Whitehead AS; Skinner M; Bruns GA; Costello W; Edge MD; Cohen AS; Sipe JD
    Mol Biol Med; 1984 Dec; 2(6):411-23. PubMed ID: 6100724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Diagnosis by recombinant DNA techniques and clinical features of familial amyloid polyneuropathy].
    Harada T
    No To Shinkei; 1988 Jul; 40(7):617-21. PubMed ID: 2852018
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical features and diagnosis by recombinant DNA techniques of familial amyloid polyneuropathy in Japan.
    Harada T; Kito S; Ishizaki F; Matsubayashi H; Katayama S; Sasaki H; Furuya H; Sakaki Y
    Res Commun Chem Pathol Pharmacol; 1989 Aug; 65(2):237-44. PubMed ID: 2587841
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Rapid prenatal diagnosis of familial amyloidotic polyneuropathy using DNA amplification].
    Murakami T; Nishiguchi S; Maeda S; Shimada K; Araki S
    Rinsho Shinkeigaku; 1990 Apr; 30(4):384-7. PubMed ID: 2167187
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial amyloid polyneuropathy related to transthyretin Gly42 in a Japanese family.
    Uemichi T; Ueno S; Fujimura H; Umekage T; Yorifuji S; Matsuzawa Y; Tarui S
    Muscle Nerve; 1992 Aug; 15(8):904-11. PubMed ID: 1353861
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type.
    Saraiva MJ; Costa PP; Goodman DS
    J Lab Clin Med; 1983 Oct; 102(4):590-603. PubMed ID: 6311926
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Amyloid neuropathy].
    Ikegawa S
    Rinsho Shinkeigaku; 1990 Dec; 30(12):1371-3. PubMed ID: 1966018
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy.
    Yoshioka K; Sasaki H; Yoshioka N; Furuya H; Harada T; Kito S; Sakaki Y
    Mol Biol Med; 1986 Aug; 3(4):319-28. PubMed ID: 3022107
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Diagnosis of familial amyloid polyneuropathy type I in Argentina].
    PĂ©rez G; Romero MC; Trigo P; Lendoire J; Imventarza O; Nesse A
    Medicina (B Aires); 2008; 68(4):273-81. PubMed ID: 18786882
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnosis of Maryland/German familial amyloidotic polyneuropathy using allele-specific, enzymatically amplified, genomic DNA.
    Mendell JR; Jiang XS; Warmolts JR; Nichols WC; Benson MD
    Ann Neurol; 1990 May; 27(5):553-7. PubMed ID: 2360796
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence].
    Adams D; Reilly M; Harding AE; Said G
    Rev Neurol (Paris); 1992; 148(12):736-41. PubMed ID: 1338934
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal detection of a gene for hereditary amyloidosis.
    Nichols WC; Padilla LM; Benson MD
    Am J Med Genet; 1989 Dec; 34(4):520-4. PubMed ID: 2516414
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.
    Koeppen AH; Wallace MR; Benson MD; Altland K
    Muscle Nerve; 1990 Nov; 13(11):1065-75. PubMed ID: 2122246
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prealbumin variants in the amyloid fibrils of Swedish familial amyloidotic polyneuropathy.
    Westermark P; Sletten K; Olofsson BO
    Clin Exp Immunol; 1987 Sep; 69(3):695-701. PubMed ID: 3117463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.
    Saraiva MJ; Birken S; Costa PP; Goodman DS
    Ann N Y Acad Sci; 1984; 435():86-100. PubMed ID: 6099706
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family.
    Wallace MR; Conneally PM; Long GL; Benson MD
    Am J Med Genet; 1986 Oct; 25(2):335-41. PubMed ID: 2877582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset.
    Nakazato M; Kurihara T; Matsukura S; Kangawa K; Matsuo H
    J Clin Invest; 1986 May; 77(5):1699-703. PubMed ID: 3457802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis of familial amyloidotic polyneuropathy: isolation of variant prealbumin.
    Suzuki T; Azuma T; Tsujino S; Mizuno R; Kishimoto S; Wada Y; Hayashi A; Ikeda S; Yanagisawa N
    Neurology; 1987 Apr; 37(4):708-11. PubMed ID: 3031544
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.