BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 1358785)

  • 1. Transthyretin Pro 36 associated with familial amyloidotic polyneuropathy in an Ashkenazic Jewish kindred.
    Jacobson DR; Rosenthal CJ; Buxbaum JN
    Hum Genet; 1992; 90(1-2):158-60. PubMed ID: 1358785
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.
    Saraiva MJ; Sherman W; Goodman DS
    J Lab Clin Med; 1986 Jul; 108(1):17-22. PubMed ID: 3011930
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy.
    Uemichi T; Murrell JR; Zeldenrust S; Benson MD
    J Med Genet; 1992 Dec; 29(12):888-91. PubMed ID: 1362222
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement.
    Jacobson DR; McFarlin DE; Kane I; Buxbaum JN
    Hum Genet; 1992 May; 89(3):353-6. PubMed ID: 1351039
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy.
    Jones LA; Skare JC; Harding JA; Cohen AS; Milunsky A; Skinner M
    Am J Hum Genet; 1991 May; 48(5):979-82. PubMed ID: 1850191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Amyloidogenic and non-amyloidogenic transthyretin Asn 90 variants.
    Alves IL; Almeida MR; Skare J; Skinner M; Kurose K; Sakaki Y; Costa PP; Saraiva MJ
    Clin Genet; 1992 Jul; 42(1):27-30. PubMed ID: 1355416
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of three transthyretin gene mutations in familial amyloidotic polyneuropathy by analysis of DNA extracted from formalin-fixed and paraffin-embedded tissues.
    Date Y; Nakazato M; Kangawa K; Shirieda K; Fujimoto T; Matsukura S
    J Neurol Sci; 1997 Sep; 150(2):143-8. PubMed ID: 9268242
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin.
    Saraiva MJ; Costa PP; Almeida Mdo R; Banzhoff A; Altland K; Ferlini A; Rubboli G; Plasmati R; Tassinari CA; Romeo G
    Hum Genet; 1988 Dec; 80(4):341-3. PubMed ID: 2848756
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy.
    Skare J; Yazici H; Erken E; Dede H; Cohen A; Milunsky A; Skinner M
    Hum Genet; 1990 Nov; 86(1):89-90. PubMed ID: 2174830
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A transthyretin variant (alanine 49) associated with familial amyloidotic polyneuropathy in a French family.
    Benson MD; Julien J; Liepnieks J; Zeldenrust S; Benson MD
    J Med Genet; 1993 Feb; 30(2):117-9. PubMed ID: 8095301
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy.
    Saraiva MJ; Alves IL; Costa PP
    Clin Chem; 1989 Jun; 35(6):1033-5. PubMed ID: 2543515
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TTR exon scanning in peripheral neuropathies.
    Torres Mde F; Almeida Mdo R; Saraiva MJ
    Neuromuscul Disord; 1995 May; 5(3):187-91. PubMed ID: 7633183
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A novel mutant (transthyretin Ile-50) related to amyloid polyneuropathy. Single-strand conformation polymorphism as a new genetic marker.
    Saeki Y; Ueno S; Takahashi N; Soga F; Yanagihara T
    FEBS Lett; 1992 Aug; 308(1):35-7. PubMed ID: 1644201
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family.
    Benson MD; Turpin JC; Lucotte G; Zeldenrust S; LeChevalier B; Benson MD
    J Med Genet; 1993 Feb; 30(2):120-2. PubMed ID: 8095302
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy.
    Murakami T; Atsumi T; Maeda S; Tanase S; Ishikawa K; Mita S; Kumamoto T; Araki S; Ando M
    Biochem Biophys Res Commun; 1992 Aug; 187(1):397-403. PubMed ID: 1520326
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy.
    Saraiva MJ; Costa PP; Goodman DS
    Neurology; 1986 Nov; 36(11):1413-7. PubMed ID: 3762958
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transthyretin Ser 6 gene frequency in individuals without amyloidosis.
    Jacobson DR; Alves IL; Saraiva MJ; Thibodeau SN; Buxbaum JN
    Hum Genet; 1995 Mar; 95(3):308-12. PubMed ID: 7868124
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.