These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 12553428)

  • 1. Laboratory assessment of transthyretin amyloidosis.
    Benson MD; Yazaki M; Magy N
    Clin Chem Lab Med; 2002 Dec; 40(12):1262-5. PubMed ID: 12553428
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
    Connors LH; Yamashita T; Yazaki M; Skinner M; Benson MD
    Amyloid; 2004 Mar; 11(1):61-6. PubMed ID: 15185501
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cardiac amyloidosis associated with the transthyretin Ile122 mutation in a Caucasian family.
    Hamidi Asl K; Nakamura M; Yamashita T; Benson MD
    Amyloid; 2001 Dec; 8(4):263-9. PubMed ID: 11791619
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His.
    Blevins G; Macaulay R; Harder S; Fladeland D; Yamashita T; Yazaki M; Hamidi Asl K; Benson MD; Donat JR
    Neurology; 2003 May; 60(10):1625-30. PubMed ID: 12771253
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of transthyretin variants by sequential proteomic and genomic analysis.
    Bergen HR; Zeldenrust SR; Butz ML; Snow DS; Dyck PJ; Dyck PJ; Klein CJ; O'Brien JF; Thibodeau SN; Muddiman DC
    Clin Chem; 2004 Sep; 50(9):1544-52. PubMed ID: 15217993
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gastrointestinal amyloidosis associated with transthyretin Phe64Ser mutation.
    Naderi AS; Farsian FN; Igarashi P
    Am J Med Sci; 2007 Sep; 334(3):219-21. PubMed ID: 17873539
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 12(8):1775-85. PubMed ID: 12876326
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis.
    Lim A; Prokaeva T; Connor LH; Falk RH; Skinner M; Costello CE
    Amyloid; 2002 Jun; 9(2):134-40. PubMed ID: 12440486
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new Arg54Gly transthyretin gene mutation associated with vitreous amyloidosis in Chinese.
    Shi Y; Li J; Hu J; Hu J; Sun L; Li H; Shi R; Yang L; Sun Y; Li C
    Eye Sci; 2011 Dec; 26(4):230-8. PubMed ID: 22187309
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A prospective evaluation of the transthyretin Ile122 allele frequency in an African-American population.
    Yamashita T; Hamidi Asl K; Yazaki M; Benson MD
    Amyloid; 2005 Jun; 12(2):127-30. PubMed ID: 16011990
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.
    Zhang Y; Deng YL; Ma JF; Zheng L; Hong Z; Wang ZQ; Sheng CY; Xiao Q; Cao L; Chen SD
    Neurodegener Dis; 2011; 8(4):187-93. PubMed ID: 21135536
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
    Magy N; Liepnieks JJ; Gil H; Kantelip B; Dupond JL; Kluve-Beckerman B; Benson MD
    Amyloid; 2003 Mar; 10(1):29-33. PubMed ID: 12762139
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amyloid fibril composition and transthyretin gene structure in senile systemic amyloidosis.
    Gustavsson A; Jahr H; Tobiassen R; Jacobson DR; Sletten K; Westermark P
    Lab Invest; 1995 Nov; 73(5):703-8. PubMed ID: 7474944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transthyretin Cardiac Amyloidosis.
    Mankad AK; Shah KB
    Curr Cardiol Rep; 2017 Aug; 19(10):97. PubMed ID: 28840452
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome.
    Takei Y; Hattori T; Yazaki M; Tokuda T; Urasawa N; Kanai S; Ikeda S
    Amyloid; 2003 Mar; 10(1):25-8. PubMed ID: 12762138
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis.
    Nie XM; Cai SJ; Xie B; Chen XW; Jiang M
    Genet Mol Res; 2016 Mar; 15(1):. PubMed ID: 27051017
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Identification of a TTR gene mutation in a family with hereditary vitreous amyloidosis].
    Xie Y; Zhao Y; Zhou JJ; Wang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):13-5. PubMed ID: 22311483
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial vitreous amyloidosis resulting from transthyretin variant Gly83Arg.
    Xie B; Cai SJ; Jiang M; Li H; Su G
    Acta Ophthalmol; 2017 Sep; 95(6):e520-e521. PubMed ID: 28266151
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel variant of transthyretin (Glu89Lys) associated with familial amyloidotic polyneuropathy.
    Nakamura M; Hamidi Asl K; Benson MD
    Amyloid; 2000 Mar; 7(1):46-50. PubMed ID: 10842705
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.