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 *

124 related articles for article (PubMed ID: 9605286)

  • 1. Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis.
    Patrosso MC; Salvi F; De Grandis D; Vezzoni P; Jacobson DR; Ferlini A
    Am J Med Genet; 1998 May; 77(2):135-8. PubMed ID: 9605286
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
    Booth DR; Tan SY; Hawkins PN; Pepys MB; Frustaci A
    Circulation; 1995 Feb; 91(4):962-7. PubMed ID: 7850982
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel hot spot' in codon 47.
    Ferlini A; Obici L; Manzati E; Biadi O; Tarantino E; Conigli P; Merlini G; D'Alessandro M; Mazzaferro V; Tassinari CA; Salvi F
    Clin Genet; 2000 Apr; 57(4):284-90. PubMed ID: 10845569
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. A new transthyretin mutation associated with amyloidotic vitreous opacities. Asparagine for isoleucine at position 84.
    Skinner M; Harding J; Skare I; Jones LA; Cohen AS; Milunsky A; Skare J
    Ophthalmology; 1992 Apr; 99(4):503-8. PubMed ID: 1350083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A second transthyretin mutation at position 33 (Leu/Phe) associated with familial amyloidotic polyneuropathy.
    Harding J; Skare J; Skinner M
    Biochim Biophys Acta; 1991 Oct; 1097(3):183-6. PubMed ID: 1932142
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
    Holmgren G; Bergström S; Drugge U; Lundgren E; Nording-Sikström C; Sandgren O; Steen L
    Clin Genet; 1992 Jan; 41(1):39-41. PubMed ID: 1353008
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.
    Murakami A; Fujiki K; Hasegawa S; Imamura S; Kawano H; Kanai A; Matsumoto T
    Am J Ophthalmol; 2002 Feb; 133(2):272-3. PubMed ID: 11812437
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new Thr49Pro transthyretin gene mutation associated with leptomeningeal amyloidosis.
    Nakagawa K; Sheikh SI; Snuderl M; Frosch MP; Greenberg SM
    J Neurol Sci; 2008 Sep; 272(1-2):186-90. PubMed ID: 18579156
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial amyloid with a transthyretin leucine 33 mutation presenting with ascites.
    Myers TJ; Kyle RA; Jacobson DR
    Am J Hematol; 1998 Nov; 59(3):249-51. PubMed ID: 9798666
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel transthyretin mutation associated with familial amyloidotic polyneuropathy.
    Murakami T; Maeda S; Yi S; Ikegawa S; Kawashima E; Onodera S; Shimada K; Araki S
    Biochem Biophys Res Commun; 1992 Jan; 182(2):520-6. PubMed ID: 1734866
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two transthyretin mutations (glu42gly, his90asn) in an Italian family with amyloidosis.
    Skare J; Jones LA; Myles N; Kane K; Milunsky A; Cohen A; Skinner M
    Clin Genet; 1994 Jun; 45(6):281-4. PubMed ID: 7923855
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis.
    Jacobson DR; Gertz MA; Buxbaum JN
    Hum Mutat; 1994; 3(4):399-401. PubMed ID: 8081397
    [No Abstract]   [Full Text] [Related]  

  • 18. Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.
    Almeida MR; Ferlini A; Forabosco A; Gawinowicz M; Costa PP; Salvi F; Plasmati R; Tassinari CA; Altland K; Saraiva MJ
    Hum Mutat; 1992; 1(3):211-5. PubMed ID: 1301926
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosis.
    Dupuy O; Blétry O; Blanc AS; Droz D; Viémont M; Delpech M; Grateau G
    Amyloid; 1998 Dec; 5(4):285-7. PubMed ID: 10036587
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.
    Ferlini A; Patrosso MC; Repetto M; Frattini A; Villa A; Fini S; Salvi F; Vezzoni P; Forabosco A
    Hum Mutat; 1994; 4(1):61-4. PubMed ID: 7951260
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.