BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 10198255)

  • 1. A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.
    Hamidi Asl K; Liepnieks JJ; Nakamura M; Parker F; Benson MD
    Biochem Biophys Res Commun; 1999 Apr; 257(2):584-8. PubMed ID: 10198255
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.
    Hamidi Asl L; Liepnieks JJ; Hamidi Asl K; Uemichi T; Moulin G; Desjoyaux E; Loire R; Delpech M; Grateau G; Benson MD
    Am J Pathol; 1999 Jan; 154(1):221-7. PubMed ID: 9916936
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene.
    Benson MD; Liepnieks JJ; Yazaki M; Yamashita T; Hamidi Asl K; Guenther B; Kluve-Beckerman B
    Genomics; 2001 Mar; 72(3):272-7. PubMed ID: 11401442
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Apolipoprotein AI and transthyretin as components of amyloid fibrils in a kindred with apoAI Leu178His amyloidosis.
    de Sousa MM; Vital C; Ostler D; Fernandes R; Pouget-Abadie J; Carles D; Saraiva MJ
    Am J Pathol; 2000 Jun; 156(6):1911-7. PubMed ID: 10854214
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.
    Booth DR; Tan SY; Booth SE; Tennent GA; Hutchinson WL; Hsuan JJ; Totty NF; Truong O; Soutar AK; Hawkins PN; Bruguera M; Caballería J; Solé M; Campistol JM; Pepys MB
    J Clin Invest; 1996 Jun; 97(12):2714-21. PubMed ID: 8675681
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.
    Booth DR; Tan SY; Booth SE; Hsuan JJ; Totty NF; Nguyen O; Hutton T; Vigushin DM; Tennent GA; Hutchinson WL
    QJM; 1995 Oct; 88(10):695-702. PubMed ID: 7493166
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26.
    Vigushin DM; Gough J; Allan D; Alguacil A; Penner B; Pettigrew NM; Quinonez G; Bernstein K; Booth SE; Booth DR
    Q J Med; 1994 Mar; 87(3):149-54. PubMed ID: 8208902
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Familial disseminated amylosis with cutaneous and cardiac predominance by apolipoprotein A1 mutation].
    Moulin G
    Ann Dermatol Venereol; 2000; 127(8-9):748. PubMed ID: 11011171
    [No Abstract]   [Full Text] [Related]  

  • 9. Extensive intimal apolipoprotein A1-derived amyloid deposits in a patient with an apolipoprotein A1 mutation.
    Amarzguioui M; Mucchiano G; Häggqvist B; Westermark P; Kavlie A; Sletten K; Prydz H
    Biochem Biophys Res Commun; 1998 Jan; 242(3):534-9. PubMed ID: 9464251
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Fibril-forming proteins: the amyloidosis. New hopes for a disease that cardiologists must know].
    Arbustini E; Gavazzi A; Merlini G
    Ital Heart J Suppl; 2002 Jun; 3(6):590-7. PubMed ID: 12116807
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.
    Benson MD; Liepnieks J; Uemichi T; Wheeler G; Correa R
    Nat Genet; 1993 Mar; 3(3):252-5. PubMed ID: 8097946
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transthyretin-derived senile systemic amyloidosis: clinicopathologic and structural considerations.
    Westermark P; Bergström J; Solomon A; Murphy C; Sletten K
    Amyloid; 2003 Aug; 10 Suppl 1():48-54. PubMed ID: 14640042
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structure, function and amyloidogenic propensity of apolipoprotein A-I.
    Obici L; Franceschini G; Calabresi L; Giorgetti S; Stoppini M; Merlini G; Bellotti V
    Amyloid; 2006 Dec; 13(4):191-205. PubMed ID: 17107880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary renal amyloidosis with a novel variant fibrinogen.
    Uemichi T; Liepnieks JJ; Benson MD
    J Clin Invest; 1994 Feb; 93(2):731-6. PubMed ID: 8113408
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial amino acid sequence of an amyloid fibril protein from unusual cutaneous cystic lesions in myeloma-associated amyloidosis.
    Akiyama T; Seishima M; Nojiri M; Satoh M; Ichiki Y; Kitajima Y
    Eur J Dermatol; 1999 Dec; 9(8):624-8. PubMed ID: 10586130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biochemical characterization of vitreous and cardiac amyloid in Ile84Ser transthyretin amyloidosis.
    Liepnieks JJ; Wilson DL; Benson MD
    Amyloid; 2006 Sep; 13(3):170-7. PubMed ID: 17062384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a novel human islet amyloid polypeptide beta-sheet domain and factors influencing fibrillogenesis.
    Jaikaran ET; Higham CE; Serpell LC; Zurdo J; Gross M; Clark A; Fraser PE
    J Mol Biol; 2001 May; 308(3):515-25. PubMed ID: 11327784
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of late onset cardiac amyloidosis with a new transthyretin variant (lysine 92).
    Saito F; Nakazato M; Akiyama H; Kitahara Y; Date Y; Iwasaki Y; Harasawa S; Hisaki R; Horie T; Kinukawa N; Watanabe T; Sakamaki T; Yagi H; Hoshii Y; Yutani C; Kanmatsuse K
    Hum Pathol; 2001 Feb; 32(2):237-9. PubMed ID: 11230714
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide.
    Obici L; Bellotti V; Mangione P; Stoppini M; Arbustini E; Verga L; Zorzoli I; Anesi E; Zanotti G; Campana C; Viganò M; Merlini G
    Am J Pathol; 1999 Sep; 155(3):695-702. PubMed ID: 10487826
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Colocalization of apolipoprotein AI in various kinds of systemic amyloidosis.
    Sakata N; Hoshii Y; Nakamura T; Kiyama M; Arai H; Omoto M; Morimatsu M; Ishihara T
    J Histochem Cytochem; 2005 Feb; 53(2):237-42. PubMed ID: 15684336
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.