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 *

231 related articles for article (PubMed ID: 3517880)

  • 1. Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C).
    Ghiso J; Jensson O; Frangione B
    Proc Natl Acad Sci U S A; 1986 May; 83(9):2974-8. PubMed ID: 3517880
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases.
    Levy E; Lopez-Otin C; Ghiso J; Geltner D; Frangione B
    J Exp Med; 1989 May; 169(5):1771-8. PubMed ID: 2541223
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary cerebral amyloid angiopathy: the amyloid fibrils contain a protein which is a variant of cystatin C, an inhibitor of lysosomal cysteine proteases.
    Ghiso J; Pons-Estel B; Frangione B
    Biochem Biophys Res Commun; 1986 Apr; 136(2):548-54. PubMed ID: 3707586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage.
    Jensson O; Gudmundsson G; Arnason A; Blöndal H; Petursdottir I; Thorsteinsson L; Grubb A; Löfberg H; Cohen D; Frangione B
    Acta Neurol Scand; 1987 Aug; 76(2):102-14. PubMed ID: 3673496
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace.
    Cohen DH; Feiner H; Jensson O; Frangione B
    J Exp Med; 1983 Aug; 158(2):623-8. PubMed ID: 6886625
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cellular processing of the amyloidogenic cystatin C variant of hereditary cerebral hemorrhage with amyloidosis, Icelandic type.
    Benedikz E; Merz GS; Schwenk V; Johansen TE; Wisniewski HM; Rushbrook JI
    Amyloid; 1999 Sep; 6(3):172-82. PubMed ID: 10524281
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Instability of the amyloidogenic cystatin C variant of hereditary cerebral hemorrhage with amyloidosis, Icelandic type.
    Wei L; Berman Y; Castaño EM; Cadene M; Beavis RC; Devi L; Levy E
    J Biol Chem; 1998 May; 273(19):11806-14. PubMed ID: 9565605
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distinct properties of wild-type and the amyloidogenic human cystatin C variant of hereditary cerebral hemorrhage with amyloidosis, Icelandic type.
    Calero M; Pawlik M; Soto C; Castaño EM; Sigurdsson EM; Kumar A; Gallo G; Frangione B; Levy E
    J Neurochem; 2001 Apr; 77(2):628-37. PubMed ID: 11299325
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular diagnosis of hereditary cystatin C amyloid angiopathy.
    Jonsdottir S; Palsdottir A
    Biochem Med Metab Biol; 1993 Apr; 49(2):117-23. PubMed ID: 8097919
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Possibly "familial" cerebral amyloid angiopathy in Japan: immunohistochemical identification of gamma-trace].
    Fujihara S; Shimode K; Kobayashi S; Tsunematsu T; Kagawa R
    Rinsho Shinkeigaku; 1988 Apr; 28(4):453-8. PubMed ID: 3063424
    [No Abstract]   [Full Text] [Related]  

  • 11. Cerebral amyloid angiopathy with the deposition of cystatin C (gamma-trace) and beta-protein.
    Fujihara S; Shimode K; Nakamura M; Kobayashi S; Tsunematsu T
    Prog Clin Biol Res; 1989; 317():939-44. PubMed ID: 2690129
    [No Abstract]   [Full Text] [Related]  

  • 12. Immunohistochemical study of cerebral amyloid angiopathy. III. Widespread Alzheimer A4 peptide in cerebral microvessel walls colocalizes with gamma trace in patients with leukoencephalopathy.
    Vinters HV; Secor DL; Pardridge WM; Gray F
    Ann Neurol; 1990 Jul; 28(1):34-42. PubMed ID: 2197973
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis for amyloidosis related to hereditary brain hemorrhage.
    Abrahamson M
    Scand J Clin Lab Invest Suppl; 1996; 226():47-56. PubMed ID: 8981667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation in the cystatin C gene causes hereditary brain hemorrhage.
    Palsdottir A; Abrahamson M; Thorsteinsson L; Arnason A; Olafsson I; Grubb A; Jensson O
    Prog Clin Biol Res; 1989; 317():241-6. PubMed ID: 2602420
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms.
    Olafsson I; Gudmundsson G; Abrahamson M; Jensson O; Grubb A
    Scand J Clin Lab Invest; 1990 Feb; 50(1):85-93. PubMed ID: 2315647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of a normal and variant Alzheimer's beta-protein gene in amyloid of hereditary cerebral hemorrhage, Dutch type: DNA and protein diagnostic assays.
    Prelli F; Levy E; van Duinen SG; Bots GT; Luyendijk W; Frangione B
    Biochem Biophys Res Commun; 1990 Jul; 170(1):301-7. PubMed ID: 2196878
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cystatin C mutation in an elderly man with sporadic amyloid angiopathy and intracerebral hemorrhage.
    Graffagnino C; Herbstreith MH; Schmechel DE; Levy E; Roses AD; Alberts MJ
    Stroke; 1995 Nov; 26(11):2190-3. PubMed ID: 7482672
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The molecular pathology of hereditary cystatin C amyloid angiopathy causing brain hemorrhage.
    Olafsson I; Thorsteinsson L; Jensson O
    Brain Pathol; 1996 Apr; 6(2):121-6. PubMed ID: 8737928
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra-CNS amyloid deposits of aged Japanese.
    Yamada M; Tsukagoshi H; Wada Y; Otomo E; Hayakawa M; Thorsteinsson L; Jensson O
    Acta Neurol Scand; 1989 Jun; 79(6):504-9. PubMed ID: 2782031
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation of a sequence encoding human cystatin C. Conservation of exon-intron structure between members of the cysteine proteinase inhibitors superfamily.
    Ghiso J; Cowan N; Frangione B
    Biol Chem Hoppe Seyler; 1988 May; 369 Suppl():205-8. PubMed ID: 3264504
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.