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Volumn 56, Issue 226, 1996, Pages 47-56

Molecular basis for amyloidosis related to hereditary brain hemorrhage

Author keywords

amyloid; cystatin; mutagenesis; point mutation; protease inhibitor; recombinant DNA

Indexed keywords

CATHEPSIN B; CYSTATIN C; CYSTATIN;

EID: 0030342083     PISSN: 0085591X     EISSN: None     Source Type: Journal    
DOI: 10.3109/00365519609168298     Document Type: Review
Times cited : (31)

References (12)
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  • 3
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    • Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastro-entero-pancreatic neuro-endocrine protein, gamma-trace
    • Cohen DH, Feiner H, Jensson O, Frangione B. Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastro-entero-pancreatic neuro-endocrine protein, gamma-trace. J Exp Med 1983;158:623-8.
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    • Cohen, D.H.1    Feiner, H.2    Jensson, O.3    Frangione, B.4
  • 4
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    • Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosis
    • Löfberg H, Grubb AO, Nilsson EK, Jensson O, Gudmundsson G, Blöndal H, Arnason A, Thorsteinsson L. Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosis. Stroke 1987;18:431-40.
    • (1987) Stroke , vol.18 , pp. 431-440
    • Löfberg, H.1    Grubb, A.O.2    Nilsson, E.K.3    Jensson, O.4    Gudmundsson, G.5    Blöndal, H.6    Arnason, A.7    Thorsteinsson, L.8
  • 5
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    • Abnormal metabolism of gamma-trace alkaline microprotein. the basic defect in hereditary cerebral hemorrhage with amyloidosis
    • Grubb A, Jensson O, Gudmundsson G, Arnason A, Löfberg H, Malm J. Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosis. N Engl J Med 1984;311:1547-9.
    • (1984) N Engl J Med , vol.311 , pp. 1547-1549
    • Grubb, A.1    Jensson, O.2    Gudmundsson, G.3    Arnason, A.4    Löfberg, H.5    Malm, J.6
  • 6
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    • 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. Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C). Proc Natl Acad Sci USA 1986; 83:2974-8.
    • (1986) Proc Natl Acad Sci USA , vol.83 , pp. 2974-2978
    • Ghiso, J.1    Jensson, O.2    Frangione, B.3
  • 7
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    • Human gamma-trace, a basic microprotein: Amino acid sequence and presence in the adenohypophysis
    • Grubb A, Löfberg H. Human gamma-trace, a basic microprotein: Amino acid sequence and presence in the adenohypophysis. Proc Natl Acad Sci USA 1982;79:3024-7.
    • (1982) Proc Natl Acad Sci USA , vol.79 , pp. 3024-3027
    • Grubb, A.1    Löfberg, H.2
  • 9
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    • Molecular cloning and sequence analysis of cDNA coding for the precursor of the human cysteine proteinase inhibitor cystatin C
    • Abrahamson M, Grubb A, Olafsson I, Lundwall Å. Molecular cloning and sequence analysis of cDNA coding for the precursor of the human cysteine proteinase inhibitor cystatin C. FEBS Lett 1987;216:229-33.
    • (1987) FEBS Lett , vol.216 , pp. 229-233
    • Abrahamson, M.1    Grubb, A.2    Olafsson, I.3    Lundwall, Å.4
  • 10
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    • Human γ-trace: Structure, function and clinical use of concentration measurements
    • Grubb A, Löfberg H. Human γ-trace: Structure, function and clinical use of concentration measurements. Scand J Clin Lab Invest 1985;45, Suppl 177:7-13.
    • (1985) Scand J Clin Lab Invest , vol.45 , Issue.177 SUPPL. , pp. 7-13
    • Grubb, A.1    Löfberg, H.2
  • 11
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    • The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20
    • Abrahamson M, Islam MQ, Szpirer J, Szpirer C, Levan G. The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20. Hum Genet 1989;82:223-6.
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    • Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2
    • Schnittger S, Gopal Rao VVN, Abrahamson M, Hansmann I. Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2. Genomics 1993;16:50-5.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.