메뉴 건너뛰기




Volumn 154, Issue 1, 1999, Pages 221-227

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; AMYLOID; APOLIPOPROTEIN A1; PROTEIN PRECURSOR;

EID: 0010287190     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9440(10)65268-6     Document Type: Article
Times cited : (95)

References (39)
  • 1
    • 0001999309 scopus 로고
    • Amyloidosis
    • Edited by Scriver CR, Beaudet AL, Sly WS, Valle D, New York, McGraw-Hill
    • Benson MD: Amyloidosis. The Metabolic Basis of Inherited Disease, ed 7. Edited by Scriver CR, Beaudet AL, Sly WS, Valle D, New York, McGraw-Hill, 1995, pp 4159-4191
    • (1995) The Metabolic Basis of Inherited Disease, Ed 7 , pp. 4159-4191
    • Benson, M.D.1
  • 3
    • 0025950987 scopus 로고
    • A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease
    • Murrell J, Farlow M, Ghetti B, Benson MD: A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease Science 1991, 254:97-99
    • (1991) Science , vol.254 , pp. 97-99
    • Murrell, J.1    Farlow, M.2    Ghetti, B.3    Benson, M.D.4
  • 4
    • 0017226393 scopus 로고
    • Characterization of amyloid fibril proteins from medullary carcinoma of the thyroid
    • Sletten K, Westermark P, Natvig JB: Characterization of amyloid fibril proteins from medullary carcinoma of the thyroid. J Exp Med 1976, 143:993-998
    • (1976) J Exp Med , vol.143 , pp. 993-998
    • Sletten, K.1    Westermark, P.2    Natvig, J.B.3
  • 5
    • 1842527698 scopus 로고    scopus 로고
    • Transthyretin amyloidosis
    • Benson MD, Uemichi T: Transthyretin amyloidosis. Amyloid 1996, 3:44-51
    • (1996) Amyloid , vol.3 , pp. 44-51
    • Benson, M.D.1    Uemichi, T.2
  • 7
    • 0025006134 scopus 로고
    • A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy
    • Nichols WC, Gregg RE, Brewer HB Jr, Benson MD: A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. Genomics 1990, 8:318-323
    • (1990) Genomics , vol.8 , pp. 318-323
    • Nichols, W.C.1    Gregg, R.E.2    Brewer H.B., Jr.3    Benson, M.D.4
  • 8
    • 0027465319 scopus 로고
    • Hereditary renal amyloidosis associated with a mutant fibrinogen α-chain
    • Benson MD, Liepnieks J, Uemichi T, Wheeler G, Correa R: Hereditary renal amyloidosis associated with a mutant fibrinogen α-chain. Nature Genet 1993, 3:252-255
    • (1993) Nature Genet , vol.3 , pp. 252-255
    • Benson, M.D.1    Liepnieks, J.2    Uemichi, T.3    Wheeler, G.4    Correa, R.5
  • 10
    • 0022481290 scopus 로고
    • 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: Hereditary cerebral amyloid angiopathy: the amyloid fibrils contain a protein which is a variant of cystatin C, an inhibitor of lysosomal cysteine proteases. Biochem Biophys Res Commun 1986, 136:548-554
    • (1986) Biochem Biophys Res Commun , vol.136 , pp. 548-554
    • Ghiso, J.1    Pons-Estel, B.2    Frangione, B.3
  • 11
    • 0014444934 scopus 로고
    • Inherited predisposition to generalized amyloidosis
    • Van Allen M, Frohlich J, Davis J: Inherited predisposition to generalized amyloidosis. Neurology 1969, 19:10-25
    • (1969) Neurology , vol.19 , pp. 10-25
    • Van Allen, M.1    Frohlich, J.2    Davis, J.3
  • 16
    • 0003163646 scopus 로고    scopus 로고
    • Local synthesis of amyloid fibril precursor in AL amyloidosis of the urinary tract
    • Hamidi Asl K, Liepnieks JJ, Bihrle R, Benson MD: Local synthesis of amyloid fibril precursor in AL amyloidosis of the urinary tract. Amyloid 1998, 5 49-54
    • (1998) Amyloid , vol.5 , pp. 49-54
    • Hamidi Asl, K.1    Liepnieks, J.J.2    Bihrle, R.3    Benson, M.D.4
  • 17
    • 0023472472 scopus 로고
    • Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1-100 kDa
    • Schagger H, Von Jagow G: Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1-100 kDa. Anal Biochem 1987, 166:368-379
    • (1987) Anal Biochem , vol.166 , pp. 368-379
    • Schagger, H.1    Von Jagow, G.2
  • 19
    • 0021635560 scopus 로고
    • Isolation and DNA sequence of full-length cDNA and of the entire gene for human apolipoprotein AI: Discovery of a new genetic polymorphism in the apo AI gene
    • Seilhamer JJ, Protter AA, Frossard P, Levy-Wilson B: Isolation and DNA sequence of full-length cDNA and of the entire gene for human apolipoprotein AI: discovery of a new genetic polymorphism in the apo AI gene. DNA 1984, 3:309-317
    • (1984) DNA , vol.3 , pp. 309-317
    • Seilhamer, J.J.1    Protter, A.A.2    Frossard, P.3    Levy-Wilson, B.4
  • 20
    • 0029844722 scopus 로고    scopus 로고
    • Primary localized amyloidosis of the eyelid: Two cases of immunoglobulin light chain-derived proteins, subtype lambda V respectively lambda VI
    • Olsen KE, Sandgren O, Sletten K, Westermark P: Primary localized amyloidosis of the eyelid: two cases of immunoglobulin light chain-derived proteins, subtype lambda V respectively lambda VI. Clin Exp Immunol 1996, 106:362-366
    • (1996) Clin Exp Immunol , vol.106 , pp. 362-366
    • Olsen, K.E.1    Sandgren, O.2    Sletten, K.3    Westermark, P.4
  • 21
    • 0019510287 scopus 로고
    • Skin involvement in familial amyloidotic polyneuropathy
    • Rubinow A, Cohen AS: Skin involvement in familial amyloidotic polyneuropathy. Neurology 1981, 31:1341-1345
    • (1981) Neurology , vol.31 , pp. 1341-1345
    • Rubinow, A.1    Cohen, A.S.2
  • 25
    • 0026410035 scopus 로고
    • Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II
    • Gorevic PD, Munoz PC, Gorgone G: Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II. N Engl J Med 1991, 325:1780-1785
    • (1991) N Engl J Med , vol.325 , pp. 1780-1785
    • Gorevic, P.D.1    Munoz, P.C.2    Gorgone, G.3
  • 27
    • 0025006121 scopus 로고
    • Clinical features of cutaneous amyloidosis
    • Wang WJ: Clinical features of cutaneous amyloidosis. Clin Dermatol 1990, 8:13-19
    • (1990) Clin Dermatol , vol.8 , pp. 13-19
    • Wang, W.J.1
  • 28
    • 0018144518 scopus 로고
    • Familial primary cutaneous amyloidosis, clinical, genetic, and immunofluorescent studies
    • Vasily DB, Bhatia SG, Uhlin SR: Familial primary cutaneous amyloidosis, clinical, genetic, and immunofluorescent studies. Arch Dermatol 1978, 114:1173-1176
    • (1978) Arch Dermatol , vol.114 , pp. 1173-1176
    • Vasily, D.B.1    Bhatia, S.G.2    Uhlin, S.R.3
  • 30
    • 0015382653 scopus 로고
    • Familial lichen amyloidosis: Report of 19 cases in 4 generations of a chinese family in Malaysia
    • Rajagopalan K, Tay CH: Familial lichen amyloidosis: report of 19 cases in 4 generations of a chinese family in Malaysia. Br J Dermatol 1972, 87:123-129
    • (1972) Br J Dermatol , vol.87 , pp. 123-129
    • Rajagopalan, K.1    Tay, C.H.2
  • 31
    • 0026462953 scopus 로고
    • Pulmonary vascular amyloidosis in aged dogs: A new form of spontaneously occurring amyloidosis derived from apolipoprotein A1
    • Johnson KH, Sletten K, Hayden DW, O'Brien TD, Roertgen KE, Westermark P: Pulmonary vascular amyloidosis in aged dogs: a new form of spontaneously occurring amyloidosis derived from apolipoprotein A1. Am J Pathol 1992, 141:1013-1019
    • (1992) Am J Pathol , vol.141 , pp. 1013-1019
    • Johnson, K.H.1    Sletten, K.2    Hayden, D.W.3    O'Brien, T.D.4    Roertgen, K.E.5    Westermark, P.6
  • 34
    • 0027476367 scopus 로고
    • The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val30→Met variant to 1.7-Å resolution
    • Hamilton JA, Steinrauf LK, Braden BC, Liepnieks J, Benson MD, Holmgren G, Sandgren O, Steen L: The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val30→Met variant to 1.7-Å resolution. J Biol Chem 1993, 268:2416-2424
    • (1993) J Biol Chem , vol.268 , pp. 2416-2424
    • Hamilton, J.A.1    Steinrauf, L.K.2    Braden, B.C.3    Liepnieks, J.4    Benson, M.D.5    Holmgren, G.6    Sandgren, O.7    Steen, L.8
  • 36
    • 0027717482 scopus 로고
    • Characterization of amyloid fibril-peptide in familial Alzheimer disease with APP 717 mutations
    • Liepnieks JJ, Ghetti B, Farlow M, Roses AD, Benson MD: Characterization of amyloid fibril-peptide in familial Alzheimer disease with APP 717 mutations. Biochem Biophys Res Commun 1993, 197:386-392
    • (1993) Biochem Biophys Res Commun , vol.197 , pp. 386-392
    • Liepnieks, J.J.1    Ghetti, B.2    Farlow, M.3    Roses, A.D.4    Benson, M.D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.