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Volumn 14, Issue 2, 2000, Pages 149-151

A new variant of apolipoprotein E (apo E Maebashi) in lipoprotein glomerulopathy

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN E;

EID: 0033974584     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670050032     Document Type: Short Survey
Times cited : (33)

References (19)
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    • (1989) Am J Kidney Dis , vol.13 , pp. 148-153
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  • 2
    • 0024575139 scopus 로고
    • A case of nephrotic syndrome with glomerular lipoprotein deposition with capillary ballooning and mesangiolysis
    • Watanabe Y, Ozaki I, Fukatsu A, Ito Y, Matsuo S, Sakamoto N (1989) A case of nephrotic syndrome with glomerular lipoprotein deposition with capillary ballooning and mesangiolysis. Nephron 51:265-270
    • (1989) Nephron , vol.51 , pp. 265-270
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  • 7
    • 0342421361 scopus 로고
    • Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with Hha I
    • Hixson JE, Vernier DT (1990) Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with Hha I. Pediatr Nephrol 11:213-214
    • (1990) Pediatr Nephrol , vol.11 , pp. 213-214
    • Hixson, J.E.1    Vernier, D.T.2
  • 8
    • 0001430252 scopus 로고
    • DNA fragments differing by single-base-pair substitutions are separated in denaturing gradient gel: Correspondence with melting theory
    • Fisher SG, Lerman LS (1983) DNA fragments differing by single-base-pair substitutions are separated in denaturing gradient gel: correspondence with melting theory. Proc Natl Acad Sci USA 80:1579-1583
    • (1983) Proc Natl Acad Sci USA , vol.80 , pp. 1579-1583
    • Fisher, S.G.1    Lerman, L.S.2
  • 9
    • 0027185201 scopus 로고
    • Identification of a splice-site mutation in the low density lipoprotein receptor gene by denaturing gradient gel electrophoresis
    • Top B, Zee A van der, Havekes LM, Hooft FM van't, Frants RR (1993) Identification of a splice-site mutation in the low density lipoprotein receptor gene by denaturing gradient gel electrophoresis. Hum Genet 91:480-484
    • (1993) Hum Genet , vol.91 , pp. 480-484
    • Top, B.1    Van Der Zee, A.2    Havekes, L.M.3    Van't Hooft, F.M.4    Frants, R.R.5
  • 10
    • 0026778830 scopus 로고
    • Rabbit very low density lipoprotein receptor: A low density lipoprotein receptor-like protein with distinct ligand specificity
    • Takahashi S, Kawarabayashi Y, Nakai T, Sakai J, Yamamoto T (1992) Rabbit very low density lipoprotein receptor: a low density lipoprotein receptor-like protein with distinct ligand specificity. Proc Natl Acad Sci USA 89:9252-9256
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 9252-9256
    • Takahashi, S.1    Kawarabayashi, Y.2    Nakai, T.3    Sakai, J.4    Yamamoto, T.5
  • 11
    • 0001665337 scopus 로고
    • Surface location and high affinity for calcium of a 500-kD liver membrane protein closely related to the LDL-receptor suggest physiological role as lipoprotein receptor
    • Herz J, Humann U (1988) Surface location and high affinity for calcium of a 500-kD liver membrane protein closely related to the LDL-receptor suggest physiological role as lipoprotein receptor. EMBO J 7:4119-4127
    • (1988) EMBO J , vol.7 , pp. 4119-4127
    • Herz, J.1    Humann, U.2
  • 13
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    • Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels
    • Knijff P de, Maagdenberg AM van den, Frants RR, Havekes LM (1994) Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels. Hum Mutat 4:178-194
    • (1994) Hum Mutat , vol.4 , pp. 178-194
    • De Knijff, P.1    Van Den Maagdenberg, A.M.2    Frants, R.R.3    Havekes, L.M.4
  • 15
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    • Type III hypercholesterolemia (dysbetalipoproteinemia): The role of apolipoprotein E in normal and abnormal lipoprotein in metabolism
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    • Mahley RW, Rall SC Jr (1995) Type III hypercholesterolemia (dysbetalipoproteinemia): the role of apolipoprotein E in normal and abnormal lipoprotein in metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular basis of inherited disease, 7th edn. MacGraw-Hill, New York, pp 1953-1980
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    • Mahley, R.W.1    Rall S.C., Jr.2
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    • A case of congenital nephrotic syndrome associated with partial deficiency of lecithin cholesterol acyltransferase (LCAT) and hypothyroidism
    • Hiramatsu M, Karashima S, Hattori S, Matsuda I, Maeda H (1984) A case of congenital nephrotic syndrome associated with partial deficiency of lecithin cholesterol acyltransferase (LCAT) and hypothyroidism. Int J Pediatr Nephrol 5:183-186
    • (1984) Int J Pediatr Nephrol , vol.5 , pp. 183-186
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.