메뉴 건너뛰기




Volumn 243, Issue 4, 1998, Pages 317-321

Identification of homozygous lipoprotein lipase gene mutation in a woman with recurrent aggravation of hypertriglyceridaemia induced by pregnancy

Author keywords

Hypertriglyceridaemia; Lipoprotein lipase deficiency; Pancreatitis; Pregnancy

Indexed keywords

CHOLESTEROL; LIPOPROTEIN LIPASE; TRIACYLGLYCEROL;

EID: 0031859494     PISSN: 09546820     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2796.1998.00306.x     Document Type: Article
Times cited : (37)

References (17)
  • 1
    • 0019986799 scopus 로고
    • Population-based lipoprotein lipid reference values for pregnant women compared to nonpregnant women classified by sex hormone usage
    • Knopp RH, Bergelin RO, Wahl PW, Walden CE, Chapman M, Irvine S. Population-based lipoprotein lipid reference values for pregnant women compared to nonpregnant women classified by sex hormone usage. Am J Obstet Gynecol 1982; 143: 626-637.
    • (1982) Am J Obstet Gynecol , vol.143 , pp. 626-637
    • Knopp, R.H.1    Bergelin, R.O.2    Wahl, P.W.3    Walden, C.E.4    Chapman, M.5    Irvine, S.6
  • 2
    • 0024500560 scopus 로고
    • Lipoprotein lipase
    • Eckel RH. Lipoprotein lipase. N Engl J Med 1989; 320: 1060-1068.
    • (1989) N Engl J Med , vol.320 , pp. 1060-1068
    • Eckel, R.H.1
  • 4
    • 0019364005 scopus 로고
    • Excessive hypertriglyceridemia and pancreatitis in pregnancy: Association with deficiency of lipoprotein lipase
    • Lykkesfeldt G, Bock JE, Pedersen FD, Meinertz H, Faergeman O. Excessive hypertriglyceridemia and pancreatitis in pregnancy: Association with deficiency of lipoprotein lipase. Acta Obstet Gynecol Scand 1980; 60: 79-82.
    • (1980) Acta Obstet Gynecol Scand , vol.60 , pp. 79-82
    • Lykkesfeldt, G.1    Bock, J.E.2    Pedersen, F.D.3    Meinertz, H.4    Faergeman, O.5
  • 5
    • 0026572179 scopus 로고
    • Management of patients with severe hypertriglyceridaemia during pregnancy: Report of two cases with familial lipoprotein lipase deficiency
    • Watts GF, Morton K, Jackson P, Lewis B. Management of patients with severe hypertriglyceridaemia during pregnancy: report of two cases with familial lipoprotein lipase deficiency. Br J Obstet Gynaecol 1992; 99: 163-66.
    • (1992) Br J Obstet Gynaecol , vol.99 , pp. 163-166
    • Watts, G.F.1    Morton, K.2    Jackson, P.3    Lewis, B.4
  • 7
    • 0025001512 scopus 로고
    • A sandwich-enzyme immunoassay for the quantification of lipoprotein lipase and hepatic triglyceride lipase in human postheparin plasma using monoclonal antibodies to the corresponding enzymes
    • Ikeda Y, Takagi A, Ohkaru Y, Nogi K, Iwanaga T, Kurooka S, Yamamoto A. A sandwich-enzyme immunoassay for the quantification of lipoprotein lipase and hepatic triglyceride lipase in human postheparin plasma using monoclonal antibodies to the corresponding enzymes. J Lipid Res 1990; 31: 1911-1924.
    • (1990) J Lipid Res , vol.31 , pp. 1911-1924
    • Ikeda, Y.1    Takagi, A.2    Ohkaru, Y.3    Nogi, K.4    Iwanaga, T.5    Kurooka, S.6    Yamamoto, A.7
  • 8
    • 0026580924 scopus 로고
    • a/b) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript
    • a/b) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript. J Clin Invest 1992; 89: 581-591.
    • (1992) J Clin Invest , vol.89 , pp. 581-591
    • Takagi, A.1    Ikeda, Y.2    Tsutsumi, Z.3    Shoji, T.4    Yamamoto, A.5
  • 10
    • 0030946073 scopus 로고
    • Development of a direct DNA sequencing method for detecting heterozygous mutations of the human lipoprotein lipase gene
    • Mori A, Takagi A, Ikeda Y, Yamamoto A. Development of a direct DNA sequencing method for detecting heterozygous mutations of the human lipoprotein lipase gene. Clin Biochem 1947; 30: 315-324.
    • (1947) Clin Biochem , vol.30 , pp. 315-324
    • Mori, A.1    Takagi, A.2    Ikeda, Y.3    Yamamoto, A.4
  • 12
    • 0026344120 scopus 로고
    • Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency
    • Gotoda T, Yamada N, Kawamura M, Kozaki K, Mori N, Ishibashi S et al. Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency. J Clin Invest 1991; 88: 1856-1864.
    • (1991) J Clin Invest , vol.88 , pp. 1856-1864
    • Gotoda, T.1    Yamada, N.2    Kawamura, M.3    Kozaki, K.4    Mori, N.5    Ishibashi, S.6
  • 13
    • 0016748922 scopus 로고
    • Lipid metabolism in pregnancy III. Altered lipid composition in intermediate, very low, low and high density lipoprotein fractions
    • Warth MR, Arky RA, Knopp RH. Lipid metabolism in pregnancy III. Altered lipid composition in intermediate, very low, low and high density lipoprotein fractions. J Endocrinol Metab 1975; 41: 649-655.
    • (1975) J Endocrinol Metab , vol.41 , pp. 649-655
    • Warth, M.R.1    Arky, R.A.2    Knopp, R.H.3
  • 14
    • 0001033625 scopus 로고
    • Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome
    • Scriver CR & Beaudet AL, eds. New York, USA: McGraw-Hill
    • Brunzell JD. Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. In: Scriver CR & Beaudet AL, eds. The Metabolic and Molecular Basis of Inherited Disease. 7th ed. New York, USA: McGraw-Hill. 1995: 1913-32.
    • (1995) The Metabolic and Molecular Basis of Inherited Disease. 7th Ed. , pp. 1913-1932
    • Brunzell, J.D.1
  • 15
    • 0026768077 scopus 로고
    • Molecular genetics of human lipoprotein lipase deficiency
    • Hayden MR, Ma Y. Molecular genetics of human lipoprotein lipase deficiency. Mol Cell Biochem 1992; 113: 171-176.
    • (1992) Mol Cell Biochem , vol.113 , pp. 171-176
    • Hayden, M.R.1    Ma, Y.2
  • 16
    • 0000808381 scopus 로고
    • Elucidation of an underlying etiology of primary type IV hyperlipoproteinemia: Heterozygous lipoprotein lipase deficiency as a causal genetic disorder
    • Yamamoto A & Nakamura H, eds. Tokyo, Japan: Churchill Livingstone Japan
    • Ikeda Y, Takagi A, Yamamoto A. Elucidation of an underlying etiology of primary type IV hyperlipoproteinemia: heterozygous lipoprotein lipase deficiency as a causal genetic disorder. In: Yamamoto A & Nakamura H, eds. Current Advances in Triglycerides and Atherosclerosis. Tokyo, Japan: Churchill Livingstone Japan. 1994; 173-86.
    • (1994) Current Advances in Triglycerides and Atherosclerosis , pp. 173-186
    • Ikeda, Y.1    Takagi, A.2    Yamamoto, A.3
  • 17
    • 0029038966 scopus 로고
    • Alcohol-induced hypertriglyceridemia in subjects with decreased lipoprotein lipase - Improvement after cessation of alcohol intake
    • Tsutsumi Z, Ikeda Y, Takagi A, Tsushima M, Higashino K, Yamamoto A. Alcohol-induced hypertriglyceridemia in subjects with decreased lipoprotein lipase - Improvement after cessation of alcohol intake-. Jpn J Gastroenterol 1995: 92: 951-59.
    • (1995) Jpn J Gastroenterol , vol.92 , pp. 951-959
    • Tsutsumi, Z.1    Ikeda, Y.2    Takagi, A.3    Tsushima, M.4    Higashino, K.5    Yamamoto, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.