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Journal Abstract Search

153 related items for PubMed ID: 9126659

  • 21. An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-II.
    Fojo SS, de Gennes JL, Chapman J, Parrott C, Lohse P, Kwan SS, Truffert J, Brewer HB.
    J Biol Chem; 1989 Dec 15; 264(35):20839-42. PubMed ID: 2592354
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  • 22. Electrophoretic screening for human apolipoprotein C-II variants: repeated identification of apolipoprotein C-II(K19T).
    Wiebusch H, Nofer JR, von Eckardstein A, Funke H, Wahrburg U, Martin H, Köhler E, Assmann G.
    J Mol Med (Berl); 1995 Jul 15; 73(7):373-8. PubMed ID: 8520970
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  • 25. A case of hyperlipidemia with homozygous apolipoprotein E5 (Glu3-->Lys).
    Kobayashi J, Shirai K, Murano T, Misawa Y, Tashiro J, Yoshida T, Shinomiya M.
    Biochim Biophys Acta; 2002 Jun 13; 1583(1):117-21. PubMed ID: 12069856
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  • 26. Association of apolipoprotein E4 and haplotypes of the apolipoprotein E gene with lobar intracerebral hemorrhage.
    Woo D, Kaushal R, Chakraborty R, Woo J, Haverbusch M, Sekar P, Kissela B, Pancioli A, Jauch E, Kleindorfer D, Flaherty M, Schneider A, Khatri P, Sauerbeck L, Khoury J, Deka R, Broderick J.
    Stroke; 2005 Sep 13; 36(9):1874-9. PubMed ID: 16100021
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  • 27. Apolipoprotein E gene polymorphism alters lipids before pancreas transplantation.
    Balakrishnan S, Colling C, Burkman T, Erickson J, Lyden E, Maheshwari H, Mack-Shipman L, Lane J, Larsen J.
    Transplantation; 2002 Oct 15; 74(7):974-7. PubMed ID: 12394840
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  • 30. ApoC-IIParis2: a premature termination mutation in the signal peptide of apoC-II resulting in the familial chylomicronemia syndrome.
    Parrott CL, Alsayed N, Rebourcet R, Santamarina-Fojo S.
    J Lipid Res; 1992 Mar 15; 33(3):361-7. PubMed ID: 1569385
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  • 31. Apolipoprotein E genotyping and phenotyping in type II diabetes mellitus patients with hypertriglyceridemia.
    Kim JH, Lee EJ, Kwon OH.
    Clin Biochem; 1997 Feb 15; 30(1):47-52. PubMed ID: 9056109
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  • 32. Novel compound heterozygous mutations for lipoprotein lipase deficiency. A G-to-T transversion at the first position of exon 5 causing G154V missense mutation and a 5' splice site mutation of intron 8.
    Ikeda Y, Takagi A, Nakata Y, Sera Y, Hyoudou S, Hamamoto K, Nishi Y, Yamamoto A.
    J Lipid Res; 2001 Jul 15; 42(7):1072-81. PubMed ID: 11441134
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  • 33. Apolipoprotein E phenotypes in patients with gout: relation with hypertriglyceridaemia.
    Moriwaki Y, Yamamoto T, Takahashi S, Tsutsumi Z, Higashino K.
    Ann Rheum Dis; 1995 May 15; 54(5):351-4. PubMed ID: 7794039
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  • 34. The familial chylomicronemia syndrome.
    Santamarina-Fojo S.
    Endocrinol Metab Clin North Am; 1998 Sep 15; 27(3):551-67, viii. PubMed ID: 9785052
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  • 35. Sandwich ELISA for the measurement of Apo-E4 levels in serum and the estimation of the allelic status of Apo-E4 isoforms.
    Uchida Y, Ito S, Nukina N.
    J Clin Lab Anal; 2000 Sep 15; 14(6):260-4. PubMed ID: 11138606
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  • 39. Apolipoprotein CII (apo CII) gene expression defect in an individual with familial apo CII deficiency.
    Davison PJ, Stalenhoef AF, Humphries SE.
    Biochem Biophys Res Commun; 1987 Oct 14; 148(1):320-8. PubMed ID: 2445343
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  • 40. Apolipoprotein E polymorphism and the distribution profile of very low density lipoproteins; an influence of the E4 allele on large (Sf > 60) particles.
    Bioletto S, Fontana P, Darioli R, James RW.
    Atherosclerosis; 1998 May 14; 138(1):207-15. PubMed ID: 9678786
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