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Journal Abstract Search

142 related items for PubMed ID: 2318821

  • 1. In vitro expression and site-specific mutagenesis of the cloned human lipoprotein lipase gene. Potential N-linked glycosylation site asparagine 43 is important for both enzyme activity and secretion.
    Semenkovich CF, Luo CC, Nakanishi MK, Chen SH, Smith LC, Chan L.
    J Biol Chem; 1990 Apr 05; 265(10):5429-33. PubMed ID: 2318821
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  • 2. Lipoprotein lipase and hepatic lipase: the role of asparagine-linked glycosylation in the expression of a functional enzyme.
    Ben-Zeev O, Stahnke G, Liu G, Davis RC, Doolittle MH.
    J Lipid Res; 1994 Sep 05; 35(9):1511-23. PubMed ID: 7806965
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  • 3. Functional role of N-linked glycosylation in human hepatic lipase: asparagine-56 is important for both enzyme activity and secretion.
    Wölle J, Jansen H, Smith LC, Chan L.
    J Lipid Res; 1993 Dec 05; 34(12):2169-76. PubMed ID: 8301235
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  • 4. Absence of N-glycosylation at asparagine 43 in human lipoprotein lipase induces its accumulation in the rough endoplasmic reticulum and alters this cellular compartment.
    Buscá R, Pujana MA, Pognonec P, Auwerx J, Deeb SS, Reina M, Vilaró S.
    J Lipid Res; 1995 May 05; 36(5):939-51. PubMed ID: 7658166
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  • 5. A missense (Asp250----Asn) mutation in the lipoprotein lipase gene in two unrelated families with familial lipoprotein lipase deficiency.
    Ishimura-Oka K, Semenkovich CF, Faustinella F, Goldberg IJ, Shachter N, Smith LC, Coleman T, Hide WA, Brown WV, Oka K.
    J Lipid Res; 1992 May 05; 33(5):745-54. PubMed ID: 1619366
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  • 6. Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His).
    Rouis M, Lohse P, Dugi KA, Lohse P, Beg OU, Ronan R, Talley GD, Brunzell JD, Santamarina-Fojo S.
    J Lipid Res; 1996 Mar 05; 37(3):651-61. PubMed ID: 8728326
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  • 7. Functional topology of a surface loop shielding the catalytic center in lipoprotein lipase.
    Faustinella F, Smith LC, Chan L.
    Biochemistry; 1992 Aug 18; 31(32):7219-23. PubMed ID: 1510914
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  • 8. A naturally occurring mutation at the second base of codon asparagine 43 in the proposed N-linked glycosylation site of human lipoprotein lipase: in vivo evidence that asparagine 43 is essential for catalysis and secretion.
    Kobayashi J, Inadera H, Fujita Y, Talley G, Morisaki N, Yoshida S, Saito Y, Fojo SS, Brewer HB.
    Biochem Biophys Res Commun; 1994 Nov 30; 205(1):506-15. PubMed ID: 7999071
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  • 9. Lipoprotein lipaseBethesda: a single amino acid substitution (Ala-176----Thr) leads to abnormal heparin binding and loss of enzymic activity.
    Beg OU, Meng MS, Skarlatos SI, Previato L, Brunzell JD, Brewer HB, Fojo SS.
    Proc Natl Acad Sci U S A; 1990 May 30; 87(9):3474-8. PubMed ID: 2110364
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  • 10. Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family.
    Faustinella F, Chang A, Van Biervliet JP, Rosseneu M, Vinaimont N, Smith LC, Chen SH, Chan L.
    J Biol Chem; 1991 Aug 05; 266(22):14418-24. PubMed ID: 1907278
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  • 11. Two naturally occurring mutations at the first and second bases of codon aspartic acid 156 in the proposed catalytic triad of human lipoprotein lipase. In vivo evidence that aspartic acid 156 is essential for catalysis.
    Ma YH, Bruin T, Tuzgol S, Wilson BI, Roederer G, Liu MS, Davignon J, Kastelein JJ, Brunzell JD, Hayden MR.
    J Biol Chem; 1992 Jan 25; 267(3):1918-23. PubMed ID: 1730727
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  • 20. Structure-function analysis of D9N and N291S mutations in human lipoprotein lipase using molecular modelling.
    Razzaghi H, Day BW, McClure RJ, Kamboh MI.
    J Mol Graph Model; 2001 Jan 25; 19(6):487-94, 587-90. PubMed ID: 11552677
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