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28. [Lipoprotein lipase: a multifunctional enzyme in lipoprotein metabolism]. Foubert L; Benlian P; Turpin G Presse Med; 1996 Feb; 25(5):207-10. PubMed ID: 8729382 [TBL] [Abstract][Full Text] [Related]
29. A mutation in the lipoprotein lipase gene associated with hyperlipoproteinemia type I in mink: studies on lipid and lipase levels in heterozygotes. Lindberg A; Nordstoga K; Christophersen B; Savonen R; van Tol A; Olivecrona G Int J Mol Med; 1998 Mar; 1(3):529-38. PubMed ID: 9852258 [TBL] [Abstract][Full Text] [Related]
30. Compound heterozygosity for a new (S259G) and a previously described (G188E) mutation in lipoprotein lipase (LpL) as a cause of chylomicronemia. Mutations in brief no. 183. Online. Evans D; Wendt D; Ahle S; Guerra A; Beisiegel U Hum Mutat; 1998; 12(3):217. PubMed ID: 10660334 [TBL] [Abstract][Full Text] [Related]
31. Familial lipoprotein lipase deficiency caused by known (G188E) and novel (W394X) LPL gene mutations. Hooper AJ; Crawford GM; Brisbane JM; Robertson K; Watts GF; van Bockxmeer FM; Burnett JR Ann Clin Biochem; 2008 Jan; 45(Pt 1):102-5. PubMed ID: 18275685 [TBL] [Abstract][Full Text] [Related]
32. Adipose cell size and distribution in familial lipoprotein lipase deficiency. Peeva E; Brun LD; Ven Murthy MR; Després JP; Normand T; Gagné C; Lupien PJ; Julien P Int J Obes Relat Metab Disord; 1992 Oct; 16(10):737-44. PubMed ID: 1330953 [TBL] [Abstract][Full Text] [Related]
33. Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries. Ma Y; Liu MS; Chitayat D; Bruin T; Beisiegel U; Benlian P; Foubert L; De Gennes JL; Funke H; Forsythe I Hum Mutat; 1994; 3(1):52-8. PubMed ID: 7906986 [TBL] [Abstract][Full Text] [Related]
34. Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s. Ueda M; Burke FM; Remaley AT; Hegele RA; Rader DJ; Dunbar RL Ann Intern Med; 2020 Apr; 172(7):500-502. PubMed ID: 31739313 [No Abstract] [Full Text] [Related]
36. Human lipoprotein lipase deficiency: does chronic dyslipidemia lead to increased oxidative stress and mitochondrial DNA damage in blood cells? Ven Murthy MR; Julien P; Singh P; Levy E Acta Biochim Pol; 1996; 43(1):227-40. PubMed ID: 8790727 [TBL] [Abstract][Full Text] [Related]
37. A novel missense mutation in the gene for lipoprotein lipase resulting in a highly conservative amino acid substitution (Asp180-->Glu) causes familial chylomicronemia (type I hyperlipoproteinemia). Haubenwallner S; Hörl G; Shachter NS; Presta E; Fried SK; Höfler G; Kostner GM; Breslow JL; Zechner R Genomics; 1993 Nov; 18(2):392-6. PubMed ID: 8288243 [TBL] [Abstract][Full Text] [Related]
38. Familial chylomicronemia syndrome: a novel mutation in the lipoprotein lipase gene. Van Biervliet S; Vande Velde S; De Bruyne P; Callewaert B; Verloo P; De Bruyne R Acta Gastroenterol Belg; 2024; 87(2):326-328. PubMed ID: 39210765 [No Abstract] [Full Text] [Related]
39. A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry. Foubert L; Bruin T; De Gennes JL; Ehrenborg E; Furioli J; Kastelein J; Benlian P; Hayden M Hum Mutat; 1997; 10(3):179-85. PubMed ID: 9298816 [TBL] [Abstract][Full Text] [Related]