158 related articles for article (PubMed ID: 1562620)
41. 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]
42. Type I hyperlipoproteinemia due to a novel loss of function mutation of lipoprotein lipase, Cys(239)-->Trp, associated with recurrent severe pancreatitis.
Hoffmann MM; Jacob S; Luft D; Schmülling RM; Rett K; März W; Häring HU; Matthaei S
J Clin Endocrinol Metab; 2000 Dec; 85(12):4795-8. PubMed ID: 11134145
[TBL] [Abstract][Full Text] [Related]
43. A 4 basepair deletion in exon 4 of the human lipoprotein lipase gene results in type I hyperlipoproteinemia.
Ma Y; Liu MS; Zhang H; Forsythe IJ; Brunzell JD; Hayden MR
Hum Mol Genet; 1993 Jul; 2(7):1049-50. PubMed ID: 8364543
[No Abstract] [Full Text] [Related]
44. A family-based study of hyperinsulinemia and hypertriglyceridemia in heterozygous lipoprotein lipase deficiency.
Ikeda Y; Takagi A; Nakata Y; Sera Y; Hyoudou S; Hamamoto K; Nishi Y; Yamamoto A
Clin Chim Acta; 2002 Feb; 316(1-2):179-85. PubMed ID: 11750290
[TBL] [Abstract][Full Text] [Related]
45. A novel substitution at the translation initiator codon (ATG-->ATC) of the lipoprotein lipase gene is mainly responsible for lipoprotein lipase deficiency in a patient with severe hypertriglyceridemia and recurrent pancreatitis.
Yu XH; Zhao TQ; Wang L; Liu ZP; Zhang CM; Chen R; Li L; Liu G; Hu WC
Biochem Biophys Res Commun; 2006 Mar; 341(1):82-7. PubMed ID: 16431216
[TBL] [Abstract][Full Text] [Related]
46. A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries.
Monsalve MV; Henderson H; Roederer G; Julien P; Deeb S; Kastelein JJ; Peritz L; Devlin R; Bruin T; Murthy MR
J Clin Invest; 1990 Sep; 86(3):728-34. PubMed ID: 1975597
[TBL] [Abstract][Full Text] [Related]
47. Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipase.
Al-Shali K; Wang J; Fellows F; Huff MW; Wolfe BM; Hegele RA
Clin Biochem; 2002 Mar; 35(2):125-30. PubMed ID: 11983347
[TBL] [Abstract][Full Text] [Related]
48. [A case of neonatal lipoprotein lipase deficiency caused by novel compound heterozygous variants of LPL gene].
Zhu L; Li G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):156-158. PubMed ID: 32034744
[TBL] [Abstract][Full Text] [Related]
49. Identification of compound heterozygous mutations (G188E/W382X) of lipoprotein lipase gene in a Japanese infant with hyperchylomicronemia: the G188E mutation was newly identified in Japanese.
Takagi A; Ikeda Y; Tachi K; Shinozuka T; Yamamoto A
Clin Chim Acta; 1999 Jul; 285(1-2):143-54. PubMed ID: 10481930
[TBL] [Abstract][Full Text] [Related]
50. 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]
51. Postheparin plasma lipoprotein lipase activity in heterozygotes of familial lipoprotein lipase deficiency.
Kondo Y; Kurobane I; Omura K; Sano R; Abe R; Chida N; Tada K
Tohoku J Exp Med; 1985 Jan; 145(1):1-6. PubMed ID: 3983953
[TBL] [Abstract][Full Text] [Related]
52. A missense mutation Pro157 Arg in lipoprotein lipase (LPLNijmegen) resulting in loss of catalytic activity.
Bruin T; Kastelein JJ; Van Diermen DE; Ma Y; Henderson HE; Stuyt PM; Stalenhoef AF; Sturk A; Brunzell JD; Hayden MR
Eur J Biochem; 1992 Sep; 208(2):267-72. PubMed ID: 1521525
[TBL] [Abstract][Full Text] [Related]
53. Molecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript.
Takagi A; Ikeda Y; Tsutsumi Z; Shoji T; Yamamoto A
J Clin Invest; 1992 Feb; 89(2):581-91. PubMed ID: 1737848
[TBL] [Abstract][Full Text] [Related]
54. Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.
Rabacchi C; Pisciotta L; Cefalù AB; Noto D; Fresa R; Tarugi P; Averna M; Bertolini S; Calandra S
Atherosclerosis; 2015 Jul; 241(1):79-86. PubMed ID: 25966443
[TBL] [Abstract][Full Text] [Related]
55. Lipoprotein lipase: recent contributions from molecular biology.
Auwerx J; Leroy P; Schoonjans K
Crit Rev Clin Lab Sci; 1992; 29(3-4):243-68. PubMed ID: 1489519
[TBL] [Abstract][Full Text] [Related]
56. 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; Shimano H; Takaku F; Yazaki Y; Furuichi Y; Murase T
J Clin Invest; 1991 Dec; 88(6):1856-64. PubMed ID: 1752947
[TBL] [Abstract][Full Text] [Related]
57. Molecular genetics of apoC-II and lipoprotein lipase deficiency.
Fojo SS; de Gennes JL; Beisiegel U; Baggio G; Stalenhoef AF; Brunzell JD; Brewer HB
Adv Exp Med Biol; 1991; 285():329-33. PubMed ID: 1858563
[No Abstract] [Full Text] [Related]
58. Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene.
Wood S; Schertzer M; Hayden M; Ma Y
Hum Genet; 1993 May; 91(4):312-6. PubMed ID: 8099055
[TBL] [Abstract][Full Text] [Related]
59. Pathogenic classification of LPL gene variants reported to be associated with LPL deficiency.
Rodrigues R; Artieda M; Tejedor D; Martínez A; Konstantinova P; Petry H; Meyer C; Corzo D; Sundgreen C; Klor HU; Gouni-Berthold I; Westphal S; Steinhagen-Thiessen E; Julius U; Winkler K; Stroes E; Vogt A; Hardt P; Prophet H; Otte B; Nordestgaard BG; Deeb SS; Brunzell JD
J Clin Lipidol; 2016; 10(2):394-409. PubMed ID: 27055971
[TBL] [Abstract][Full Text] [Related]
60. Lipoprotein lipase activity in heterozygotes for lipoprotein lipase gene mutations reveals a gender bias.
Murase T; Ebara T; Okubo M
Ann Clin Biochem; 2014 Mar; 51(Pt 2):294-7. PubMed ID: 24081181
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
