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2. Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene. Matsunaga T; Hiasa Y; Yanagi H; Maeda T; Hattori N; Yamakawa K; Yamanouchi Y; Tanaka I; Obara T; Hamaguchi H Proc Natl Acad Sci U S A; 1991 Apr; 88(7):2793-7. PubMed ID: 1901417 [TBL] [Abstract][Full Text] [Related]
3. Expression of the human serum apolipoprotein AI and AII genes in Xenopus laevis oocytes. Lipid-associated secretion of gene products. Haase A; Stoffel W Biol Chem Hoppe Seyler; 1988 Jul; 369(7):585-93. PubMed ID: 2852015 [TBL] [Abstract][Full Text] [Related]
4. [Apolipoprotein A I-C III-A IV deficiency]. Kato H Nihon Rinsho; 1994 Dec; 52(12):3253-6. PubMed ID: 7853719 [TBL] [Abstract][Full Text] [Related]
5. Apolipoprotein AI and AII metabolism in patients with primary high-density lipoprotein deficiency associated with familial hypertriglyceridemia. Saku K; Gartside PS; Hynd BA; Mendoza SG; Kashyap ML Metabolism; 1985 Aug; 34(8):754-64. PubMed ID: 3927110 [TBL] [Abstract][Full Text] [Related]
6. G to A substitution in the promoter region of the apolipoprotein AI gene is associated with elevated serum apolipoprotein AI and high density lipoprotein cholesterol concentrations. Jeenah M; Kessling A; Miller N; Humphries S Mol Biol Med; 1990 Jun; 7(3):233-41. PubMed ID: 1977072 [TBL] [Abstract][Full Text] [Related]
8. A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities. Funke H; von Eckardstein A; Pritchard PH; Karas M; Albers JJ; Assmann G J Clin Invest; 1991 Jan; 87(1):371-6. PubMed ID: 1898657 [TBL] [Abstract][Full Text] [Related]
9. Molecular basis of congenital lp(a) deficiency: a frequent apo(a) 'null' mutation in caucasians. Ogorelkova M; Gruber A; Utermann G Hum Mol Genet; 1999 Oct; 8(11):2087-96. PubMed ID: 10484779 [TBL] [Abstract][Full Text] [Related]
10. High-density lipoprotein composition is altered by a common DNA polymorphism adjacent to apoprotein AII gene in man. Scott J; Knott TJ; Priestley LM; Robertson ME; Mann DV; Kostner G; Miller GJ; Miller NE Lancet; 1985 Apr; 1(8432):771-3. PubMed ID: 2858663 [TBL] [Abstract][Full Text] [Related]
11. The human apolipoprotein AII gene: structural organization and sites of expression. Knott TJ; Wallis SC; Robertson ME; Priestley LM; Urdea M; Rall LB; Scott J Nucleic Acids Res; 1985 Sep; 13(17):6387-98. PubMed ID: 2995928 [TBL] [Abstract][Full Text] [Related]
12. Comparison of the human apolipoprotein genes. Apo AII presents a unique functional intron-exon junction. Shelley CS; Sharpe CR; Baralle FE; Shoulders CC J Mol Biol; 1985 Nov; 186(1):43-51. PubMed ID: 3935800 [TBL] [Abstract][Full Text] [Related]
13. Deletion analysis of a unique 3' splice site indicates that alternating guanine and thymine residues represent an efficient splicing signal. Shelley CS; Baralle FE Nucleic Acids Res; 1987 May; 15(9):3787-99. PubMed ID: 3108860 [TBL] [Abstract][Full Text] [Related]
14. Characterization of apolipoprotein A-I- and A-II-containing lipoproteins in a new case of high density lipoprotein deficiency resembling Tangier disease and their effects on intracellular cholesterol efflux. Cheung MC; Mendez AJ; Wolf AC; Knopp RH J Clin Invest; 1993 Feb; 91(2):522-9. PubMed ID: 8432861 [TBL] [Abstract][Full Text] [Related]
15. A novel truncated apolipoprotein B (apo B55) in a patient with familial hypobetalipoproteinemia and atypical retinitis pigmentosa. Talmud PJ; Converse C; Krul E; Huq L; McIlwaine GG; Series JJ; Boyd P; Schonfeld G; Dunning A; Humphries S Clin Genet; 1992 Aug; 42(2):62-70. PubMed ID: 1424233 [TBL] [Abstract][Full Text] [Related]
16. Familial HDL deficiency due to marked hypercatabolism of normal apoA-I. Emmerich J; Vergès B; Tauveron I; Rader D; Santamarina-Fojo S; Shaefer J; Ayrault-Jarrier M; Thiéblot P; Brewer HB Arterioscler Thromb; 1993 Sep; 13(9):1299-306. PubMed ID: 8364014 [TBL] [Abstract][Full Text] [Related]
17. Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia. Ng DS; Leiter LA; Vezina C; Connelly PW; Hegele RA J Clin Invest; 1994 Jan; 93(1):223-9. PubMed ID: 8282791 [TBL] [Abstract][Full Text] [Related]
18. Donor splice site mutation in the apolipoprotein (Apo) C-II gene (Apo C-IIHamburg) of a patient with Apo C-II deficiency. Fojo SS; Beisiegel U; Beil U; Higuchi K; Bojanovski M; Gregg RE; Greten H; Brewer HB J Clin Invest; 1988 Nov; 82(5):1489-94. PubMed ID: 3263393 [TBL] [Abstract][Full Text] [Related]
19. A G+1 to C mutation in a donor splice site of intron 2 in the apolipoprotein (apo) C-II gene in a patient with apo C-II deficiency. A possible interaction between apo C-II deficiency and apo E4 in a severely hypertriglyceridemic patient. Okubo M; Hasegawa Y; Aoyama Y; Murase T Atherosclerosis; 1997 Apr; 130(1-2):153-60. PubMed ID: 9126659 [TBL] [Abstract][Full Text] [Related]
20. Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency. Pisciotta L; Miccoli R; Cantafora A; Calabresi L; Tarugi P; Alessandrini P; Bittolo Bon G; Franceschini G; Cortese C; Calandra S; Bertolini S Atherosclerosis; 2003 Apr; 167(2):335-45. PubMed ID: 12818417 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]