These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
134 related items for PubMed ID: 2614276
1. The molecular basis of truncated forms of apolipoprotein B in a kindred with compound heterozygous hypobetalipoproteinemia. Talmud P, King-Underwood L, Krul E, Schonfeld G, Humphries S. J Lipid Res; 1989 Nov; 30(11):1773-9. PubMed ID: 2614276 [Abstract] [Full Text] [Related]
2. Low plasma cholesterol levels caused by a short deletion in the apolipoprotein B gene. Young SG, Northey ST, McCarthy BJ. Science; 1988 Jul 29; 241(4865):591-3. PubMed ID: 3399894 [Abstract] [Full Text] [Related]
3. Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100. Young SG, Bertics SJ, Curtiss LK, Dubois BW, Witztum JL. J Clin Invest; 1987 Jun 29; 79(6):1842-51. PubMed ID: 3473077 [Abstract] [Full Text] [Related]
4. Hypobetalipoproteinemia due to an apolipoprotein B gene exon 21 deletion derived by Alu-Alu recombination. Huang LS, Ripps ME, Korman SH, Deckelbaum RJ, Breslow JL. J Biol Chem; 1989 Jul 05; 264(19):11394-400. PubMed ID: 2567736 [Abstract] [Full Text] [Related]
5. ApoB-75, a truncation of apolipoprotein B associated with familial hypobetalipoproteinemia: genetic and kinetic studies. Krul ES, Parhofer KG, Barrett PH, Wagner RD, Schonfeld G. J Lipid Res; 1992 Jul 05; 33(7):1037-50. PubMed ID: 1431583 [Abstract] [Full Text] [Related]
6. ApoB-54.8, a truncated apolipoprotein found primarily in VLDL, is associated with a nonsense mutation in the apoB gene and hypobetalipoproteinemia. Wagner RD, Krul ES, Tang J, Parhofer KG, Garlock K, Talmud P, Schonfeld G. J Lipid Res; 1991 Jun 05; 32(6):1001-11. PubMed ID: 1940616 [Abstract] [Full Text] [Related]
7. Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins. Young SG, Hubl ST, Smith RS, Snyder SM, Terdiman JF. J Clin Invest; 1990 Mar 05; 85(3):933-42. PubMed ID: 2312735 [Abstract] [Full Text] [Related]
8. 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 05; 42(2):62-70. PubMed ID: 1424233 [Abstract] [Full Text] [Related]
9. Four new mutations in the apolipoprotein B gene causing hypobetalipoproteinemia, including two different frameshift mutations that yield truncated apolipoprotein B proteins of identical length. Young SG, Pullinger CR, Zysow BR, Hofmann-Radvani H, Linton MF, Farese RV, Terdiman JF, Snyder SM, Grundy SM, Vega GL. J Lipid Res; 1993 Mar 05; 34(3):501-7. PubMed ID: 8468533 [Abstract] [Full Text] [Related]
10. Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B. Tarugi P, Lonardo A, Ballarini G, Grisendi A, Pulvirenti M, Bagni A, Calandra S. Gastroenterology; 1996 Oct 05; 111(4):1125-33. PubMed ID: 8831609 [Abstract] [Full Text] [Related]
11. A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia. Welty FK, Hubl ST, Pierotti VR, Young SG. J Clin Invest; 1991 May 05; 87(5):1748-54. PubMed ID: 2022744 [Abstract] [Full Text] [Related]
12. Two distinct truncated apolipoprotein B species in a kindred with hypobetalipoproteinemia. Krul ES, Kinoshita M, Talmud P, Humphries SE, Turner S, Goldberg AC, Cook K, Boerwinkle E, Schonfeld G. Arteriosclerosis; 1989 May 05; 9(6):856-68. PubMed ID: 2574033 [Abstract] [Full Text] [Related]
13. Two apolipoprotein B gene defects in a kindred with hypobetalipoproteinemia, one of which results in a truncated variant, apoB-61, in VLDL and LDL. Pullinger CR, Hillas E, Hardman DA, Chen GC, Naya-Vigne JM, Iwasa JA, Hamilton RL, Lalouel JM, Williams RR, Kane JP. J Lipid Res; 1992 May 05; 33(5):699-710. PubMed ID: 1619363 [Abstract] [Full Text] [Related]
14. Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46). Young SG, Hubl ST, Chappell DA, Smith RS, Claiborne F, Snyder SM, Terdiman JF. N Engl J Med; 1989 Jun 15; 320(24):1604-10. PubMed ID: 2725600 [No Abstract] [Full Text] [Related]
15. A truncated species of apolipoprotein B (B-38.7) in a patient with homozygous hypobetalipoproteinemia associated with diabetes mellitus. Ohashi K, Ishibashi S, Yamamoto M, Osuga J, Yazaki Y, Yukawa S, Yamada N. Arterioscler Thromb Vasc Biol; 1998 Aug 15; 18(8):1330-4. PubMed ID: 9714141 [Abstract] [Full Text] [Related]
16. A truncated species of apolipoprotein B, B-83, associated with hypobetalipoproteinemia. Farese RV, Garg A, Pierotti VR, Vega GL, Young SG. J Lipid Res; 1992 Apr 15; 33(4):569-77. PubMed ID: 1527480 [Abstract] [Full Text] [Related]
18. A gene-targeted mouse model for familial hypobetalipoproteinemia. Low levels of apolipoprotein B mRNA in association with a nonsense mutation in exon 26 of the apolipoprotein B gene. Kim E, Ambroziak P, Véniant MM, Hamilton RL, Young SG. J Biol Chem; 1998 Dec 18; 273(51):33977-84. PubMed ID: 9852051 [Abstract] [Full Text] [Related]
19. Donor splice mutation generates a lipid-associated apolipoprotein B-27.6 in a patient with homozygous hypobetalipoproteinemia. Talmud PJ, Krul ES, Pessah M, Gay G, Schonfeld G, Humphries SE, Infante R. J Lipid Res; 1994 Mar 18; 35(3):468-77. PubMed ID: 8014581 [Abstract] [Full Text] [Related]
20. Hypobetalipoproteinemia associated with apo B-48.4, a truncated protein only 14 amino acids longer than apo B-48. Ruotolo G, Zanelli T, Tettamanti C, Ragogna F, Parlavecchia M, Viganò F, Catapano AL. Atherosclerosis; 1998 Mar 18; 137(1):125-31. PubMed ID: 9568744 [Abstract] [Full Text] [Related] Page: [Next] [New Search]