287 related articles for article (PubMed ID: 2312735)
1. 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; 85(3):933-42. PubMed ID: 2312735
[TBL] [Abstract][Full Text] [Related]
2. 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; 79(6):1842-51. PubMed ID: 3473077
[TBL] [Abstract][Full Text] [Related]
3. 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; 87(5):1748-54. PubMed ID: 2022744
[TBL] [Abstract][Full Text] [Related]
4. Low plasma cholesterol levels caused by a short deletion in the apolipoprotein B gene.
Young SG; Northey ST; McCarthy BJ
Science; 1988 Jul; 241(4865):591-3. PubMed ID: 3399894
[TBL] [Abstract][Full Text] [Related]
5. 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; ViganĂ² F; Catapano AL
Atherosclerosis; 1998 Mar; 137(1):125-31. PubMed ID: 9568744
[TBL] [Abstract][Full Text] [Related]
6. Characterization of an abnormal species of apolipoprotein B, apolipoprotein B-37, associated with familial hypobetalipoproteinemia.
Young SG; Bertics SJ; Curtiss LK; Witztum JL
J Clin Invest; 1987 Jun; 79(6):1831-41. PubMed ID: 3584472
[TBL] [Abstract][Full Text] [Related]
7. Apolipoprotein B-32: a new truncated mutant of human apolipoprotein B capable of forming particles in the low density lipoprotein range.
McCormick SP; Fellowes AP; Walmsley TA; George PM
Biochim Biophys Acta; 1992 Apr; 1138(4):290-6. PubMed ID: 1562615
[TBL] [Abstract][Full Text] [Related]
8. 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; 34(3):501-7. PubMed ID: 8468533
[TBL] [Abstract][Full Text] [Related]
9. 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; 9(6):856-68. PubMed ID: 2574033
[TBL] [Abstract][Full Text] [Related]
10. Dual mechanisms for the low plasma levels of truncated apolipoprotein B proteins in familial hypobetalipoproteinemia. Analysis of a new mouse model with a nonsense mutation in the Apob gene.
Kim E; Cham CM; VĂ©niant MM; Ambroziak P; Young SG
J Clin Invest; 1998 Mar; 101(6):1468-77. PubMed ID: 9502790
[TBL] [Abstract][Full Text] [Related]
11. Lipoproteins containing the truncated apolipoprotein, Apo B-89, are cleared from human plasma more rapidly than Apo B-100-containing lipoproteins in vivo.
Parhofer KG; Barrett PH; Bier DM; Schonfeld G
J Clin Invest; 1992 Jun; 89(6):1931-7. PubMed ID: 1602000
[TBL] [Abstract][Full Text] [Related]
12. Decreased production rates of VLDL triglycerides and ApoB-100 in subjects heterozygous for familial hypobetalipoproteinemia.
Elias N; Patterson BW; Schonfeld G
Arterioscler Thromb Vasc Biol; 1999 Nov; 19(11):2714-21. PubMed ID: 10559016
[TBL] [Abstract][Full Text] [Related]
13. A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5).
Tarugi P; Lonardo A; Ballarini G; Erspamer L; Tondelli E; Bertolini S; Calandra S
J Hepatol; 2000 Sep; 33(3):361-70. PubMed ID: 11019990
[TBL] [Abstract][Full Text] [Related]
14. 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; 111(4):1125-33. PubMed ID: 8831609
[TBL] [Abstract][Full Text] [Related]
15. 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; 320(24):1604-10. PubMed ID: 2725600
[No Abstract] [Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. Homozygous hypobetalipoproteinemia with spared chylomicron formation.
Harano Y; Kojima H; Nakano T; Harada M; Kashiwagi A; Nakajima Y; Hidaka TH; Ohtsuki T; Suzuki T; Tamura A
Metabolism; 1989 Jan; 38(1):1-7. PubMed ID: 2909827
[TBL] [Abstract][Full Text] [Related]
18. A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: genetic and metabolic studies.
Srivastava N; Noto D; Averna M; Pulai J; Srivastava RA; Cole TG; Latour MA; Patterson BW; Schonfeld G
Metabolism; 1996 Oct; 45(10):1296-304. PubMed ID: 8843188
[TBL] [Abstract][Full Text] [Related]
19. Recent progress in understanding apolipoprotein B.
Young SG
Circulation; 1990 Nov; 82(5):1574-94. PubMed ID: 1977530
[TBL] [Abstract][Full Text] [Related]
20. 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; 33(7):1037-50. PubMed ID: 1431583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]