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.
128 related articles for article (PubMed ID: 8014581)
21. Apolipoprotein B-38.9 does not associate with apo[a] and forms two distinct HDL density particle populations that are larger than HDL. Groenewegen WA; Averna MR; Pulai J; Krul ES; Schonfeld G J Lipid Res; 1994 Jun; 35(6):1012-25. PubMed ID: 8077841 [TBL] [Abstract][Full Text] [Related]
22. Known mutations of apoB account for only a small minority of hypobetalipoproteinemia. Wu J; Kim J; Li Q; Kwok PY; Cole TG; Cefalu B; Averna M; Schonfeld G J Lipid Res; 1999 May; 40(5):955-9. PubMed ID: 10224165 [TBL] [Abstract][Full Text] [Related]
23. Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia. Di Leo E; Magnolo L; Pinotti E; Martini S; Cortella I; Vitturi N; Rabacchi C; Wunsch A; Pucci F; Bertolini S; Calandra S; Tarugi P Mol Genet Metab; 2009 Feb; 96(2):66-72. PubMed ID: 19084451 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. Exome sequencing identifies novel ApoB loss-of-function mutations causing hypobetalipoproteinemia in type 1 diabetes. Gao F; Luo H; Fu Z; Zhang CT; Zhang R Acta Diabetol; 2015 Jun; 52(3):531-7. PubMed ID: 25430706 [TBL] [Abstract][Full Text] [Related]
26. Dysbetalipoproteinemia in a kindred with hypobetalipoproteinemia due to mutations in the genes for ApoB (ApoB-70.5) and ApoE (ApoE2). Groenewegen WA; Krul ES; Averna MR; Pulai J; Schonfeld G Arterioscler Thromb; 1994 Nov; 14(11):1695-704. PubMed ID: 7947592 [TBL] [Abstract][Full Text] [Related]
27. Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia. Di Leo E; Magnolo L; Lancellotti S; Crocè L; Visintin L; Tiribelli C; Bertolini S; Calandra S; Tarugi P J Med Genet; 2007 Mar; 44(3):219-24. PubMed ID: 17158591 [TBL] [Abstract][Full Text] [Related]
28. Targeted modification of the apolipoprotein B gene results in hypobetalipoproteinemia and developmental abnormalities in mice. Homanics GE; Smith TJ; Zhang SH; Lee D; Young SG; Maeda N Proc Natl Acad Sci U S A; 1993 Mar; 90(6):2389-93. PubMed ID: 8460149 [TBL] [Abstract][Full Text] [Related]
29. 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; 33(5):699-710. PubMed ID: 1619363 [TBL] [Abstract][Full Text] [Related]
30. Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations. Di Leo E; Magnolo L; Bertolotti M; Bourbon M; Carmo Pereira S; Pirisi M; Calandra S; Tarugi P Clin Genet; 2008 Sep; 74(3):267-73. PubMed ID: 18492086 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Genetic variants of ApoE account for variability of plasma low-density lipoprotein and apolipoprotein B levels in FHBL. Yue P; Isley WL; Harris WS; Rosipal S; Akin CD; Schonfeld G Atherosclerosis; 2005 Jan; 178(1):107-13. PubMed ID: 15585207 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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; 137(1):125-31. PubMed ID: 9568744 [TBL] [Abstract][Full Text] [Related]
35. Hypobetalipoproteinemic mice with a targeted apolipoprotein (Apo) B-27.6-specifying mutation: in vivo evidence for an important role of amino acids 1254-1744 of ApoB in lipid transport and metabolism of the apoB-containing lipoprotein. Chen Z; Fitzgerald RL; Schonfeld G J Biol Chem; 2002 Apr; 277(16):14135-45. PubMed ID: 11839763 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene. Martín-Morales R; García-Díaz JD; Tarugi P; González-Santos P; Saavedra-Vallejo P; Magnolo L; Mesa-Latorre JM; di Leo E; Valdivielso P Gene; 2013 Nov; 531(1):92-6. PubMed ID: 24001780 [TBL] [Abstract][Full Text] [Related]
39. Homozygous hypobetalipoproteinemia: transcriptional regulation and 5'-flanking sequence analysis in an apolipoprotein B deficiency state. Ross RS; Hoeg JM; Higuchi K; Schumacher UK; Fojo S; Gregg RE; Brewer HB Biochim Biophys Acta; 1989 Jul; 1004(1):29-35. PubMed ID: 2742871 [TBL] [Abstract][Full Text] [Related]
40. Novel mutations of APOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia. Yue P; Yuan B; Gerhard DS; Neuman RJ; Isley WL; Harris WS; Schonfeld G Hum Mutat; 2002 Aug; 20(2):110-6. PubMed ID: 12124991 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]