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.
213 related articles for article (PubMed ID: 16728468)
1. Assessment of tocopherol metabolism and oxidative stress in familial hypobetalipoproteinemia. Clarke MW; Hooper AJ; Headlam HA; Wu JH; Croft KD; Burnett JR Clin Chem; 2006 Jul; 52(7):1339-45. PubMed ID: 16728468 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia. Whitfield AJ; Marais AD; Robertson K; Barrett PH; van Bockxmeer FM; Burnett JR Hum Mutat; 2003 Aug; 22(2):178. PubMed ID: 12872264 [TBL] [Abstract][Full Text] [Related]
4. Vitamin E and oxidative stress in abetalipoproteinemia and familial hypobetalipoproteinemia. Burnett JR; Hooper AJ Free Radic Biol Med; 2015 Nov; 88(Pt A):59-62. PubMed ID: 26086616 [TBL] [Abstract][Full Text] [Related]
5. Supplementation with mixed tocopherols increases serum and blood cell gamma-tocopherol but does not alter biomarkers of platelet activation in subjects with type 2 diabetes. Clarke MW; Ward NC; Wu JH; Hodgson JM; Puddey IB; Croft KD Am J Clin Nutr; 2006 Jan; 83(1):95-102. PubMed ID: 16400056 [TBL] [Abstract][Full Text] [Related]
6. Familial hypobetalipoproteinemia: genetics and metabolism. Schonfeld G; Lin X; Yue P Cell Mol Life Sci; 2005 Jun; 62(12):1372-8. PubMed ID: 15818469 [TBL] [Abstract][Full Text] [Related]
7. Apoprotein B-100 production is decreased in subjects heterozygous for truncations of apoprotein B. Aguilar-Salinas CA; Barrett PH; Parhofer KG; Young SG; Tessereau D; Bateman J; Quinn C; Schonfeld G Arterioscler Thromb Vasc Biol; 1995 Jan; 15(1):71-80. PubMed ID: 7749818 [TBL] [Abstract][Full Text] [Related]
8. Apolipoprotein B gene mutations and fatty liver in Japanese hypobetalipoproteinemia. Katsuda S; Kawashiri MA; Inazu A; Tada H; Tsuchida M; Kaneko Y; Nozue T; Nohara A; Okada T; Kobayashi J; Michishita I; Mabuchi H; Yamagishi M Clin Chim Acta; 2009 Jan; 399(1-2):64-8. PubMed ID: 18848826 [TBL] [Abstract][Full Text] [Related]
11. Homozygous familial hypobetalipoproteinemia. Increased LDL catabolism in hypobetalipoproteinemia due to a truncated apolipoprotein B species, apo B-87Padova. Gabelli C; Bilato C; Martini S; Tennyson GE; Zech LA; Corsini A; Albanese M; Brewer HB; Crepaldi G; Baggio G Arterioscler Thromb Vasc Biol; 1996 Sep; 16(9):1189-96. PubMed ID: 8792774 [TBL] [Abstract][Full Text] [Related]
12. [Homozygous familial hypobetalipoproteinemia caused by APOB gene variations: a case report and review of literature]. Zhang YQ; Wang JS Zhonghua Er Ke Za Zhi; 2023 Jan; 61(1):70-75. PubMed ID: 36594125 [No Abstract] [Full Text] [Related]
13. Lipoprotein metabolism in an apoB-80 familial hypobetalipoproteinemia heterozygote. Hooper AJ; Robertson K; Champain D; Hua J; Song S; Parhofer KG; Barrett PHR; van Bockxmeer FM; Burnett JR Clin Biochem; 2016 Jun; 49(9):720-722. PubMed ID: 26916057 [TBL] [Abstract][Full Text] [Related]
14. Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias. Bordat C; Vairo D; Cuerq C; Halimi C; Peiretti F; Penhoat A; Vieille-Marchiset A; Gonzalez T; Michalski MC; Nowicki M; Peretti N; Reboul E Nutrients; 2023 Jan; 15(3):. PubMed ID: 36771214 [TBL] [Abstract][Full Text] [Related]
15. Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia. Magnolo L; Najah M; Fancello T; Di Leo E; Pinotti E; Brini I; Gueddiche NM; Calandra S; Slimene NM; Tarugi P Gene; 2013 Jan; 512(1):28-34. PubMed ID: 23043934 [TBL] [Abstract][Full Text] [Related]
16. Homozygous familial hypobetalipoproteinemia: two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature. Cefalù AB; Norata GD; Ghiglioni DG; Noto D; Uboldi P; Garlaschelli K; Baragetti A; Spina R; Valenti V; Pederiva C; Riva E; Terracciano L; Zoja A; Grigore L; Averna MR; Catapano AL Atherosclerosis; 2015 Mar; 239(1):209-17. PubMed ID: 25618028 [TBL] [Abstract][Full Text] [Related]
17. Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia. Di Filippo M; Moulin P; Roy P; Samson-Bouma ME; Collardeau-Frachon S; Chebel-Dumont S; Peretti N; Dumortier J; Zoulim F; Fontanges T; Parini R; Rigoldi M; Furlan F; Mancini G; Bonnefont-Rousselot D; Bruckert E; Schmitz J; Scoazec JY; Charrière S; Villar-Fimbel S; Gottrand F; Dubern B; Doummar D; Joly F; Liard-Meillon ME; Lachaux A; Sassolas A J Hepatol; 2014 Oct; 61(4):891-902. PubMed ID: 24842304 [TBL] [Abstract][Full Text] [Related]
18. Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia. Rimbert A; Pichelin M; Lecointe S; Marrec M; Le Scouarnec S; Barrak E; Croyal M; Krempf M; Le Marec H; Redon R; Schott JJ; Magré J; Cariou B Atherosclerosis; 2016 Jul; 250():52-6. PubMed ID: 27179706 [TBL] [Abstract][Full Text] [Related]
19. Cigarette smokers have decreased lymphocyte and platelet alpha-tocopherol levels and increased excretion of the gamma-tocopherol metabolite gamma-carboxyethyl-hydroxychroman (gamma-CEHC). Jeanes YM; Hall WL; Proteggente AR; Lodge JK Free Radic Res; 2004 Aug; 38(8):861-8. PubMed ID: 15493460 [TBL] [Abstract][Full Text] [Related]
20. gamma-Tocopherol biokinetics and transformation in humans. Galli F; Lee R; Atkinson J; Floridi A; Kelly FJ Free Radic Res; 2003 Nov; 37(11):1225-33. PubMed ID: 14703735 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]