212 related articles for article (PubMed ID: 12124991)
1. 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]
2. Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation.
Pulai JI; Zakeri H; Kwok PY; Kim JH; Wu J; Schonfeld G
Am J Med Genet; 1998 Nov; 80(3):218-20. PubMed ID: 9843041
[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. 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]
5. Identification of a novel mutation in the ANGPTL3 gene in two families diagnosed of familial hypobetalipoproteinemia without APOB mutation.
Martín-Campos JM; Roig R; Mayoral C; Martinez S; Martí G; Arroyo JA; Julve J; Blanco-Vaca F
Clin Chim Acta; 2012 Mar; 413(5-6):552-5. PubMed ID: 22155345
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genetic variation of apolipoprotein B can produce both low and high levels of apoB-containing lipoproteins in plasma.
Schonfeld G
Can J Cardiol; 1995 Oct; 11 Suppl G():86G-92G. PubMed ID: 7585299
[TBL] [Abstract][Full Text] [Related]
8. Absence of fatty liver in familial hypobetalipoproteinemia linked to chromosome 3p21.
Yue P; Tanoli T; Wilhelm O; Patterson B; Yablonskiy D; Schonfeld G
Metabolism; 2005 May; 54(5):682-8. PubMed ID: 15877300
[TBL] [Abstract][Full Text] [Related]
9. Pediatric gallstone disease in familial hypobetalipoproteinemia.
Lancellotti S; Zaffanello M; Di Leo E; Costa L; Lonardo A; Tarugi P
J Hepatol; 2005 Jul; 43(1):188-91. PubMed ID: 15894400
[TBL] [Abstract][Full Text] [Related]
10. The hypobetalipoproteinemias.
Schonfeld G
Annu Rev Nutr; 1995; 15():23-34. PubMed ID: 8527219
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Lengths of truncated forms of apolipoprotein B (apoB) determine their intestinal production.
Krul ES; Tang J; Kettler TS; Clouse RE; Schonfeld G
Biochem Biophys Res Commun; 1992 Dec; 189(2):1069-76. PubMed ID: 1472017
[TBL] [Abstract][Full Text] [Related]
13. Genetic heterogeneity in familial hypobetalipoproteinemia: linkage and non-linkage to the apoB gene in Caucasian families.
Pulai JI; Neuman RJ; Groenewegen AW; Wu J; Schonfeld G
Am J Med Genet; 1998 Feb; 76(1):79-86. PubMed ID: 9508071
[TBL] [Abstract][Full Text] [Related]
14. 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; 32(6):1001-11. PubMed ID: 1940616
[TBL] [Abstract][Full Text] [Related]
15. Identification and molecular analysis of two apoB gene mutations causing low plasma cholesterol levels.
Welty FK; Ordovas J; Schaefer EJ; Wilson PW; Young SG
Circulation; 1995 Oct; 92(8):2036-40. PubMed ID: 7554178
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.
Noto D; Cefalù AB; Valenti V; Fayer F; Pinotti E; Ditta M; Spina R; Vigna G; Yue P; Kathiresan S; Tarugi P; Averna MR
Arterioscler Thromb Vasc Biol; 2012 Mar; 32(3):805-9. PubMed ID: 22247256
[TBL] [Abstract][Full Text] [Related]
18. Cryptogenic cirrhosis in a patient with familial hypocholesterolemia due to a new truncated form of apolipoprotein B.
Bonnefont-Rousselot D; Condat B; Sassolas A; Chebel S; Bittar R; Federspiel MC; Cazals-Hatem D; Bruckert E
Eur J Gastroenterol Hepatol; 2009 Jan; 21(1):104-8. PubMed ID: 19060634
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Diabetes mellitus in a new kindred with familial hypobetalipoproteinemia and an apolipoprotein B truncation (apoB-55).
Pulai JI; Latour MA; Kwok PY; Schonfeld G
Atherosclerosis; 1998 Feb; 136(2):289-95. PubMed ID: 9543100
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
