Yue P - Search Results

1

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. Noto D, et al. Among authors: yue p. Arterioscler Thromb Vasc Biol. 2012 Mar;32(3):805-9. doi: 10.1161/ATVBAHA.111.238766. Epub 2012 Jan 12. Arterioscler Thromb Vasc Biol. 2012. PMID: 22247256

2

Plasma non-cholesterol sterols in primary hypobetalipoproteinemia.

Noto D, Cefalù AB, Barraco G, Fayer F, Minà M, Yue P, Tarugi P, Schonfeld G, Averna MR. Noto D, et al. Among authors: yue p. Atherosclerosis. 2011 Jun;216(2):409-13. doi: 10.1016/j.atherosclerosis.2010.10.050. Epub 2011 Feb 1. Atherosclerosis. 2011. PMID: 21492858

3

The c.43_44insCTG variation in PCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population.

Yue P, Averna M, Lin X, Schonfeld G. Yue P, et al. Hum Mutat. 2006 May;27(5):460-6. doi: 10.1002/humu.20316. Hum Mutat. 2006. PMID: 16619215

4

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.

Musunuru K, Pirruccello JP, Do R, Peloso GM, Guiducci C, Sougnez C, Garimella KV, Fisher S, Abreu J, Barry AJ, Fennell T, Banks E, Ambrogio L, Cibulskis K, Kernytsky A, Gonzalez E, Rudzicz N, Engert JC, DePristo MA, Daly MJ, Cohen JC, Hobbs HH, Altshuler D, Schonfeld G, Gabriel SB, Yue P, Kathiresan S. Musunuru K, et al. Among authors: yue p. N Engl J Med. 2010 Dec 2;363(23):2220-7. doi: 10.1056/NEJMoa1002926. Epub 2010 Oct 13. N Engl J Med. 2010. PMID: 20942659 Free PMC article.

5

A targeted apoB38.9 mutation in mice is associated with reduced hepatic cholesterol synthesis and enhanced lipid peroxidation.

Lin X, Chen Z, Yue P, Averna MR, Ostlund RE Jr, Watson MA, Schonfeld G. Lin X, et al. Among authors: yue p. Am J Physiol Gastrointest Liver Physiol. 2006 Jun;290(6):G1170-6. doi: 10.1152/ajpgi.00402.2005. Epub 2006 Feb 2. Am J Physiol Gastrointest Liver Physiol. 2006. PMID: 16455790 Free article.

6

Fatty liver in familial hypobetalipoproteinemia: triglyceride assembly into VLDL particles is affected by the extent of hepatic steatosis.

Schonfeld G, Patterson BW, Yablonskiy DA, Tanoli TS, Averna M, Elias N, Yue P, Ackerman J. Schonfeld G, et al. Among authors: yue p. J Lipid Res. 2003 Mar;44(3):470-8. doi: 10.1194/jlr.M200342-JLR200. Epub 2002 Dec 1. J Lipid Res. 2003. PMID: 12562873 Free article. Clinical Trial.

7

Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds.

Neuman RJ, Yuan B, Gerhard DS, Liu KY, Yue P, Duan S, Averna M, Schonfeld G. Neuman RJ, et al. Among authors: yue p. J Lipid Res. 2002 Mar;43(3):407-15. J Lipid Res. 2002. PMID: 11893777 Free article.

8

Hepatic fatty acid synthesis is suppressed in mice with fatty livers due to targeted apolipoprotein B38.9 mutation.

Lin X, Schonfeld G, Yue P, Chen Z. Lin X, et al. Among authors: yue p. Arterioscler Thromb Vasc Biol. 2002 Mar 1;22(3):476-82. doi: 10.1161/hq0302.105271. Arterioscler Thromb Vasc Biol. 2002. PMID: 11884293

9

Fatty liver in familial hypobetalipoproteinemia: roles of the APOB defects, intra-abdominal adipose tissue, and insulin sensitivity.

Tanoli T, Yue P, Yablonskiy D, Schonfeld G. Tanoli T, et al. Among authors: yue p. J Lipid Res. 2004 May;45(5):941-7. doi: 10.1194/jlr.M300508-JLR200. Epub 2004 Feb 16. J Lipid Res. 2004. PMID: 14967820 Free article.

10

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. Yue P, et al. Hum Mutat. 2002 Aug;20(2):110-6. doi: 10.1002/humu.10101. Hum Mutat. 2002. PMID: 12124991

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