Yue P - Search Results

1

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.

2

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

3

Familial hypobetalipoproteinemia: genetics and metabolism.

Schonfeld G, Lin X, Yue P. Schonfeld G, et al. Among authors: yue p. Cell Mol Life Sci. 2005 Jun;62(12):1372-8. doi: 10.1007/s00018-005-4473-0. Cell Mol Life Sci. 2005. PMID: 15818469 Review.

4

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

5

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

6

Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families.

Sherva R, Yue P, Schonfeld G, Neuman RJ. Sherva R, et al. Among authors: yue p. J Lipid Res. 2007 Dec;48(12):2632-9. doi: 10.1194/jlr.M700078-JLR200. Epub 2007 Sep 23. J Lipid Res. 2007. PMID: 17890784 Free article.

7

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

8

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. Yue P, et al. Atherosclerosis. 2005 Jan;178(1):107-13. doi: 10.1016/j.atherosclerosis.2004.06.020. Atherosclerosis. 2005. PMID: 15585207

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

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.

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