Bu X - Search Results

1

Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22.

Wu DA, Bu X, Warden CH, Shen DD, Jeng CY, Sheu WH, Fuh MM, Katsuya T, Dzau VJ, Reaven GM, Lusis AJ, Rotter JI, Chen YD. Wu DA, et al. Among authors: bu x. J Clin Invest. 1996 May 1;97(9):2111-8. doi: 10.1172/JCI118648. J Clin Invest. 1996. PMID: 8621801 Free PMC article.

2

Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus.

DeMeester CA, Bu X, Gray RJ, Lusis AJ, Rotter JI. DeMeester CA, et al. Among authors: bu x. Am J Hum Genet. 1995 Jan;56(1):287-93. Am J Hum Genet. 1995. PMID: 7825589 Free PMC article.

3

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes.

Dallinga-Thie GM, van Linde-Sibenius Trip M, Rotter JI, Cantor RM, Bu X, Lusis AJ, de Bruin TW. Dallinga-Thie GM, et al. Among authors: bu x. J Clin Invest. 1997 Mar 1;99(5):953-61. doi: 10.1172/JCI119260. J Clin Invest. 1997. PMID: 9062353 Free PMC article.

Familial combined hyperlipidemia (FCH) is a common genetic lipid disorder in Western societies. In a recent report (Dallinga-Thie, G.M., X.D. Bu, M. van Linde-Sibenius Trip, J.I. Rotter, A.J. Lusis, and T.W.A. de Bruin. ...

Familial combined hyperlipidemia (FCH) is a common genetic lipid disorder in Western societies. In a recent report (Dallinga-Thie, G.M., …

4

Leber hereditary optic neuropathy: estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locus.

Bu X, Rotter JI. Bu X, et al. Clin Genet. 1992 Sep;42(3):143-8. doi: 10.1111/j.1399-0004.1992.tb03226.x. Clin Genet. 1992. PMID: 1395084

5

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.

Bu XD, Rotter JI. Bu XD, et al. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):8198-202. doi: 10.1073/pnas.88.18.8198. Proc Natl Acad Sci U S A. 1991. PMID: 1896469 Free PMC article.

6

Multilocus genetic determinants of LDL particle size in coronary artery disease families.

Rotter JI, Bu X, Cantor RM, Warden CH, Brown J, Gray RJ, Blanche PJ, Krauss RM, Lusis AJ. Rotter JI, et al. Among authors: bu x. Am J Hum Genet. 1996 Mar;58(3):585-94. Am J Hum Genet. 1996. PMID: 8644718 Free PMC article.

7

Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III.

Dallinga-Thie GM, Bu XD, van Linde-Sibenius Trip M, Rotter JI, Lusis AJ, de Bruin TW. Dallinga-Thie GM, et al. Among authors: bu xd. J Lipid Res. 1996 Jan;37(1):136-47. J Lipid Res. 1996. PMID: 8820109 Free article.

8

Two-locus mitochondrial and nuclear gene models for mitochondrial disorders.

Bu X, Yang HY, Shohat M, Rotter JI. Bu X, et al. Genet Epidemiol. 1992;9(1):27-44. doi: 10.1002/gepi.1370090105. Genet Epidemiol. 1992. PMID: 1634105

9

Evidence for linkage of the apolipoprotein A-II locus to plasma apolipoprotein A-II and free fatty acid levels in mice and humans.

Warden CH, Daluiski A, Bu X, Purcell-Huynh DA, De Meester C, Shieh BH, Puppione DL, Gray RM, Reaven GM, Chen YD, et al. Warden CH, et al. Among authors: bu x. Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10886-90. doi: 10.1073/pnas.90.22.10886. Proc Natl Acad Sci U S A. 1993. PMID: 8248186 Free PMC article.

10

Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13.

Fischel-Ghodsian N, Bu X, Prezant TR, Oeztas S, Huang ZS, Bohlman MC, Rotter JI, Shohat M. Fischel-Ghodsian N, et al. Among authors: bu x. Am J Med Genet. 1993 Jul 1;46(6):689-93. doi: 10.1002/ajmg.1320460619. Am J Med Genet. 1993. PMID: 8362911

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