Hunt SC - Search Results

1

Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease.

Lingenhel A, Kollerits B, Schwaiger JP, Hunt SC, Gress R, Hopkins PN, Schoenborn V, Heid IM, Kronenberg F. Lingenhel A, et al. Among authors: hunt sc. Exp Gerontol. 2008 Dec;43(12):1102-7. doi: 10.1016/j.exger.2008.08.047. Epub 2008 Aug 26. Exp Gerontol. 2008. PMID: 18790042 Free PMC article.

2

Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred.

Haddad L, Day IN, Hunt S, Williams RR, Humphries SE, Hopkins PN. Haddad L, et al. J Lipid Res. 1999 Jun;40(6):1113-22. J Lipid Res. 1999. PMID: 10357843 Free article.

3

Low-renin hypertension, altered sodium homeostasis, and an alpha-adducin polymorphism.

Grant FD, Romero JR, Jeunemaitre X, Hunt SC, Hopkins PN, Hollenberg NH, Williams GH. Grant FD, et al. Among authors: hunt sc. Hypertension. 2002 Feb;39(2):191-6. doi: 10.1161/hy0202.104273. Hypertension. 2002. PMID: 11847182

4

Angiotensinogen genotype affects renal and adrenal responses to angiotensin II in essential hypertension.

Hopkins PN, Hunt SC, Jeunemaitre X, Smith B, Solorio D, Fisher ND, Hollenberg NK, Williams GH. Hopkins PN, et al. Among authors: hunt sc. Circulation. 2002 Apr 23;105(16):1921-7. doi: 10.1161/01.cir.0000014684.75359.68. Circulation. 2002. PMID: 11997278 Clinical Trial.

5

Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees.

Kronenberg F, Coon H, Ellison RC, Borecki I, Arnett DK, Province MA, Eckfeldt JH, Hopkins PN, Hunt SC. Kronenberg F, et al. Among authors: hunt sc. Eur J Hum Genet. 2002 Jun;10(6):367-74. doi: 10.1038/sj.ejhg.5200818. Eur J Hum Genet. 2002. PMID: 12080388

6

A genome scan for loci influencing anti-atherogenic serum bilirubin levels.

Kronenberg F, Coon H, Gutin A, Abkevich V, Samuels ME, Ballinger DG, Hopkins PN, Hunt SC. Kronenberg F, et al. Among authors: hunt sc. Eur J Hum Genet. 2002 Sep;10(9):539-46. doi: 10.1038/sj.ejhg.5200842. Eur J Hum Genet. 2002. PMID: 12173031

7

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

Hunt SC, Hasstedt SJ, Coon H, Camp NJ, Cawthon RM, Wu LL, Hopkins PN. Hunt SC, et al. Kidney Int. 2002 Oct;62(4):1143-8. doi: 10.1111/j.1523-1755.2002.kid557.x. Kidney Int. 2002. PMID: 12234284 Free article.

8

Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred.

Takada D, Emi M, Ezura Y, Nobe Y, Kawamura K, Iino Y, Katayama Y, Xin Y, Wu LL, Larringa-Shum S, Stephenson SH, Hunt SC, Hopkins PN. Takada D, et al. Among authors: hunt sc. J Hum Genet. 2002;47(12):656-64. doi: 10.1007/s100380200101. J Hum Genet. 2002. PMID: 12522687

9

Apolipoprotein H variant modifies plasma triglyceride phenotype in familial hypercholesterolemia: a molecular study in an eight-generation hyperlipidemic family.

Takada D, Ezura Y, Ono S, Iino Y, Katayama Y, Xin Y, Wu LL, Larringa-Shum S, Stephenson SH, Hunt SC, Hopkins PN, Emi M. Takada D, et al. Among authors: hunt sc. J Atheroscler Thromb. 2003;10(2):79-84. doi: 10.5551/jat.10.79. J Atheroscler Thromb. 2003. PMID: 12740481 Free article.

10

Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study.

Hopkins PN, Heiss G, Ellison RC, Province MA, Pankow JS, Eckfeldt JH, Hunt SC. Hopkins PN, et al. Among authors: hunt sc. Circulation. 2003 Aug 5;108(5):519-23. doi: 10.1161/01.CIR.0000081777.17879.85. Epub 2003 Jul 7. Circulation. 2003. PMID: 12847072

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