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Results: 11

1.

Genetic determinants of statin intolerance.

Oh J, Ban MR, Miskie BA, Pollex RL, Hegele RA.

Lipids Health Dis. 2007 Mar 21;6:7.

PMID:
17376224
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imaging.

Al-Attar SA, Pollex RL, Robinson JF, Miskie BA, Walcarius R, Little CH, Rutt BK, Hegele RA.

BMC Med Imaging. 2007 Mar 12;7:3.

PMID:
17352814
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Semi-automated segmentation and quantification of adipose tissue in calf and thigh by MRI: a preliminary study in patients with monogenic metabolic syndrome.

Al-Attar SA, Pollex RL, Robinson JF, Miskie BA, Walcarius R, Rutt BK, Hegele RA.

BMC Med Imaging. 2006 Aug 31;6:11.

PMID:
16945131
[PubMed]
Free PMC Article
4.

Treatment of dyslipidemia with lovastatin and ezetimibe in an adolescent with cholesterol ester storage disease.

Tadiboyina VT, Liu DM, Miskie BA, Wang J, Hegele RA.

Lipids Health Dis. 2005 Oct 28;4:26.

PMID:
16255772
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Rigid spine muscular dystrophy due to SEPN1 mutation presenting as cor pulmonale.

Venance SL, Koopman WJ, Miskie BA, Hegele RA, Hahn AF.

Neurology. 2005 Jan 25;64(2):395-6. No abstract available.

PMID:
15668457
[PubMed - indexed for MEDLINE]
6.

Optimizing RNA extraction yield from whole blood for microarray gene expression analysis.

Wang J, Robinson JF, Khan HM, Carter DE, McKinney J, Miskie BA, Hegele RA.

Clin Biochem. 2004 Sep;37(9):741-4.

PMID:
15329310
[PubMed - indexed for MEDLINE]
7.

Assembly and secretion of very low density lipoproteins containing apolipoprotein B48 in transfected McA-RH7777 cells. Lack of evidence that palmitoylation of apolipoprotein B48 is required for lipoprotein secretion.

Vukmirica J, Tran K, Liang X, Shan J, Yuan J, Miskie BA, Hegele RA, Resh MD, Yao Z.

J Biol Chem. 2003 Apr 18;278(16):14153-61. Epub 2003 Feb 11.

PMID:
12582154
[PubMed - indexed for MEDLINE]
Free Article
8.

A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia.

Burnett JR, Shan J, Miskie BA, Whitfield AJ, Yuan J, Tran K, McKnight CJ, Hegele RA, Yao Z.

J Biol Chem. 2003 Apr 11;278(15):13442-52. Epub 2003 Jan 27.

PMID:
12551903
[PubMed - indexed for MEDLINE]
Free Article
9.

Elevated serum C-reactive protein and free fatty acids among nondiabetic carriers of missense mutations in the gene encoding lamin A/C (LMNA) with partial lipodystrophy.

Hegele RA, Kraw ME, Ban MR, Miskie BA, Huff MW, Cao H.

Arterioscler Thromb Vasc Biol. 2003 Jan 1;23(1):111-6.

PMID:
12524233
[PubMed - indexed for MEDLINE]
Free Article
10.

Functional promoter polymorphism in SREBP cleavage-activating protein (SCAP).

Cao H, Miskie BA, Hegele RA.

J Hum Genet. 2002;47(9):492-6.

PMID:
12202990
[PubMed - indexed for MEDLINE]
11.

Acanthocytosis in a patient with homozygous familial hypobetalipoproteinemia due to a novel APOB splice site mutation.

Hegele RA, Miskie BA.

Clin Genet. 2002 Feb;61(2):101-3.

PMID:
11940084
[PubMed - indexed for MEDLINE]

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