Hegele RA - Search Results

1

Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.

Wang J, Hegele RA. Wang J, et al. Among authors: hegele ra. Hum Mutat. 2000 Mar;15(3):294-5. doi: 10.1002/(SICI)1098-1004(200003)15:3<294::AID-HUMU14>3.0.CO;2-E. Hum Mutat. 2000. PMID: 10679949

2

Human hepatic lipase mutations and polymorphisms.

Hegele RA, Tu L, Connelly PW. Hegele RA, et al. Hum Mutat. 1992;1(4):320-4. doi: 10.1002/humu.1380010410. Hum Mutat. 1992. PMID: 1301939

3

Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal Canadians.

Hegele RA, Harris SB, Zinman B, Wang J, Cao H, Hanley AJ, Tsui LC, Scherer SW. Hegele RA, et al. J Clin Endocrinol Metab. 1998 Nov;83(11):3980-3. doi: 10.1210/jcem.83.11.5219. J Clin Endocrinol Metab. 1998. PMID: 9814479

4

A microdeletion within DAX-1 in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.

Wang J, Killinger DW, Hegele RA. Wang J, et al. Among authors: hegele ra. J Investig Med. 1999 May;47(5):232-5. J Investig Med. 1999. PMID: 10361383

5

The ADD1 G460W polymorphism is not associated with variation in blood pressure in Canadian Oji-Cree.

Busch CP, Harris SB, Hanley AJ, Zinman B, Hegele RA. Busch CP, et al. Among authors: hegele ra. J Hum Genet. 1999;44(4):225-9. doi: 10.1007/s100380050148. J Hum Genet. 1999. PMID: 10429360

6

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.

Cao H, Hegele RA. Cao H, et al. Among authors: hegele ra. Hum Mol Genet. 2000 Jan 1;9(1):109-12. doi: 10.1093/hmg/9.1.109. Hum Mol Genet. 2000. PMID: 10587585

7

Human C-reactive protein (CRP) 1059G/C polymorphism.

Cao H, Hegele RA. Cao H, et al. Among authors: hegele ra. J Hum Genet. 2000;45(2):100-1. doi: 10.1007/s100380050022. J Hum Genet. 2000. PMID: 10721674

8

Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes.

Hegele RA, Anderson CM, Wang J, Jones DC, Cao H. Hegele RA, et al. Genome Res. 2000 May;10(5):652-8. doi: 10.1101/gr.10.5.652. Genome Res. 2000. PMID: 10810087 Free PMC article.

9

A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.

Krahn AD, Wang J, Spindler B, Skanes AC, Yee R, Klein GJ, Hegele RA. Krahn AD, et al. Among authors: hegele ra. Am Heart J. 2000 Jul;140(1):146-9. doi: 10.1067/mhj.2000.106599. Am Heart J. 2000. PMID: 10874277

10

Common and rare ABCA1 variants affecting plasma HDL cholesterol.

Wang J, Burnett JR, Near S, Young K, Zinman B, Hanley AJ, Connelly PW, Harris SB, Hegele RA. Wang J, et al. Among authors: hegele ra. Arterioscler Thromb Vasc Biol. 2000 Aug;20(8):1983-9. doi: 10.1161/01.atv.20.8.1983. Arterioscler Thromb Vasc Biol. 2000. PMID: 10938021

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