Hegele RA - Search Results

1

Genomic organization and evolution of the CX3CR1/CCR8 chemokine receptor locus.

DeVries ME, Cao H, Wang J, Xu L, Kelvin AA, Ran L, Chau LA, Madrenas J, Hegele RA, Kelvin DJ. DeVries ME, et al. Among authors: hegele ra. J Biol Chem. 2003 Apr 4;278(14):11985-94. doi: 10.1074/jbc.M211422200. Epub 2003 Jan 27. J Biol Chem. 2003. PMID: 12551893 Free article.

2

G protein beta3 subunit gene variant and blood pressure variation in Canadian Oji-Cree.

Hegele RA, Harris SB, Hanley AJ, Cao H, Zinman B. Hegele RA, et al. Hypertension. 1998 Oct;32(4):688-92. doi: 10.1161/01.hyp.32.4.688. Hypertension. 1998. PMID: 9774364

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

The hepatic nuclear factor-1alpha G319S variant is associated with early-onset type 2 diabetes in Canadian Oji-Cree.

Hegele RA, Cao H, Harris SB, Hanley AJ, Zinman B. Hegele RA, et al. J Clin Endocrinol Metab. 1999 Mar;84(3):1077-82. doi: 10.1210/jcem.84.3.5528. J Clin Endocrinol Metab. 1999. PMID: 10084598

5

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

6

Mannose-binding lectin gene variation and cardiovascular disease in Canadian Inuit.

Hegele RA, Busch CP, Young TK, Connelly PW, Cao H. Hegele RA, et al. Clin Chem. 1999 Aug;45(8 Pt 1):1283-5. Clin Chem. 1999. PMID: 10430797 No abstract available.

7

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

8

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

9

Human aryl hydrocarbon receptor nuclear translocator gene (ARNT) D/N511 polymorphism.

Cao H, Hegele RA. Cao H, et al. Among authors: hegele ra. J Hum Genet. 2000;45(2):92-3. doi: 10.1007/s100380050018. J Hum Genet. 2000. PMID: 10721670

10

Human cathepsin S gene (CTSS) promoter -25G/A polymorphism.

Cao H, Hegele RA. Cao H, et al. Among authors: hegele ra. J Hum Genet. 2000;45(2):94-5. doi: 10.1007/s100380050019. J Hum Genet. 2000. PMID: 10721671

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