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Results:
1-16
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Results: 16
Authors:
Cao, HN
Hegele, RA
Citation: Hn. Cao et Ra. Hegele, Single nucleotide polymorphisms of the resistin (RSTN) gene, J HUM GENET, 46(9), 2001, pp. 553-555
Authors:
Hegele, RA
Cao, HN
Citation: Ra. Hegele et Hn. Cao, Single nucleotide polymorphisms of RXRA encoding retinoid X receptor alpha, J HUM GENET, 46(7), 2001, pp. 423-425
Authors:
Hegele, RA
Ramdath, DD
Ban, MR
Carruthers, MN
Carrington, CV
Cao, HN
Citation: Ra. Hegele et al., Polymorphisms in PNLIP, encoding pancreatic lipase, and associations with metabolic traits, J HUM GENET, 46(6), 2001, pp. 320-324
Authors:
Hegele, RA
Yuen, J
Cao, HN
Citation: Ra. Hegele et al., Single-nucleotide polymorphisms of the nuclear lamina proteome, J HUM GENET, 46(6), 2001, pp. 351-354
Authors:
Cao, HN
Hegele, RA
Citation: Hn. Cao et Ra. Hegele, Human aryl hydrocarbon receptor nuclear translocator gene (ARNT) D/N511 polymorphism, J HUM GENET, 45(2), 2000, pp. 92-93
Authors:
Cao, HN
Hegele, RA
Citation: Hn. Cao et Ra. Hegele, Human cathepsin S gene (CTSS) promoter-25G/A polymorphism, J HUM GENET, 45(2), 2000, pp. 94-95
Authors:
Cao, HN
Hegele, RA
Citation: Hn. Cao et Ra. Hegele, Human hepatocyte nuclear factor-1 beta (HNF1B) 1968A/G polymorphism, J HUM GENET, 45(2), 2000, pp. 98-99
Authors:
Cao, HN
Hegele, RA
Citation: Hn. Cao et Ra. Hegele, Human C-reactive protein (CRP) 1059G/C polymorphism, J HUM GENET, 45(2), 2000, pp. 100-101
Authors:
Hegele, RA
Cao, HN
Harris, SB
Zinman, B
Hanley, AJ
Anderson, CM
Citation: Ra. Hegele et al., Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians, PHYSIOL GEN, 3(1), 2000, pp. 39-44
Authors:
Hegele, RA
Anderson, CM
Wang, J
Jones, DC
Cao, HN
Citation: Ra. Hegele et al., Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes, GENOME RES, 10(5), 2000, pp. 652-658
Authors:
Hegele, RA
Cao, HN
Harris, SB
Hanley, AJG
Zinman, B
Connelly, PW
Citation: Ra. Hegele et al., The private hepatocyte nuclear factor-1 alpha G319S variant is associated with plasma lipoprotein variation in Canadian Oji-Cree, ART THROM V, 20(1), 2000, pp. 217-222
Authors:
Hegele, RA
Anderson, CM
Cao, HN
Citation: Ra. Hegele et al., Lamin A/C mutation in a woman and her two daughters with Dunnigan-type partial lipodystrophy and insulin resistance, DIABET CARE, 23(2), 2000, pp. 258-259
Authors:
Hegele, RA
Cao, HN
Huff, MW
Anderson, CM
Citation: Ra. Hegele et al., LMNA R482Q mutation in partial lipodystrophy associated with reduced plasma leptin concentration, J CLIN END, 85(9), 2000, pp. 3089-3093
Authors:
Hegele, RA
Cao, HN
Anderson, CM
Hramiak, IM
Citation: Ra. Hegele et al., Heterogeneity of nuclear lamin A mutations in Dunnigan-type familial partial lipodystrophy, J CLIN END, 85(9), 2000, pp. 3431-3435
Authors:
Fehlner-Gardiner, CC
Cao, HN
Jackson-Boeters, L
Nakamura, T
Elliott, BE
Uniyal, S
Chan, BMC
Citation: Cc. Fehlner-gardiner et al., Characterization of a functional relationship between hepatocyte growth factor and mouse bone marrow-derived mast cells, DIFFERENTIA, 65(1), 1999, pp. 27-42
Authors:
Hegele, RA
Busch, CP
Young, TK
Connelly, PW
Cao, HN
Citation: Ra. Hegele et al., Mannose-binding lectin gene variation and cardiovascular disease in Canadian inuit, CLIN CHEM, 45(8), 1999, pp. 1283-1285
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1-16
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