Search Results - "Sale, M.M."

Variants in Intron 13 of the ELMO1 Gene are Associated with Diabetic Nephropathy in African Americans by Leak, T. S., Perlegas, P. S., Smith, S. G., Keene, K. L., Hicks, P. J., Langefeld, C. D., Mychaleckyj, J. C., Rich, S. S., Kirk, J. K., Freedman, B. I., Bowden, D. W., Sale, M. M.

“…Summary Variants in the engulfment and cell motility 1 (ELMO1) gene are associated with nephropathy due to type 2 diabetes mellitus (T2DM) in a Japanese…”
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Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk by HSU, F.-C, SIDES, E. G, FURIE, K. L, SALE, M. M, MYCHALECKYJ, J. C, WORRALL, B. B, ELIAS, G. A, LIU, Y, CHEN, W.-M, COULL, B. M, TOOLE, J. F, RICH, S. S

“…The Vitamin Intervention for Stroke Prevention trial found an association between baseline poststroke homocysteine (Hcy) and recurrent stroke. We investigated…”
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Genetic admixture is associated with plasma hemostatic factor levels in self‐identified African Americans and Hispanics: the Multi‐Ethnic Study of Atherosclerosis by LUTSEY, P. L., WASSEL, C. L., CUSHMAN, M., SALE, M. M., DIVERS, J., FOLSOM, A. R.

“…Background: Epidemiologic studies report that self‐identified African Americans typically have higher hemostatic factor levels than do self‐identified…”
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Retinopathy of prematurity: recent advances in our understanding by Wheatley, C M, Dickinson, J L, Mackey, D A, Craig, J E, Sale, M M

“…Retinopathy of prematurity (ROP) has been recognised as an important cause of childhood visual impairment and blindness since the 1940s when improved…”
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Investigation of crystallin genes in familial cataract, and report of two disease associated mutations by Burdon, K P, Wirth, M G, Mackey, D A, Russell-Eggitt, I M, Craig, J E, Elder, J E, Dickinson, J L, Sale, M M

“…Aims: Mutations of seven crystallin genes have been shown to cause familial cataract. The authors aimed to identify disease causing crystallin mutations in…”
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Association between birth weight and adolescent systolic blood pressure in a caucasian birth cohort differs according to skin type, CRH promoter or 11 -HSD2 genotype by Dwyer, T, Blizzard, L, Patterson, B, Ponsonby, A-L, Martin, K, Quinn, S, Sale, M M, Richards, S M, Morley, R, Rich, S, Dickinson, J L

“…Objective: To examine whether the inverse association between birth weight and blood pressure varies by skin pigmentation and/or related genotypes. Study…”
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Retinopathy of prematurity: recent advances in our understanding by Wheatley, C M, Dickinson, J L, Mackey, D A, Craig, J E, Sale, M M

“…Retinopathy of prematurity (ROP) has been recognised as an important cause of childhood visual impairment and blindness since the 1940s when improved…”
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Loci Contributing to Adult Height and Body Mass Index in African American Families Ascertained for Type 2 Diabetes by Sale, M.M., Freedman, B. I., Hicks, P. J., Williams, A. H., Langefeld, C. D., Gallagher, C. J., Bowden, D. W., Rich, S. S.

“…Summary Height and body mass index (BMI) have high heritability in most studies. High BMI and reduced height are well‐recognized as important risk factors for…”
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Investigation of crystallin genes in familial cataract, and report of two disease associated mutations by Burdon, K P, Wirth, M G, Mackey, D A, Russell-Eggitt, I M, Craig, J E, Elder, J E, Dickinson, J L, Sale, M M

“…Conclusions: Although mutations in the five crystallin genes comprehensively screened in this study account for 38% of paediatric cataract mutations in the…”
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