Search Results - "Day, I. N. M"

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    Polymorphism in the Growth Hormone Gene, Weight in Infancy, and Adult Bone Mass by Dennison, E. M., Syddall, H. E., Rodriguez, S., Voropanov, A., Day, I. N. M., Cooper, C.

    “…Epidemiological studies point to the importance of gene-environment interactions during early life as determinants of later osteoporosis and fracture. We…”
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    The thermolabile variant of MTHFR is associated with depression in the British Women's Heart and Health Study and a meta-analysis by LEWIS, S. J, LAWLOR, D. A, SMITH, G. Davey, ARAYA, R, TIMPSON, N, DAY, I. N. M, EBRAHIM, S

    Published in Molecular psychiatry (01-04-2006)
    “…Low dietary folate intake has been implicated as a risk factor for depression. However, observational epidemiological studies are plagued by problems of…”
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    PARL Leu262Val is not associated with fasting insulin levels in UK populations by FAWCETT, K. A, WAREHAM, N. J, LUAN, J, SYDDALL, H, COOPER, C, O'RAHILLY, S, DAY, I. N. M, SANDHU, M. S, BARROSO, I

    Published in Diabetologia (01-11-2006)
    “…PARL, the gene encoding presenilins-associated rhomboid-like protein, maps to chromosome 3q27 within a quantitative trait locus that influences components of…”
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    IGF1, growth pathway polymorphisms and schizophrenia: A pooling study by Gunnell, D., Lewis, S., Wilkinson, J., Georgieva, L., Davey, G. Smith, Day, I.N.M., Holly, J.M.P., O'Donovan, M.C., Owen, M.J., Kirov, G., Zammit, S.

    “…It has been hypothesized that insulin‐like growth factors (IGFs) and components of the growth‐hormone (GH)‐IGF axis may underlie reported associations of poor…”
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    The use of long PCR to confirm three common alleles at the CYP2A6 locus and the relationship between genotype and smoking habit by GU, D. F., HINKS, L. J., MORTON, N. E., DAY, I. N. M.

    Published in Annals of human genetics (01-09-2000)
    “…Long PCR followed by nested PCR has previously been used to determine CYP2A6 160H alleles, but the method proved unreliable. We have optimized this approach in…”
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    Journal Article Conference Proceeding
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    Genotype of galectin 2 (LGALS2) is associated with insulin-glucose profile in the British Women's Heart and Health Study by Christensen, M. B, Lawlor, D. A, Gaunt, T. R, Howell, M.W, Davey Smith, G, Ebrahim, S, Day, I. N. M

    Published in Diabetologia (01-04-2006)
    “…Aims/hypothesis It has been suggested that the gene encoding lymphotoxin-alpha (LTA) is associated with insulin resistance, and genetic association studies in…”
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    A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress by Marchbanks, R.M., Ryan, Margaret, Day, I.N.M., Owen, M., McGuffin, P., Whatley, S.A.

    Published in Schizophrenia research (01-12-2003)
    “…We have previously reported a changed mitochondrial ( mt) gene expression in brain from patients with schizophrenia [Schizophr. Res. 14 (1995) 203]; now, we…”
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    IGF2BP1 , IGF2BP2 and IGF2BP3 genotype, haplotype and genetic model studies in metabolic syndrome traits and diabetes by Rodriguez, S, Eiriksdottir, G, Gaunt, T.R, Harris, T.B, Launer, L.J, Gudnason, V, Day, I.N.M

    Published in Growth hormone & IGF research (01-08-2010)
    “…Abstract Objective Genetic variation at the insulin-like binding protein 2 ( IGF2BP2 ) gene has been associated with type 2 diabetes (T2D) by genome-wide…”
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    Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traits by Abdollahi, M R, Gaunt, T R, Syddall, H E, Cooper, C, Phillips, D I W, Ye, S, Day, I N M

    Published in Journal of medical genetics (01-05-2005)
    “…Background: The renin angiotensin system is important in the regulation of vascular tone and fluid and electrolyte balance. The angiotensin converting enzyme…”
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    Epistatic interaction between variations in the angiotensin I converting enzyme and angiotensin II type 1 receptor genes in relation to extent of coronary atherosclerosis by Ye, S, Dhillon, S, Seear, R, Dunleavey, L, Day, L B, Bannister, W, Day, I N M, Simpson, I

    Published in Heart (British Cardiac Society) (01-10-2003)
    “…Objective: To test the hypothesis that gene–gene interaction of the renin–angiotensin system is associated with an effect on the extent of coronary…”
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    Refined Association Mapping for a Quantitative Trait: Weight in the H19‐IGF2‐INS‐TH Region by Zhang, W., Maniatis, N., Rodriguez, S., Miller, G. J., Day, I. N. M., Gaunt, T. R., Collins, A., Morton, N. E.

    Published in Annals of human genetics (01-11-2006)
    “…Summary Previous analyses have provided evidence for one or more loci affecting body weight in the H19‐IGF2‐INS‐TH region on chromosome 11p15. To identify the…”
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    Level of Ex Vivo Interleukin 6 Expression in Human Peripheral Fat Compared with Other Tissues by Sonnenberg, S, Shearman, C.P, Baxter, S, Morris, G.E, Cumming, D.V.E, Montgomery, H.E, Rose-Zerilli, M.J, Day, I.N.M

    “…Objectives Adipose tissue is able to secrete a variety of active mediators into the circulation. One of these is Interleukin 6 (IL6). IL6 may play a causal…”
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    Methylation patterns in the human muscle-specific enolase gene (ENO3) by PESHAVARIA, M, DAY, I. N. M

    Published in Biochemical journal (15-06-1993)
    “…The methylation status in the human-muscle enolase gene (ENO3) was assayed. Previous sequence data and MspI cleavage sites indicate the presence of a 5'…”
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    Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindreds by HADDAD, L., DAY, L. B., ATTWOOD, J., POVEY, S., HUMPHRIES, S. E., DAY, I. N. M.

    Published in Annals of human genetics (01-11-1997)
    “…Co-segregation studies based on a selection of intragenic restriction fragment length polymorphisms of the low density lipoprotein receptor (LDLR) gene have…”
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    Journal Article Conference Proceeding
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    The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14 by Edwards, Y H, Fox, M F, Povey, S, Hinks, L J, Thompson, R J, Day, I N

    Published in Annals of human genetics (01-10-1991)
    “…Ubiquitin carboxy terminal hydrolase 1, UCHL1, is a neurone-specific protein involved in the ubiquitin-mediated proteolytic pathway. The gene for human UCHL1…”
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    The association of the paraoxonase (PON1) Q192R polymorphism with depression in older women: findings from the British Women’s Heart and Health Study by Lawlor, Debbie A, Day, Ian N M, Gaunt, Tom R, Hinks, Lesley J, Timpson, Nick, Ebrahim, Shah, Davey Smith, George

    “…Background: The association between the R allele of PON1 Q192R and symptoms reported by sheep dippers and Gulf War veterans has been used to suggest a…”
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