AAAAAA

   
Results: 1-7 |
Results: 7
Linear dichroism for the detection of single base pair mutations
Authors: Halsall, DJ Rodger, A Dafforn, TR
Citation: Dj. Halsall et al., Linear dichroism for the detection of single base pair mutations, CHEM COMMUN, (23), 2001, pp. 2410-2411
Uncoupling protein 3 genetic variants in human obesity: the c-55t promoterpolymorphism is negatively correlated with body mass index in a UK Caucasian population
Authors: Halsall, DJ Luan, J Saker, P Huxtable, S Farooqi, IS Keogh, J Wareham, NJ O'Rahilly, S
Citation: Dj. Halsall et al., Uncoupling protein 3 genetic variants in human obesity: the c-55t promoterpolymorphism is negatively correlated with body mass index in a UK Caucasian population, INT J OBES, 25(4), 2001, pp. 472-477
Evidence for gene-nutrient interaction at the PPAR gamma locus
Authors: Luan, J Browne, PO Harding, AH Halsall, DJ O'Rahilly, S Chatterjee, VKK Wareham, NJ
Citation: J. Luan et al., Evidence for gene-nutrient interaction at the PPAR gamma locus, DIABETES, 50(3), 2001, pp. 686-689
A common apolipoprotein B signal peptide polymorphism modifies the relation between plasma non-esterified fatty acids and triglyceride concentration in men
Authors: Halsall, DJ Martensz, ND Luan, J Maison, P Wareham, NJ Hales, CN Byrne, CD
Citation: Dj. Halsall et al., A common apolipoprotein B signal peptide polymorphism modifies the relation between plasma non-esterified fatty acids and triglyceride concentration in men, ATHEROSCLER, 152(1), 2000, pp. 9-17
The CART gene and human obesity - Mutational analysis and population genetics
Authors: Challis, BG Yeo, GSH Farooqi, IS Luan, J Aminian, S Halsall, DJ Keogh, JM Wareham, NJ O'Rahilly, S
Citation: Bg. Challis et al., The CART gene and human obesity - Mutational analysis and population genetics, DIABETES, 49(5), 2000, pp. 872-875
Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
Authors: Robson, KJH Merryweather-Clark, AT Pointon, JJ Shearman, JD Halsall, DJ Kelly, A Cox, TM Rosenberg, WM Howell, M Eccles, D Patch, C Fowler, AV Wallace, DF Camaschella, C Roetto, A Zecchina, G De Gobbi, M Gasparini, P Cadet, E Vandwalle, JL Capron, D Rochette, J Borot, N Demangel, C Dery, R Vinel, JP Pascal, JP Coppin, H Roth, MP
Citation: Kjh. Robson et al., Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience, BR J HAEM, 108(1), 2000, pp. 31-39
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
Authors: Merryweather-Clarke, AT Pointon, JJ Shearman, JD Robson, KJH Jouanolle, AM Mosser, A David, V Le Gall, JY Halsall, DJ Elsey, TS Kelly, A Cox, TM Clare, M Bomford, A Vandwalle, JL Rochette, J Borot, N Coppin, H Roth, MP Ryan, E Crowe, J Totaro, A Gasparini, P Roetto, A Gamaschella, C Darke, C Wallace, DF Saeb-Parsy, K Dooley, JS Worwood, M Walker, AP
Citation: At. Merryweather-clarke et al., Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results, NAT GENET, 23(3), 1999, pp. 271-271
Risultati: 1-7 |