Zobrazeno 1 - 10
of 76
pro vyhledávání: '"A Likidlilid"'
Autor:
A Likidlilid, P Thanomsuk
Publikováno v:
Siriraj Medical Journal, Vol 51, Iss 7 (1999)
There is much evidence suggesting a possible role of reactive oxygen species and other free radicals as mediators of phenotypic and genotypic changes that lead from mutation to cancer. The imbalance in cancer cell antioxidant defense mechanism can in
Externí odkaz:
https://doaj.org/article/353b56b3eb874072a8acbf4203549652
Autor:
Damrus Tresukosol, Bhoom Suktitipat, Saowalak Hunnangkul, Ruttakarn Kamkaew, Saiphon Poldee, Boonrat Tassaneetrithep, Atip Likidlilid
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e110188 (2014)
Clopidogrel is an antiplatelet prodrug that is recommended to reduce the risk of recurrent thrombosis in coronary artery disease (CAD) patients. Paraoxonase 1 (PON1) is suggested to be a rate-limiting enzyme in the conversion of 2-oxo-clopidogrel to
Externí odkaz:
https://doaj.org/article/6423afbc34c34773886c2b4ca5dfedd2
Autor:
Chaudhary Rajesh, Likidlilid Atip, Peerapatdit Thavatchai, Tresukosol Damras, Srisuma Sorachai, Ratanamaneechat Suphachai, Sriratanasathavorn Charn
Publikováno v:
Cardiovascular Diabetology, Vol 11, Iss 1, p 36 (2012)
Abstract Background The most common apolipoprotein E (apoE) gene polymorphism has been found to influence plasma lipid concentration and its correlation with coronary artery disease (CAD) has been extensively investigated in the last decade. It is, h
Externí odkaz:
https://doaj.org/article/d1062163a1334323b82263d11df93044
Publikováno v:
Acta Cardiologica. 65:681-691
Objective - Two common polymorphisms of the paraoxonase (PON 1) gene, L55M and Q192R, were proven to mitigate atherosclerosis pathogenesis by protecting lipoproteins against peroxidation. This study was to evaluate the associations between both PON1
Autor:
Rajesh Chaudhary, Suphachai Ratanamaneechat, Atip Likidlilid, Damras Tresukosol, Thavatchai Peerapatdit, Sorachai Srisuma, Charn Sriratanasathavorn
Publikováno v:
Cardiovascular Diabetology
Cardiovascular Diabetology, Vol 11, Iss 1, p 36 (2012)
Cardiovascular Diabetology, Vol 11, Iss 1, p 36 (2012)
Background The most common apolipoprotein E (apoE) gene polymorphism has been found to influence plasma lipid concentration and its correlation with coronary artery disease (CAD) has been extensively investigated in the last decade. It is, however, u
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 90(9)
Diabetic (DM) patients are claimed to be under oxidative stress because of hyperglycemia. The influence of free radical production by this hyperglycemic induction may involve cardiovascular complications in diabetes. The present study aimed to compar
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 89
In Type 1 diabetes mellitus (DM), hyperglycemia is considered a primary cause of diabetic vascular complications and is associated with oxidative stress. The role of antioxidants, particularly alpha tocopherol, in Type 1 DM and its contribution in th
Autor:
Thavatchai, Peerapatdit, Natchai, Patchanans, Atip, Likidlilid, Saiphon, Poldee, Charn, Sriratanasathavorn
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 89
Observation shows diabetic patients to be more prone to oxidative stress because of hyperglycemia. The elevation of free radical production by this hyperglycemic production may exacerbate cardiovascular complication in diabetes. This study aims to in
Autor:
Thavatchai Peerapatdit, Atip Likidlilid, Natchai Patchanans, Nednapis Tirawanchai, Charn Sriratanasathavorn
Publikováno v:
Siriraj Medical Journal, Vol 56, Iss 2 (2004)
Objectives : Hyperglycemia is claimed to cause oxidative stress in diabetic (DM) patients. The influence of free radical production by hyperglycemia may exacerbate the cardiovascular complications in diabetes. However, the effects of glycemic control
Autor:
K U, Pongrapeeporn, V, Sutthikhum, A, Likidlilid, S, Poldee, A, Futrakul, P, Yamwong, A, Amornrattana, S, Ong-Ajyooth
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 83
A mutation in low density lipoprotein (LDL) receptor gene causes an autosomal codominant disorder namely familial hypercholesterolemia (FH). Mutations in the LDL receptor gene are very heterogeneous at the DNA levels, occurring in all 18 exons of the