All Stories

  1. Analysis of GPR126 polymorphisms and their relationship with scoliosis in Marfan syndrome and Marfan-like syndrome in Mexican patients
  2. Bioinformatics Study of the DNA and RNA Viruses Infecting Plants and Bacteria that Could Potentially Affect Animals and Humans
  3. Effect of the Melanocortin 4-Receptor Ile269Asn Mutation on Weight Loss Response to Dietary, Phentermine and Bariatric Surgery Interventions
  4. Increased Carotid Intima-Media Thickness in Asymptomatic Individuals Is Associated with the PCSK9 (rs2149041) Gene Polymorphism in the Mexican Mestizo Population: Results of the GEA Cohort
  5. Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
  6. Effect of metabolic control on recurrent major adverse cardiovascular events and cardiovascular mortality in patients with premature coronary artery disease: Results of the Genetics of Atherosclerotic Disease study
  7. Long-Term Exposure to Ozone and Fine Particulate Matter and Risk of Premature Coronary Artery Disease: Results from Genetics of Atherosclerotic Disease Mexican Study
  8. Association of the rs17574 DPP4 Polymorphism with Premature Coronary Artery Disease in Diabetic Patients: Results from the Cohort of the GEA Mexican Study
  9. Osteoprotegerin Gene Polymorphisms Are Associated with Subclinical Atherosclerosis in the Mexican Mestizo Population
  10. FOXA3 Polymorphisms Are Associated with Metabolic Parameters in Individuals with Subclinical Atherosclerosis and Healthy Controls—The GEA Mexican Study
  11. The rs8176740 T/A and rs512770 T/C Genetic Variants of the ABO Gene Increased the Risk of COVID-19, as well as the Plasma Concentration Platelets
  12. ACE and ACE2 Gene Variants Are Associated With Severe Outcomes of COVID-19 in Men
  13. Bioinformatics-Based Characterization of Proteins Related to SARS-CoV- 2 Using the Polarity Index Method® (PIM®) and Intrinsic Disorder Predisposition
  14. Characterization of Proteins from Putative Human DNA and RNA Viruses
  15. DNA Methylation Levels of the TBX5 Gene Promoter Are Associated with Congenital Septal Defects in Mexican Paediatric Patients
  16. Los polimorfismos rs4783961 y rs708272 del gen CETP son asociados con la enfermedad arterial coronaria y no con la restenosis tras el implante de un stent coronario
  17. Association Analysis Between the Functional Single Nucleotide Variants in miR-146a, miR-196a-2, miR-499a, and miR-612 With Acute Lymphoblastic Leukemia
  18. Osteopontin Gene Polymorphisms Are Associated with Cardiovascular Risk Factors in Patients with Premature Coronary Artery Disease
  19. Genome-Wide Association Study Identifies a Functional SIDT2 Variant Associated With HDL-C (High-Density Lipoprotein Cholesterol) Levels and Premature Coronary Artery Disease
  20. Native Low-Density Lipoproteins Act in Synergy with Lipopolysaccharide to Alter the Balance of Human Monocyte Subsets and Their Ability to Produce IL-1 Beta, CCR2, and CX3CR1 In Vitro and In Vivo: Implications in Atherogenesis
  21. Heterogeneity of Genetic Admixture Determines SLE Susceptibility in Mexican
  22. Trp Fluorescence Redshift during HDL Apolipoprotein Denaturation Is Increased in Patients with Coronary Syndrome in Acute Phase: A New Assay to Evaluate HDL Stability
  23. Dipeptidylpeptidase-4 levels and DPP4 gene polymorphisms in patients with COVID-19. Association with disease and with severity
  24. The rs12617336 and rs17574 Dipeptidyl Peptidase-4 Polymorphisms Are Associated With Hypoalphalipoproteinemia and Dipeptidyl Peptidase-4 Serum Levels: A Case-Control Study of the Genetics of Atherosclerotic Disease (GEA) Cohort
  25. The rs508487, rs236911, and rs236918 Genetic Variants of the Proprotein Convertase Subtilisin–Kexin Type 7 (PCSK7) Gene Are Associated with Acute Coronary Syndrome and with Plasma Concentrations of HDL-Cholesterol and Triglycerides
  26. Association of the IL-37 Polymorphisms with Transaminases and Alkaline Phosphatase Levels in Premature Coronary Artery Disease Patients and Healthy Controls. Results of the Genetics of Atherosclerotic (GEA) Mexican Study
  27. BLK and BANK1 variants and interactions are associated with susceptibility for primary Sjögren’s syndrome and with some clinical features
  28. Variants of PCSK9 Gene Are Associated with Subclinical Atherosclerosis and Cardiometabolic Parameters in Mexicans. The GEA Project
  29. Influence of COMT polymorphism in cognitive performance on dementia in community-dwelling elderly Mexican (SADEM study)
  30. Interferon Regulatory Factor 5 (IRF5) Gene Haplotypes Are Associated with Premature Coronary Artery Disease. Association of the IRF5 Polymorphisms with Cardiometabolic Parameters. The Genetics of Atherosclerotic Disease (GEA) Mexican Study
  31. Are functional variants of the microRNA-146a gene associated with primary knee OA? Evidence in Mexican mestizo population
  32. A high-throughput multiplexed microfluidic device for COVID-19 serology assays
  33. Association between congenital heart disease and NKX2.5 gene polymorphisms: systematic review and meta-analysis
  34. Two genetic variants in the promoter region of the CCL5 gene are associated with the risk of acute coronary syndrome and with a lower plasma CCL5 concentration
  35. Epstein-Barr virus-induced gene 3 (EBI3) single nucleotide polymorphisms and their association with central obesity and risk factors for cardiovascular disease: The GEA study
  36. Genetic Variants and Haplotypes in OPG Gene Are Associated with Premature Coronary Artery Disease and Traditional Cardiovascular Risk Factors in Mexican Population: The GEA Study
  37. Variability in genes related to SARS-CoV-2 entry into host cells (ACE2, TMPRSS2, TMPRSS11A, ELANE, and CTSL) and its potential use in association studies
  38. IL-37 Gene and Cholesterol Metabolism: Association of Polymorphisms with the Presence of Hypercholesterolemia and Cardiovascular Risk Factors. The GEA Mexican Study
  39. The c.*52 A/G and c.*773 A/G Genetic Variants in the UTR′3 of the LDLR Gene Are Associated with the Risk of Acute Coronary Syndrome and Lower Plasma HDL-Cholesterol Concentration
  40. Genomic study of dilated cardiomyopathy in a group of Mexican patients using site‐directed next generation sequencing
  41. Association of ERAP2 polymorphisms in Colombian HLA-B27+ or HLA-B15+ patients with SpA and its relationship with clinical presentation: axial or peripheral predominance
  42. Microencapsulated Pomegranate Modifies the Composition and Function of High-Density Lipoproteins (HDL) in New Zealand Rabbits
  43. IL-12B Polymorphisms Are Associated with the Presence of Premature Coronary Artery Disease and with Cardiovascular Risk Factors: The Genetics of Atherosclerotic Disease Mexican Study
  44. The rs46522 Polymorphism of the Ubiquitin-Conjugating Enzyme E2Z Gene Is Associated with Abnormal Metabolic Parameters in Patients with Myocardial Infarction: The Genetics of Atherosclerosis Disease Mexican Study
  45. <p>Bone Morphogenetic Protein-2 and Osteopontin Gene Expression in Epicardial Adipose Tissue from Patients with Coronary Artery Disease Is Associated with the Presence of Calcified Atherosclerotic Plaques</p>
  46. HLA genes in Amerindians from Mexico San Vicente Tancuayalab Teenek/Huastecos
  47. Study of HLA genes in Mexico Mayo/Yoremes Amerindians: Further support of gene exchange with Pacific Islanders
  48. Coronary Artery Calcium is Associated with LPA Gene Variant RS7765803-C in Mexican Mestizo Population. The GEA Project
  49. Genetic polymorphisms of IL17A associated with Chagas disease: results from a meta-analysis in Latin American populations
  50. The Branched-chain Amino Acid Transaminase 1 -23C/G Polymorphism Confers Protection Against Acute Coronary Syndrome
  51. The Ser290Asn and Thr715Pro Polymorphisms of the SELP Gene Are Associated with A Lower Risk of Developing Acute Coronary Syndrome and Low Soluble P-Selectin Levels in A Mexican Population
  52. The role of socioeconomic status in the susceptibility to develop systemic lupus erythematosus in Mexican patients
  53. Common Variants in IL-20 Gene are Associated with Subclinical Atherosclerosis, Cardiovascular Risk Factors and IL-20 Levels in the Cohort of the Genetics of Atherosclerotic Disease (GEA) Mexican Study
  54. SREBF1c and SREBF2 gene polymorphisms are associated with acute coronary syndrome and blood lipid levels in Mexican population
  55. The rs10455872-G allele of the LPA gene is associated with high lipoprotein(a) levels and increased aortic valve calcium in a Mexican adult population
  56. Interleukin 10 gene polymorphisms and frailty syndrome in elderly Mexican people: (Sadem study)
  57. Association Of Il-37 Rs2708965 Polymorphism With Cardiovascular Risk Factors In Individuals With Coronary Artery Disease, Subclinical Atherosclerosis And Healthy Controls. The Gea Mexican Study.
  58. Association of vitamin D receptor polymorphisms and nephrolithiasis: A meta-analysis
  59. The Dpp-4 Rs12617336 Y Rs12617656 Polymorphisms Are Associated With Premature Coronary Artery Disease And Cardiovascular Risk Factors. The Gea Mexican Study.
  60. The rs2066808 Polymorphism Located Near the IL-23A Gene Is Associated with Premature Coronary Artery Disease in Mexican Population (GEA Study)
  61. Microencapsulated Pomegranate Reverts High-Density Lipoprotein (HDL)-Induced Endothelial Dysfunction and Reduces Postprandial Triglyceridemia in Women with Acute Coronary Syndrome
  62. MRE11A Polymorphisms Are Associated With Subclinical Atherosclerosis and Cardiovascular Risk Factors. A Case-Control Study of the GEA Mexican Project
  63. Atorvastatin and Fenofibrate Increase the Content of Unsaturated Acyl Chains in HDL and Modify In Vivo Kinetics of HDL-Cholesteryl Esters in New Zealand White Rabbits
  64. Atorvastatin and Fenofibrate Exert Opposite Effects on the Vascularization and Characteristics of Visceral Adipose Tissue in New Zealand White Rabbits
  65. Polymorphisms in B-Adrenergic Receptors Are Associated with Increased Risk to Have a Positive Head-Up Tilt Table Test in Patients with Vasovagal Syncope
  66. Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease
  67. Interleukin 27 polymorphisms, their association with insulin resistance and their contribution to subclinical atherosclerosis. The GEA Mexican study
  68. The rs1805193, rs5361, and rs5355 single nucleotide polymorphisms in the E-selectin gene (SEL-E) are associated with subclinical atherosclerosis: The Genetics of Atherosclerotic Disease (GEA) Mexican study
  69. Raet1e Polymorphisms Are Associated with Increased Risk of Developing Premature Coronary Artery Disease and with Some Cardiometabolic Parameters: The GEA Mexican Study
  70. miR-196a2 (rs11614913) polymorphism is associated with coronary artery disease, but not with in-stent coronary restenosis
  71. The −44 C/G (rs1800972) polymorphism of the β‐defensin 1 is associated with increased risk of developing type 2 diabetes mellitus
  72. HDL-Mediated Lipid Influx to Endothelial Cells Contributes to Regulating Intercellular Adhesion Molecule (ICAM)-1 Expression and eNOS Phosphorylation
  73. Fast Morphological Gallbladder Changes Triggered by a Hypercholesterolemic Diet
  74. Interleukin 10 gene polymorphisms are associated with a decreased risk of developing premature coronary artery disease and some clinical and metabolic parameters. The gea study
  75. The MRE11A RS13447720 and RS499952 polymorphisms are associated with decreased risk of developing subclinical atherosclerosis and with some cardiovascular risk factors. The gea mexican study
  76. HHIPL-1 (rs2895811) gene polymorphism is associated with cardiovascular risk factors and cardiometabolic parameters in Mexicans patients with myocardial infarction
  77. The IL-10-1082 (rs1800896) G allele is associated with a decreased risk of developing premature coronary artery disease and some IL-10 polymorphisms were associated with clinical and metabolic parameters. The GEA study
  78. The UCP2 -866G/A, Ala55Val and UCP3 -55C/T polymorphisms are associated with premature coronary artery disease and cardiovascular risk factors in Mexican population
  79. Vitamin D Deficiency is not Associated with Fatty Liver in a Mexican Population
  80. C-reactive protein (CRP) polymorphisms and haplotypes are associated with SLE susceptibility and activity but not with serum CRP levels in Mexican population
  81. Characterization of immortalized human dermal microvascular endothelial cells (HMEC-1) for the study of HDL functionality
  82. Innate Immunity in Coronary Disease. The Role of Interleukin-12 Cytokine Family in Atherosclerosis
  83. CETP and LCAT Gene Polymorphisms Are Associated with High-Density Lipoprotein Subclasses and Acute Coronary Syndrome
  84. Class I HLA alleles are associated with influenza A H1N1 susceptibility.
  85. Deficiencia de vitamina D y su asociación con enfermedad arterial coronaria en población mexicana: estudio Genético de la Enfermedad Aterosclerosa
  86. IL-15 polymorphisms are associated with subclinical atherosclerosis and cardiovascular risk factors. The Genetics of Atherosclerosis Disease (GEA) Mexican Study
  87. Association of the I148M/PNPLA3 (rs738409) polymorphism with premature coronary artery disease, fatty liver, and insulin resistance in type 2 diabetic patients and healthy controls. The GEA study
  88. Prevalencia y extensión de la calcificación arterial coronaria en población mexicana asintomática cardiovascular: estudio Genética de la Enfermedad Aterosclerosa
  89. The T>A (rs11646213) gene polymorphism of cadherin-13 (CDH13) gene is associated with decreased risk of developing hypertension in Mexican population
  90. Hyperuricemia is Associated with Increased Apo AI Fractional Catabolic Rates and Dysfunctional HDL in New Zealand Rabbits
  91. Differential expression of osteopontin, and osteoprotegerin mRNA in epicardial adipose tissue between patients with severe coronary artery disease and aortic valvular stenosis: association with HDL subclasses
  92. Interleukin-35 polymorphisms are associated with decreased risk of premature coronary artery disease, metabolic parameters and IL-35 levels: the mexican genetics of atherosclerotic disease (GEA) study
  93. Raet1e polymorphisms are associated with increased risk of developing coronary artery disease and with some cardiometabolic parameters. The genetics of atherosclerotic disease (GEA) mexican study
  94. Vascular Calcification
  95. Interaction between FTO rs9939609 and the Native American-origin ABCA1 rs9282541 affects BMI in the admixed Mexican population
  96. The NLRP3 and CASP1 gene polymorphisms are associated with developing of acute coronary syndrome: a case-control study
  97. Prevalencia y asociación de la calcificación valvular aórtica con factores de riesgo y aterosclerosis coronaria en población mexicana
  98. Interleukin-27 polymorphisms are associated with premature coronary artery disease and metabolic parameters in the Mexican population: the genetics of atherosclerotic disease (GEA) Mexican study
  99. Receptor-interacting protein 2 (RIP2) gene polymorphisms are associated with increased risk of subclinical atherosclerosis and clinical and metabolic parameters. The Genetics of Atherosclerotic Disease (GEA) Mexican study
  100. The rs7044343 Polymorphism of the Interleukin 33 Gene Is Associated with Decreased Risk of Developing Premature Coronary Artery Disease and Central Obesity, and Could Be Involved in Regulating the Production of IL-33
  101. Corrigendum to “Association of Nuclear Factor-Erythroid 2-Related Factor 2, Thioredoxin Interacting Protein, and Heme Oxygenase-1 Gene Polymorphisms with Diabetes and Obesity in Mexican Patients”
  102. Interleukin 35 Polymorphisms Are Associated with Decreased Risk of Premature Coronary Artery Disease, Metabolic Parameters, and IL-35 Levels: The Genetics of Atherosclerotic Disease (GEA) Study
  103. Association of Adiponectin with Subclinical Atherosclerosis in a Mexican-Mestizo Population
  104. Small HDL subclasses become cholesterol-poor during postprandial period after a fat diet intake in subjects with high triglyceridemia increases
  105. Association of human leukocyte A, B, and DR antigens in Colombian patients with diagnosis of spondyloarthritis
  106. Possible role of intronic polymorphisms in the PHACTR1 gene on the development of cardiovascular disease
  107. Adipose tissue dysfunction increases fatty liver association with pre diabetes and newly diagnosed type 2 diabetes mellitus
  108. Vitamin D and its effects on cardiovascular diseases: a comprehensive review
  109. Association of interleukin-10 polymorphisms with risk factors of Alzheimer’s disease and other dementias (SADEM study)
  110. The RS16900627 polymorphism of the receptor-interacting protein 2 ( RIP2 ) gene is associated with subclinical atherosclerosis. The genetics of atherosclerotic disease (GEA) Mexican study
  111. Interleukin-27 polymorphisms are associated with premature coronary artery disease and insulin resistance. The genetics of atherosclerotic disease (GEA) Mexican study
  112. PHACTR1 Gene Polymorphism Is Associated with Increased Risk of Developing Premature Coronary Artery Disease in Mexican Population
  113. Polymorphisms of APLN-APLNR system are associated with essential hypertension in Mexican-Mestizo individuals
  114. The Effect of Resveratrol and Quercetin Treatment on PPAR Mediated Uncoupling Protein (UCP-) 1, 2, and 3 Expression in Visceral White Adipose Tissue from Metabolic Syndrome Rats
  115. Angiotensin II Type 1 receptor (AGTR1) gene polymorphisms are associated with vascular manifestations in patients with systemic sclerosis (SSc)
  116. Polimorfismos genéticos de interleucina-22 en pacientes con colitis ulcerosa
  117. Protective role of Interleukin 27 (IL-27) gene polymorphisms in patients with ulcerative colitis
  118. HDL-sphingomyelin reduction after weight loss by an energy-restricted diet is associated with the improvement of lipid profile, blood pressure, and decrease of insulin resistance in overweight/obese patients
  119. Increased HDL Size and Enhanced Apo A-I Catabolic Rates Are Associated With Doxorubicin-Induced Proteinuria in New Zealand White Rabbits
  120. Association of Nuclear Factor-Erythroid 2-Related Factor 2, Thioredoxin Interacting Protein, and Heme Oxygenase-1 Gene Polymorphisms with Diabetes and Obesity in Mexican Patients
  121. Insulin Resistance in Adipose Tissue but Not in Liver Is Associated with Aortic Valve Calcification
  122. rs3918242 MMP9 gene polymorphism is associated with myocardial infarction in Mexican patients
  123. Serum magnesium is inversely associated with coronary artery calcification in the Genetics of Atherosclerotic Disease (GEA) study
  124. Dietary fat and carbohydrate modulate the effect of the ATP-binding cassette A1 (ABCA1) R230C variant on metabolic risk parameters in premenopausal women from the Genetics of Atherosclerotic Disease (GEA) Study
  125. Analysis of HLA-B15 and HLA-B27 in spondyloarthritis with peripheral and axial clinical patterns
  126. C3435T polymorphism of the ABCB1 gene is associated with poor clopidogrel responsiveness in a Mexican population undergoing percutaneous coronary intervention
  127. The interleukin-1β-511 T>C (rs16944) gene polymorphism is associated with risk of developing silent myocardial ischemia in diabetic patients
  128. Monocyte chemoattractant protein-1 gene ( MCP-1 ) polymorphisms are associated with risk of premature coronary artery disease in Mexican patients from the Genetics of Atherosclerotic Disease (GEA) study
  129. MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients
  130. Fatty liver and abdominal fat relationships with high C-reactive protein in adults without coronary heart disease
  131. The C4280A (rs5705) gene polymorphism of the renin (REN) gene is associated with risk of developing coronary artery disease, but not with restenosis after coronary stenting
  132. Functional Polymorphism rs13306560 of the MTHFR Gene Is Associated With Essential Hypertension in a Mexican-Mestizo Population
  133. Epicardial adipose tissue mrna expression of genes coding for proteins related with calcium deposit is related to HDL subclasses in patients with coronary artery disease
  134. Adipose Tissue in Metabolic Syndrome: Onset and Progression of Atherosclerosis
  135. The rs10833 and rs1057972 polymorphisms of the IL-15 gene are associated with subclinical atherosclerosis. Results from the genetic of atherosclerotic disease Mexican study
  136. Atorvastatin and fenofibrate combination induces the predominance of the large HDL subclasses and increased apo AI fractional catabolic rates in New Zealand white rabbits with exogenous hypercholesterolemia
  137. Identification of Copy Number Variations in Isolated Tetralogy of Fallot
  138. Identification of genetic variants in the TNF promoter associated with COPD secondary to tobacco smoking and its severity
  139. HLA Class I and II Blocks Are Associated to Susceptibility, Clinical Subtypes and Autoantibodies in Mexican Systemic Sclerosis (SSc) Patients
  140. Role of adiponectin and free fatty acids on the association between abdominal visceral fat and insulin resistance
  141. Low concentrations of phospholipids and plasma HDL cholesterol subclasses in asymptomatic subjects with high coronary calcium scores
  142. The variant rs8048002 T>C in intron 3 of the MHC2TA gene is associated with risk of developing acute coronary syndrome
  143. The T29C (rs1800470) polymorphism of the transforming growth factor-β1 (TGF-β1) gene is associated with restenosis after coronary stenting in Mexican patients
  144. Hepatic lipase (LIPC) C-514T gene polymorphism is associated with cardiometabolic parameters and cardiovascular risk factors but not with fatty liver in Mexican population
  145. Interleukin-17A Gene Haplotypes Are Associated with Risk of Premature Coronary Artery Disease in Mexican Patients from the Genetics of Atherosclerotic Disease (GEA) Study
  146. Next generation sequencing for molecular confirmation of hereditary sudden cardiac death syndromes
  147. Novel Mutationsin the Transcriptional Activator Domain of the Human TBX20 in Patients with Atrial Septal Defect
  148. Association of the C-type lectin-like domain family-16A (CLEC16A) gene polymorphisms with acute coronary syndrome in Mexican patients
  149. Protective role of DDAH2 (rs805304) gene polymorphism in patients with myocardial infarction
  150. Association of the suppressor of cytokine signaling 1 (SOCS1) gene polymorphisms with acute coronary syndrome in Mexican patients
  151. Síndrome de Andersen-Tawil: una revisión del diagnóstico genético y clínico con énfasis en sus manifestaciones cardíacas
  152. High-resolution HLA analysis of primary and secondary Sjögren’s syndrome: a common immunogenetic background in Mexican patients
  153. Mixtec Mexican Amerindians: an HLA Alleles Study for America Peopling, Pharmacogenomics and Transplantation
  154. Early endothelial nitrosylation and increased abdominal adiposity in Wistar rats after long-term consumption of food fried in canola oil
  155. IL-24 Gene Polymorphisms Are Associated with Cardiometabolic Parameters and Cardiovascular Risk Factors But Not with Premature Coronary Artery Disease: The Genetics of Atherosclerotic Disease Mexican Study
  156. Distribution of ABCB1, CYP3A5, CYP2C19, and P2RY12 gene polymorphisms in a Mexican Mestizos population
  157. Haplotypes of the angiotensin-converting enzyme (ACE) gene are associated with coronary artery disease but not with restenosis after coronary stenting
  158. Angiotensin-1-converting enzyme (ACE) polymorphisms are associated with coronary artery disease but not with restenosis after coronary stenting
  159. Interleukin-33 polymorphisms are associated with premature coronary artery disease and central obesity
  160. TIMP2 gene polymorphisms are associated with hypertension in patients with myocardial infarction
  161. The −974C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients
  162. The HIF1A rs2057482 polymorphism is associated with risk of developing premature coronary artery disease and with some metabolic and cardiovascular risk factors. The Genetics of Atherosclerotic Disease (GEA) Mexican Study
  163. Premature and severe cardiovascular disease in a Mexican male with markedly low high-density-lipoprotein-cholesterol levels and a mutation in the lecithin:cholesterol acyltransferase gene: A family study
  164. INTERLEUKIN-33 POLYMORPHISMS ARE ASSOCIATED WITH PREMATURE CORONARY ARTERY DISEASE AND CENTRAL OBESITY: RESULTS FROM THE GENETICS OF ATHEROSCLEROTIC DISEASE MEXICAN STUDY
  165. Association of the interleukin 15 (IL-15) gene polymorphisms with the risk of developing ulcerative colitis in Mexican individuals
  166. The (G>A) rs11573191 Polymorphism ofPLA2G5Gene Is Associated with Premature Coronary Artery Disease in the Mexican Mestizo Population: The Genetics of Atherosclerotic Disease Mexican Study
  167. The TGF-B1 and IL-10 gene polymorphisms are associated with risk of developing silent myocardial ischemia in the diabetic patients
  168. Value of EQ-5D in Mexican city older population with and without dementia (SADEM study)
  169. Toll-like receptor 4 gene polymorphisms and acute coronary syndrome: No association in a Mexican population
  170. The MHC2TA 1614 C>G gene polymorphism is associated with risk of developing acute coronary syndrome
  171. HLA Class I and Class II Conserved Extended Haplotypes and Their Fragments or Blocks in Mexicans: Implications for the Study of Genetic Diversity in Admixed Populations
  172. Variants in toll-like receptor 9 gene influence susceptibility to tuberculosis in a Mexican population
  173. Single Nucleotide Polymorphisms within LIPA (Lysosomal Acid Lipase A) Gene Are Associated with Susceptibility to Premature Coronary Artery Disease. A Replication in the Genetic of Atherosclerotic Disease (GEA) Mexican Study
  174. The Interleukin-1 Gene Cluster Polymorphisms Are Associated with Takayasu's Arteritis in Mexican Patients
  175. Single Nucleotide Polymorphisms of the Angiotensin-Converting Enzyme (ACE) Gene Are Associated with Essential Hypertension and Increased ACE Enzyme Levels in Mexican Individuals
  176. Corrigendum to “HLA genes in Cubans and the detection of Amerindian alleles” [Mol. Immunol. 44 (March (7)) (2007) 2426–2435]
  177. Normal HDL–apo AI turnover and cholesterol enrichment of HDL subclasses in New Zealand rabbits with partial nephrectomy
  178. LOW CHOLESTEROL AND PHOSPHATIDYLCHOLINE PLASMA CONCENTRATIONS OF HIGH-DENSITY LIPOPROTEINS SUBCLASSES IN SUBJECTS WITH CORONARY CALCIUM SCORE ABOVE THE 75TH PERCENTILE FOR AGE AND GENDER
  179. PROTECTIVE ROLE OF DDAH2 GENE HAPLOTYPES IN PATIENTS WITH MYOCARDIAL INFARCTION
  180. Detecting Polymorphisms in Human Longevity Studies: HLA Typing and SNP Genotyping by Amplicon Sequencing
  181. Genetic polymorphisms of interleukin 20 (IL-20) in patients with ulcerative colitis
  182. Aldosterone synthase gene polymorphism and renal histopathologic changes in kidney transplant patients receiving a calcineurin inhibitor
  183. Shift of high-density lipoprotein size distribution toward large particles in patients with proteinuria
  184. The ABCA1 Gene R230C Variant Is Associated with Decreased Risk of Premature Coronary Artery Disease: The Genetics of Atherosclerotic Disease (GEA) Study
  185. Distribution of theIL-1RN,IL-6,IL-10,INF-γ, andTNF-αGene Polymorphisms in the Mexican Population
  186. The MHC2TA gene polymorphisms are not associated with restenosis after coronary stenting in Mexican patients
  187. The T29C polymorphism of the transforming growth factor-β1 (TGF-β1) gene is associated with genetic susceptibility to acute coronary syndrome in Mexican patients
  188. The Srb1+1050T Allele Is Associated with Metabolic Syndrome in Children but Not with Cholesteryl Ester Plasma Concentrations of High-Density Lipoprotein Subclasses
  189. A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia
  190. The Matrix Metalloproteinase 2-1575 gene Polymorphism is Associated with the Risk of Developing Myocardial Infarction in Mexican Patients
  191. Overweight and obesity as markers for the evaluation of disease risk in older adults
  192. Protective role of interleukin-19 gene polymorphisms in patients with ulcerative colitis
  193. Tumor necrosis factor alpha promoter polymorphisms in Mexican patients with dengue fever
  194. Association of angiotensin II type 1-receptor gene polymorphisms with the risk of developing hypertension in Mexican individuals
  195. Genetic variants associated with severe pneumonia in A/H1N1 influenza infection
  196. Alleles and haplotypes of the interleukin 10 gene polymorphisms are associated with risk of developing acute coronary syndrome in Mexican patients
  197. Interleukin 1 β (IL-1B) and IL-1 Antagonist Receptor (IL-1RN) Gene Polymorphisms are Associated With the Genetic Susceptibility and Steroid Dependence in Patients With Ulcerative Colitis
  198. Lipid plasma concentrations of HDL subclasses determined by enzymatic staining on polyacrylamide electrophoresis gels in children with metabolic syndrome
  199. Human Leukocyte Antigen-DRB1 Class II Genes in Mexican Amerindian Mazahuas: Genes and Languages Do Not Correlate
  200. The Interleukin 6 - 572 G>C (rs1800796) Polymorphism Is Associated with the Risk of Developing Acute Coronary Syndrome
  201. 415 Abnormal Lipid Composition of Hdl Subclasses in Children with Metabolic Syndrome is Independent of Srbi (+1050T/C) and Adiponectin (+45T/G, +246G/T)Polymorphisms.
  202. HLA genes in Wayu Amerindians from Colombia
  203. HLA-Class II Genes in Mexican Amerindian Mayas: Relatedness with Guatemalan Mayans and Other Populations
  204. Depressive symptoms and APOE polymorphisms in an elderly population-based sample
  205. Interleukin 1 receptor antagonist polymorphisms are associated with the risk of developing acute coronary syndrome in Mexicans
  206. PDCD1 gene polymorphisms in different Mexican ethnic groups and their role in the susceptibility to hypersensitivity pneumonitis
  207. Enzymatic assessment of cholesterol on electrophoresis gels for estimating HDL size distribution and plasma concentrations of HDL subclasses
  208. Cost-effective analysis of genotyping using oral cells in the geriatric population
  209. Distribution of HLA Class II Alleles and Haplotypes in Mexican Mestizo Population: Comparison with Other Populations
  210. HLA class I and II polymorphisms in Mexican Mestizo patients with dengue fever
  211. Reduction of serum lipids by soy protein and soluble fiber is not associated with the ABCG5/G8, apolipoprotein E, and apolipoprotein A1 polymorphisms in a group of hyperlipidemic Mexican subjects
  212. Human Leukocyte Antigens I and II Haplotypes Associated With Human Papillomavirus 16-Positive Invasive Cervical Cancer in Mexican Women
  213. Protective KIR–HLA interactions for HCV infection in intravenous drug users
  214. Tumor Necrosis Factor Alpha and Interleukin 10 Promoter Polymorphisms in Mexican Patients with Restenosis After Coronary Stenting
  215. Association of adrenergic receptor gene polymorphisms with different fibromyalgia syndrome domains
  216. Relationship Between the Angiotensin I–Converting Enzyme Insertion/Deletion (I/D) Polymorphism and Cardiovascular Risk Factors in Healthy Young Mexican Women
  217. Rosiglitazone modifies HDL structure and increases HDL-apo AI synthesis and catabolic rates
  218. High resolution human leukocyte antigen (HLA) class I and class II allele typing in Mexican mestizo women with sporadic breast cancer: case-control study
  219. HLA-DR Allele Frequencies in Mexican Mestizos with Autoimmune Liver Diseases Including Overlap Syndromes
  220. Association BetweenIL-1BandIL-1RNGene Polymorphisms and Chagas' Disease Development Susceptibility
  221. Mixomas cardiacos y complejo de Carney
  222. No association found between the insertion/deletion of a 287-bp alu repeat sequence within intron 16 of the angiotensin-I-converting enzyme (ACE) gene in Mexican patients and binary restenosis after coronary stenting
  223. Comparative study of the residues 63 and 67 on the HLA-B molecule in patients with Takayasu's arteritis and tuberculosis
  224. Allelic diversity at the primate MHC-DMB locus: presence of a conserved tyrosine inhibitory motif in the cytoplasmic tail
  225. Genetic admixture and diversity estimations in the Mexican Mestizo population from Mexico City using 15 STR polymorphic markers
  226. Transporter associated with antigen processing (TAP) 1 gene polymorphisms in patients with hypersensitivity pneumonitis
  227. HLA class I and class II haplotypes in admixed families from several regions of Mexico
  228. The interleukin 1B–511 polymorphism is associated with the risk of developing restenosis after coronary stenting in Mexican patients
  229. Apolipoprotein E polymorphisms in Mexican patients with coronary artery disease
  230. MCP-1, RANTES, and SDF-1 polymorphisms in Mexican patients with systemic lupus erythematosus
  231. Prospective meta-analysis of interleukin 1 gene complex polymorphisms confirms associations with ankylosing spondylitis
  232. HLA Genes in Mayos Population from Northeast Mexico
  233. HLA-DRB1*0101 is associated with the genetic susceptibility to develop lichen planus in the Mexican Mestizo population
  234. Association of HLA-DRB1*16 with chronic discoid lupus erythematosus in Mexican mestizo patients
  235. The risk of developing cervical cancer in Mexican women is associated to CYP1A1 MspI polymorphism
  236. Class I and class II major histocompatibility complex genes in Mexican patients with actinic prurigo
  237. Comparison Distribution of HLA-B Alleles in Mexican Patients with Takayasu Arteritis and Tuberculosis
  238. The Arg389Gly β1-adrenergic receptor gene polymorphism and susceptibility to faint during head-up tilt test
  239. HLA-DR association with the genetic susceptibility to develop ashy dermatosis in Mexican Mestizo patients
  240. HLA-E polymorphism in Amerindians from Mexico (Mazatecans), Colombia (Wayu) and Chile (Mapuches): evolution of MHC-E gene
  241. HLA genes in Cubans and the detection of Amerindian alleles
  242. Palmitic acid in HDL is associated to low apo A-I fractional catabolic rates in vivo
  243. HLA-DRB1*08 allele may help to distinguish between type 1 diabetes mellitus and type 2 diabetes mellitus in Mexican children
  244. MHC class II genes in Mexican patients with idiopathic dilated cardiomyopathy
  245. Origin of Mexican Nahuas (Aztecs) according to HLA genes and their relationships with worldwide populations
  246. Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia
  247. Angiotensin-I-converting enzyme (ACE) insertion/deletion polymorphism in Mexican patients with coronary artery disease. Association with the disease but not with lipid levels
  248. Tumor Necrosis Factor-α Promoter Polymorphisms in Mexican Patients With Spondyloarthritis
  249. β1-adrenergic receptor gene polymorphisms in Mexican patients with idiopathic dilated cardiomyopathy
  250. Low grade radiographic sacroiliitis as prognostic factor in patients with undifferentiated spondyloarthritis fulfilling diagnostic criteria for ankylosing spondylitis throughout follow up
  251. HLA genes in Mexican Teeneks: HLA genetic relationship with other worldwide populations
  252. Distribution of paraoxonase PON1 gene polymorphisms in Mexican populations. Its role in the lipid profile
  253. Role of the HLA-DQ locus in the development of chronic gastritis and gastric carcinoma in Mexican patients
  254. Tumor necrosis factor-alpha promoter polymorphism in Mexican patients with Chagas’ disease
  255. Tumor necrosis factor-alpha −308 promoter polymorphism contributes independently to HLA alleles in the severity of rheumatoid arthritis in Mexicans
  256. Comparative study of the residues 63 and 67 on the HLA-B molecule in patients with Takayasu's Arteritis
  257. Cytochrome P4501A1 polymorphisms in the Amerindian and Mestizo populations of Mexico
  258. Matrix γ-Carboxyglutamic Acid Protein (MGP) G-7A and T-138C Gene Polymorphisms in Indian (Mayo and Teenek) and Mestizo Populations from Mexico
  259. β 1 Adrenergic Receptor Polymorphisms Arg389Gly and Ser49Gly in the Amerindian and Mestizo Populations of Mexico
  260. Association study of LMP gene polymorphisms in Mexican patients with spondyloarthritis
  261. HLA-DQA1, -DQB1 and -DRB1 alleles in Mazatecan population from Mexico
  262. Polymorphisms in the promoter region of tumor necrosis factor alpha (TNF-α) and the HLA-DRB1 locus in Mexican Mestizo patients with ulcerative colitis
  263. Different evolutionary pathway of B*570101 and B*5801 ( B17 group) alleles based in intron sequences
  264. HLA-DRB1 alleles encoding the “shared epitope” are associated with susceptibility to developing rheumatoid arthritis whereas HLA-DRB1 alleles encoding an aspartic acid at position 70 of the β-chain are protective in Mexican mestizos
  265. MHC class I and class II genes in mexican patients with Chagas disease
  266. MHC class II alleles in Mexican patients with rheumatic heart disease
  267. HLA class II genotypes in Mexican Mestizo patients with myasthenia gravis
  268. Tumor necrosis factor-alpha promoter polymorphisms in Mexican patients with rheumatic heart disease
  269. Distribution of HLA-B alleles in Mexican Amerindian populations
  270. Familial collapsing glomerulopathy: Clinical, pathological and immunogenetic features
  271. Angiotensin-Converting Enzyme Gene (ACE) Insertion/Deletion Polymorphism in Mexican Populations
  272. Clinical and genetic heterogeneity in Mexican patients with ulcerative colitis
  273. Endothelial Nitric Oxide Synthase Gene Polymorphism in the Indian and Mestizo Populations of Mexico
  274. HLA-DR antigen frequencies in Mexican patients with dengue virus infection: HLA-DR4 as a possible genetic resistance factor for dengue hemorrhagic fever
  275. LMP2 and LMP7 gene polymorphism in Mexican populations: Mestizos and Amerindians
  276. Effect of HLA-B and HLA-DR genes on susceptibility to and severity of spondyloarthropathies in Mexican patients
  277. Distribution of class I and class III MHC antigens in the Tarasco Amerindians
  278. HLA Study on Two Mexican Mestizo Families with Autoimmune Thyroid Disease
  279. Heat shock protein 70 gene polymorphisms in Mexican patients with spondyloarthropathies
  280. rpoB Gene Mutations in Rifampin-Resistant Mycobacterium tuberculosis Identified by Polymerase Chain Reaction Single-Stranded Conformational Polymorphism
  281. Tumor necrosis factor-α promoter polymorphisms in Mexican patients with systemic lupus erythematosus (SLE)
  282. Class II allele and haplotype frequencies in Mexican systemic lupus erythematosus patients: the relevance of considering homologous chromosomes in determining susceptibility
  283. Polymorphism and distribution of HLA-DR2 alleles in Mexican populations
  284. Influence of the Apolipoprotein E Polymorphism on Plasma Lipoproteins in a Mexican Population
  285. HLA genes in Mexican Mazatecans, the peopling of the Americas and the uniqueness of Amerindians
  286. DNA sequencing of HLA-B alleles in Mexican patients with Takayasu arteritis
  287. Lack of association between the polymorphism at the heat-shock protein (HSP70-2) gene and systemic lupus erythematosus (SLE) in the Mexican Mestizo population
  288. HLA-DR4 allele frequencies on Indian and Mestizo population from Mexico
  289. HLA-DRB and HLA-DQB loci in the genetic susceptibility to develop glaucoma in Mexicans
  290. Heat-shock protein (HSP70-2) allelic frequencies in three distinct Mexican populations
  291. Genetic features of Mexican women predisposing to cancer of the uterine cervix
  292. Evolutionary relationships between HLA‐B alleles as indicated by an analysis of intron sequences
  293. Intron 2 and exon 3 sequences of HLA-B alleles may be involved in the susceptibility to develop Takayasu arteritis
  294. Complotype SC30 Is Associated With Susceptibility to Develop Ulcerative Colitis in Mexicans
  295. Primate Mhc-E and -G alleles
  296. Haplotype Distribution of Class II MHC Genes in Mexican Patients with Systemic Lupus Erythematosus
  297. HLA-DR7 in Association with Chlorpromazine-induced Lupus Anticoagulant (LA)
  298. Generation of the HLA-B35, -B5, -B16, and B15 groups of alleles studied by intron 1 and 2 sequence analysis
  299. Description of HLA - A * 6803 and A * 68N in Mazatecan Indians from Mexico
  300. Primate Mhc-E and -G alleles
  301. Description of a new HLA-B40 allele (B * 4011) found in a Mexican individual of Nahua (Aztec) descent
  302. Further evidence of the role of HLA-DR4 in the genetic susceptibility to actinic prurigo
  303. Differences in intron 2 sequences between B * 39061 and B * 39062 in Amerindians: comparison with those of B * 3901, B * 5101, and B * 52012 alleles
  304. Description of a New HLA-E (E∗01031) Allele and Its Frequency in the Spanish Population
  305. High polymorphism of Mhc-E locus in non-human primates: alleles with identical exon 2 and 3 are found in two different species
  306. Frequencies of HLA-A and HLA-B alleles in a Mexico City mestizo sample
  307. Relationship of anticardiolipin antibodies and antiphospholipid syndrome to HLA-DR7 in Mexican patients with systemic lupus erythematosus (SLE)
  308. A new sequence (Mhc-BJ ) showing similarity both to Mhc-B alleles and to the HLA-J pseudogene in Macaca mulatta
  309. HLA-DR6 (possibly DRB1*1301) is associated with susceptibility to Takayasu arteritis in Mexicans
  310. A novel HLA-B35 (B*3517) allele found in a Mexican of Otomi descent
  311. The role of HLA-DR alleles and complotypes through the ethnic barrier in systemic lupus erythematosus in Mexicans
  312. An HLA class I PCR-SSP typing study in Caucasoid Siberians
  313. A new HLA-B35 (B * 3516) allele found in a Mexican of Nahua (Aztec) descent
  314. Description of a novel HLA-B35 (B∗3514) allele found in a mexican family of Nahua Aztec descent
  315. HLA DR and DQ polymorphism in Ashkenazi and non‐Ashkenazi Jews: comparison with other Mediterraneans
  316. A newHLA-B35 (B * 3516) allele found in a Mexican of Nahua (Aztec) descent
  317. Independent Associations of the HLA-B27 Antigen and the Complement Haplotype SC21 in Chronic Anterior Uveitis
  318. Association of hla–dr5 (possibly drb1*1201) with the primary antiphospholipid syndrome in mexican patients
  319. Immunogenetic Aspects in Primary Open-angle Glaucoma in Family Members of Mexican Mestizo Glaucomatous Patients
  320. HLA-B alleles and complotypes in Mexican patients with seronegative spondyloarthropathies.