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S. M. Ren, Yang, G. L., Liu, C. Z., Zhang, C. X., Shou, Q. H., Yu, S. F., Li, W. C., and Su, X. L., Association between HLA-A and -B polymorphisms and susceptibility to Henoch-Schönlein purpura in Han and Mongolian children from Inner Mongolia, vol. 11, pp. 221-228, 2012.
Amoli MM, Thomson W, Hajeer AH, Calvino MC, et al. (2002). HLA-B35 association with nephritis in Henoch-Schonlein purpura. J. Rheumatol. 29: 948-949. PMid:12022355 Fan YL, Xia GQ, Cao LF, Jie J, et al. (2006). MHC-II (DQ) gene polymorphism and Henoch-Schöenlein purpura. Hei Long Jiang Med. J. 30: 94-96. Flomenberg N, Baxter-Lowe LA, Confer D, Fernandez-Vina M, et al. (2004). Impact of HLA class I and class II high-resolution matching on outcomes of unrelated donor bone marrow transplantation: HLA-C mismatching is associated with a strong adverse effect on transplantation outcome. Blood 104: 1923-1930. PMid:15191952 Hughes EH, Collins RW, Kondeatis E, Wallace GR, et al. (2005). Associations of major histocompatibility complex class I chain-related molecule polymorphisms with Behcet’s disease in Caucasian patients. Tissue Antigens 66: 195-199. PMid:16101830 Kawasaki K, Komura H, Nakahara Y, Shiraishi M, et al. (2006). Factor XIII in Henoch-Schönlein purpura with isolated gastrointestinal symptoms. Pediatr. Int. 48: 413-415. PMid:16911090 Liu Y, Sun LW, Li LH, Zhao YL, et al. (2008). Analysis of relevance between Henoch-Schöenlein purpura and HLA-DRB1 in children. Chin. J. Lab. Diagnosis 12: 1375-1377. Luo JM, Sun WB, Huang XG, Li WH, et al. (2008). Correlation between the HLA-A, B alleles polymorphism and hemorrhagic fever with renal syndrome of Han nationality in Zunyi area. Chin. J. Microbiol. Immunol. 24: 430-435. Ozen S, Ruperto N, Dillon MJ, Bagga A, et al. (2006). EULAR/PReS endorsed consensus criteria for the classification of childhood vasculitides. Ann. Rheum. Dis. 65: 936-941. PMid:16322081    PMCid:1798210 Peru H, Soylemezoglu O, Gonen S, Cetinyurek A, et al. (2008). HLA class 1 associations in Henoch Schönlein purpura: increased and decreased frequencies. Clin. Rheumatol. 27: 5-10. PMid:17487448 Ren SM, Yang GL, Tong LH, Yu HL, et al. (2003). Association between clinical characteristics and HLA-DRB1 in Mongolian and Han children with Henoch-Schönlein purpura. Chin. J. Rheumatol. 7: 469-473. Shen CM, Zhu BF and Li SB (2008). Analysis of gene polymorphism of HLA-A, B, DRB1 of Mongolian in Inner Mongolia. Hereditas 30: 164-168. PMid:18244920 Shin JI, Park JM, Shin YH, Hwang DH, et al. (2006). Predictive factors for nephritis, relapse, and significant proteinuria in childhood Henoch-Schönlein purpura. Scand. J. Rheumatol. 35: 56-60. PMid:16467044 Soylemezoglu O, Peru H, Gonen S, Cetinyurek A, et al. (2008a). CTLA-4 +49 A/G genotype and HLA-DRB1 polymorphisms in Turkish patients with Henoch-Schönlein purpura. Pediatr. Nephrol. 23: 1239-1244. PMid:18449568 Soylemezoglu O, Peru H, Gonen S, Cetinyurek A, et al. (2008b). HLA-DRB1 alleles and Henoch-Schönlein purpura: susceptibility and severity of disease. J. Rheumatol. 35: 1165-1168. PMid:18412308 Sun YP, Song CX, Li SL, Gao XJ, et al. (1984). Comparative study of Chinese human leucocyte antigen. Chin. J. Microbiol. Immunol. 4: 205-211. Volz A, Boyle JM, Cann HM, Cottingham RW, et al. (1994). Report of the second international workshop on human chromosome 6. Genomics 21: 464-472. PMid:8088851 Xu SB, Tao YF, Huang XQ, Chu ZT, et al. (2004). Polymorphism of HLA-DRB1 in Han population in Yunnan and comparison with 9 Han populations. Yi Chuan 26: 787-792. PMid:15640103 Yan CX, Song YP, Lai SP, Lai JH, et al. (2002). Research on HLA-A polymorphism of Chinese Han and Uighur nationality by PCR-SSOP. J. Genet. Genomics 29: 384-389. Yang GL, Ren SM, Shou QH, Su XL, et al. (2007). Susceptibility of HLA-A, B gene to Henoch-Schöenlein purpura in children. Chin. Clin. Med. 23: 850-853. Zhang HB, Gao F, Kang LL and Li SB (2005). Polymorphism of HLA-A, B, DRB1 of Menba population in Tibet. Chin. J. Med. Genet. 22: 344-346.
L. P. Wang, Zhao, L. R., Cui, H. W., Yan, M. R., Yang, L., and Su, X. L., Association between PPARγ2 Pro12Ala polymorphism and myocardial infarction and obesity in Han Chinese in Hohhot, China, vol. 11, pp. 2929-2938, 2012.
Akiyama TE, Sakai S, Lambert G, Nicol CJ, et al. (2002). Conditional disruption of the peroxisome proliferator-activated receptor gamma gene in mice results in lowered expression of ABCA1, ABCG1, and apoE in macrophages and reduced cholesterol efflux. Mol. Cell Biol. 22: 2607-2619. PMid:11909955 PMCid:133709   Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, et al. (2000). The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat. Genet. 26: 76-80. PMid:10973253   Beamer BA, Yen CJ, Andersen RE, Muller D, et al. (1998). Association of the Pro12Ala variant in the peroxisome proliferator-activated receptor-gamma2 gene with obesity in two Caucasian populations. Diabetes 47: 1806-1808. PMid:9792554   Black MH, Fingerlin TE, Allayee H, Zhang W, et al. (2008). Evidence of interaction between PPARG2 and HNF4A contributing to variation in insulin sensitivity in Mexican Americans. Diabetes 57: 1048-1056. 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Relations between metabolic syndrome, oxidative stress and inflammation and cardiovascular disease. Verh. K. Acad. Geneeskd. Belg. 70: 193-219. PMid:18669160   Hsueh WA and Bruemmer D (2004). Peroxisome proliferator-activated receptor gamma: implications for cardiovascular disease. Hypertension 43: 297-305. PMid:14732733   Hu Q, Zhang XJ, Liu CX, Wang XP, et al. (2010). PPARgamma1-induced caveolin-1 enhances cholesterol efflux and attenuates atherosclerosis in apolipoprotein E-deficient mice. J. Vasc. Res. 47: 69-79. PMid:19729954   Issemann I and Green S (1990). Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators. Nature 347: 645-650. PMid:2129546   Iwai M, Kanno H, Senba I, Nakaoka H, et al. (2011). Irbesartan increased PPARgamma activity in vivo in white adipose tissue of atherosclerotic mice and improved adipose tissue dysfunction. Biochem. Biophys. Res. Commun. 406: 123-126. PMid:21296052   Ji Y, Liu J, Wang Z, Liu N, et al. (2009). PPARgamma agonist, rosiglitazone, regulates angiotensin II-induced vascular inflammation through the TLR4-dependent signaling pathway. Lab. Invest. 89: 887-902. PMid:19451898   Kagawa Y, Yanagisawa Y, Hasegawa K, Suzuki H, et al. (2002). Single nucleotide polymorphisms of thrifty genes for energy metabolism: evolutionary origins and prospects for intervention to prevent obesity-related diseases. Biochem. Biophys. Res. Commun. 295: 207-222.   Kim KS, Choi SM, Shin SU, Yang HS, et al. (2004). Effects of peroxisome proliferator-activated receptor-gamma 2 Pro12Ala polymorphism on body fat distribution in female Korean subjects. Metabolism 53: 1538-1543. PMid:15562396   Kolehmainen M, Uusitupa MI, Alhava E, Laakso M, et al. (2003). Effect of the Pro12Ala polymorphism in the peroxisome proliferator-activated receptor (PPAR) gamma2 gene on the expression of PPARgamma target genes in adipose tissue of massively obese subjects. J. Clin. Endocrinol. Metab. 88: 1717-1722. 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PMid:10702770   Miyazaki Y, Mahankali A, Matsuda M, Glass L, et al. (2001). Improved glycemic control and enhanced insulin sensitivity in type 2 diabetic subjects treated with pioglitazone. Diabetes Care 24: 710-719. PMid:11315836   Moran CS, Cullen B, Campbell JH and Golledge J (2009). Interaction between angiotensin II, osteoprotegerin, and peroxisome proliferator-activated receptor-gamma in abdominal aortic aneurysm. J. Vasc. Res. 46: 209-217. PMid:18931513   Mori H, Ikegami H, Kawaguchi Y, Seino S, et al. (2001). The Pro12 →Ala substitution in PPAR-gamma is associated with resistance to development of diabetes in the general population: possible involvement in impairment of insulin secretion in individuals with type 2 diabetes. Diabetes 50: 891-894. PMid:11289058   Mori Y, Kim-Motoyama H, Katakura T, Yasuda K, et al. (1998). Effect of the Pro12Ala variant of the human peroxisome proliferator-activated receptor gamma 2 gene on adiposity, fat distribution, and insulin sensitivity in Japanese men. Biochem. Biophys. Res. Commun. 251: 195-198. PMid:9790929   Pan XF, Song XB, Wang LL, Li LX, et al. (2009). Association of the Pro12Ala polymorphism in peroxisome proliferators activated receptor-gamma gene with rheumatoid arthritis in Sichuan Province of China. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 26: 87-90. PMid:19199260   Ren Y, Sun C, Sun Y, Tan H, et al. (2009). PPAR gamma protects cardiomyocytes against oxidative stress and apoptosis via Bcl-2 upregulation. Vascul. Pharmacol. 51: 169-174. PMid:19540934   Ridker PM, Cook NR, Cheng S, Erlich HA, et al. (2003). Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction. Arterioscler. Thromb. Vasc. Biol. 23: 859-863. PMid:12663371   Rose GA and Blackburn H (1982). Cardiovascular Survey Methods. World Health Organization. WHO Monograph Series, Geneva.   Schaffler A, Barth N, Schmitz G, Zietz B, et al. (2001). Frequency and significance of Pro12Ala and Pro115Gln polymorphism in gene for peroxisome proliferation-activated receptor-gamma regarding metabolic parameters in a Caucasian cohort. Endocrine. 14: 369-373.   Stefanski A, Majkowska L, Ciechanowicz A, Frankow M, et al. (2006). Lack of association between the Pro12Ala polymorphism in PPAR-gamma2 gene and body weight changes, insulin resistance and chronic diabetic complications in obese patients with type 2 diabetes. Arch. Med. Res. 37: 736-743. PMid:16824933   Tamori Y, Masugi J, Nishino N and Kasuga M (2002). Role of peroxisome proliferator-activated receptor-gamma in maintenance of the characteristics of mature 3T3-L1 adipocytes. Diabetes 51: 2045-2055. PMid:12086932   Tavares V, Hirata RD, Rodrigues AC, Monte O, et al. (2005). Association between Pro12Ala polymorphism of the PPAR-gamma2 gene and insulin sensitivity in Brazilian patients with type-2 diabetes mellitus. Diabetes Obes. Metab. 7: 605-611. PMid:16050954   Wang G, Wei J, Guan Y, Jin N, et al. (2005). Peroxisome proliferator-activated receptor-gamma agonist rosiglitazone reduces clinical inflammatory responses in type 2 diabetes with coronary artery disease after coronary angioplasty. Metabolism 54: 590-597. PMid:15877288   Wei Q, Jacobs DR, Jr., Schreiner PJ, Siscovick DS, et al. (2006). Patterns of association between PPARgamma genetic variation and indices of adiposity and insulin action in African-Americans and whites: the CARDIA Study. J. Mol. Med. 84: 955-965. PMid:16955276   Yamamoto Y, Hirose H, Miyashita K, Nishikai K, et al. (2002). PPAR(gamma)2 gene Pro12Ala polymorphism may influence serum level of an adipocyte-derived protein, adiponectin, in the Japanese population. Metabolism 51: 1407- 1409. PMid:12404189   Yen CJ, Beamer BA, Negri C, Silver K, et al. (1997). Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation. Biochem. Biophys. Res. Commun. 241: 270-274. PMid:9425261   Zafarmand MH, van der Schouw YT, Grobbee DE, de Leeuw PW, et al. (2008). Peroxisome proliferator-activated receptor gamma-2 P12A polymorphism and risk of acute myocardial infarction, coronary heart disease and ischemic stroke: a case-cohort study and meta-analyses. Vasc. Health Risk Manag. 4: 427-436. PMid:18561518 PMCid:2496990
T. Hasi, Hao, L., Yang, L., and Su, X. L., Acetaldehyde dehydrogenase 2 SNP rs671 and susceptibility to essential hypertension in Mongolians: a case control study, vol. 10, pp. 537-543, 2011.
Amamoto K, Okamura T, Tamaki S, Kita Y, et al. (2002). Epidemiologic study of the association of low-Km mitochondrial acetaldehyde dehydrogenase genotypes with blood pressure level and the prevalence of hypertension in a general population. Hypertens. Res. 25: 857-864. PMid:12484509   Beilin LJ (1995). Alcohol, hypertension and cardiovascular disease. J. Hypertens. 13: 939-942. PMid:8586827   Chen WJ, Loh EW, Hsu YP and Cheng AT (1997). Alcohol dehydrogenase and aldehyde dehydrogenase genotypes and alcoholism among Taiwanese aborigines. Biol. Psychiatry 41: 703-709.   Chen CC, Lu RB, Chen YC, Wang MF, et al. (1999). Interaction between the functional polymorphisms of the alcohol-metabolism genes in protection against alcoholism. Am. J. Hum. Genet. 65: 795-807. PMid:10441588 PMCid:1377988   Chen L, Davey SG, Harbord RM and Lewis SJ (2008). Alcohol intake and blood pressure: a systematic review implementing a Mendelian randomization approach. PLoS. Med. 5: e52. PMid:18318597 PMCid:2265305   Ferguson RA and Goldberg DM (1997). Genetic markers of alcohol abuse. Clin. Chim. Acta 257: 199-250.   Hui P, Nakayama T, Morita A, Sato N, et al. (2007). Common single nucleotide polymorphisms in Japanese patients with essential hypertension: aldehyde dehydrogenase 2 gene as a risk factor independent of alcohol consumption. Hypertens. Res. 30: 585-592. PMid:17785925   Itoh T, Matsumoto M, Nakamura M, Okada A, et al. (1997). Effects of daily alcohol intake on the blood pressure differ depending on an individual's sensitivity to alcohol: oriental flushing as a sign to stop drinking for health reasons. J. Hypertens. 15: 1211-1217. PMid:9383169   Minami J, Todoroki M, Ishimitsu T, Yamamoto H, et al. (2002). Effects of alcohol intake on ambulatory blood pressure, heart rate, and heart rate variability in Japanese men with different ALDH2 genotypes. J. Hum. Hypertens. 16: 345-351. PMid:12082496   Morimoto K and Takeshita T (1996). Low Km aldehyde dehydrogenase (ALDH2) polymorphism, alcohol-drinking behavior, and chromosome alterations in peripheral lymphocytes. Environ. Health Perspect. 104 (Suppl 3): 563-567. PMid:8781384 PMCid:1469639   Nishiyori A, Shibata A, Ogimoto I, Uchimura N, et al. (2005). Alcohol drinking frequency is more directly associated with alcohol use disorder than alcohol metabolizing enzymes among male Japanese. Psychiatry Clin. Neurosci. 59: 38-44. PMid:15679538   Saito K, Yokoyama T, Yoshiike N, Date C, et al. (2003). Do the ethanol metabolizing enzymes modify the relationship between alcohol consumption and blood pressure? J. Hypertens. 21: 1097-1105. PMid:12777946   Takagi S, Baba S, Iwai N, Fukuda M, et al. (2001). The aldehyde dehydrogenase 2 gene is a risk factor for hypertension in Japanese but does not alter the sensitivity to pressor effects of alcohol: the Suita study. Hypertens. Res. 24: 365-370. PMid:11510748   Tsuchihashi-Makaya M, Serizawa M, Yanai K, Katsuya T, et al. (2009). Gene-environmental interaction regarding alcohol-metabolizing enzymes in the Japanese general population. Hypertens. Res. 32: 207-213. PMid:19262484   Wang D (2005). Report on Nutrition and Health Survey of Chinese, 2002 Comprehensive Report. People's Medical Publishing House, Beijing,   Yamamoto K, Ueno Y, Mizoi Y and Tatsuno Y (1993). Genetic polymorphism of alcohol and aldehyde dehydrogenase and the effects on alcohol metabolism. Arukoru Kenkyu to Yakubutsu Izon 28: 13-25. PMid:8512495
X. L. Su, Dong, H. R., Yan, M. R., Cui, H. W., Yang, L., and Han, F. Q., Association between peroxisome proliferator-activated receptor gamma coactivator-1 alpha polymorphism and hypertension in Mongolians in Inner Mongolia, vol. 10, pp. 3930-3936, 2011.
Andersen G, Wegner L, Jensen DP, Glumer C, et al. (2005). PGC-1alpha Gly482Ser polymorphism associates with hypertension among Danish whites. Hypertension 45: 565-570. PMid:15738346   Bhat A, Koul A, Rai E, Sharma S, et al. (2007). PGC-1alpha Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study. Hum. Genet. 121: 609-614. PMid:17390150   Chen S, Yan W, Huang J, Yang W, et al. (2004). Peroxisome proliferator-activated receptor-gamma coactivator-1alpha polymorphism is not associated with essential hypertension and type 2 diabetes mellitus in Chinese population. Hypertens. Res. 27: 813-820. PMid:15824463   Ek J, Andersen G, Urhammer SA, Gaede PH, et al. (2001). Mutation analysis of peroxisome proliferator-activated receptor-gamma coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus. Diabetologia 44: 2220-2226. 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Epigenetic regulation of PPARGC1A in human type 2 diabetic islets and effect on insulin secretion. Diabetologia 51: 615-622. PMid:18270681 PMCid:2270364   Michael LF, Wu Z, Cheatham RB, Puigserver P, et al. (2001). Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1. Proc. Natl. Acad. Sci. U. S. A. 98: 3820-3825. PMid:11274399 PMCid:31136   Muller YL, Bogardus C, Pedersen O and Baier L (2003). A Gly482Ser missense mutation in the peroxisome proliferator-activated receptor gamma coactivator-1 is associated with altered lipid oxidation and early insulin secretion in Pima Indians. Diabetes 52: 895-898. PMid:12606537   Nelson TL, Fingerlin TE, Moss L, Barmada MM, et al. (2007). The peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene (PGC-1alpha) is not associated with type 2 diabetes mellitus or body mass index among Hispanic and non Hispanic Whites from Colorado. Exp. Clin. Endocrinol. 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P. Y. Chang, Zhao, L. G., and Su, X. L., Association of TSC gene variants and hypertension in Mongolian and Han populations, vol. 10, pp. 902-909, 2011.
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