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MeSH:(NADPH Oxidases/genetics*)

1.DUOX2 mutations in children with congenital hypothyroidism.

Jian CHAI ; Xiao-Long YANG ; Ming-Zhen GUO ; Lu LIU ; Shi-Guo LIU ; Sheng-Li YAN ; Yin-Lin GE

Chinese Journal of Contemporary Pediatrics 2015;17(1):40-44

2.DUOX2 gene mutation in patients with congenital goiter with hypothyroidism.

Zhi-ping LÜ ; Gui-hua LI ; Wen-jie LI ; Shi-guo LIU

Chinese Journal of Pediatrics 2011;49(12):943-946

3.Progress in the studies on the relationship between the polymorphism of P22phox gene and coronary heart disease.

Jian-gong ZHAO ; Dong-feng GU

Acta Academiae Medicinae Sinicae 2002;24(1):105-104

4.Expression of NADPH oxidase and production of reactive oxygen species in aorta in an active immunization mouse model with AT1-EC2 peptide.

Yumiao WEI ; Yaoqi CHEN ; Zhi LI ; Wenping ZHOU ; Yuanyuan LV ; Zihua ZHOU ; Xiang CHENG ; Yuhua LIAO

Journal of Huazhong University of Science and Technology (Medical Sciences) 2012;32(4):490-494

5.The role and mechanism of NADPH oxidase in leptin-induced reactive oxygen species production in hepatic stellate cells.

Wen-hua HE ; Bo LI ; Xuan ZHU ; Kun-he ZHANG ; Bi-min LI ; Zhi-jian LIU ; Ge-yun LIU ; Jian WANG

Chinese Journal of Hepatology 2010;18(11):849-854

6.Relationship between expression of endothelial nitric oxide synthase and NADPH oxidase in lungs of mice exposed to chronic hypoxia.

Xi-Ling WU ; Li-Zhong DU ; Xue-Feng XU

Chinese Journal of Contemporary Pediatrics 2015;17(9):1001-1006

7.Correlation between neutrophil cytosolic factor 1 gene C923T polymorphism and cerebral hemorrhage in the Han in Changsha.

Xiaosong HUANG ; Qidong YANG

Journal of Central South University(Medical Sciences) 2011;36(4):301-306

8.Association of nicotinamide adenine dinucleotide phosphate oxidase p22phox gene 549C>T polymorphism with coronary artery disease.

Tong-tao LIU ; Li-li WANG ; Sheng-xia FANG ; Chong-qi JIA

Chinese Medical Journal 2012;125(8):1416-1419

9.Pioglitazone inhibits the expression of nicotinamide adenine dinucleotide phosphate oxidase and p38 mitogen-activated protein kinase in rat mesangial cells.

Shan WANG ; Shan-Dong YE ; Wen-Jia SUN ; Yuan-Yuan HU

Chinese Medical Journal 2013;126(21):4054-4059

10.Clinical features and molecular analysis of 2 Chinese children with autosomal recessive chronic granulomatous disease caused by CYBA mutations.

Jian-xin HE ; Shun-ying ZHAO ; Bao-ping XU ; Ying-hui HU ; Kun-ling SHEN ; Zai-fang JIANG

Chinese Journal of Pediatrics 2011;49(11):853-857

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