EPHX1 Antibody

1. The substrate specificity of microsomal epoxide hydrolase should therefore be expanded to include not only epoxides but also the oxetanyl ring system present in AZD1979. PMID: 27256986
2. EPHX1 variants were significantly associated with higher metabolic ratio of carbamazepine PMID: 27276192
3. Single nucleotide polymorphisms in EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population. PMID: 27193053
4. This study showed that polymorphisms of EPHX1 and VKORC1L1 could be determinants of stable warfarin doses. PMID: 29054760
5. The Tyr113His T/C variant of rs1051740 and very slow phenotype alters EPHX1, miR-26b-5p and miR-1207-5p expression, and contributes towards low blood iron levels and low birthweights. PMID: 28789952
6. Structural characterization of human microsomal epoxide hydrolase by combined homology modeling, molecular dynamics simulations, and molecular docking calculations has been reported. PMID: 28120429
7. Y113H polymorphism in EPHX1 gene contributed to increased susceptibility to COPD in the Kazakhstan population. PMID: 28464990
8. EPHX1 polymorphisms were not associated with sporadic colorectal neoplasms. PMID: 28018104
9. This study demonstrated that two SNPs might play roles in the process of nicotine metabolism and abstinence, rs1051740 being more important; and EPHX SNPs (rs1051740 and rs2234922) are associated with the effectiveness of Nicotine Replacement Therapy . PMID: 27783326
10. No association was found between EPHX1 and COPD; however, a minor effect of EPHX1 on COPD risk was not completely excluded. PMID: 27173271
11. The SCN1A IVS5-91G>A SNP is associated with susceptibility to epilepsy. SNPs in EPHX1 gene are influencing CBZ metabolism and disposition PMID: 26555147
12. In conclusion, GSTs, EPHX1, and XPD are potential genetic factors for arsenic-induced skin cancers. The roles of these genes for arsenic-induced skin carcinogenesis need to be further evaluated. PMID: 26295053
13. the EPHX1 Tyr113His polymorphism may be a risk factor for lung cancer in Asians, whereas it may be a decreased risk factor among Caucasians. However, this polymorphism was not found to be associated with breast cancer. PMID: 25222243
14. To be poly(ADP-ribose)polymerase-1 (PARP-1) bound to the EPHX1 proximal promoter. PMID: 25992604
15. Polymorphism in the EPHX1 gene may have a significant role in differential responses to treatment with N-acetylcysteine in patients with COPD. PMID: 25999707
16. This review and meta-analysis suggests that EPHX1 Tyr113His polymorphism may be a risk factor for Head and Neck Cancer, while the EPHX1 His139Arg polymorphism has no association with Head and Neck Cancer risk. PMID: 25923690
17. Studies suggest that the presence of microsomal epoxide hydrolase 1 (EPHX1) single nucleotide polymorphisms (SNPs) may significantly affect the risk of lung, upper aerodigestive tract, breast, bladder, and ovarian carcinomas. PMID: 26216302
18. the genetic associations exist between mEH polymorphisms and lung cancer susceptibility in Asian populations PMID: 25312477
19. These results demonstrate that 2-AG is an endogenous substrate for EPHX1, a potential role of EPHX1 in the endocannabinoid signaling and a new AA biosynthetic pathway. PMID: 24958911
20. EPHX1 rs2292566 polymorphism may affect the maintenance dose of warfarin in Caucasians. PMID: 25629049
21. His/His genotype of EPHX1 Tyr113His polymorphism is a risk factor for developing caner for Asian and mixed population, while no evidence was found for the association between the EPHX1 His139Arg polymorphism and increased cancer risk. PMID: 25261893
22. EPHX1 Tyr113His and His139Arg polymorphism are not associated with esophageal cancer risk. PMID: 25714851
23. This meta-analysis suggests that EPHX1 Tyr113His polymorphism contributes to HCC risk. PMID: 26065263
24. No clear effect is evident for EPHX1 polymorphisms for different radon concentrations on the risk of lung cancer. PMID: 24852519
25. Review/Meta-analysis: suggest p.Tyr113His and p.His139Arg polymorphisms in EPHX1 may not be associated with esophageal cancer development. PMID: 24803829
26. This study provides direct evidence that methylation plays an important role in PCOS and demonstrates a novel role for EPHX1 in female reproduction. PMID: 24505354
27. Meta-analysis showed that the Tyr113His polymorphism was a stronger power trend towards risk for esophageal cancer using a recessive model PMID: 24615030
28. The association of EPHX1 polymorphism with the HELLP syndrome and eclampsia may hint to EPHX being a further key player in the pathogenesis of preeclampsia. PMID: 24013430
29. Results suggest that Exons 3 and 4 polymorphisms of the mEH gene may contribute to lung cancer susceptibility through disturbed antioxidant balance. PMID: 23928928
30. The C allele and C-G diplotype of EPHX1 may play important roles in increasing the risk of CBZ-SJS/toxic epidermal necrolysis development of epilepsy in Chinese Han patients. PMID: 24861996
31. Chinese epilepsy patients with variant EPHX1 c.416A>G genotype have higher plasma carbamazepine concentrations compared to those with the wild type genotype. PMID: 24125961
32. No evidence of an association of EPHX1 Tyr113His or His139Arg polymorphisms with risk for development of esophageal cancer. [Meta-analysis] PMID: 24222229
33. EPHX1 genetic polymorphisms were not associated with the risk of HCC. PMID: 23955801
34. The study showed that microsomal epoxide hydrolase exon 3 113Tyr-139Arg was associated with gastric cancer in presence of H. pylori, though in its absence, it appeared to be protective. PMID: 23580125
35. Sp1 and Sp3 are functionally involved as transcriptional integrators regulating the basal expression of the derived microsomal epoxide hydrolase E1b variant transcript. PMID: 24315822
36. Genotype frequencies for EPHX1 polymorphisms did not show any correlation with lymphoma. PMID: 23651475
37. This meta-analysis suggests that EPHX1 His139Arg polymorphism is associated with decreased risk of esophageal cancer in Caucasians. PMID: 23681797
38. There is substantial evidence that mEH polymorphisms interact synergistically with other genes and the environment to modulate risk of HCC PMID: 23451147
39. findings suggest that benzene exposure may be associated with hypermethylation in ERCC3, and that genetic variants in EPHX1 may play an important role in epigenetic changes and hematotoxicity among benzene-exposed workers PMID: 23797950
40. This is the first report that examined HIF1A polymorphisms in chronic obstructive pulmonary disease and demonstrated a possible role of HIF-1alpha in COPD, as well as GSTP1 and EPHX1. PMID: 21651746
41. EPHX1 transcript, termed E1-b', drives EPHX1 expression primarily in the ovary. PMID: 23564882
42. EPHX1 gene polymorphisms and haplotypes are associated with an increased risk for alcoholism in the Kota Indian population PMID: 22257321
43. minor Tyr113 allele of mEPHX1 polymorphism had a higher risk of type 2 diabetes mellitus PMID: 22555758
44. Microsomal epoxide hydrolase 1 T113C polymorphism is associated with lung cancer. PMID: 23378225
45. the maternal EPHX1 rs1051740 genotype (RR = 3.26, P = .01) was associated with medulloblastoma risk. PMID: 22994552
46. Meta-analyses of available data supported the concept of EPHX1 A139G polymorphism as a genetic susceptibility factor for lung cancer PMID: 23055191
47. EPHX1 gene polymorphisms and haplotypes were not involved in the susceptibility to oral cancer in South Indian subjects. PMID: 21453055
48. EPHX1 Tyr113His polymorphism may be not associated with CRC development PMID: 22928041
49. Study analyzed the association between four SNPs in the EPHX1 and EPHX2 and the risk of oligozoospermia and asthenospermia; rs1051740, rs2234922 and rs751141 were not associated with oligozoospermia and asthenospermia and rs1042064 was a protective factor in idiopathic male infertility. PMID: 22986331
50. microsomal epoxide hydrolase polymorphism is associated with chromosomal instability of 1,3-butadiene exposed workers. PMID: 22156006

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HGNC: 3401

OMIM: 132810

KEGG: hsa:2052

STRING: 9606.ENSP00000272167

UniGene: Hs.89649