INT100254
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Recording of both neural D- and I- MEPs and SEPs is feasible under high sole i.v. | |||||||||||||||
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The associations between SELS genotype and BP in the whole cohort remained significant also when omitting subjects on antihypertensive treatment. | |||||||||||||||
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It has been speculated that the interaction between the SAA1 protein and the putative receptor SELS [6] could be involved in the development of insulin resistance, and a recent study in rats showed that the expression level of SELS in liver was higher in diabetic rats compared with both healthy rats and diabetic rats treated with the insulin sensitizer rosiglitazone [25]. | |||||||||||||||
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The gender-genotype interaction analysis supports our previous findings for USF1 and SEPS1 variants in which the disease risk was limited to women [30], [31], providing a gender-genotype interaction p-values<0.01 for the USF1 variant rs2774279 and for two SEPS1 variants, rs4965814 and rs9874. | |||||||||||||||
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For ischemic stroke, only one SEPS1 variant, rs7178239, was associated at p? | |||||||||||||||
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The gender-genotype interaction analysis supports our previous findings for USF1 and SEPS1 variants in which the disease risk was limited to women [30], [31], providing a gender-genotype interaction p-values<0.01 for the USF1 variant rs2774279 and for two SEPS1 variants, rs4965814 and rs9874. | |||||||||||||||
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For ischemic stroke, we identified a variant in F5 as conferring gender-specific risk, in addition to our previously reported association between SEPS1 variants and ischemic stroke in women [30]. | |||||||||||||||
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General Comments
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