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1.Of or designating a pair of crosses in which the male parent in one cross is of the same genotype or phenotype as the female parent in the other cross.
倒易移位的属于或表明一对混血种的，其中一个混血种的父亲与另一个混血种的母亲具有相同的基因型或表现型收藏指正
2.At the same time, there was no difference in SBP, DBP and PP (P>0.05) between II and ID genotype in male EH group.
同时,EH组II、ID基因型的男性的收缩压、舒张压、脉压差异均无统计学意义(P>0·05)。收藏指正
3.Results: The frequencies of DD genotype were 41 4% and 22 0%, ID genotype, 31 0% and 41 5%, II genotype, 27 6% and 36 6% in myocardial infaction and normal human respectively. The frequency of DD genotype in patients was higher than that in the control group, χ 2=4 21,P<0 05. There is no significant difference of DD genotype between male and female.
结果　病例组和对照组ACE基因多态性分布频率 ,DD型分别为 41 4%和 2 2 0 %、ID型分别为 31 0 %和 41 5 %、II型分别为 2 7 6 %和 36 6 % ,病例组DD型高于对照组 ,χ2 =4 2 1,P <0 0 5。收藏指正
4.Stratification analysis showed that the increased risk of ESCC related to the LL genotype was limited in male subjects, with the OR being 1.54 (95% CI = 1.02-2.32).
性别分层后LL基因型与食管癌风险的关系主要表现在男性(校正OR=1.54，95％CI=1.02～2.32)，女性则不相关(校正OR=1.21，95％CI=0.64-2.30)。收藏指正
5.Results The genotype frequency of Gln223 Arg variant in leptin receptor gene was related with obesity which happened in male hypertensive patients; Allele A was associated with increased systolic blood pressure(P=0.023)and diastolic blood pressure(P=0.036)and BMI(P=0.031)in male hypertensive patients complicated with obesity.
结果瘦素受体基因Gln223Arg变异与男性高血压合并肥胖相关,A等位基因与男性患者的体质指数、收缩压及舒张压相关,P值分别为0.031,0.023,0.036。收藏指正
6.(2)Logistic regression analysis showed that DD genotype, age, male gender and essential hypertension contributed significantly to the formation of carotid atherosclerosis in type 2 diabetic patients (OR=3.869, 1.081, 2.447, 2.173,respectively, P <0.05).
(2 )Logistic回归分析显示 ,ACE基因DD型、年龄、合并高血压及男性是糖尿病颈动脉硬化性病变的危险因素 (OR分别为 3 .86 9,1.0 81,2 .44 7,2 .173,P <0 .0 5 )。收藏指正
7.P = 0.047 within GNB3 CC+CT genotype. The results suggest that ACE, or a nearby gene, is a male-specific susceptible gene for hypertension, and that there may exist epistatic gene-gene interaction between ACE D allele and GNB3 825C allele.
P=0.047.结果暗示,血管紧张素转换酶基因或附近的某个基因是具有男性性别倾向的高血压易感侯选基因,同时,在血管紧张素转换酶基因基因的D等位基因和G蛋白beta3亚基基因的825C等位基因之间,可能存在具有上位效应的基因-基因相互作用.收藏指正
8.The risk of chromosomal damage induced by VCM for individuals carrying XRCC1 c. 194 Arg/Arg genotype was 0.6898(95% CI 0.4997-0.9333,P=0.0195)of those carrying Arg/Trp,Trp/Trp genotypes. The risk of chromosomal damage for female VCM exposure workers was 1.6000(95% CI 1.2284-2.0699, P=0.0004)of male workers.
多因素poisson回归分析结果表明,女性发生染色体损伤的危险性是男性的1.6倍(95%CI1.2284~2.0699,P=0.0004),XRCC1194Arg/Arg基因型个体发生染色体损伤的危险性是Arg/Trp、Trp/Trp基因型个体的0.6898倍,(95%CI0.4997~0.9333,P=0.0195)。收藏指正
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