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1.Results We mapped the gene to 15q11.1-q12, SPG6 loeus (Lod Score: 4.55) .
结果 我们将这一家系的致病基因定位于15q11.1-q12,SPG6的位点(Lod Score 4.55).收藏指正
2.a novel locus of SPG was mapped to 1p21.3-p31.2 (Maximum Lod score=2.62 at Θ=0.00;) within a region of about 9.08cM flanked by markers D1S2865 and D1S2753;
第二个家系被定位于1p21.3-31.2区域(最大Lod值2.62; 重组率Θ=0.00),区间为D1s2865到D1s2753之间9.08cM范围内。收藏指正
3.Results: The results produced by MLINK program are as follows: In three pedigrees including HY-01, CY-01 and CY-02, the maximum sum two-point LOD score of 2.151 for D16S3131 was obtained at recombination rates of 0.000 under autosomal dominant model with 90% penetrance.
结果:连锁分析结果显示:在标记位点D16S3131处,家系HY-01、CY-01和CY-02在AD模式下,重组率为0.000,外显率为90%时,获得最大LOD值总和为2.151。收藏指正
4.The LOD score was 2.689.45.Three QTLs qGL-5,qGWt-1a and qGWt-1b were both detected under upland and lowland environments(common QTL). Two co-localized QTLs(qGL-1a and qGWt-1a,and qGL-1b and qGWt-1b) controlling GL and GW were detected.
其中控制粒长的qGL-5及控制粒重的qGWt-1 a和qGWt-1b在水、旱条件下均能检测到,在抗旱育种中可用于分子标记辅助选择籽粒性状。收藏指正
5.2. All affected individuals displayed bilateral lens opacities, and pulverulentcataract cataract with variable severity. 3. The LOD score of each selected markers ADCC in FANS family was negative. 4. An abnormal band was found by SSCP in a patient, and sequence analysis proved a deletion of CA in none coding region of GJA3 gene.
2.2 基因连锁分析:选取分布在晶状体蛋白基因(CRYAA、CRYAB、CRYBA1/A3、CRYBB1、CRYBB2、CRYGC、CRYGD)、膜运输蛋白基因(MAF)、念珠状纤维蛋白基因(BFSP2)、热休克蛋白基因(HSF4)及MAF基因上下约10厘摩(centimorgan,cM)范围内的微卫星标记;收藏指正
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