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1.The internal transcribed spacer (ITS) regions of nuclear ribosomal DNA (including 5.8 S rDNA) of 6 Laminaria cultivars (CUL002, CUL860, CUL1170, CUL901, CUL018) with clear genetic backgrounds and variant phenotypes, as well as L. longissima planted in China were amplified and sequenced. The phylogenetic relationships of 7 Laminaria spp.
对遗传背景清晰且具有明显的表型差异的 6 个海带栽培品系(CUL002,CUL860,CUL1170,CUL017,CUL018,CUL901)和长海带的转录间隔区(ITS区)进行了 PCR 扩增和序列测定,并分析了 8 个种 17 个品系(其中 7 种共 10株从 GenBank 中获得)海带之间的系统进化关系。收藏指正
2.Simultaneously, to explore the value of fluorescence in situ hybridization (FISH) and multiplex fluorescence in situ hybridization (M-FISH) techniques in the detection of genetic changes in CML carrying variant Philadelphia translocation (vPh).
同时探讨荧光原位杂交(FISH)及多重荧光原位杂交(M-FISH)技术在检测伴变异型Ph易位(vPh)的CML中遗传学改变的意义。收藏指正
3.Genetic polymorphism of CYP2A6 has been found in Caucasians, Oriental and African American population, which includes from CYP2A6*1 to CYP2A6*12, totally 12 variant alleles.
CYP2A6基因多态性存在于白种人、东方人及非洲裔美国人群中 ,包括CYP2A6 1至CYP2A6 12 ,总共 12个变异等位基因。收藏指正
4.Univariate (single-marker) family-based association tests (FBATs) demonstrated that variant alleles at a SNP, rs384288, in exon 3 of FcγRIIIA gene were significantly associated with genetic susceptibility to SLE in additive model (Z=2.271,P=0.023) and recessive model( Z=2.031 , P=0.042 ) .
FcγRⅢA基因101位点和270位点PCR扩增后，用RFLP的方法没有酶切成功，可能不存在酶切位点，没有检出SNP。 FBAT软件分析显示118位点基因多态性与SLE发病相关：附加模型(Z=2.271，P=0.023)以及隐性模型(Z=2.031，P=0.042)。收藏指正
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