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constitutive exon 组成型外显子
It is a missense mutation in exon III. 它是位于外显子III的错义突变。
The fifth exon codes for the transmembrane domain. 第五个外显子编码跨膜结构域。
No mutation was found in exon 5, 8 of FHIT gene. 而正常人FHIT基因外显子5和8无1例缺失；
The constitutive institution may provide for these matters. 组织文件可对这些事项作出规定。
Almost all the cell contain the constitutive Nitric Oxide. 几乎所有细胞都含有原生型一氧化氮合酶。
Constitutive activation of STATS was present in BEL-7402 cells. 肝癌细胞中Wnt异常信号转导途径对细胞增殖及迁移的影响
Perhaps constitutive equation has to be fortified by experimental evidence. 本构方程或许还得用试验数据予以验证。
Exon rearrangement of parkin gene exists in Chinese patients with isolated EOP. 我国散发EOP患者存在parkin基因外显子重排突变。
UCP2 Exon 8 Ins/Del polymorphism is associated with REE/kg in OW/OB group. UCP2Exon 8Ins/Del多态位点与超重 /肥胖者REE/kg有关 ,参与其超重 /肥胖程度的不同。
The effect of skipping just one exon can be dramatic for an organism. 仅仅略过一段表现子，就可能对生物体造成显著的影响。
This means that constitutive equations must be framed in tensor language. 这意味着建立本构方程必须采用张量符号。
EFFECT OF VIBRATION FREQUENCY ON DYNAMIC CONSTITUTIVE RELATIONSHIP OF LOESS? 振动频率对原状黄土动本构关系的影响?
Parameters of linearized constitutive relationship of the fabric are obtained. 在试验中引入了云纹干涉完成了大应变的量测。
KEY WORDS Anisotropic, Constitutive model, Viscoplastic, Turbine blade. 关键词：正交异性，本构模型，粘塑性，涡轮叶片
Objecties. To determine the allelic distribution of the exon 12 polymorphism within a sample of families with FIS. 目的：决定在具有家族性特发性脊柱侧凸（FIS）的家族样本中外显子12多态现象的等位基因的分配。
Splice donor site -- the junction between the end of an exon and the start of the downstream introns, commencing with the dinucleotide GT. 剪接提供位--位在表现子终端和下一个表现子之间的接合点;由GT核苷对起始.
A homolygous loss was found in SU DHL 9 while mutations of P16 exon 2 in SU DHL 1 and Daudi. 检出1例纯合缺失 ,2例 P16基因第二外显子突变。
Vein blood samples 4-6ml were collected and Genomic DNA were extracted. Exon 9 of CFH gene was PCR amplified . 抽取外周抗凝血4-6ml,用酚-氯仿抽提法提取全基因组DNA,聚合酶链反应(Polymerase chain reaction ,PCR)扩增外显子9片断并进行直接测序。
A transition in exon 9 in SH3BP2 gene was detected in the family,which led to a missensemutation(Arg 415 Pro). 该家系中的每位患者均存在SH3BP2基因的第9外显子的单碱基突变,导致编码第415位氨基酸的密码子由CGA 替换为CCA,其编码的氨基酸中精氨酸(Arg)变为脯氨酸(Pro)。