网络框内缺失;符合读框的缺失;缺失突变属框内缺失 网络释义
in-frame deletion 专业医学词典 框内缺失,符合读框的缺失 与"in-frame deletion"相近的词条 ... In-flight Medical Support System in-flight nuclear interaction inflow in force in fragmentis in-frame in-frame deletion in-frame fusion in-frame insertion in-frame start codon in-frame stop codon in-...
网络号外显子的框内缺失 网络释义 1. 号外显子的框内缺失 最常见的 激活突变是 19号外显子的框内缺失(in-framedeletion)同突变和 858 密码子的一个错义突 变 (导致精氨酸被亮氨酸 … wenku.baidu.com|基于2个网页
In-Frame DeletionDefinition An in-frame deletion is a mutation in the coding region of a gene, resulting in the loss of normal DNA sequence, which does not alter the normal triplet reading frame between the mutation site and the carboxyterminus of the polypeptide. Heritable Skin Disorders...
1)in-frame deletion框内缺失突变 英文短句/例句 1.Construction of Streptococcus mutans comE Mutant Strain Using In-frame Deletion System框内缺失突变法构建变形链球菌comE基因突变株 2.excision repair deficient mutant剪切修复缺失突变型 3.The Effect and Mechanism of mtDNA4834bp Deletion in Model of Inner ...
2.Clone the gene into any convenient vector 3.Make your in-frame deletion. We do this by PCRing out from the edges of the gene, in effect PCRing the edges of the gene, the flanking DNA, and the vector without the internal part of the gene. We make the primers to contain a ...
et al. In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy. Eur J Hum Genet 17, 656–663 (2009). https://doi.org/10.1038/ejhg.2008.226 Download citation Received11 June 2008 Revised20 October 2008 Accepted28 October 2008 Published...
Differences in virulence of pneumolysin and autolysin mutants constructed by insertion du- plication mutagenesis and in-frame deletion in Streptococcus pneumoniae[J]. BMCBiotechnol, 2014, 14(1): 16.Liu, E. Y., Chang, F. Y., Chang, J. C., and Fung, C. P. (2014). Differences in ...
A novel in-frame deletion affecting the BAR domain of OPHN1 in a family with intellectual disability and hippocampal alterations.doi:10.1038/ejhg.2013.216Oligophrenin-1 (OPHN1) is one of at least seven genes located on chromosome X that take part in Rho GTPase-dependent signaling pathways ...
This in-frame deletion within the BAR domain could be responsible for the hippocampal alterations that were not detected in patients with a complete loss of OPHN1. PATIENTS AND METHODS The propositus (III.2; Figure 1) was referred to the Human Genetics Service at the State University of Rio...