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
框内缺失突变,in-frame deletion 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 mtDNA4834...
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...
in frame deletion The following is what we found works best for making markerless mutations.1.Amplify the gene of interest along with sufficient flanking DNA (at least 500bp) on each side to mediate homologous recombination. (I found that using Easy A polymerase from Stratagene gives high fideli...
In patients from an unrelated family a 12-nucleotide deletion (c.2997_3008del) in FLNC resulting in a predicted in-frame four-residue deletion (p.Val930_Thr933del) in the seventh repeat of filamin C was identified. Both affected family members, mother and daughter, but not unrelated ...
IMPORTANCE Hidradenitis suppurativa (HS) is a complex trait that has a monogenic etiology in a subset of patients. Variation in genes that encode proteins of the ? secretase complex, particularly NCSTN, account for few patients who exhibit familial forms of HS. Thus far, extensive genotype-phenoty...
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...
Traeger-Synodinos J, Harteveld CL, Kanavakis E, Giordano PC, Kattamis C, Bernini LF. Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemia. Hemoglobin. 1999; 23 :317–324. doi: 10.3109/03630269909090747. [ Cross Ref ]...