查询词典 mutations

Furthermore, 27 of 35 of the IGHV sequences (77%) had mutations, with similar distributions after stratification either below or above the median time between the collection of the prediagnostic blood sample and the subsequent CLL diagnosis.

此外，35个IGHV序列中有27个（77 ％）有突变，对诊断前血液样本收集和随后CLL诊断的中位时间进行分层，突变具有类似的分布。

We studied the mutation of PDS gene in children diagnosed to have prelingual non-syndromic hearing loss with concomitant bilateral large vestibular aqueduct and Mondini's dysplasia. We tried to find the correlation between non-syndromic hearing loss in local patients and PDS gene, and to establish the basic data of PDS gene mutations in Taiwan.

本篇研究之目的，乃对於患有非症候群学语前听障并合并双侧大前庭导水管及Mondini氏发育异常（Mondini's dysplasia）的儿童，作基因的分析，尝试找出本土非症候群听障与PDS基因的关连性，以建立台湾地区PDS基因突变的基本资料。

Therefore, base on our findings, we have developed a simple molecular test for the 235deC, 299-300delAT and 551G to A mutations and it should be considerable help to those families in understanding the cause of their children having the prelingual deafness.

这些结果可以对於已知遗传成因的学习语言前期非症候群听障家属提供遗传谘询。

We have sequenced the coding region of Cx26 gene from 190 Taiwanese patients with prelingual deafness and 120 unrelated normal individuals. In the deaf patients, three mutations were found: missense mutation, 551G to A and deletion, 235delC and 299-300delAT.

收集120位听力正常人及190位听障孩童对Cx26基因进行多型性比对发现有5种多型性，其中有4种多型性是之前已被发表的：79G→A(V27I)、109G→A(V37I)、341A→G(E114G)及608T→C(I203T)，另发现有一个新的多型性(558G→A)。

Mutations in the promotor region of ALOX5 and LTC4S genes reduce response to leukotriene modifiers.

在ALOX5与LTC4S基因突变的病人对白三烯素调节剂的反应下降。

Mutations in LRP5, a coreceptor for Wnt proteins, cause the disease osteoporosis pseudoglioma.

突变LRP5是一个Wnt蛋白信号受体，能导致骨质疏松症假性神经胶质瘤。

Due to severe amplification by his mutations, this power can psychically reshape the battlefield perceived by all sides for a short duration.

而且随着他的变异加深，这项能力也得到了加强，现在&地狱&能力可以在一段时间内重塑战场上所有人对战况的感知意思就是所有部队的士气好坏都要看他的意思。。

Results No mutations were found in GJA8 gene and GJA3 gene in all patients of this pulverulent cataract family.

结果 在该粉尘状白内障家系GJA8基因和GJA3基因的外显子及其邻近的内含子中，均未发现任何突变。

There were CD34+ mono-nucleus cells and pyramidate cells with mutations in transplantation group 48 hours after operation while none in the brain of other side and control group.

对侧脑组织、对照组大鼠的脑组织均未见CD34阳性细胞。

The researchers, led by Raif Geha, MD, and Emanuela Castigli, PhD, in the Division of Immunology at Children's Hospital Boston, found mutations in a gene known as TACI in 4 of 19 unrelated patients with CVID and in 1 of 16 unrelated patients with IgA deficiency.

研究员，由Raif Geha， MD，和Emanuela Castigli 带领， PhD，在免疫学分部在儿童医院波士顿，发现了变化在基因以TACI 著名在4 19 名无关的患者中与CVID 和在1 有IgA 缺乏16 名无关的病人中。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。