- 更多网络例句与发育异常的相关的网络例句 [注：此内容来源于网络，仅供参考]
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For investigation of genetic mechanisms of leaf polarity formation, we screened for Arabidopsis mutants with aber...
通过EMS化学诱变，寻找到一些形态相似，叶发育异常的突变体，遗传实验证明这些突变体可以被分成两类。
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ABSTRACT Agenesis of one or more teeth constitutes one of the most common developmental anomalies in man.
牙齿的发育不全是一种人类常见的发育异常，先天缺牙是牙齿发育异常的表现之一，可伴随遗传性的综合征出现，也可能是单独的症状以散发病例或家系遗。。。
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Objective To evaluate the clinical application of multi-slice spiral CT angiography in developmental anomaly of aorta.
目的 探讨多层螺旋CT血管成像对主动脉发育异常的诊断价值。
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Methods DAS consisting of 36 physical and dermatoglyphics items was rated in 101 RD children (70 males and 31 females) and 66 controls (40 males and 26 females).
根据遗传发育神经生物学理论和有关文献编制发育异常评定量表，对101例汉族RD儿童和66名正常儿童作发育异常的评定分析。
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The aberrant epigenetic reprogramme is an important cause for abnormal development of nuclear transfer embryos.
表观重编程异常是核移植胚胎发育异常的重要原因。
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The morphological observation has identified 37 mutant lines, the majority ofwhich showed anomalies in axis and somite formation. Ten of them are kept forfurther study.
表型观察法筛选了约 200 个 F2 家族，获得了 37 个突变品系，其中以体轴和体节发育异常的突变体为主，将其中 10 个品系保种，以备进一步研究。
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" Turner's syndrome: Chromosomal disorder (from the presence of only one sex chromosome, X, in all or some of the body's cells) that causes abnormal sexual development in females."
特纳氏症候群：可致女人性发育异常的染色体疾病(所有或某些体细胞中只具有1个性染色体X)。
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" Turner's syndrome: Chromosomal disorder (from the presence of only one sex chromosome, X, in all or some of the body's cells) that causes abnormal sex ual development in females."
特纳氏症候群：可致女人性发育异常的染色体疾病(所有或某些体细胞中只具有1个性染色体X)。
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Hypohidrosis ectodermal dysplasia is a rare congenital disorder that results in abnormalities in the structures of ectodermal origin tissues, such as teeth, eccrine sweat glands, hair and nails.
少汗型外胚层发育不良症是一种罕见的起源于外胚层组织，如牙、汗腺、毛发等发育异常的遗传性疾病。
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At the one-cell stage, each embryo was injected with gradient doses of 2-8ng MO. The control morpholino, was purchased from Gene-Tools.To test the knockdown effectiveness of the morpholino, the tbx2-EGFP (enhanced green fluorescent protein) construct was generated. And coinjection of morpholino with mRNA tests its specificity of the morpholino. Overexpression of tbx2 via mRNA microinjection helps us understand gaining function of tbx2. Results The tbx2-EGFP construct tests the knockdown effectiveness of the morpholino. Zebrafish embryos lacking tbx2 function have defects in cardiac contractility, rhythm and morphology in a dose-dependent manner. The embryos with c-MO are normal in development. Coinjection of morpholino with mRNA rescue the phenotype of tbx2 knocking down. The phenotypes include pericardial edema, hypogenetic ventricle, dilation of atria, arrhythmia, bradycardia, asystole, abnormal atrioventricular canal, aberrant valve and blood regurgitation.
结果荧光蛋白融合标记实验验证了tbx2-MO可以很好得阻抑斑马鱼胚胎tbx2的表达，tbx2-MO组胚胎在心脏收缩性、节律和形态学发生上出现了异常，心脏畸形随着注射剂量的增加而出现比较一致的表型，而c-MO组胚胎没有出现明显的畸形；tbx2-mRNA和tbx2-MO的共注射减少了tbx2-MO胚胎心脏畸形的发生率及减轻了心脏畸形的程度，验证了所设计合成的tbx2-MO对tbx2基因的抑制作用具有特异性；tbx2-MO组胚胎心脏缺陷包括心室发育不良、心房扩张、房室管和瓣膜异常以及心率缓慢、心律不齐、心脏停搏、血液返流等，并根据心脏发育异常的程度分为轻、中、重度畸形组tbx2-mRNA基因过表达胚胎没有见到心腔的形成。
- 更多网络解释与发育异常的相关的网络解释 [注：此内容来源于网络，仅供参考]
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achondroplasia：软骨发育不良
[正文快照] 软骨发育不良(Achondroplasia)是认识最一早的、典型的先天性骨发育异常. 临床上以不成比例性积、儒为特征. 虽然在X线诊断上比较容易,但和其它骨发育不良性疾病的鉴别诊断问题仍有重视的的必要. 本组报告8例.
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cretin：克汀病
临床按照其程度分为克汀病(cretin)和亚克汀病(subcretin),其一致的神经损伤模式反映出对胎儿神经系统发育导致骨骼系统发育异常的弥漫性损害[1]. 甲状腺激素是维持胚胎和胎儿生长发育、新陈代谢的最重要的内分泌之一.
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gonadal dysgenesis：性腺发育不全
4、性腺发育不全 由于胚胎时期卵巢发育异常而致卵巢没有其功能,称性腺发育不全(Gonadal dysgenesis),这些病人主要是存在染色体数量的异常,性腺发育异常可致原发性闭经或卵巢早衰.
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Dysplasia：发育异常
PSC伴随CUC时,发生结肠恶性肿瘤的危险度增加,其发生率为10%,甚至有报道结肠癌发生于肝移植之后,PSC与CUC同时存在时,结肠发育异常(dysplasia)为45%,单纯CUC组为16%.
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shell tooth：薄壳牙:牙本质发育异常而釉质基本正常致使髓室及根管极度增大,牙如空壳状
screw-driver teeth 旋凿状牙:同Hutchinson餾 teeth | shell tooth 薄壳牙:牙本质发育异常而釉质基本正常致使髓室及根管极度增大,牙如空壳状 | snaggle tooth 凸牙,歪牙:在牙列中排列不整的牙
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alloplastic：兴趣外向的
alloplasia 发育异常 | alloplastic 兴趣外向的 | alloplasty 外向性力
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dysplastic：发育异常的
dysplasia 发育异常 | dysplastic 发育异常的 | dysplastic type 变态型
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Dysplastic nodule：发育异常的结节
Duodenum 十二指肠 | Dysplastic nodule 发育异常的结节 | Endoscopic retrograde cholangiography 内窥镜逆行胆管胰腺造影
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heterophoric：隐斜视的 (形)
heterophoria 隐斜视 (名) | heterophoric 隐斜视的 (形) | heteroplasia 发育异常, 再生异常 (名)
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heteroplastic：异质形成术的; 异体造形术的 (形)
heteroplasia 发育异常, 再生异常 (名) | heteroplastic 异质形成术的; 异体造形术的 (形) | heteroplasty 异体植皮术; 异体造形术 (名)