纤维化不良的

基本解释 (translations)

dysepulotic

与纤维化不良的相关的网络例句 [注：此内容来源于网络，仅供参考]

Objective Oxygen toxicity plays a major role in the pathogenesis of bronchopulmonary dysplasiain neonates requiring ventilation.

支气管肺发育不良(bronchopulmonary dysplasia， BPD)是一种因长期用氧，氧毒性使肺组织纤维化及肺萎陷的病变［1］。

This study indicates that the apoptosis-inducing strategy to treat liver fibrosis has high potential, but it will be necessary to develop an HSC-specific therapy to prevent adverse effects.

本研究表明诱导凋亡策略治疗肝纤维化有很高的可行性，但必须建立一个针对肝星状细胞的特异疗法以避免不良反应。

Aminoglycosides suppress termination at nonsense codons and result in functional improvement in a cystic fibrosis bronchial epithelial cell line, in muscle cells from mdx mice and in fibroblasts from individuals with Hurler syndrome.

氨基糖苷类物质可以通过抑制无意义密码子的终止作用，改善囊性纤维化的支气管上皮细胞、患肌营养不良的肌细胞和Hurler综合征病人的成纤维细胞的功能。

Objective To explore the changes of apoptosis of cells in the lung tissue of rats with silica instillation and to its significance in silicosis, and to clarify the role of caspase-3 in the apoptosis progress.

肺纤维化是一组由多种病因所引起的肺破坏性疾病，目前的治疗一直未能改善其不良的预后，故加深对肺纤维化的认识，并在此基础上发展新的治疗策略已尤为迫切[1]。

The reisions are intended to highlight the risk for nephrogenic systemic fibrosis (NSF; also known as nephrogenic fibrosing dermopathy ) after GBCA exposure in certain patient populations, according to an alert sent from MedWatch, the FDA's safety information and aderse eent reporting program.

根据一个来自MedWatch（美国食品和药物管理局安全信息和不良反应的报告程序）的警报，这些修改建议意味着突出钆基造影剂对某些特定患者的肾源性系统纤维化（NSF；也可以称之为肾源性纤维性皮肤病）的危险。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

分别编码端粒末端转移酶反转录酶和端粒酶RNA的hTERT和hTR基因的种系突变导致常染色体显性先天性角化不良，它是一种罕见的因为再生障碍性贫血和肺纤维化而早亡的遗传性疾病。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

端粒酶逆转录酶的编码基因hTERT和端粒酶RNA的编码基因hTR发生种系突变时，可引起常染色体显性先天性角化不良，这是一种罕见的遗传性疾病，它与再生障碍性贫血和肺纤维变性所致的早产儿死亡具有相关性。