a推测原因可能是由于P53 阴性表达使P53具有的DNA修复及稳定功能缺失 Extrapolated the reason possibly is because the P53 negative expression causes the DNA repair and the stable function flaw which P53 has[translate] a•ok when guys are around 14 正在翻译,请等待...[translate] ...
P53 is found often in familial melanoma cases. The gene, when it operates normally, helps the body repair mutated cells to prevent, amongst other things, cancer from developing. However when p53 is altered it can’t operate its job properly and allow cancers to grow. Heavy UV light that da...
声明: 本网站大部分资源来源于用户创建编辑，上传，机构合作，自有兼职答题团队，如有侵犯了你的权益，请发送邮箱到feedback@deepthink.net.cn 本网站将在三个工作日内移除相关内容,刷刷题对内容所造成的任何后果不承担法律上的任何义务或责任
(S4999) 38 Negative comments about a genetic cause by respondents with CF or SCD addressed deliberations over having children and disappointment that their parents had failed to prevent the disease, a sign perhaps, of ignorance on their parents' part. Nobody knew of it. I mean, the only ...
【题目】题序主题体裁难度词数建议用时实际用时评价D人生经历记叙文★★★70812分钟(名师原创题)KEY -P53I cannot remember what it was like to have two legs and it was just 14 years ago. I mean, the reasonwhy is because I know that, that is the old me, that is not the new me, and...
19 out of 37 (51%) of BRCA1-positive ovarian cancer patients and 21 out of 55 (39%) BRCA1-positive breast cancer [patients] had negative family history of breast and/or ovarian cancer among first- and second-degree relatives. In ovarian cancer patients, negative family history was more ...
What Equity, the Promise Economy, and Cognition Mean for How Fiduciary Law Should Develop 来自 学术范 喜欢 0 阅读量: 29 作者: HJ Pace 年份: 2018 收藏 引用 批量引用 报错 分享 全部来源 免费下载 求助全文 scholarship.law.upenn.edu 学术范 学术范 (全网免费下载) ...
The investigators suggest that some of the anxiety disorders prevalent among HD patients may be caused by loss of normal HTT function in the hippocampus and cortex, particularly with regards to BDNF transport, due to a dominant negative effect of mHTT (although Her and Goldste...
In particular, some biomarkers may be useful in predicting positive (a high TMB) or negative responses (mutations in STK11 and KEAP1) to treatment with ICIs [312,313]. Certain mutations, such as those in STK11, can also open up new avenues of targeted therapies and may be detected with...
Unfortunately, there are still a small number of studies conducted in humans, which does not mean that it should be ignored. In fact, there is a strong rationale for continuing a long-term study, due to increasing environmental pollution [66]. It is worth adding that the new discovery of ...