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Deletion of macrophage HO-1 reduced expression of the dormancy regulon.

巨噬细胞HO-1清除可以降低休眠调节达。

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He amended his speech by making some additions and deletions.

他对讲稿作了些增删修改。

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Dentin matrix protein 1 (DMP1) is expressed in both pulp and odontoblast cells and deletion of the Dmp1 gene leads to defects in odontogenesis and mineralization.

牙本质基质蛋白-1(DMP1)在牙髓和成牙本质细胞中均有达,Dmp1基因缺失可导致牙齿发育和矿化障碍。

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Here, we show that deletions of VPS28 and VPS32 increase the susceptibility of C. albicans to cell wall disruption agents, echinocandin and azole antifungal agents.

【文献摘要】Vps28p and Vps32p act in both the endocytic and the pH signaling pathways in yeasts and are required for Candida albicans virulence.

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The addition and deletion of picks in the Linescan portion of Interactive Interpretation works the same as Interactive Interpretation in earlier versions of RADAN.

添加和删除线扫描中挑选部分作互动释义相同交互式旧版RADAN 。

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In mice, widespread deletion of the tumor suppressor Phosphatase and tensin homolog (PTEN) generates hamartomatous intestinal polyps with epithelial and stromal inolement.

在小鼠,广泛删除肿瘤抑制因磷酸酶和张力蛋白同源物〔PTEN〕产生错构小肠隐窝,含有上皮和间质。

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The deque class is like a vector, but also supports fast insertion and deletion at the front of the deque.

顺序容器共享一组通用已标准化:如果两种顺序容器都提供某一操作,那么该操作具有相同和含义。

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Furthermore, PTP1B deletion significantly reduced gene expression of 3 1-adrenergic receptor subtypes, consistent with blunted constriction to phenylephrine.

此外PTP1B缺乏明显减少31-肾上腺受体亚型基因达,与对苯福林收缩反应迟钝有关。

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Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者现为抗凝血酶基因外显6区13389G缺失,引起移码突变。

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TED 2019年度大会(语)

Cutting a DNA sequence in your genome also disrupts the function of the cut gene, typically, by causing the insertion and deletion of random mixtures of DNA letters at the cut site.

切割基因组中的DNA序列也会破坏切割基因的功能,通常,是通过在切割位点和除随机的DNA字母混。

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语版 TED-Ed 演讲精选

In the end, the Congress made a few, minor word changes, and one big deletion.

最后,国会修改了很小一部分的语句,并除了一大块。

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Osmosis-内分泌

So both an MYCN amplification or ALK gene fusion, where the oncogene is " turned on, " or a PHOX2B and chromosome 1 and 11 deletions, where tumor suppressor genes are " turned off, " can potentially cause uncontrolled cell growth.

因此,MYCN基因扩增或ALK基因的融,即致癌基因被激活,或PHOX2B与1号、11号染色体缺失,即抑癌基因的失活,都可能导致细胞生长不受控制。

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经济学(汇总)

A public figure's stupid tweets are more likely than most to be screen-captured by others, so that even deletion won't help (and may suggest a guilty conscience).

相较于大多数,公众欠妥的推文要更容易被其他截屏,所以即使除也无济于事(还可能昭示博主心里有鬼)。

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科学60秒-科学美国 2022年8月集

Or you can have an insertion or deletion where a note is either inserted or deleted from the sequence or a nucleotide is inserted or deleted from the sequence.

你也可以在音符被/除的模进中,或在核苷酸被/除的基因序列中,进行或除。

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Osmosis-心血管

The cause of this TA is unknown, although a lot of cases seem to be associated with 22q11.2 deletion syndrome, also known as DiGeorge Syndrome.

TA的诱因尚不明确,但不少病例似乎与22q11.2染色体微缺失综征(或称DiGeorge综征)相关。

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VOA常速英语_美洲

The American Car Rental Association is part of a coalition asking the U.S. Congress to pass a law to govern data deletion.

美国汽车租赁协会也要求美国国会通过一项法律来管理数据除。

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Osmosis-肌骨

Most of these gene mutations are deletions or duplications of one or more exons, and a small amount are point mutations.

基因突变大多数为一个或多个外显子的缺失或重复,小部分是点突变。

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Osmosis-解剖与生理

Once the pathogen is destroyed, most of the clonally expanded cells die off, that's called clonal deletion.

一旦病原体被摧毁了,大部分克隆扩增的细胞会死亡,这被称为克隆清除。

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VOA Special 2023年12月集

The company said the deletion process will start with Google accounts that were created, but never used again.

该公司表示,除程序将会从创建但从未再使用过的谷歌账户开始。

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Osmosis-遗传

With gene editing, targeted changes are made like deletions and insertions right in an organism's genome.

通过基因编辑,可以在生的基因组上做出除、等特定的改变。

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Osmosis-遗传

And alpha thalassemia is caused by mutations in the alpha genes, most commonly a gene deletion.

而α地中海贫血是由α基因变异引起的,最常见的原因是基因缺失。

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Osmosis-遗传

The most common one is a deletion on the paternal genes spanning Prader-Willi region.

最常见的原因是父源染色体相关基因的缺陷。

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Osmosis-遗传

So the Prader-Willi patients with deletions that encompass OCA2 can have a light complexion.

因此OCA2基因缺失的普拉德-威利综征患者肤色较浅。

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Osmosis-遗传

All right, as a quick recap: alpha thalassemia is an autosomal recessive disorder caused by deletion of alpha globin genes on chromosome 16.

得!快速回顾一下:α地中海贫血是一种常染色体隐性遗传病,由16号染色体上的α珠蛋白基因缺陷引起。

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The Boring Talks

The question also remains of who actually did the deletion.

除操作实际上是谁执行的,这个问题也仍然存在。

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