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Live Science on MSN
2 天
New CRISPR system pauses genes, rather than turning them off permanently
Researchers in Lithuania present the molecular structure of a new, more-versatile CRISPR system for gene editing.
2 天
Combining AI and Crispr Will Be Transformational
The genome-editing technology can be supercharged by artificial intelligence—and the results are already being felt.
studyfinds
5 小时
Genetic breakthrough may pave way to creating hypoallergenic cats
For millions of people who adore cats but are plagued by allergies, the dream of snuggling a furry friend without sneezing ...
TipRanks on MSN
14 小时
CRISPR Therapeutics (NASDAQ:CRSP) Boasts Solid Potential and Limited Risk
CRISPR Therapeutics ($CRSP) has endured a tough year since gaining several important regulatory approvals for its ...
腾讯网
10 天
潜在首款!持久降低疾病指标超90%达2年,体内CRISPR基因编辑疗法登 ...
Nex-z是一款基于Intellia公司专有的非病毒平台,利用脂质纳米颗粒(LNP)向肝脏输送由两部分组成的体内CRISPR/Cas9基因编辑系统:靶向TTR基因的特异性引导RNA(gRNA)和编码Cas9酶的mRNA。通过体内失活TTR基因,nex ...
Frontiers
2 天
Silenced Voices: The Role of Marginalized Groups in Debates on the Regulation of CRISPR-Cas ...
CRISPR gene editing is widely regarded as one of the most important leaps in biomedical and agricultural research, with ...
Yahoo Malaysia
2 小时
How evolution evolved: the risks and rewards of gene-editing technology
India Block speaks to paediatrician and TV writer Dr Neal Baer about the controversial technology and how it could reshape ...
生物谷
12 天
Science封面:华人学者开发AI模型,学会生命的语言,生成新型CRISPR ...
人工智能基础模型的出现,为生物序列建模指明了一条有前景的道路,但尚未实现全基因组水平的建模。DNA序列非常长,例如我们人类有着30亿碱基对,简单如大肠杆菌也有这数百万碱基对。要想充分理解进化的影响,需要具有单个核苷酸分辨率的分辨率,这些问题使得大规模 ...
News Medical on MSN
2 天
First U.S. trial uses non-viral CRISPR to correct sickle cell mutation
UCSF Benioff Children's Hospital Oakland is enrolling patients in an innovative clinical trial that seeks to cure sickle cell ...
gmwatch.org
6 天
CRISPR gene editing causes large-scale genetic damage while correcting mutant genes
CRISPR-based gene-editing tools are being developed to correct specific defective sections of the genome to cure inherited genetic diseases, with some applications already in clinical trials. However, ...
New Scientist
3 天
Why gene editors want to treat fetuses when they are still in the womb
Gene editing in the womb could be more effective than the same treatment after birth, as it is easier to deliver the ...
9 天
on MSN
CRISPR-based system labels extracellular vesicles with 'barcodes' to better understand cell ...
Cell-to-cell communication through nanosized particles, working as messengers and carriers, can now be analyzed in a whole ...
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