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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.
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 ...
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 ...
11 小时
on MSN
How evolution evolved: the risks and rewards of gene-editing technology
How evolution evolved: the risks and rewards of gene-editing technology - India Block speaks to paediatrician and TV writer ...
来自MSN
11 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 ...
5 天
on MSN
RNA editing is the next frontier in gene therapy—here's what you need to know
The United States Food and Drug Administration has just approved the first-ever clinical trial that uses CRISPR-Cas13 RNA ...
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, ...
2 天
PPSC gets grant to develop research into gene-editing
Pikes Peak State College (PPSC), in partnership with the University of Colorado at Colorado Springs (UCCS), has been awarded ...
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 ...
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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