资讯

时令 发自 凹非寺 糖尿病治疗迎来新突破! 最新研究显示,科学家首次将CRISPR编辑的胰岛细胞移植到一名1型糖尿病患者体内。 这些细胞不仅在数月内持续分泌胰岛素,还能逃避免疫检测,使植入接受者无需服用免疫抑制剂。 此研究于已发表在《新英格兰医学杂志 ...
1型糖尿病是一种 自身免疫性疾病 ,患者的免疫系统会错误地攻击胰腺中分泌胰岛素的细胞。 针对这一问题,华盛顿西雅图 Sana Biotechnology公司 提出了一项新研究,为全球约950万1型糖尿病病人带来了治愈的希望。
记者:刘 霞 利用CRISPR基因编辑技术可提高马匹肌肉力量。图片来源:《自然》网站 随着CRISPR基因编辑技术的不断进步,科学家已将其应用于马、绵羊、猪等动物的遗传改良。
The placenta is a unique organ that exists only during pregnancy, growing at tumour-like speed to the size of a small dinner ...
Flagship Pioneering’s Lila Sciences has landed a substantial $235 million series A as it looks to exceed the current limits ...
The global research antibodies and reagents market is projected to grow at a CAGR of 7% from 2025 to 2030, driven by ...
The study will interest researchers studying genome organisation in mitosis. Genomes assume a complex 3D architecture in the interphase cell nucleus. Yet, the molecular mechanisms that determine ...
The field of microbiology has emerged as a cornerstone for green technology, playing a crucial role in fostering sustainable ...
CRISPR gene-edited cell therapy improves quality of life in patients with transfusion-dependent beta-thalassemia, research suggests.
Discover how Simplify Health Care ETF outperforms with active healthcare stock selection, offering alpha where others see ...
Xenotransplantation, leveraging genetic engineering and CRISPR, offers a promising solution to the organ shortage crisis ...
来自国际顶尖团队的研究人员通过CRISPR-Cas9全基因组敲除筛选,发现脂肪酸延长酶ELOVL6可选择性降解KRAS-G12V突变蛋白,破坏其膜定位并抑制肿瘤生长。该研究揭示了KRAS突变癌细胞的代谢弱点,为开发首创新药靶向清除KRAS-G12V提供了理论依据。 这项突破性研究揭示了KRAS癌蛋白令人惊讶的代谢软肋。KRAS作为癌症中最常突变的原癌基因,其G12V热点突变一直缺乏有效靶向策略。通 ...