相关实验视频

Updated: Sep 9, 2025

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
11:15

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors

Published on: September 20, 2016

24.5K

跨物种分析发现肺腺癌的基因型驱动弱点

Angeliki Karatza, Maayan Pour, Jaylen M Powell

    bioRxiv : the preprint server for biology
    |September 5, 2025
    PubMed
    概括

    这项研究揭示了由STK11,KRAS和EGFR突变驱动的肺腺癌 (LUAD) 独特的免疫微环境. 了解这些基因型特异性免疫特征和代谢依赖性对于开发向的LUAD疗法至关重要.

    更多相关视频

    Author Spotlight: Exploring the Role of Inflammation in the Co-occurrence of Primary Sjogren's Syndrome and Lung Adenocarcinoma10:21

    Author Spotlight: Exploring the Role of Inflammation in the Co-occurrence of Primary Sjogren's Syndrome and Lung Adenocarcinoma

    Published on: September 20, 2024

    540
    Ex Vivo Organoid Model of Adenovirus-Cre Mediated Gene Deletions in Mouse Urothelial Cells09:16

    Ex Vivo Organoid Model of Adenovirus-Cre Mediated Gene Deletions in Mouse Urothelial Cells

    Published on: May 5, 2022

    2.7K

    相关概念视频

    Single Nucleotide Polymorphisms-SNPs01:05

    Single Nucleotide Polymorphisms-SNPs

    A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
    15.8K