DNA repair protein XRCC4 - Wikipedia
DNA repair protein XRCC4 (hXRCC4) also known as X-ray repair cross-complementing protein 4 is a protein that in humans is encoded by the XRCC4 gene. XRCC4 is also expressed in many …
XRCC4 Gene - GeneCards | XRCC4 Protein | XRCC4 Antibody
2024年12月25日 · XRCC4 (X-Ray Repair Cross Complementing 4) is a Protein Coding gene. Diseases associated with XRCC4 include Short Stature, Microcephaly, And Endocrine …
Systematic analysis identifies XRCC4 as a potential immunological …
2023年2月10日 · XRCC4 is a NHEJ factor identified recently that plays a vital role in repairing DNA double-stranded breaks. Studies have reported the associations between abnormal …
X 光修复交叉补 4（XRCC4）基因 | MCE - MCE-生物活性分子 ...
由该基因编码的蛋白质与 DNA 连接酶 IV 和 DNA 依赖性蛋白激酶一起发挥修复 DNA 双链断裂的作用。 该蛋白在非同源末端连接和 V (D) J 重组的完成中均发挥作用。 该基因的突变可导致 …
Interplay of p53 and DNA-repair protein XRCC4 in tumorigenesis …
2000年4月20日 · XRCC4 is a non-homologous end-joining protein employed in DNA double strand break repair and in V (D)J recombination 1, 2. In mice, XRCC4-deficiency causes a …
XRCC4 X-ray repair cross complementing 4 [ (human)]
XRCC4 and MRE11 Roles and Transcriptional Response to Repair of TALEN-Induced Double-Strand DNA Breaks. X-ray scattering reveals disordered linkers and dynamic interfaces in …
Mol Cell：细胞凋亡阶段Caspase切割核蛋白XRCC4调节细胞膜磷脂结构的改变 …
通过高通量的CRISPR-cas9突变筛选，作者发现了一种叫做XRCC4的蛋白，此前研究表明XRCC4是DNA损伤修复复合体的成分，而该研究表明XRCC4蛋白的缺失会显著影响Xkr4蛋白 …
Reciprocal regulation of RIG-I and XRCC4 connects DNA repair ... - Nature
2021年4月12日 · Reciprocally, XRCC4, while suppressed for its DNA repair function, has a critical role in RIG-I immune signaling through RIG-I interaction. XRCC4 promotes RIG-I signaling by …
Systematic analysis identifies XRCC4 as a potential ... - PubMed
2023年2月10日 · Studies have reported the associations between abnormal expression of XRCC4 and tumor susceptibility and radiosensitivity, but the potential biological mechanisms by which …
Entry - *194363 - X-RAY REPAIR CROSS COMPLEMENTING 4; XRCC4 …
2016年10月4日 · In mice, XRCC4 deficiency causes late embryonic lethality accompanied by defective lymphogenesis and defective neurogenesis manifested by extensive apoptotic death …