XK disease is a multisystem neurodegenerative disorder caused by mutations in the XK gene that codes for the lipid scram...
...XK) pathway, nonoxidative pentose phosphate pathway (PPP), and nonoxidative glycolysis (NOG) pathway in K. phaffii to in...
...XK nuclease superfamily, has been shown to play a vital role in plant development and responses to abiotic stresses. How...
...Xk, ΓK) of number-theoretic origin. Specifically, we analyze the shift space Xk, defined as the closure of the set Vk of...
...Xk|k⟩, where the squared amplitudes Pk=|Xk|2 are outcome probabilities. However, the meaning of the phase factors eiϕk i...
...XK-type nuclease domain, designated EndoDinGs, has remained uncharacterized. Here, we report the first structural and fu...
...XK endonuclease motif within MDV UL24, suggesting involvement in nuclear processes critical for replication. Collectivel...
...XK mutation (c.664C>T, p.(Arg222*)), confirming McLeod syndrome. This case highlights that bilateral striatal hypometabo...
...XK at near-atomic resolution. VPS13A interacts with XK via its pleckstrin homology domain, priming VPS13A's bridge-like ...
...Xk-related protein 8 (XKR8), a plasma membrane phospholipid scramblase, as a pivotal regulator of NETs formation. Upon N...
山东省济南市章丘区文博路2号
齐鲁师范学院 genelibs生信实验室
山东省济南市高新区舜华路750号
大学科技园北区F座4单元2楼
电话: 0531-88819269