Suchergebnisse - "Zeng, Zhen"

PubPharm (907)

91

Lung tumor-infiltrating T_reghave divergent transcriptional profiles and function linked to checkpoint blockade response

enthalten in: bioRxiv.org | 2023

von Dykema, A. | Zhang, J. | Zhang, B. | +34

92

The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria

enthalten in: Journal of molecular medicine (Berlin, Germany) | 2023

von Chen, H. | Yang, P. | Yang, D. | +11

93

Integrated bioinformatic and physiological analyses reveal the pivotal role of hydrogen sulfide in enhancing low-temperature tolerance in alfalfa

enthalten in: Physiologia plantarum | 2023

von Gao, S. | Wang, Y. | Zeng, Z. | +8

94

Exploring the binding effects and inhibiting mechanism of hyperoside to lipase using multi-spectroscopic approaches, isothermal titration calorimetry, inhibition kinetics and molecular dynamics

enthalten in: RSC advances | 2023

von Zeng, Z. | Wu, D. | Tang, L. | +3

95

Organocatalytic asymmetric deoxygenation of sulfones to access chiral sulfinyl compounds

enthalten in: Nature chemistry | 2023

von Huang, S. | Zeng, Z. | Zhang, N. | +3

96

Five-Year Clinical Outcomes after Neoadjuvant Nivolumab in Resectable Non-Small Cell Lung Cancer

enthalten in: Clinical cancer research : an official journal of the American Association for Cancer Research | 2023

von Rosner, S. | Reuss, J. | Zahurak, M. | +14

97

The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria

enthalten in: Journal of molecular medicine | 2023

von Chen, H. | Yang, P. | Yang, D. | +11

98

Phosphoproteomics of cellular mechanosensing reveals NFATC4 as a regulator of myofibroblast activity

enthalten in: bioRxiv.org | 2023

von Mattner, L. | Zeng, Z. | Mayr, C. | +12

99

Genetic association of PRKCD and CARD9 polymorphisms with Vogt-Koyanagi-Harada disease in the Chinese Han population

enthalten in: Human genomics | 2023

von Zhou, C. | Cai, S. | Xie, Y. | +8

100

Genetic association of PRKCD and CARD9 polymorphisms with Vogt–Koyanagi–Harada disease in the Chinese Han population

enthalten in: Human genomics | 2023

von Zhou, C. | Cai, S. | Xie, Y. | +8