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/vufind/Search/Results?lookfor=%22Wang%2C+Yanan%22&type=Person&page=8
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PubPharm (2.263)
71
Design and optimization of a multidirectional photodetector in optoelectronic integration
enthalten in:
Optics letters
| 2024
von
Chen, J.
|
Kuang, H.
|
Wang, Y.
| +3
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72
Non-adiabatic conformation distortion charge transfer enables dual emission of thermally activated delayed fluorescence and room temperature phosphorescence
enthalten in:
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
| 2024
von
Guo, Y.
|
Guan, H.
|
Li, P.
| +4
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73
Monocytes in allo-HSCT with aged donors secrete IL-1/IL-6/TNF to increase the risk of GVHD and damage the aged HSCs
enthalten in:
iScience
| 2024
von
Li, X.
|
Zhang, W.
|
Wang, Y.
| +12
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74
Targeting oxidative phosphorylation to increase the efficacy of immune-combination therapy in renal cell carcinoma
enthalten in:
Journal for immunotherapy of cancer
| 2024
von
Tian, J.
|
Luo, J.
|
Zeng, X.
| +7
ErratumIn: J Immunother Cancer. 2024 Mar 5;12(3):. - PMID 38448039
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75
Genetic analysis of albinism caused by compound heterozygous mutation of OCA2 gene in a Chinese family
enthalten in:
ResearchSquare.com
| 2024
von
Wang, Y.
|
Chang, Y.
|
Gao, M.
| +2
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76
Gliclazide Reduces Colitis-Associated Colorectal Cancer Formation by Deceasing Colonic Inflammation and Regulating AMPK-NF-κB Signaling Pathway
enthalten in:
Digestive diseases and sciences
| 2024
von
Li, S.
|
Wang, Y.
|
Zhang, D.
| +4
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77
First-trimester noninvasive prenatal diagnosis of seven facioscapulohumeral muscular dystrophy type 1 families using SNP-based amplicon sequencing : An earlier, rapid and safer way
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Fu, X.
|
Zhao, Z.
|
Kong, L.
| +7
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78
A Lightweight Hybrid Model Using Multiscale Markov Transition Field for Real-Time Quality Assessment of Photoplethysmography Signals
enthalten in:
IEEE journal of biomedical and health informatics
| 2024
von
Liu, J.
|
Hu, S.
|
Wang, Y.
| +3
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79
Genetic analysis of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family
enthalten in:
Hereditas
| 2024
von
Wang, Y.
|
Chang, Y.
|
Gao, M.
| +2
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80
Genetic analysis of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family
enthalten in:
Hereditas
| 2024
von
Wang, Y.
|
Chang, Y.
|
Gao, M.
| +2
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