Suchergebnisse - "Xu, Xiaowei"

PubPharm (986)

71

A Novel Fluorescent Probe for the Detection of Hydrogen Peroxide

enthalten in: Biosensors | 2023

von Wang, K. | Yao, T. | Xue, J. | +2

72

Less Is More : Surgical Phase Recognition From Timestamp Supervision

enthalten in: IEEE transactions on medical imaging | 2023

von Ding, X. | Yan, X. | Wang, Z. | +4

73

Microfluidic Biosensor Integrated with Signal Transduction and Enhancement Mechanism for Ultrasensitive Noncompetitive Assay of Multiple Mycotoxins

enthalten in: Analytical chemistry | 2023

von Xiang, X. | Song, M. | Xu, X. | +5

74

Structure and oxygen vacancy engineered CuCo-layered double oxide nanotube arrays as advanced bifunctional electrocatalysts for overall water splitting

enthalten in: Dalton transactions (Cambridge, England : 2003) | 2023

von Zeng, Z. | Gao, Z. | Guo, Z. | +7

75

Correction : sFRP2 Supersedes VEGF as an Age-related Driver of Angiogenesis in Melanoma, Affecting Response to Anti-VEGF Therapy in Older Patients

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

von Fane, M. | Ecker, B. | Kaur, A. | +16

ErratumFor: Clin Cancer Res. 2020 Nov 1;26(21):5709-5719. - PMID 33097493

76

Graph matching and deep neural networks based whole heart and great vessel segmentation in congenital heart disease

enthalten in: Scientific reports | 2023

von Yao, Z. | Xie, W. | Zhang, J. | +5

77

Phase I Trial of Autologous RNA-electroporated cMET-directed CAR T Cells Administered Intravenously in Patients with Melanoma and Breast Carcinoma

enthalten in: Cancer research communications | 2023

von Shah, P. | Huang, A. | Xu, X. | +22

78

Review of Konjac Glucomannan Structure, Properties, Gelation Mechanism, and Application in Medical Biology

enthalten in: Polymers | 2023

von Sun, Y. | Xu, X. | Zhang, Q. | +6

79

A distinct pattern of growth and RAC1 signaling in melanoma brain metastasis cells

enthalten in: Neuro-oncology | 2023

von Stejerean-Todoran, I. | Gimotty, P. | Watters, A. | +21

80

Correction : Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report

enthalten in: Italian journal of pediatrics | 2023

von Wu, J. | Lei, M. | Wang, X. | +5

ErratumFor: Ital J Pediatr. 2022 Dec 29;48(1):204. - PMID 36582000