Xiaodong Wang
Researcher Next ID · RN-026638
Researcher · Biochemistry, Genetics and Molecular Biology
Taipei, China
- Works count
- 438
- Citation count
- 79,403
- H-index
- 98
- i10-index
- 251
Research interests
Publications
Construction of 1D Heterostructure NiCo@C/ZnO Nanorod with Enhanced Microwave Absorption
Nano-Micro Letters · 2021 · https://doi.org/10.1007/s40820-021-00704-5
Application of local fully Convolutional Neural Network combined with YOLO v5 algorithm in small target detection of remote sensing image
PLoS ONE · 2021 · https://doi.org/10.1371/journal.pone.0259283
Preparation of two-dimensional titanium carbide (Ti3C2Tx) and NiCo2O4 composites to achieve excellent microwave absorption properties
Composites Part B Engineering · 2019 · https://doi.org/10.1016/j.compositesb.2019.107577
Deep Learning Recommendation Model for Personalization and Recommendation Systems
arXiv (Cornell University) · 2019 · https://doi.org/10.48550/arxiv.1906.00091
Radar and Communication Coexistence: An Overview: A Review of Recent Methods
IEEE Signal Processing Magazine · 2019 · https://doi.org/10.1109/msp.2019.2907329
Applied Machine Learning at Facebook: A Datacenter Infrastructure Perspective
Journal · 2018 · https://doi.org/10.1109/hpca.2018.00059
Heat transfer enhancement in microchannel heat sink by wavy channel with changing wavelength/amplitude
International Journal of Thermal Sciences · 2017 · https://doi.org/10.1016/j.ijthermalsci.2017.05.013
Mixed Lineage Kinase Domain-like Protein MLKL Causes Necrotic Membrane Disruption upon Phosphorylation by RIP3
Molecular Cell · 2014 · https://doi.org/10.1016/j.molcel.2014.03.003
The Mitochondrial Phosphatase PGAM5 Functions at the Convergence Point of Multiple Necrotic Death Pathways
Cell · 2012 · https://doi.org/10.1016/j.cell.2011.11.030
Mixed Lineage Kinase Domain-like Protein Mediates Necrosis Signaling Downstream of RIP3 Kinase
Cell · 2012 · https://doi.org/10.1016/j.cell.2011.11.031
Toll-like receptors activate programmed necrosis in macrophages through a receptor-interacting kinase-3–mediated pathway
Proceedings of the National Academy of Sciences · 2011 · https://doi.org/10.1073/pnas.1116302108
Receptor Interacting Protein Kinase-3 Determines Cellular Necrotic Response to TNF-α
Cell · 2009 · https://doi.org/10.1016/j.cell.2009.05.021
TNF-α Induces Two Distinct Caspase-8 Activation Pathways
Cell · 2008 · https://doi.org/10.1016/j.cell.2008.03.036
Argonaute2 Cleaves the Anti-Guide Strand of siRNA during RISC Activation
Cell · 2005 · https://doi.org/10.1016/j.cell.2005.10.020
Mule/ARF-BP1, a BH3-Only E3 Ubiquitin Ligase, Catalyzes the Polyubiquitination of Mcl-1 and Regulates Apoptosis
Cell · 2005 · https://doi.org/10.1016/j.cell.2005.06.009
Cytochrome C -Mediated Apoptosis
Annual Review of Biochemistry · 2004 · https://doi.org/10.1146/annurev.biochem.73.011303.073706
Three-Dimensional Structure of the Apoptosome
Molecular Cell · 2002 · https://doi.org/10.1016/s1097-2765(02)00442-2
Endonuclease G is an apoptotic DNase when released from mitochondria
Nature · 2001 · https://doi.org/10.1038/35083620
Structural basis of IAP recognition by Smac/DIABLO
Nature · 2000 · https://doi.org/10.1038/35050012
Smac, a Mitochondrial Protein that Promotes Cytochrome c–Dependent Caspase Activation by Eliminating IAP Inhibition
Cell · 2000 · https://doi.org/10.1016/s0092-8674(00)00008-8
Structural and biochemical basis of apoptotic activation by Smac/DIABLO
Nature · 2000 · https://doi.org/10.1038/35022514
Biochemical Pathways of Caspase Activation During Apoptosis
Annual Review of Cell and Developmental Biology · 1999 · https://doi.org/10.1146/annurev.cellbio.15.1.269
Iterative (turbo) soft interference cancellation and decoding for coded CDMA
IEEE Transactions on Communications · 1999 · https://doi.org/10.1109/26.774855
An APAF-1·Cytochrome c Multimeric Complex Is a Functional Apoptosome That Activates Procaspase-9
Journal of Biological Chemistry · 1999 · https://doi.org/10.1074/jbc.274.17.11549
Bid, a Bcl2 Interacting Protein, Mediates Cytochrome c Release from Mitochondria in Response to Activation of Cell Surface Death Receptors
Cell · 1998 · https://doi.org/10.1016/s0092-8674(00)81589-5
Apaf-1, a Human Protein Homologous to C. elegans CED-4, Participates in Cytochrome c–Dependent Activation of Caspase-3
Cell · 1997 · https://doi.org/10.1016/s0092-8674(00)80501-2
DFF, a Heterodimeric Protein That Functions Downstream of Caspase-3 to Trigger DNA Fragmentation during Apoptosis
Cell · 1997 · https://doi.org/10.1016/s0092-8674(00)80197-x
Prevention of Apoptosis by Bcl-2: Release of Cytochrome c from Mitochondria Blocked
Science · 1997 · https://doi.org/10.1126/science.275.5303.1129
Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade
Cell · 1997 · https://doi.org/10.1016/s0092-8674(00)80434-1
Induction of Apoptotic Program in Cell-Free Extracts: Requirement for dATP and Cytochrome c
Cell · 1996 · https://doi.org/10.1016/s0092-8674(00)80085-9
SREBP-1, a membrane-bound transcription factor released by sterol-regulated proteolysis
Cell · 1994 · https://doi.org/10.1016/0092-8674(94)90234-8
SREBP-1, a basic-helix-loop-helix-leucine zipper protein that controls transcription of the low density lipoprotein receptor gene
Cell · 1993 · https://doi.org/10.1016/s0092-8674(05)80095-9
Structural parts involved in activation and inactivation of the sodium channel
Nature · 1989 · https://doi.org/10.1038/339597a0
Current projects
No projects listed.