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Publications by Cheng Zhang

Peer reviewed

Articles

[3]
[4]
A. Kaynar et al., "Discovery of a Therapeutic Agent for Glioblastoma Using a Systems Biology-Based Drug Repositioning Approach," International Journal of Molecular Sciences, vol. 25, no. 14, 2024.
[5]
E. Mohammadi et al., "Drug repositioning for immunotherapy in breast cancer using single-cell analysis," npj Systems Biology and Applications, vol. 10, no. 1, 2024.
[7]
[8]
S. Lee et al., "Global compositional and functional states of the human gut microbiome in health and disease," Genome Research, vol. 34, no. 6, pp. 967-978, 2024.
[10]
L. Meng et al., "Multi-omics analysis reveals the key factors involved in the severity of the Alzheimer's disease," Alzheimer's Research & Therapy, vol. 16, no. 1, 2024.
[12]
A. B. Ceyhan et al., "Novel drug targets and molecular mechanisms for sarcopenia based on systems biology," Biomedicine and Pharmacotherapy, vol. 176, 2024.
[18]
[19]
[24]
X. Li et al., "The acute effect of different NAD+ precursors included in the combined metabolic activators," Free Radical Biology & Medicine, vol. 205, pp. 77-89, 2023.
[25]
L. Voland et al., "Tissue pleiotropic effect of biotin and prebiotic supplementation in established obesity," American Journal of Physiology. Endocrinology and Metabolism, vol. 325, no. 4, pp. E390-E405, 2023.
[28]
M. Karlsson et al., "Genome-wide annotation of protein-coding genes in pig," BMC Biology, vol. 20, no. 1, 2022.
[31]
M. Zeybel et al., "Multiomics Analysis Reveals the Impact of Microbiota on Host Metabolism in Hepatic Steatosis," Advanced Science, vol. 9, no. 11, pp. 2104373, 2022.
[34]
M. Karlsson et al., "A single-cell type transcriptomics map of human tissues," Science Advances, vol. 7, no. 31, 2021.
[36]
Ö. Altay et al., "Combined Metabolic Activators Accelerates Recovery in Mild-to-Moderate COVID-19," Advanced Science, vol. 8, no. 17, 2021.
[43]
A. Bayraktar et al., "Revealing the Molecular Mechanisms of Alzheimer's Disease Based on Network Analysis," International Journal of Molecular Sciences, vol. 22, no. 21, 2021.
[44]
D. Mahdessian et al., "Spatiotemporal dissection of the cell cycle with single-cell proteogenomics," Nature, vol. 590, no. 7847, 2021.
[47]
A. Kaynar et al., "Systems Biology Approaches to Decipher the Underlying Molecular Mechanisms of Glioblastoma Multiforme," International Journal of Molecular Sciences, vol. 22, no. 24, pp. 13213, 2021.
[48]
M. Arif et al., "iNetModels 2.0 : an interactive visualization and database of multi-omics data.," Nucleic Acids Research, vol. 49, no. W1, pp. W271-W276, 2021.
[49]
S. Lam et al., "A systems biology approach for studying neurodegenerative diseases," Drug Discovery Today, vol. 25, no. 7, pp. 1146-1159, 2020.
[50]
E. Sjöstedt et al., "An atlas of the protein-coding genes in the human, pig, and mouse brain," Science, vol. 367, no. 6482, pp. 1090-+, 2020.
[51]
E. C. Sayitoglu et al., "Boosting Natural Killer Cell-Mediated Targeting of Sarcoma Through DNAM-1 and NKG2D," Frontiers in Immunology, vol. 11, 2020.
[53]
C. Lieven et al., "Correction: MEMOTE for standardized genome-scale metabolic model testing (vol 38, pg 272, 2020)," Nature Biotechnology, vol. 38, no. 4, pp. 504-504, 2020.
[55]
T. Abdellah et al., "Integration of molecular profiles in a longitudinal wellness profiling cohort," Nature Communications, vol. 11, no. 1, 2020.
[56]
C. Lieven et al., "MEMOTE for standardized genome-scale metabolic model testing," Nature Biotechnology, vol. 38, no. 3, pp. 272-276, 2020.
[59]
M. Uhlén et al., "A genome-wide transcriptomic analysis of protein-coding genes in human blood cells," Science, vol. 366, no. 6472, pp. 1471-+, 2019.
[60]
C. Pineau et al., "Cell Type-Specific Expression of Testis Elevated Genes Based on Transcriptomics and Antibody-Based Proteomics," Journal of Proteome Research, vol. 18, no. 12, pp. 4215-4230, 2019.
[66]
C. Cadenas et al., "LIPG-promoted lipid storage mediates adaptation to oxidative stress in breast cancer," International Journal of Cancer, vol. 145, no. 4, pp. 901-915, 2019.
[72]
G. Bidkhori et al., "Metabolic network-based stratification of hepatocellular carcinoma reveals three distinct tumor subtypes," Proceedings of the National Academy of Sciences of the United States of America, 2018.
[73]
A. Olin et al., "Stereotypic Immune System Development in Newborn Children," Cell, vol. 174, no. 5, pp. 1277-+, 2018.
[76]
M. Uhlén et al., "A pathology atlas of the human cancer transcriptome," Science, vol. 357, no. 6352, pp. 660-+, 2017.
[77]
P. J. Thul et al., "A subcellular map of the human proteome," Science, vol. 356, no. 6340, 2017.
[80]
[82]
S. Lee et al., "TCSBN: a database of tissue and cancer specific biological networks," Nucleic Acids Research, vol. 46, no. D1, pp. D595-D600, 2017.
[83]
[84]
S. Lee et al., "Dysregulated signaling hubs of liver lipid metabolism reveal hepatocellular carcinoma pathogenesis," Nucleic Acids Research, vol. 44, no. 12, pp. 5529-5539, 2016.
[89]
[90]
D. Gu et al., "Reframed genome-scale metabolic model to facilitate genetic design and integration with expression data," IEEE/ACM Transactions on Computational Biology & Bioinformatics, 2016.
[91]
[92]
A. Mardinoglu et al., "The gut microbiota modulates host amino acid and glutathione metabolism in mice," Molecular Systems Biology, vol. 11, no. 10, 2015.

Non-peer reviewed

Articles

[93]
H. Yang et al., "Revisiting the role of serine metabolism in hepatic lipogenesis," Nature Metabolism, vol. 5, no. 5, pp. 760-761, 2023.
[96]
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2024-12-01 04:24:07