Exploring the hub Genes and Potential Mechanisms of Complement system-related Genes in Parkinson Disease: Based on Transcriptome Sequencing and Mendelian Randomization-Reference-Cited by-同舟云学术

Exploring the hub Genes and Potential Mechanisms of Complement system-related Genes in Parkinson Disease: Based on Transcriptome Sequencing and Mendelian Randomization

Published:2024-10-07 Issue:4 Volume:74 Page:
ISSN:1559-1166
Container-title:Journal of Molecular Neuroscience
language:en
Short-container-title:J Mol Neurosci

Author:

Wang Xin^ORCID,Yang Gaoming,Lai Yali,Li Yuanyuan,Liu Xindong

Funder

the Chengdu Health Commission Foundation

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s12031-024-02272-w.pdf

Reference76 articles.

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2. Armstrong MJ, Okun MS (2020) Diagnosis and treatment of Parkinson Disease: A Review. JAMA 323(6):548. https://doi.org/10.1001/jama.2019.22360

3. Berg D, Lang AE, Postuma RB, Maetzler W, Deuschl G, Gasser T, Siderowf A et al (2013) Changing the Research Criteria for the Diagnosis of Parkinson’s Disease: Obstacles and Opportunities. The Lancet Neurology 12(5):514–524. https://doi.org/10.1016/S1474-4422(13)70047-4

4. Beyer M, Mallmann MR, Xue J, Staratschek-Jox A, Vorholt D, Krebs W, Sommer D et al (2012) High-resolution transcriptome of human macrophages. PLoS ONE 7(9):e45466. https://doi.org/10.1371/journal.pone.0045466

5. Bohlson SS, Silva R, Fonseca MI, Tenner AJ (2005) CD93 is rapidly shed from the Surface of Human myeloid cells and the Soluble form is detected in human plasma. J Immunol 175(2):1239–1247. https://doi.org/10.4049/jimmunol.175.2.1239

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