Associated Papers
Genetic Insights into Circulating Complement Proteins in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Potential Inflammatory Subgroup.
Maya J et al.
International Journal of Molecular Sciences, 2026
Encoding and decoding selectivity and promiscuity in the human chemokine-GPCR interaction network.
Kleist AB et al.
Cell, 2025
40273912 (PubMed )
Supplement: NIHMS2076408-supplement-MMC5.xlsx › CK_GENEATLAS
Whole-Exome Sequencing Characterized the Landscape of Somatic Mutations and Pathways in Colorectal Cancer Liver Metastasis.
Feng L et al.
Journal of Oncology, 2019
31814826 (PubMed )
Supplement: 2684075.f1.zip › 2684075.f1 › Supplemental_Table_2.xlsx › Sheet1
Pathway-focused genetic evaluation of immune and inflammation related genes with chronic fatigue syndrome.
Rajeevan MS et al.
Human Immunology, 2015
CXCL16 haplotypes in patients with human carotid atherosclerosis: preliminary results.
Zivković M et al.
Journal of Atherosclerosis and Thrombosis, 2015
Triangulation of the human, chimpanzee, and Neanderthal genome sequences identifies potentially compensated mutations.
Zhang G et al.
Human Mutation, 2010
21064102 (PubMed )
Supplement: supplement_1.pdf
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