List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Cerebrospinal fluid levels of Alzheimer's disease-related proteins. The EFO term CCL4 measurement, Alzheimers disease, Alzheimer's disease biomarker measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
JS Kauwe, MH Bailey, PG Ridge, R Perry, ME Wadsworth, KL Hoyt, LA Staley, CM Karch, O Harari, C Cruchaga, BJ Ainscough, K Bales, EH Pickering, S Bertelsen, AM Fagan, DM Holtzman, JC Morris, AM Goate
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Protein quantitative trait loci. The EFO term CCL4 measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
D Melzer, JR Perry, D Hernandez, AM Corsi, K Stevens, I Rafferty, F Lauretani, A Murray, JR Gibbs, G Paolisso, S Rafiq, J Simon-Sanchez, H Lango, S Scholz, MN Weedon, S Arepalli, N Rice, N Washecka, A Hurst, A Britton, W Henley, J van de Leemput, R Li, AB Newman, G Tranah, T Harris, V Panicker, C Dayan, A Bennett, MI McCarthy, A Ruokonen, MR Jarvelin, J Guralnik, S Bandinelli, TM Frayling, A Singleton, L Ferrucci
A CC chemokine with specificity for CCR5 RECEPTORS. It is a chemoattractant for NK CELLS; MONOCYTES and a variety of other immune cells. This chemokine is encoded by multiple genes.
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The production of 12 out of 27 measured factors was induced by CEsHUT including IL-1β, TNF and IL-1Ra. In contrast to sIL-1Ra production, that of IL-1β and TNF was inhibited by HDL, corroborating previous results. In addition, CEsHUT induced monocytes to produce factors involved in their localization, survival and differentiation such as CCL5 (RANTES), CCL2 (MCP-1), interferon-γ (IFNγ), granulocyte-macrophage colony-stimulating factor (GM-CSF), and macrophage-CSF (M-CSF). The production of the latter was moderate and it was not affected by HDL.
Authors:
Gruaz L, Delucinge-Vivier C, Descombes P, Dayer JM, Burger D
Since HDL preparations may contain several particle subpopulations, we first ascertained that the inhibitory activity of the HDL preparation used in this study was due to apo A–I. As shown in Figure 1Figure 1, the inhibitory activity of HDL was reversed in a dose-dependent manner by antibodies to apo A–I. Antibodies to apo A–I alone did not affect IL-1β and TNF production by human monocytes. Similarly, they did not change CEsHUT-induced production of IL-1β or TNF in the absence of HDL.
Authors:
Gruaz L, Delucinge-Vivier C, Descombes P, Dayer JM, Burger D
CCR receptors with specificity for CHEMOKINE CCL3; CHEMOKINE CCL4; and CHEMOKINE CCL5. They are expressed at high levels in T-LYMPHOCYTES; B-LYMPHOCYTES; MACROPHAGES; MAST CELLS; and NK CELLS. The CCR5 receptor is used by the HUMAN IMMUNODEFICIENCY VIRUS to infect cells.
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Genes significantly downregulated (p < 0.05) in peripheral blood mononuclear cells (PBMC) specimens from SARS-CoV2 patients compared to healthy donors. Genes were taken from the PBMC DEGs tab of Supplementary File 1 with value = "Up" in "Tag" column. Values are log2 fold change. Genes were entered as base Ensemble IDs. The following gene identifiers were not in GeneWeaver at the time of loading: ENSG00000277739, ENSG00000236213, ENSG00000273824, ENSG00000285366, ENSG00000267523, ENSG00000260719, ENSG00000257176, ENSG00000261324, ENSG00000236449, ENSG00000279884, ENSG00000226380, ENSG00000276136, ENSG00000174171, ENSG00000260891, ENSG00000253736, ENSG00000253720, ENSG00000276853, ENSG00000279908, ENSG00000272256, ENSG00000273319, ENSG00000231858, ENSG00000286145, ENSG00000283674, ENSG00000284707, ENSG00000228655, ENSG00000251034, ENSG00000257802, ENSG00000278962, ENSG00000257277, ENSG00000233392, ENSG00000250696, ENSG00000287195, ENSG00000228140, ENSG00000231769, ENSG00000258875, ENSG00000273066, ENSG00000234156, ENSG00000273160, ENSG00000287218, ENSG00000273038, ENSG00000261208, ENSG00000287070, ENSG00000285847, ENSG00000234268, ENSG00000273284, ENSG00000287425, ENSG00000255545, ENSG00000264063, ENSG00000280614, ENSG00000281181, ENSG00000277437, ENSG00000280800, ENSG00000281383, ENSG00000268154, ENSG00000227598, ENSG00000285730.
Authors:
Yong Xiong, Yuan Liu, Liu Cao, Dehe Wang, Ming Guo, Ao Jiang, Dong Guo, Wenjia Hu, Jiayi Yang, Zhidong Tang, Honglong Wu, Yongquan Lin, Meiyuan Zhang, Qi Zhang, Mang Shi, Yingle Liu, Yu Zhou, Ke Lan, Yu Chen
Inflammatory cytokines significantly downregulated (p < 0.05) in peripheral blood mononuclear cells (PBMC) specimens from SARS-CoV2 patients compared to healthy donors. Genes were taken from starred genes in Figure 4B and which have value = "Down" in "Tag" column of the PBMC DEGs tab of Supplementary File 1. This tab is also the source of the values, which are log2 fold change, and the gene IDs, which were entered as base Ensemble IDs.
Authors:
Yong Xiong, Yuan Liu, Liu Cao, Dehe Wang, Ming Guo, Ao Jiang, Dong Guo, Wenjia Hu, Jiayi Yang, Zhidong Tang, Honglong Wu, Yongquan Lin, Meiyuan Zhang, Qi Zhang, Mang Shi, Yingle Liu, Yu Zhou, Ke Lan, Yu Chen
49 genes associated with sustained inflammatory effects in humans. Peripheral blood mononuclear cells (PBMCs) from 7 opioid-dependent and 7 non-dependent human subjects were isolated from blood samples and analyzed via scRNA-seq. Data taken from Supplementary Table 1. Values presented are "1" to represent presence. Cell-hashing scRNA-seq data available at GEO (accession: GSE128879).
Authors:
Tanya T Karagiannis, John P Cleary, Busra Gok, Andrew J Henderson, Nicholas G Martin, Masanao Yajima, Elliot C Nelson, Christine S Cheng
Differentially expressed genes in male Sprague-Dawley rats (300-375 g or 250-300 g) following cocaine administration. Some animals expressed the H3.3 Q5A vector, which led to down-regulation of histone H3 glutamine 5 dopaminylation (H3Q5dop), which is involved in midbrain plasticity in response to cocaine. Gene expression was evaluated via RNA-seq. Data taken from Supplemental Table S4 (associated with Fig 2. E, G, and I). Values presented are p-values. Data available at GEO with accession number GSE124055.
Authors:
Ashley E Lepack, Craig T Werner, Andrew F Stewart, Sasha L Fulton, Ping Zhong, Lorna A Farrelly, Alexander C W Smith, Aarthi Ramakrishnan, Yang Lyu, Ryan M Bastle, Jennifer A Martin, Swarup Mitra, Richard M O'Connor, Zi-Jun Wang, Henrik Molina, Gustavo Turecki, Li Shen, Zhen Yan, Erin S Calipari, David M Dietz, Paul J Kenny, Ian Maze
Inflammatory chemokine and receptor genes that are upregulated in the presence of LPS and differentially expressed in response to CBD + LPS. Mouse BV-2 microglial cells were pretreated with 10 uM CBD for 2 h, followed by addition of LPS for an additional 4 h. Gene expression was evaluated via microarray analysis. Data taken from Supplementary Table S2. Values presented are fold-change. Data available at GEO with accession number GSE70689.
Authors:
Ana Juknat, Maciej Pietr, Ewa Kozela, Neta Rimmerman, Rivka Levy, Fuying Gao, Giovanni Coppola, Daniel Geschwind, Zvi Vogel
Inflammatory chemokine and receptor genes that are upregulated in the presence of LPS and differentially expressed in response to THC + LPS. Mouse BV-2 microglial cells were pretreated with 10 uM THC for 2 h, followed by addition of LPS for an additional 4 h. Gene expression was evaluated via microarray analysis. Data taken from Supplementary Table S2. Values presented are fold-change. Data available at GEO with accession number GSE70689.
Authors:
Ana Juknat, Maciej Pietr, Ewa Kozela, Neta Rimmerman, Rivka Levy, Fuying Gao, Giovanni Coppola, Daniel Geschwind, Zvi Vogel
Inflammatory chemokine and receptor genes that are upregulated in the presence of LPS and differentially expressed in response to CBD. Mouse BV-2 microglial cells were pretreated with 10 uM CBD for 2 h. Gene expression was evaluated via microarray analysis. Data taken from Supplementary Table S2. Values presented are fold-change. Data available at GEO with accession number GSE70689.
Authors:
Ana Juknat, Maciej Pietr, Ewa Kozela, Neta Rimmerman, Rivka Levy, Fuying Gao, Giovanni Coppola, Daniel Geschwind, Zvi Vogel
Inflammatory chemokine and receptor genes that are upregulated in the presence of LPS and differentially expressed in response to THC. Mouse BV-2 microglial cells were pretreated with 10 uM THC for 2 h. Gene expression was evaluated via microarray analysis. Data taken from Supplementary Table S2. Values presented are fold-change. Data available at GEO with accession number GSE70689.
Authors:
Ana Juknat, Maciej Pietr, Ewa Kozela, Neta Rimmerman, Rivka Levy, Fuying Gao, Giovanni Coppola, Daniel Geschwind, Zvi Vogel
Genes up-regulated in various immune cells cells present in blood from MIS-C patients compared to healthy child donors. Genes which exhibited increased expression in some cell types and decreased expression in other cell types were included in this set. Genes from each tab (NaïveCD8, MemoryCD8, NKcell, NaïveCD4, MemoryCD4, Treg, NaïveB, MemoryB, Monocytes, Neutrophils, cDCs, pDCs) of s3-table-S6-mmc3.xlxs were assigned a category based on their cell type (indcated by the tab name) and whether they were up or down regulated (indicated by a positive or negative value in the "avg_logFC" column, e.g. either "NaïveCD8 up" or "NaïveCD8 down" for markers present in the "NaïveCD8" tab. Gene were entered as HGNC IDs. 13 Markers could not be mapped at HGNC (43893, 44075, AC004865.2, AC007952.4, AC020636.1, AC020656.1, AC119396.1, AC243960.1, AC245014.3, AL360270.1, AL445524.1).
Authors:
Anjali Ramaswamy, Nina N Brodsky, Tomokazu S Sumida, Michela Comi, Hiromitsu Asashima, Kenneth B Hoehn, Ningshan Li, Yunqing Liu, Aagam Shah, Neal G Ravindra, Jason Bishai, Alamzeb Khan, William Lau, Brian Sellers, Neha Bansal, Pamela Guerrerio, Avraham Unterman, Victoria Habet, Andrew J Rice, Jason Catanzaro, Harsha Chandnani, Merrick Lopez, Naftali Kaminski, Charles S Dela Cruz, John S Tsang, Zuoheng Wang, Xiting Yan, Steven H Kleinstein, David van Dijk, Richard W Pierce, David A Hafler, Carrie L Lucas
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Cerebrospinal fluid levels of Alzheimer's disease-related proteins. The EFO term Alzheimers disease, Alzheimer's disease biomarker measurement, CCL2 measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
JS Kauwe, MH Bailey, PG Ridge, R Perry, ME Wadsworth, KL Hoyt, LA Staley, CM Karch, O Harari, C Cruchaga, BJ Ainscough, K Bales, EH Pickering, S Bertelsen, AM Fagan, DM Holtzman, JC Morris, AM Goate
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Cerebrospinal fluid levels of Alzheimer's disease-related proteins. The EFO term matrix metalloproteinase measurement, Alzheimers disease, Alzheimer's disease biomarker measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
JS Kauwe, MH Bailey, PG Ridge, R Perry, ME Wadsworth, KL Hoyt, LA Staley, CM Karch, O Harari, C Cruchaga, BJ Ainscough, K Bales, EH Pickering, S Bertelsen, AM Fagan, DM Holtzman, JC Morris, AM Goate
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Cerebrospinal fluid levels of Alzheimer's disease-related proteins. The EFO term Alzheimers disease, interleukin-6 measurement, Alzheimer's disease biomarker measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
JS Kauwe, MH Bailey, PG Ridge, R Perry, ME Wadsworth, KL Hoyt, LA Staley, CM Karch, O Harari, C Cruchaga, BJ Ainscough, K Bales, EH Pickering, S Bertelsen, AM Fagan, DM Holtzman, JC Morris, AM Goate
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Cerebrospinal fluid levels of Alzheimer's disease-related proteins. The EFO term angiotensin-converting enzyme measurement, Alzheimers disease, Alzheimer's disease biomarker measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
JS Kauwe, MH Bailey, PG Ridge, R Perry, ME Wadsworth, KL Hoyt, LA Staley, CM Karch, O Harari, C Cruchaga, BJ Ainscough, K Bales, EH Pickering, S Bertelsen, AM Fagan, DM Holtzman, JC Morris, AM Goate
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