C-reactive Protein

Complement

Walport, M. J. (2001) · New England Journal of Medicine · doi:10.1056/nejm200104053441406 · Cited by 2,921 · see citing works

Serological reactions in pneumonia with a non-protein somatic fraction of Pneumococcus

Tillett, W. S., & Francis, T. (1930) · Journal of Experimental Medicine · doi:10.1084/jem.52.4.561 · Cited by 1,482 · see citing works

Demonstration That C-Reactive Protein Decreases eNOS Expression and Bioactivity in Human Aortic Endothelial Cells

Venugopal, S. K., Devaraj, S., Yuhanna, I. S., Shaul, P. W., & Jialal, I. (2002) · Circulation · doi:10.1161/01.cir.0000033116.22237.f9 · Cited by 849 · see citing works

C-Reactive Protein–Mediated Low Density Lipoprotein Uptake by Macrophages

Zwaka, T. P., Hombach, V., & Torzewski, J. (2001) · Circulation · doi:10.1161/01.cir.103.9.1194 · Cited by 845 · see citing works

The physiological structure of human C-reactive protein and its complex with phosphocholine

Thompson, D., Pepys, M. B., & Wood, S. P. (1999) · Structure · doi:10.1016/s0969-2126(99)80023-9 · Cited by 818 · see citing works

C-Reactive Protein Binds to Apoptotic Cells, Protects the Cells from Assembly of the Terminal Complement Components, and Sustains an Antiinflammatory Innate Immune Response

Gershov, D., Kim, S., Brot, N., & Elkon, K. B. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.9.1353 · Cited by 695 · see citing works

C-Reactive Protein: Risk Marker or Mediator in Atherothrombosis?

Jialal, I., Devaraj, S., & Venugopal, S. K. (2004) · Hypertension · doi:10.1161/01.hyp.0000130484.20501.df · Cited by 569 · see citing works

C-reactive protein binds to both oxidized LDL and apoptotic cells through recognition of a common ligand: Phosphorylcholine of oxidized phospholipids

Chang, M.-K., Binder, C. J., Torzewski, M., & Witztum, J. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.192399699 · Cited by 517 · see citing works

Specificity of C-Reactive Protein for Choline Phosphate Residues of Pneumococcal C-Polysaccharide

Volanakis, J. E., & Kaplan, M. H. (1971) · Experimental Biology and Medicine · doi:10.3181/00379727-136-35323 · Cited by 398 · see citing works

C-Reactive Protein Accelerates the Progression of Atherosclerosis in Apolipoprotein E–Deficient Mice

Paul, A., Ko, K. W. S., Li, L., Yechoor, V. K., McCrory, M. A., Szalai, A. J., & Chan, L. (2004) · Circulation · doi:10.1161/01.cir.0000114526.50618.24 · Cited by 373 · see citing works

Induction of inflammatory cytokine release from cultured human monocytes by C-reactive protein

Ballou, S. P., & Lozanski, G. (1992) · Cytokine · doi:10.1016/1043-4666(92)90079-7 · Cited by 371 · see citing works

The Crystal Structure of the Globular Head of Complement Protein C1q Provides a Basis for Its Versatile Recognition Properties

Gaboriaud, C., Juanhuix, J., Gruez, A., Lacroix, M., Darnault, C., Pignol, D., Verger, D., Fontecilla-Camps, J. C., & Arlaud, G. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307764200 · Cited by 362 · see citing works

Three dimensional structure of human C-reactive protein

Shrive, A., Gheetham, G. M. T., Holden, D., Myles, D., Turnell, W., Volanakis, J., Pepys, M., Bloomer, A., & Greenhough, T. (1996) · Nature Structural Biology · doi:10.1038/nsb0496-346 · Cited by 349 · see citing works

Regulation of complement activation by C-reactive protein

Mold, C., Gewurz, H., & Du Clos, T. W. (1999) · Immunopharmacology · doi:10.1016/s0162-3109(99)00007-7 · Cited by 326 · see citing works

Phosphorylcholine on the Lipopolysaccharide of Haemophilus influenzae Contributes to Persistence in the Respiratory Tract and Sensitivity to Serum Killing Mediated by C-reactive Protein

Weiser, J. N., Pan, N., McGowan, K. L., Musher, D. M., Martin, A., & Richards, J. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.4.631 · Cited by 304 · see citing works

Polymorphism at the C-reactive protein locus influences gene expression and predisposes to systemic lupus erythematosus

Russell, A. I. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddh021 · Cited by 294 · see citing works

Increased Thrombosis After Arterial Injury in Human C-Reactive Protein–Transgenic Mice

Danenberg, H. D., Szalai, A. J., Swaminathan, R. V., Peng, L., Chen, Z., Seifert, P. A., Fay, W. P., Simon, D. I., & Edelman, E. R. (2003) · Circulation · doi:10.1161/01.cir.0000085568.13915.1e · Cited by 283 · see citing works

Conformational Rearrangement in C-Reactive Protein Is Required for Proinflammatory Actions on Human Endothelial Cells

Khreiss, T., József, L., Potempa, L. A., & Filep, J. G. (2004) · Circulation · doi:10.1161/01.cir.0000125527.41598.68 · Cited by 279 · see citing works

Antiinflammatory properties of hepatic acute phase proteins: preferential induction of interleukin 1 (IL-1) receptor antagonist over IL-1 beta synthesis by human peripheral blood mononuclear cells.

Tilg, H., Vannier, E. G., Vachino, G., Dinarello, C. A., & Mier, J. W. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.178.5.1629 · Cited by 256 · see citing works

C-reactive protein is protective against Streptococcus pneumoniae infection in mice.

Mold, C., Nakayama, S., Holzer, T. J., Gewurz, H., & Clos, T. W. D. (1981) · The Journal of Experimental Medicine · doi:10.1084/jem.154.5.1703 · Cited by 243 · see citing works

Interaction of C-reactive protein with artificial phosphatidylcholine bilayers

Volanakis, J. E., & WIRTZ, K. W. A. (1979) · Nature · doi:10.1038/281155a0 · Cited by 238 · see citing works

Human C-reactive protein is protective against fatal Streptococcus pneumoniae infection in transgenic mice

Szalai, A. J., Briles, D. E., & Volanakis, J. E. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.155.5.2557 · Cited by 205 · see citing works

Topology and Structure of the C1q-Binding Site on C-Reactive Protein

Agrawal, A. C., Shrive, A. K., Greenhough, T. J., & Volanakis, J. E. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.6.3998 · Cited by 187 · see citing works

A role for secretory phospholipase A2 and C-reactive protein in the removal of injured cells

Hack, C. E., Wolbink, G., Schalkwijk, C., Speijer, H., Hermens, W. T., & van den BOSCH, H. (1997) · Immunology Today · doi:10.1016/s0167-5699(97)01002-5 · Cited by 183 · see citing works

C-Reactive Protein Mediates Protection from Lipopolysaccharide Through Interactions With FcγR

Mold, C., Rodriguez, W., Rodic-Polic, B., & Clos, T. W. D. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.12.7019 · Cited by 162 · see citing works

Transgenic mice expressing rabbit C-reactive protein are resistant to endotoxemia

Xia, D., & Samols, D. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.6.2575 · Cited by 156 · see citing works

The position of phosphorylcholine on the lipopolysaccharide of Haemophilus influenzae affects binding and sensitivity to C‐reactive protein‐mediated killing

Lysenko, E., Richards, J. C., Cox, A. D., et al. (2000) · Molecular Microbiology · doi:10.1046/j.1365-2958.2000.01707.x · Cited by 155 · see citing works

C-reactive protein levels during disease exacerbations and infections in systemic lupus erythematosus: a prospective longitudinal study.

ter Borg, E. J., Horst, G., Limburg, P. C., van Rijswijk, M. H., & Kallenberg, C. (1990) · PubMed · Cited by 155 · see citing works

Serum Amyloid P Component and C-Reactive Protein Mediate Phagocytosis Through Murine FcγRs

Mold, C., Gresham, H. D., & Clos, T. W. D. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.2.1200 · Cited by 148 · see citing works

Protection from Streptococcus pneumoniae Infection by C-Reactive Protein and Natural Antibody Requires Complement But Not Fcγ Receptors

Mold, C., Rodic-Polic, B., & Clos, T. W. D. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.12.6375 · Cited by 139 · see citing works

Stimulating effect of C-reactive protein on phagocytosis of various species of pathogenic bacteria.

Kindmark, C. O. (1971) · PubMed · Cited by 135 · see citing works

Serum Amyloid P Component and C-Reactive Protein Opsonize Apoptotic Cells for Phagocytosis through Fcγ Receptors

Mold, C., Baca, R., & Clos, T. W. D. (2002) · Journal of Autoimmunity · doi:10.1006/jaut.2002.0615 · Cited by 134 · see citing works

C-reactive protein is produced by a small number of normal human peripheral blood lymphocytes.

Kuta, A. E., & Baum, L. L. (1986) · The Journal of Experimental Medicine · doi:10.1084/jem.164.1.321 · Cited by 132 · see citing works

Human C-Reactive Protein Is Protective against FatalSalmonella entericaSerovar Typhimurium Infection in Transgenic Mice

Szalai, A. J., VanCott, J. L., McGhee, J. R., Volanakis, J. E., & Benjamin, W. H. (2000) · Infection and Immunity · doi:10.1128/iai.68.10.5652-5656.2000 · Cited by 113 · see citing works

Delayed lupus onset in (NZB × NZW)F1 mice expressing a human C‐reactive protein transgene

Szalai, A. J., Weaver, C. T., McCrory, M. A., van Ginkel, F. W., Reiman, R. M., Kearney, J. F., Marion, T. N., & Volanakis, J. E. (2003) · Arthritis & Rheumatism · doi:10.1002/art.11026 · Cited by 100 · see citing works

C-Reactive Protein: Structural Biology and Host Defense Function

Szalai, A. J., Agrawal, A., Greenhough, T. J., et al. (1999) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.1999.046 · Cited by 90 · see citing works

Experimental Allergic Encephalomyelitis Is Inhibited in Transgenic Mice Expressing Human C-Reactive Protein

Szalai, A. J., Nataf, S., Hu, X., & Barnum, S. R. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.11.5792 · Cited by 89 · see citing works

The antimicrobial activity of C-reactive protein

Szalai, A. J. (2002) · Microbes and Infection · doi:10.1016/s1286-4579(01)01528-3 · Cited by 86 · see citing works

C-Reactive Protein Upregulates Complement-Inhibitory Factors in Endothelial Cells

Li, S., Szmitko, P. E., Weisel, R. D., Wang, C., Fedak, P. W. M., Li, R., Mickle, D. A. G., & Verma, S. (2004) · Circulation · doi:10.1161/01.cir.0000117087.27524.0e · Cited by 84 · see citing works

Decreased Autoantibody Levels and Enhanced Survival of (NZB × NZW) F1 Mice Treated with C-Reactive Protein

Clos, T. W. D., Zlock, L. T., Hicks, P., & Mold, C. (1994) · Clinical Immunology and Immunopathology · doi:10.1006/clin.1994.1005 · Cited by 84 · see citing works

A C-Reactive Protein Mutant That Does Not Bind to Phosphocholine and Pneumococcal C-Polysaccharide

Agrawal, A. C., Simpson, M. J., Black, S., et al. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.6.3217 · Cited by 78 · see citing works

Probing the C1q-binding site on human C-reactive protein by site-directed mutagenesis.

Agrawal, A., & Volanakis, J. E. (1994) · The Journal of Immunology · doi:10.4049/jimmunol.152.11.5404 · Cited by 75 · see citing works

Transgenic Mice Expressing Rabbit C-Reactive Protein Exhibit Diminished Chemotactic Factor-Induced Alveolitis

Ahmed, N., Thorley, R., Xia, D., Samols, D. R., & Webster, R. O. (1996) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.153.3.8630558 · Cited by 62 · see citing works

Do Post‐transcriptional Mechanisms Participate in Induction of C‐reactive Protein and Serum Amyloid A by IL‐6 and IL‐I?a

Kushner, I., JIANG, S., ZHANG, D., Lozanski, G., & Samols, D. R. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb32318.x · Cited by 62 · see citing works

C-Reactive Protein Induces Signaling Through FcγRIIa on HL-60 Granulocytes,

Chi, M., Tridandapani, S., Zhong, W., Coggeshall, K. M., & Mortensen, R. F. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.3.1413 · Cited by 55 · see citing works

Transcription factor c-Rel enhances C-reactive protein expression by facilitating the binding of C/EBPβ to the promoter

Agrawal, A. C. (2003) · Molecular Immunology · doi:10.1016/s0161-5890(03)00148-2 · Cited by 54 · see citing works

The phosphocholine and the polycation-binding sites on rabbit C-reactive protein are structurally and functionally distinct

Black, S., Agrawal, A., & Samols, D. R. (2003) · Molecular Immunology · doi:10.1016/s0161-5890(03)00031-2 · Cited by 38 · see citing works

A hypothesis resolving the apparently disparate activities of native and altered forms of human C-reactive protein

Shields, M. J. (1993) · Immunologic Research · doi:10.1007/bf02918367 · Cited by 27 · see citing works

Expression of host defense scavenger receptors in spondylarthropathy

McBeth (2001) · Pure Amsterdam UMC · doi:10.1002/1529-0131(200104)44:4 · Cited by 1 · see citing works

Untitled work

(2001) · doi:10.1002/1521-4141(200112)31:12

Consensus definition of sarcopenia, cachexia and pre-cachexia: joint document elaborated by Special Interest Groups (SIG) “cachexia-anorexia in chronic wasting diseases” and “nutrition in geriatrics”

Muscaritoli, M., Anker, S. D., Argilés, J., Aversa, Z., Bauer, J. M., Biolo, G., Boirie, Y., Bosaeus, I., Cederholm, T., Costelli, P., et al. (2010) · Clinical Nutrition · doi:10.1016/j.clnu.2009.12.004 · Cited by 1,732 · see citing works

Rethinking IL-6 and CRP: Why they are more than inflammatory biomarkers, and why it matters

Del Giudice, M., & Gangestad, S. W. (2018) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2018.02.013 · Cited by 779 · see citing works

The pivotal role of the complement system in aging and age-related macular degeneration: Hypothesis re-visited

Anderson, D. H., Radeke, M. J., Gallo, N. B., Chapin, E. A., Johnson, P. T., Curletti, C. R., Hancox, L. S., Hu, J., Ebright, J. N., Malek, G., et al. (2010) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2009.11.003 · Cited by 727 · see citing works

Elevated C-Reactive Protein Levels, Psychological Distress, and Depression in 73 131 Individuals

Wium-Andersen, M. K., Ørsted, D. D., Nielsen, S. F., & Nordestgaard, B. G. (2013) · JAMA Psychiatry · doi:10.1001/2013.jamapsychiatry.102 · Cited by 489 · see citing works

Hepatocytes: a key cell type for innate immunity

Zhou, Z., Xu, M.-J., & Gao, B. (2016) · Cellular & Molecular Immunology · doi:10.1038/cmi.2015.97 · Cited by 472 · see citing works

Complement activation by photooxidation products of A2E, a lipofuscin constituent of the retinal pigment epithelium

Zhou, J., Jang, Y. P., Kim, S. R., & Sparrow, J. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604255103 · Cited by 358 · see citing works

Complement Factor H Polymorphism, Complement Activators, and Risk of Age-Related Macular Degeneration

Despriet, D. D. G., Klaver, C. C. W., Witteman, J. C. M., Bergen, A. A. B., Kardys, I., de Maat, M. P. M., Boekhoorn, S. S., Vingerling, J. R., Hofman, A., Oostra, B. A., et al. (2006) · JAMA · doi:10.1001/jama.296.3.301 · Cited by 348 · see citing works

Childhood adversity and inflammatory processes in youth: a prospective study

Slopen, N., Kubzansky, L. D., McLaughlin, K. A., & Koenen, K. C. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.05.013 · Cited by 330 · see citing works

Reduction in C-reactive protein through cardiac rehabilitation and exercise training

Milani, R. V., Lavie, C. J., & Mehra, M. R. (2004) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2003.10.041 · Cited by 302 · see citing works

Circulating Levels of Inflammatory Cytokines and Risk of Colorectal Adenomas

Kim, S., Keku, T. O., Martin, C., Galanko, J., Woosley, J. T., Schroeder, J. C., Satia, J. A., Halabi, S., & Sandler, R. S. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-2924 · Cited by 298 · see citing works

Individuals homozygous for the age-related macular degeneration risk-conferring variant of complement factor H have elevated levels of CRP in the choroid

Johnson, P. T., Betts, K. E., Radeke, M. J., Hageman, G. S., Anderson, D. H., & Johnson, L. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606234103 · Cited by 223 · see citing works

Early environments and the ecology of inflammation

McDade, T. W. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202244109 · Cited by 218 · see citing works

Correlates of Serum C-Reactive Protein (CRP) — No Association With Sleep Duration or Sleep Disordered Breathing

Taheri, S., Austin, D., Lin, L., Nieto, F. J., Young, T., & Mignot, E. (2007) · Sleep · doi:10.1093/sleep/30.8.991 · Cited by 189 · see citing works

Dietary nitrite prevents hypercholesterolemic microvascular inflammation and reverses endothelial dysfunction

Stokes, K. Y., Dugas, T. R., Tang, Y., Garg, H., Guidry, E., & Bryan, N. S. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01291.2008 · Cited by 171 · see citing works

Periodontal therapy and cardiovascular risk

Orlandi, M., Graziani, F., & D'Aiuto, F. (2020) · Periodontology 2000 · doi:10.1111/prd.12299 · Cited by 155 · see citing works

C-reactive protein: structure, function, regulation, and role in clinical diseases

Zhou, H.-H., Tang, Y.-L., Xu, T.-H., & Cheng, B. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1425168 · Cited by 162 · see citing works

Dietary Patterns during Pregnancy Are Associated with Risk of Gestational Diabetes Mellitus

Shin, D., Lee, K., & Song, W. (2015) · Nutrients · doi:10.3390/nu7115472 · Cited by 133 · see citing works

Development of VAX128, a recombinant hemagglutinin (HA) influenza-flagellin fusion vaccine with improved safety and immune response

Taylor, D. N., Treanor, J. J., Sheldon, E. A., Johnson, C., Umlauf, S., Song, L., Kavita, U., Liu, G., Tussey, L., Ozer, K., et al. (2012) · Vaccine · doi:10.1016/j.vaccine.2012.06.086 · Cited by 132 · see citing works

Inflammation and long-term mortality in acute congestive heart failure

Mueller, C., Laule-Kilian, K., Christ, A., Brunner–La Rocca, H. P., & Perruchoud, A. P. (2006) · American Heart Journal · doi:10.1016/j.ahj.2005.06.046 · Cited by 131 · see citing works

Curcumin and/or omega-3 polyunsaturated fatty acids supplementation reduces insulin resistance and blood lipids in individuals with high risk of type 2 diabetes: A randomised controlled trial

Thota, R. N., Acharya, S. H., & Garg, M. L. (2019) · Lipids in Health and Disease · doi:10.1186/s12944-019-0967-x · Cited by 127 · see citing works

Effect of Periodontal Treatment on Serum C‐Reactive Protein Levels: A Systematic Review and Meta‐Analysis

Ioannidou, E., Malekzadeh, T., & Dongari‐Bagtzoglou, A. (2006) · Journal of Periodontology · doi:10.1902/jop.2006.050443 · Cited by 118 · see citing works

Associations of high sensitivity C-reactive protein levels in schizophrenia and comparison groups

Joseph, J., Depp, C., Martin, A. S., Daly, R. E., Glorioso, D. K., Palmer, B. W., & Jeste, D. V. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.08.019 · Cited by 109 · see citing works

Systemic inflammation following non-surgical and surgical periodontal therapy

Graziani, F., Cei, S., Tonetti, M., Paolantonio, M., Serio, R., Sammartino, G., Gabriele, M., & D'Aiuto, F. (2010) · Journal Of Clinical Periodontology · doi:10.1111/j.1600-051x.2010.01585.x · Cited by 107 · see citing works

Serum Amyloid A Is an Endogenous Ligand That Differentially Induces IL-12 and IL-23

He, R., Shepard, L. W., Chen, J., Pan, Z. K., & Ye, R. D. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.6.4072 · Cited by 100 · see citing works

Levels of C-reactive protein (CRP) in patients with schizophrenia, unipolar depression and bipolar disorder

Wysokiński, A., Margulska, A., Strzelecki, D., & Kłoszewska, I. (2015) · Nordic Journal of Psychiatry · doi:10.3109/08039488.2014.984755 · Cited by 94 · see citing works

Exercise intervention and inflammatory markers in coronary artery disease: A meta-analysis

Swardfager, W., Herrmann, N., Cornish, S., Mazereeuw, G., Marzolini, S., Sham, L., & Lanctôt, K. L. (2012) · American Heart Journal · doi:10.1016/j.ahj.2011.12.017 · Cited by 91 · see citing works

T helper 17 cells may drive neuroprogression in major depressive disorder: Proposal of an integrative model

Slyepchenko, A., Maes, M., Köhler, C. A., Anderson, G., Quevedo, J., Alves, G. S., Berk, M., Fernandes, B. S., & Carvalho, A. F. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.02.002 · Cited by 89 · see citing works

Polymorphisms of the CRP gene inhibit inflammatory response and increase susceptibility to depression: The Health in Men Study

Almeida, O. P., Norman, P. E., Allcock, R., Bockxmeer, F. V., Hankey, G. J., Jamrozik, K., & Flicker, L. (2009) · International Journal of Epidemiology · doi:10.1093/ije/dyp199 · Cited by 80 · see citing works

Prognostic value of serum albumin combined with serum C-reactive protein levels in older hospitalized patients: continuing importance of serum albumin

Iwata, M., Kuzuya, M., Kitagawa, Y., & Iguchi, A. (2006) · Aging Clinical and Experimental Research · doi:10.1007/bf03324664 · Cited by 73 · see citing works

A randomized placebo-controlled pilot study of pravastatin as an adjunctive therapy in schizophrenia patients: Effect on inflammation, psychopathology, cognition and lipid metabolism

Vincenzi, B., Stock, S., Borba, C. P. C., Cleary, S. M., Oppenheim, C. E., Petruzzi, L. J., Fan, X., Copeland, P. M., Freudenreich, O., Cather, C., et al. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.08.021 · Cited by 67 · see citing works

A Perspective of AMD Through the Eyes of Immunology

Copland, D. A., Theodoropoulou, S., Liu, J., & Dick, A. D. (2018) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.18-23893 · Cited by 66 · see citing works

Elevated C-Reactive Protein Is Associated with Cognitive Decline in Outpatients of a General Hospital: The Project in Sado for Total Health (PROST)

Watanabe, Y., Kitamura, K., Nakamura, K., Sanpei, K., Wakasugi, M., Yokoseki, A., Onodera, O., Ikeuchi, T., Kuwano, R., Momotsu, T., et al. (2016) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000442585 · Cited by 65 · see citing works

Pathways leading to muscle insulin resistance – The muscle – fat connection

Sell, H., Eckel, J., & Dietze-Schroeder, D. (2006) · Archives of Physiology and Biochemistry · doi:10.1080/13813450600711540 · Cited by 61 · see citing works

Pioglitazone for secondary prevention after ischemic stroke and transient ischemic attack: Rationale and design of the Insulin Resistance Intervention after Stroke Trial

Viscoli, C. M., Brass, L. M., Carolei, A., Conwit, R., Ford, G. A., Furie, K. L., Gorman, M., Guarino, P. D., Inzucchi, S. E., Lovejoy, A. M., et al. (2014) · American Heart Journal · doi:10.1016/j.ahj.2014.07.016 · Cited by 50 · see citing works

The effect of aerobic training on serum adiponectin and leptin levels and inflammatory markers of coronary heart disease in obese men.

Akbarpour, M. (2013) · Biology of Sport · doi:10.5604/20831862.1029817 · Cited by 48 · see citing works

Cytokines are associated with longitudinal changes in cognitive performance among urban adults

Beydoun, M. A., Weiss, J., Obhi, H. K., Beydoun, H. A., Dore, G. A., Liang, H., Evans, M. K., & Zonderman, A. B. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.04.027 · Cited by 45 · see citing works

Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study

Russell, A. E., Ford, T., Gunnell, D., Heron, J., Joinson, C., Moran, P., Relton, C., Suderman, M., Hemani, G., & Mars, B. (2020) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2020.05.065 · Cited by 39 · see citing works

Inflammation and Oral Contraceptive Use in Female Athletes Before the Rio Olympic Games

Larsen, B., Cox, A., Colbey, C., Drew, M., McGuire, H., Fazekas de St Groth, B., Hughes, D., Vlahovich, N., Waddington, G., Burke, L., et al. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00497 · Cited by 38 · see citing works

Advanced oxidation protein products and inflammatory markers in liver cirrhosis: a comparison between alcohol-related and HCV-related cirrhosis.

Zuwała-Jagiełło, J., Pazgan-Simon, M., Simon, K., & Warwas, M. (2011) · Acta Biochimica Polonica · doi:10.18388/abp.2011_2286 · Cited by 38 · see citing works

Biological Profiling of Prospective Antidepressant Response in Major Depressive Disorder: Associations with (Neuro)Inflammation, Fatty Acid Metabolism, and Amygdala-Reactivity

Mocking, R. J. T., Nap, T. S., Westerink, A. M., Assies, J., Vaz, F. M., Koeter, M. W. J., Ruhé, H. G., & Schene, A. H. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.02.019 · Cited by 34 · see citing works

Stress-induced parasympathetic control and its association with inflammatory reactivity.

Woody, A., Figueroa, W. S., Benencia, F., & Zoccola, P. M. (2017) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000426 · Cited by 33 · see citing works

Angiotensin II Induces C-Reactive Protein Expression via AT1-ROS-MAPK-NF-κB Signal Pathway in Hepatocytes

Zhao, J., Liu, J., Pang, X., Wang, S., Wu, D., Zhang, X., & Feng, L. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000354461 · Cited by 31 · see citing works

C-reactive protein (CRP) is essential for efficient systemic transduction of recombinant adeno-associated virus vector 1 (rAAV-1) and rAAV-6 in mice

Denard, J., Marolleau, B., Jenny, C., Rao, T. N., Fehling, H. J., Voit, T., & Svinartchouk, F. (2013) · Journal of Virology · doi:10.1128/jvi.01813-13 · Cited by 31 · see citing works

A high sensitivity assay is more accurate than a classical assay for the measurement of plasma CRP levels in endometriosis

Vodolazkaia, A., Bossuyt, X., Fassbender, A., Kyama, C. M., Meuleman, C., Peeraer, K., Tomassetti, C., & D'Hooghe, T. M. (2011) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-9-113 · Cited by 28 · see citing works

Safety and efficacy assessment of an mRNA rabies vaccine in dogs, rodents, and cynomolgus macaques

Li, J., Yu, P., Liu, Q., Xu, L., Chen, Y., Li, Y., Zhang, F., Zhu, W., & Peng, Y. (2024) · npj Vaccines · doi:10.1038/s41541-024-00925-w · Cited by 24 · see citing works

Positive antibody response to vaccination in adolescence predicts lower C‐reactive protein concentration in young adulthood in the philippines

Mcdade, T. W., Adair, L., Feranil, A. B., & Kuzawa, C. (2011) · American Journal of Human Biology · doi:10.1002/ajhb.21128 · Cited by 22 · see citing works

Inflammation Through a Psychoneuroimmunological Lens

Bennett, J. M., Gillie, B. L., Lindgren, M. E., Fagundes, C. P., & Kiecolt-Glaser, J. K. (2013) · Handbook of Systems and Complexity in Health · doi:10.1007/978-1-4614-4998-0_19 · Cited by 15 · see citing works

Discussion on pathogenesis levels of hypertension

Wang, Q. (2007) · Zhongyi-yao xuebao

Exploration on relationship of basic pathogenesis and disease symptom

Zhang, Y. (2010) · Journal of Tianjin University of Traditional Chinese Medicine

Analysis of Pathogenesis and Correlative Factors of Acute Upper Gastrointestinal Hemorrhage

Qu, J. (2013) · Xiandai shengwu yixue jinzhan

[Interaction between NOD-like receptor protein 3 inflammatory corpuscles and mitochondrial dysfunction in the pathogenesis of septic cardiomyopathy].

Yuan, Y., Shen, Q., & Jin, J. (2024) · PubMed · doi:10.3760/cma.j.cn121430-20230518-00379 · Cited by 1 · see citing works

Update on pathogenesis in idiopathic inflammatory myopathies

Wen-tao, W. (2005) · Yixue yanjiusheng xuebao