What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Cytokine
His scientific interests lie mostly in Immunology, Virology, Innate immune system, Immune system and Virus.
Mark J. Cameron combines subjects such as Endocrinology and Nod with his study of Immunology.
His Virology study combines topics from a wide range of disciplines, such as RNA, Transcription, Gene and Gene expression.
The Innate immune system study combines topics in areas such as Acquired immune system and Interferon.
His Virus research includes themes of CXCL10 and Gene expression profiling.
As part of one scientific family, Mark J. Cameron deals mainly with the area of Insulitis, narrowing it down to issues related to the Pancreatic islets, and often T cell.
His most cited work include:
- Yellow fever vaccine induces integrated multilineage and polyfunctional immune responses (448 citations)
- SARS-CoV-2 Reverse Genetics Reveals a Variable Infection Gradient in the Respiratory Tract. (420 citations)
- Activation of HIV transcription with short-course vorinostat in HIV-infected patients on suppressive antiretroviral therapy. (332 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Immunology, Immune system, Virology, T cell and Innate immune system.
His study in Immunity, Interferon, Antibody, Vaccination and NOD mice is carried out as part of his Immunology studies.
The concepts of his NOD mice study are interwoven with issues in Pancreas and Pancreatic islets.
Mark J. Cameron has researched Virology in several fields, including CXCL10 and Gene expression profiling.
His research in T cell intersects with topics in Cytotoxic T cell, Cell, Cancer research and Cell biology.
He specializes in Innate immune system, namely CCL18.
He most often published in these fields:
- Immunology (63.70%)
- Immune system (29.45%)
- Virology (23.97%)
What were the highlights of his more recent work (between 2018-2021)?
- Immunology (63.70%)
- Psoriasis (7.53%)
- Cancer research (8.22%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Immunology, Psoriasis, Cancer research, Transcriptome and Immune system.
Mark J. Cameron frequently studies issues relating to Peripheral blood mononuclear cell and Immunology.
His work deals with themes such as Computational biology, Systems biology and Subclinical atherosclerosis, which intersect with Psoriasis.
His Cancer research study incorporates themes from Spleen and Homing.
The Transcriptome study which covers Cell that intersects with Innate lymphoid cell, Transforming growth factor beta, B cell, Germinal center and Extracellular matrix.
Immune system is closely attributed to Endogeny in his study.
Between 2018 and 2021, his most popular works were:
- SARS-CoV-2 Reverse Genetics Reveals a Variable Infection Gradient in the Respiratory Tract. (420 citations)
- Human Immunodeficiency Virus (HIV)-Antibody Repertoire Estimates Reservoir Size and Time of Antiretroviral Therapy Initiation in Virally Suppressed Perinatally HIV-Infected Children. (14 citations)
- Integrated systems approach defines the antiviral pathways conferring protection by the RV144 HIV vaccine. (13 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
His main research concerns Immunology, Inflammation, Microbiome, Microbiology and Tumor necrosis factor alpha.
His biological study spans a wide range of topics, including Cytotoxic T cell and Peripheral blood mononuclear cell.
His Inflammation research is multidisciplinary, incorporating perspectives in Cancer research, Dyslipidemia, Cytokine, Glucocorticoid receptor and FOXP3.
His work investigates the relationship between Microbiome and topics such as Antibiotics that intersect with problems in Immune system.
The Regulatory T cell research Mark J. Cameron does as part of his general Immune system study is frequently linked to other disciplines of science, such as Ileitis, therefore creating a link between diverse domains of science.
His Tumor necrosis factor alpha research incorporates elements of CD163, Liver X receptor and Receptor, Innate immune system, TLR4.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
