What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Enzyme
His primary scientific interests are in Matrix metalloproteinase, Immunology, Macrophage, Inflammation and Macrophage elastase.
His studies deal with areas such as Molecular biology, Extracellular matrix, In situ hybridization and In vivo as well as Matrix metalloproteinase.
His Immunology study integrates concerns from other disciplines, such as Cancer, Cancer research and Signal transduction, Cell biology.
His Macrophage research includes themes of Bronchoalveolar lavage, Lung and Monocyte.
His Inflammation research integrates issues from Proteases and Cytokine.
His Macrophage elastase research includes elements of Elastase and Pathology.
His most cited work include:
- MMP-9/Gelatinase B Is a Key Regulator of Growth Plate Angiogenesis and Apoptosis of Hypertrophic Chondrocytes (1535 citations)
- Requirement for Macrophage Elastase for Cigarette Smoke-Induced Emphysema in Mice (1298 citations)
- Targeted gene disruption of matrix metalloproteinase-9 (gelatinase B) suppresses development of experimental abdominal aortic aneurysms (708 citations)
What are the main themes of his work throughout his whole career to date?
Steven D. Shapiro spends much of his time researching Immunology, Matrix metalloproteinase, Pathology, Lung and COPD.
His work deals with themes such as Bronchoalveolar lavage, Macrophage and Cancer research, which intersect with Immunology.
His Matrix metalloproteinase research is multidisciplinary, relying on both Molecular biology, Extracellular matrix, Cell biology and Macrophage elastase.
Steven D. Shapiro specializes in Lung, namely Lung injury.
The various areas that Steven D. Shapiro examines in his COPD study include Pulmonary disease, Disease and Pathogenesis.
His Inflammation research is included under the broader classification of Internal medicine.
He most often published in these fields:
- Immunology (29.91%)
- Matrix metalloproteinase (19.63%)
- Pathology (18.38%)
What were the highlights of his more recent work (between 2011-2021)?
- Immunology (29.91%)
- COPD (14.33%)
- Cancer research (9.66%)
In recent papers he was focusing on the following fields of study:
Immunology, COPD, Cancer research, Internal medicine and Lung cancer are his primary areas of study.
His Immunology research includes elements of Receptor, Peroxisome proliferator-activated receptor and Bronchoalveolar lavage, Lung.
His research in Receptor focuses on subjects like Lung structure, which are connected to Pathology.
Steven D. Shapiro has included themes like Genetics, Anesthesia, Disease and Candidate gene in his COPD study.
His Cancer research research integrates issues from Cell, DNA methylation, Inflammation, Cancer cell and Immune system.
His studies deal with areas such as Endocrinology, Oncology and Cardiology as well as Internal medicine.
Between 2011 and 2021, his most popular works were:
- Peripheral Blood Mononuclear Cell Gene Expression Profiles Predict Poor Outcome in Idiopathic Pulmonary Fibrosis (171 citations)
- Doubling Times and CT Screen–Detected Lung Cancers in the Pittsburgh Lung Screening Study (65 citations)
- Emerging genetics of COPD (62 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Enzyme
Steven D. Shapiro mainly investigates Immunology, COPD, Lung, Cancer research and Candidate gene.
His Immunology research is multidisciplinary, incorporating perspectives in Reverse transcription polymerase chain reaction, Cell culture, Epithelium, NFKB1 and Signal transduction.
His work carried out in the field of COPD brings together such families of science as Apoptosis, Peroxisome proliferator-activated receptor, Chemokine, Rosiglitazone and Bronchoalveolar lavage.
The concepts of his Lung study are interwoven with issues in Autophagy, TFEB and Lung cancer.
Steven D. Shapiro combines subjects such as Proteostasis, Genetic enhancement and Respiratory system with his study of Cancer research.
His research in Annexin intersects with topics in Inflammation and Macrophage.
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