What is he best known for?
The fields of study he is best known for:
- Gene
- DNA
- Cellular differentiation
His primary areas of investigation include Reprogramming, Cell biology, Induced pluripotent stem cell, Cellular differentiation and Embryonic stem cell.
He usually deals with Reprogramming and limits it to topics linked to Transcription factor and Cell.
His Cell biology research includes elements of SOX2, Molecular biology and Somatic cell.
His research integrates issues of Endothelial stem cell, Stem cell transplantation for articular cartilage repair, Amniotic epithelial cells, Adult stem cell and Progenitor cell in his study of SOX2.
Jose M. Polo focuses mostly in the field of Somatic cell, narrowing it down to matters related to DNA methylation and, in some cases, Endoderm and Mesoderm.
His biological study spans a wide range of topics, including Epithelial–mesenchymal transition and Proteome.
His most cited work include:
- Cell type of origin influences the molecular and functional properties of mouse induced pluripotent stem cells (980 citations)
- Immortalization eliminates a roadblock during cellular reprogramming into iPS cells (773 citations)
- A Molecular Roadmap of Reprogramming Somatic Cells into iPS Cells (609 citations)
What are the main themes of his work throughout his whole career to date?
Cell biology, Reprogramming, Induced pluripotent stem cell, Embryonic stem cell and Transcription factor are his primary areas of study.
His biological study focuses on Stem cell.
His study in the field of Progenitor cell and Haematopoiesis is also linked to topics like Population and Trophoblast.
The various areas that Jose M. Polo examines in his Reprogramming study include Nuclear reprogramming, Computational biology and Cell type.
The study incorporates disciplines such as SOX2, Molecular biology, Cellular differentiation and Somatic cell in addition to Induced pluripotent stem cell.
His study on Transcription factor also encompasses disciplines like
- Regulation of gene expression which connect with Disease,
- Cell fate determination most often made with reference to Gene expression.
He most often published in these fields:
- Cell biology (122.75%)
- Reprogramming (75.66%)
- Induced pluripotent stem cell (67.72%)
What were the highlights of his more recent work (between 2019-2021)?
- Cell biology (122.75%)
- Stem cell (48.15%)
- Induced pluripotent stem cell (67.72%)
In recent papers he was focusing on the following fields of study:
Jose M. Polo mainly investigates Cell biology, Stem cell, Induced pluripotent stem cell, Transcriptome and Reprogramming.
His Cell biology study also includes
- Embryonic stem cell which is related to area like Chromatin,
- Transcription factor, which have a strong connection to Homeobox protein NANOG.
His Stem cell study combines topics in areas such as Organoid and Function.
His Induced pluripotent stem cell research is multidisciplinary, relying on both Neuroscience and Blood–brain barrier.
Chromatin remodeling is closely connected to Wnt signaling pathway in his research, which is encompassed under the umbrella topic of Transcriptome.
His Reprogramming study incorporates themes from Blastocyst and Somatic cell.
Between 2019 and 2021, his most popular works were:
- Reprogramming roadmap reveals route to human induced trophoblast stem cells. (15 citations)
- Reprogramming roadmap reveals route to human induced trophoblast stem cells. (15 citations)
- Reprogramming roadmap reveals route to human induced trophoblast stem cells. (15 citations)
In his most recent research, the most cited papers focused on:
- Gene
- DNA
- Cellular differentiation
Jose M. Polo spends much of his time researching Cell biology, Stem cell, Trophoblast, Reprogramming and Induced pluripotent stem cell.
The concepts of his Cell biology study are interwoven with issues in Oxidative stress and Olfactory system.
His Stem cell research is multidisciplinary, incorporating perspectives in Epidermal growth factor, Regeneration, Protein kinase B and Organoid.
His Trophoblast research spans across into fields like Epiblast, Embryogenesis, Gene mutation, Cell and Blastocyst.
His work deals with themes such as Chromatin, Transcriptome and Somatic cell, which intersect with Induced pluripotent stem cell.
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