What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Cell biology, Cellular differentiation, Transcription factor, Stem cell and Regulation of gene expression.
His work on Regeneration is typically connected to Paneth cell as part of general Cell biology study, connecting several disciplines of science.
His Cellular differentiation research includes elements of Chromatin, Histone H3, Molecular biology and Transcriptome.
His Transcriptome research is multidisciplinary, incorporating elements of Reprogramming and Induced pluripotent stem cell.
His Stem cell study incorporates themes from Single-cell analysis, Multicellular organism, Organoid and Cell Cycle Protein.
His biological study spans a wide range of topics, including Promoter, Retina, DNA microarray and Cell fate determination.
His most cited work include:
- PIK3CA(H1047R) induces multipotency and multi-lineage mammary tumours. (184 citations)
- PIK3CA(H1047R) induces multipotency and multi-lineage mammary tumours. (184 citations)
- Early molecular response to posttransplantation imatinib determines outcome in MRD+ Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL) (166 citations)
What are the main themes of his work throughout his whole career to date?
Michael B. Stadler spends much of his time researching Cell biology, Genetics, Transcription factor, Chromatin and Internal medicine.
The various areas that he examines in his Cell biology study include Embryonic stem cell, Regulation of gene expression and Cellular differentiation.
Michael B. Stadler has researched Cellular differentiation in several fields, including Reprogramming, Histone H3 and Molecular biology.
His study connects Computational biology and Genetics.
His Transcription factor study combines topics in areas such as Breast cancer, Gene expression and Nucleosome.
His Chromatin study integrates concerns from other disciplines, such as Promoter, Histone and Epigenetics.
He most often published in these fields:
- Cell biology (85.14%)
- Genetics (39.86%)
- Transcription factor (41.22%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (85.14%)
- Transcription factor (41.22%)
- Organoid (12.16%)
In recent papers he was focusing on the following fields of study:
Michael B. Stadler mainly investigates Cell biology, Transcription factor, Organoid, Embryonic stem cell and Cell type.
His work in the fields of Cell biology, such as Stem cell, overlaps with other areas such as Chemistry.
His study in Transcription factor is interdisciplinary in nature, drawing from both Signal transduction, Gene expression and Nucleosome.
His work in Organoid tackles topics such as Cell which are related to areas like Retina, Transcriptome, Epithelium and Biological system.
His work carried out in the field of Embryonic stem cell brings together such families of science as CRISPR, Cytoplasm, PI3K/AKT/mTOR pathway and GTPase.
He combines subjects such as Zinc finger transcription factor, Zinc finger, Reprogramming and Cellular differentiation with his study of Chromatin.
Between 2018 and 2021, his most popular works were:
- Self-organization and symmetry breaking in intestinal organoid development (118 citations)
- Self-organization and symmetry breaking in intestinal organoid development (118 citations)
- Mammalian ISWI and SWI/SNF selectively mediate binding of distinct transcription factors. (59 citations)
In his most recent research, the most cited papers focused on:
Cell biology, Organoid, Cell, Cell type and Retina are his primary areas of study.
His research integrates issues of Transcription factor and Gene in his study of Cell biology.
His research in Transcription factor intersects with topics in CRISPR, GTPase and PI3K/AKT/mTOR pathway, Signal transduction.
His study in the field of Cell Cycle Protein and Single-cell analysis also crosses realms of Paneth cell.
His Cell type research incorporates themes from Epithelium and Transcriptome.
His Stem cell research integrates issues from Phenotype, Intestinal epithelium, Enterocyte differentiation, Nuclear receptor and Retinoic acid.
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