What is he best known for?
The fields of study he is best known for:
Molecular biology, Osteoblast, Type I collagen, Gene expression and Transgene are his primary areas of study.
His research integrates issues of Promoter, Reporter gene, Chloramphenicol acetyltransferase, Cre recombinase and Tandem repeat in his study of Molecular biology.
Alexander C. Lichtler has researched Osteoblast in several fields, including Stromal cell, Internal medicine, Endocrinology and Cell biology.
His Cell biology research incorporates elements of Osteoclast and Genetically modified mouse.
Alexander C. Lichtler has included themes like Cell culture and Fibroblast in his Type I collagen study.
His Gene expression study combines topics in areas such as Procollagen peptidase, Messenger RNA and Transcription.
His most cited work include:
- Use of Type I Collagen Green Fluorescent Protein Transgenes to Identify Subpopulations of Cells at Different Stages of the Osteoblast Lineage (327 citations)
- Basic fibroblast growth factor inhibits type I collagen gene expression in osteoblastic MC3T3-E1 cells. (189 citations)
- Specification of Region-Specific Neurons Including Forebrain Glutamatergic Neurons from Human Induced Pluripotent Stem Cells (156 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Molecular biology, Cell biology, Osteoblast, Gene expression and Type I collagen.
His research in Molecular biology intersects with topics in Genetically modified mouse, Transgene, Reporter gene, Chloramphenicol acetyltransferase and Regulation of gene expression.
His Cell biology study combines topics from a wide range of disciplines, such as Cartilage, Immunology, Bone morphogenetic protein 2 and DLX5.
The concepts of his Osteoblast study are interwoven with issues in Stromal cell, Internal medicine, Bone marrow, Endocrinology and Cellular differentiation.
His Gene expression course of study focuses on Messenger RNA and Transcription and Protein biosynthesis.
Alexander C. Lichtler interconnects Transfection and Green fluorescent protein in the investigation of issues within Type I collagen.
He most often published in these fields:
- Molecular biology (50.88%)
- Cell biology (27.19%)
- Osteoblast (25.44%)
What were the highlights of his more recent work (between 2009-2020)?
- Cell biology (27.19%)
- Induced pluripotent stem cell (7.02%)
- Progenitor cell (5.26%)
In recent papers he was focusing on the following fields of study:
Alexander C. Lichtler mainly focuses on Cell biology, Induced pluripotent stem cell, Progenitor cell, Embryonic stem cell and Molecular biology.
The Cell biology study combines topics in areas such as Cartilage, Immunology and Osteoblast.
His study brings together the fields of Bone cell and Osteoblast.
His Progenitor cell study combines topics from a wide range of disciplines, such as In vivo and Green fluorescent protein.
In his study, which falls under the umbrella issue of Embryonic stem cell, Directed differentiation, Anatomy and RUNX2 is strongly linked to Cellular differentiation.
He combines Molecular biology and Epigenomics in his studies.
Between 2009 and 2020, his most popular works were:
- Specification of Region-Specific Neurons Including Forebrain Glutamatergic Neurons from Human Induced Pluripotent Stem Cells (156 citations)
- Direct cell-cell contact between mature osteoblasts and osteoclasts dynamically controls their functions in vivo. (67 citations)
- Stepwise Differentiation of Pluripotent Stem Cells into Osteoblasts Using Four Small Molecules under Serum-free and Feeder-free Conditions (63 citations)
In his most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Cell biology, Cellular differentiation, Induced pluripotent stem cell, Immunology and Osteoblast.
His research in Cell biology intersects with topics in Amelogenin, Secretion, Cell type and Dentinal Tubule.
Alexander C. Lichtler usually deals with Cellular differentiation and limits it to topics linked to Embryonic stem cell and Progenitor cell.
His Induced pluripotent stem cell research is multidisciplinary, incorporating perspectives in Sendai virus, Peripheral blood mononuclear cell, Stem cell marker and Virology.
His Bone marrow study in the realm of Immunology connects with subjects such as CD146.
His research integrates issues of Cell culture, Bone cell and Bone healing in his study of Osteoblast.
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