What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Cell biology, Transient receptor potential channel, TRPC5, TRPC and Biochemistry.
Michael Schaefer interconnects XCL1 and Chemokine receptor CCR5 in the investigation of issues within Cell biology.
His Transient receptor potential channel course of study focuses on Biophysics and TRPV1, TRPV5, Homomeric and Transmembrane domain.
His TRPC5 study integrates concerns from other disciplines, such as TRPC Cation Channels and TRPC4.
Michael Schaefer has researched TRPC Cation Channels in several fields, including TRPC3, TRPC1, TRPC6 Cation Channel, Calcium signaling and Receptor tyrosine kinase.
His Biochemistry research is multidisciplinary, incorporating elements of Alzheimer's disease and Amyloid precursor protein secretase.
His most cited work include:
- Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol. (1241 citations)
- Superior antigen cross-presentation and XCR1 expression define human CD11c+CD141+ cells as homologues of mouse CD8+ dendritic cells (635 citations)
- Subunit composition of mammalian transient receptor potential channels in living cells (631 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Cell biology, Biochemistry, Receptor, Transient receptor potential channel and Biophysics.
His Cell biology research is multidisciplinary, relying on both Protein subunit, TRPC Cation Channels and Förster resonance energy transfer.
His TRPC Cation Channels study combines topics from a wide range of disciplines, such as TRPC3, Receptor tyrosine kinase and TRPC6 Cation Channel.
Michael Schaefer studied Receptor and Molecular biology that intersect with HEK 293 cells.
His biological study spans a wide range of topics, including Extracellular and Intracellular.
His study focuses on the intersection of Biophysics and fields such as Homomeric with connections in the field of TRPV.
He most often published in these fields:
- Cell biology (34.78%)
- Biochemistry (21.74%)
- Receptor (17.39%)
What were the highlights of his more recent work (between 2008-2021)?
- Cell biology (34.78%)
- Cognitive psychology (3.26%)
- Intracellular (8.70%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Cell biology, Cognitive psychology, Intracellular, Förster resonance energy transfer and Clinical psychology.
His specific area of interest is Cell biology, where Michael Schaefer studies G protein-coupled receptor.
His Cognitive psychology study deals with Interpersonal Reactivity Index intersecting with Personal distress and Empathic concern.
His Intracellular research integrates issues from APLP1, Crosstalk, Ectodomain, Subcellular localization and APLP2.
His work deals with themes such as Endocrinology, Live cell imaging, Melanocortin, Sequence and Binding site, which intersect with Förster resonance energy transfer.
The study incorporates disciplines such as Pill and Randomized controlled trial in addition to Clinical psychology.
Between 2008 and 2021, his most popular works were:
- Superior antigen cross-presentation and XCR1 expression define human CD11c+CD141+ cells as homologues of mouse CD8+ dendritic cells (635 citations)
- Selective Expression of the Chemokine Receptor XCR1 on Cross-presenting Dendritic Cells Determines Cooperation with CD8+ T Cells (270 citations)
- Subcellular localization and dimerization of APLP1 are strikingly different from APP and APLP2 (78 citations)
In his most recent research, the most cited papers focused on:
Michael Schaefer mainly investigates Cell biology, XCL1, Chemokine receptor CCR5, CC chemokine receptors and CCL25.
His Cell biology research includes themes of Subcellular localization, Ectodomain and Förster resonance energy transfer.
XCL1 is closely attributed to XCR1 in his study.
His research in Chemokine receptor CCR5 intersects with topics in CXCL16, XCL2 and C-C chemokine receptor type 6.
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