What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Cell biology, Inositol, Voltage-dependent calcium channel, Receptor and Biochemistry.
His is involved in several facets of Cell biology study, as is seen by his studies on Endoplasmic reticulum, Intracellular, Calcium signaling and Golgi apparatus.
Ludwig Missiaen has included themes like Ruthenium red, Calcium, Molecular biology and Biophysics in his Inositol study.
His research integrates issues of Xestospongin C and Endocrinology in his study of Calcium.
His research in Voltage-dependent calcium channel tackles topics such as Calmodulin which are related to areas like Phosphorylation.
He is interested in Inositol trisphosphate receptor, which is a branch of Receptor.
His most cited work include:
- Spontaneous calcium release from inositol trisphosphate-sensitive calcium stores (317 citations)
- Endoplasmic-Reticulum Calcium Depletion and Disease (266 citations)
- Molecular physiology of the SERCA and SPCA pumps (263 citations)
What are the main themes of his work throughout his whole career to date?
Ludwig Missiaen mostly deals with Cell biology, Inositol, Biochemistry, Receptor and Endoplasmic reticulum.
Many of his studies on Cell biology involve topics that are commonly interrelated, such as Autophagy.
The study incorporates disciplines such as Calcium, Biophysics, Adenosine triphosphate, Cytosol and Stimulation in addition to Inositol.
His Receptor study combines topics in areas such as Signal transduction, Cell type, Binding site and Voltage-dependent calcium channel.
The various areas that Ludwig Missiaen examines in his Voltage-dependent calcium channel study include Molecular biology and Calmodulin.
The Endoplasmic reticulum study combines topics in areas such as SERCA, Mitochondrion and Gene isoform.
He most often published in these fields:
- Cell biology (43.23%)
- Inositol (35.81%)
- Biochemistry (33.19%)
What were the highlights of his more recent work (between 2009-2018)?
- Cell biology (43.23%)
- Endoplasmic reticulum (27.51%)
- Receptor (31.44%)
In recent papers he was focusing on the following fields of study:
Cell biology, Endoplasmic reticulum, Receptor, Intracellular and Autophagy are his primary areas of study.
His Cell biology study combines topics from a wide range of disciplines, such as Apoptosis and Programmed cell death.
His biological study spans a wide range of topics, including Signal transduction, Inositol trisphosphate receptor and Voltage-dependent calcium channel.
He combines subjects such as Molecular biology, Peptide sequence and Lumen with his study of Inositol trisphosphate receptor.
He works in the field of Receptor, focusing on Inositol in particular.
His Intracellular study integrates concerns from other disciplines, such as Biophysics and Ion transporter.
Between 2009 and 2018, his most popular works were:
- Endoplasmic-Reticulum Calcium Depletion and Disease (266 citations)
- Intracellular Ca2+ storage in health and disease: a dynamic equilibrium. (147 citations)
- Selective regulation of IP3-receptor-mediated Ca2+ signaling and apoptosis by the BH4 domain of Bcl-2 versus Bcl-Xl. (130 citations)
In his most recent research, the most cited papers focused on:
His main research concerns Cell biology, Endoplasmic reticulum, Calcium signaling, Programmed cell death and Autophagy.
His Cell biology study incorporates themes from Apoptosis and Inositol trisphosphate receptor, Inositol.
Ludwig Missiaen works mostly in the field of Inositol trisphosphate receptor, limiting it down to topics relating to Plasma protein binding and, in certain cases, Molecular biology, as a part of the same area of interest.
His Inositol research incorporates themes from Bcl-xL and Structure–activity relationship.
As part of the same scientific family, Ludwig Missiaen usually focuses on Endoplasmic reticulum, concentrating on Signal transduction and intersecting with Ryanodine receptor and SERCA.
His studies examine the connections between Calcium signaling and genetics, as well as such issues in Unfolded protein response, with regards to Voltage-dependent calcium channel.
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