What is he best known for?
The fields of study he is best known for:
- Enzyme
- Gene
- Organic chemistry
Matthias U. Kassack mainly focuses on Receptor, Biochemistry, Stereochemistry, Suramin and Agonist.
His Receptor research focuses on subjects like Calcium, which are linked to Nucleotide, Platelet activation and Platelet.
His study connects Molecular biology and Biochemistry.
His Stereochemistry research incorporates themes from Conformational isomerism, Disiloxane and Aqueous solution.
His Agonist research includes themes of Stimulation and G protein-coupled receptor.
His studies examine the connections between Intracellular and genetics, as well as such issues in DNA repair, with regards to Cell culture.
His most cited work include:
- Common variants in P2RY11 are associated with narcolepsy (173 citations)
- Comparison of the usefulness of the MTT, ATP, and calcein assays to predict the potency of cytotoxic agents in various human cancer cell lines. (172 citations)
- Structure–Activity Studies on Suramin Analogues as Inhibitors of NAD+‐Dependent Histone Deacetylases (Sirtuins) (149 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Stereochemistry, Biochemistry, Receptor, Cell culture and Suramin.
His studies in Stereochemistry integrate themes in fields like Endophytic fungus and Cytotoxicity.
His study in Biochemistry concentrates on Agonist, Structure–activity relationship, Intracellular, In vitro and Potency.
His Receptor research incorporates themes from Xenopus and Pharmacology.
His Cell culture study combines topics from a wide range of disciplines, such as Cytotoxic T cell, Apoptosis and Cancer research.
Matthias U. Kassack is studying Suramin Sodium, which is a component of Suramin.
He most often published in these fields:
- Stereochemistry (30.87%)
- Biochemistry (31.54%)
- Receptor (24.83%)
What were the highlights of his more recent work (between 2018-2021)?
- Cancer research (14.09%)
- Histone deacetylase (10.74%)
- Biochemistry (31.54%)
In recent papers he was focusing on the following fields of study:
Matthias U. Kassack mainly investigates Cancer research, Histone deacetylase, Biochemistry, HDAC6 and Cell culture.
His work deals with themes such as Caspase 3, Ovarian cancer and DNA damage, which intersect with Histone deacetylase.
His Biochemistry research focuses on Bacillus subtilis and how it relates to Fermentation.
His work focuses on many connections between HDAC6 and other disciplines, such as Cytotoxicity, that overlap with his field of interest in Proteasome inhibitor, Plasma protein binding, Enzyme, Daunorubicin and Structure–activity relationship.
His study looks at the intersection of Cell culture and topics like Clonostachys rosea with Stereochemistry.
With his scientific publications, his incorporates both Stereochemistry and Coniella fragariae.
Between 2018 and 2021, his most popular works were:
- Histone deacetylase inhibitor LMK235 attenuates vascular constriction and aortic remodelling in hypertension (12 citations)
- Class I-Histone Deacetylase (HDAC) Inhibition is Superior to pan-HDAC Inhibition in Modulating Cisplatin Potency in High Grade Serous Ovarian Cancer Cell Lines (11 citations)
- Cryptic Secondary Metabolites from the Sponge-Associated Fungus Aspergillus ochraceus (11 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Gene
- Organic chemistry
His main research concerns Histone deacetylase, Cancer research, Acetylation, Ovarian cancer and Caspase 3.
Histone deacetylase is closely attributed to Cancer cell in his work.
His research on Cancer cell often connects related areas such as Histone H3.
His work carried out in the field of Acetylation brings together such families of science as Regulation of gene expression, Histone, DNA and Cell biology.
His study in Ovarian cancer is interdisciplinary in nature, drawing from both Panobinostat, Survivin, Downregulation and upregulation, Entinostat and HDAC6.
His Caspase 3 research is multidisciplinary, incorporating perspectives in HDAC3, Cell culture and HDAC1.
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