What is he best known for?
The fields of study he is best known for:
- Gene
- Enzyme
- Internal medicine
Klaus-Armin Nave mostly deals with Myelin, Neuroscience, Cell biology, Oligodendrocyte and Proteolipid protein 1.
Klaus-Armin Nave combines subjects such as White matter, Biochemistry and Nervous system with his study of Myelin.
His Neuroscience study combines topics from a wide range of disciplines, such as NMDA receptor, Schwann cell and Signal transduction, ErbB.
Klaus-Armin Nave studies Axon, a branch of Cell biology.
The concepts of his Oligodendrocyte study are interwoven with issues in Axonal loss and Embryonic stem cell.
His Proteolipid protein 1 study incorporates themes from Mutant, Null allele, Molecular biology, Exon and Myelin proteolipid protein.
His most cited work include:
- Multiple Sclerosis: An Immune or Neurodegenerative Disorder? (1192 citations)
- Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity (790 citations)
- Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination (760 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Myelin, Cell biology, Neuroscience, Oligodendrocyte and Proteolipid protein 1.
His Myelin research focuses on Axon and how it relates to Neuroglia.
His research in Cell biology intersects with topics in Myelin basic protein, Biochemistry, Mutant and Microglia.
His work carried out in the field of Neuroscience brings together such families of science as White matter, Neurodegeneration, Transgene and Neuregulin 1.
His research ties Neuron and Oligodendrocyte together.
His Proteolipid protein 1 research is multidisciplinary, relying on both Myelin proteolipid protein, Molecular biology and Pelizaeus–Merzbacher disease.
He most often published in these fields:
- Myelin (52.08%)
- Cell biology (42.59%)
- Neuroscience (39.81%)
What were the highlights of his more recent work (between 2015-2021)?
- Myelin (52.08%)
- Cell biology (42.59%)
- Neuroscience (39.81%)
In recent papers he was focusing on the following fields of study:
Klaus-Armin Nave mainly investigates Myelin, Cell biology, Neuroscience, Oligodendrocyte and Axon.
His Myelin research includes elements of White matter, Schwann cell and Nervous system.
His Cell biology study combines topics in areas such as Astrocyte, Biochemistry, Mutant and Proteolipid protein 1.
In his study, Conditional gene knockout is inextricably linked to Neurodegeneration, which falls within the broad field of Neuroscience.
His work deals with themes such as Neuroinflammation, Amyotrophic lateral sclerosis and Cellular differentiation, which intersect with Oligodendrocyte.
His research integrates issues of Pelizaeus–Merzbacher disease, Leukodystrophy and Myelin sheath in his study of Axon.
Between 2015 and 2021, his most popular works were:
- Oligodendrocytes: Myelination and Axonal Support (269 citations)
- New Horizons in Diabetic Neuropathy: Mechanisms, Bioenergetics, and Pain (228 citations)
- Oligodendroglial NMDA receptors regulate glucose import and axonal energy metabolism. (199 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Enzyme
- Internal medicine
The scientist’s investigation covers issues in Myelin, Neuroscience, Cell biology, Axon and Oligodendrocyte.
His Myelin research is multidisciplinary, incorporating elements of White matter and Nervous system.
Klaus-Armin Nave has included themes like Glucose transporter, Glucose import, Schwann cell and Glutamate receptor in his Neuroscience study.
His studies deal with areas such as Demyelinating disease, Lipid metabolism, Biochemistry and In vivo as well as Cell biology.
As part of one scientific family, he deals mainly with the area of Axon, narrowing it down to issues related to the Multiple sclerosis, and often Neurotransmission, Process, Nerve fiber, Adenosine triphosphate and Action potential.
His research investigates the connection between Oligodendrocyte and topics such as Cellular differentiation that intersect with issues in Endocrinology, Internal medicine, Erythropoietin and Neurogenesis.
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