David N. Drechsel - Genetic Mutations

Author Information

David N. Drechsel is affiliated with the Max Planck Institute of Molecular Cell Biology and Genetics, located at Pfotenhauerstrasse 108, 01307, Dresden, Germany. His work primarily focuses on genetics and cellular biology.

Research Contributions

David N. Drechsel has made significant contributions to the field of genetics and molecular cell biology. His research includes groundbreaking work on human-specific genes, such as ARHGAP11B, and its role in expanding neocortical progenitors by glutaminolysis. He has also extensively studied protein expression systems, particularly using baculovirus vectors in insect cells. Another notable area of his research is the molecular mechanisms governing phase separation of RNA-binding proteins, and the development of tools like MS Western for multiplexed absolute protein quantification. His research has applications in understanding molecular functions during limb regeneration and imaging techniques for live cells and tissues.

Aliases

David N. Drechsel is also known by several aliases including D N Drechsel, David N. Drechsel, David N Drechsel, D. Drechsel, David Drechsel, and D Drechsel.

Publication and Citation Metrics

Metric	Value
Total Citation Count	10,815
H-Index	33
Paper Count	57

Publications:

Human-Specific ARHGAP11B Acts in Mitochondria to Expand Neocortical Progenitors by Glutaminolysis

DOI: 10.1016/j.neuron.2019.11.027

Year: 2020

FlexiBAC: a versatile, open-source baculovirus vector system for protein expression, secretion, and proteolytic processing

DOI: 10.1186/s12896-019-0512-z

Year: 2019

Baculovirus-driven protein expression in insect cells: A benchmarking study.

DOI: 10.1016/j.jsb.2018.03.004

Year: 2018

FlexiBAC: a versatile, open-source baculovirus vector system for protein expression, secretion, and proteolytic processing

DOI: 10.1101/470955

Year: 2018

Pseudotyped baculovirus is an effective gene expression tool for studying molecular function during axolotl limb regeneration.

DOI: 10.1016/j.ydbio.2017.10.008

Year: 2018

A Molecular Grammar Governing the Driving Forces for Phase Separation of Prion-like RNA Binding Proteins

DOI: 10.1016/j.cell.2018.06.006

Year: 2018

Author response: A tunable refractive index matching medium for live imaging cells, tissues and model organisms

DOI: 10.7554/ELIFE.27240.022

Year: 2017

A tunable refractive index matching medium for live imaging cells, tissues and model organisms

DOI: 10.7554/eLife.27240

Year: 2017

MS Western, a Method of Multiplexed Absolute Protein Quantification is a Practical Alternative to Western Blotting*

DOI: 10.1074/mcp.O117.067082

Year: 2017

Serum Proteases Potentiate BMP-Induced Cell Cycle Re-entry of Dedifferentiating Muscle Cells during Newt Limb Regeneration.

DOI: 10.1016/j.devcel.2017.03.002

Year: 2017

What Genetic Mutations Affect Hemoglobin?

What are the sources of PAH exposure?

How Can Harmful Mutations Be Managed or Treated?

What Are the Types of Phylogenetic Trees?

How Do Mutagens Interact with DNA?

Can Autosomal Recessive Disorders be Treated or Managed?

What is BLAST?

Are There Any Risks Associated with Beneficial Mutations?

How Does Sanger Sequencing Compare to Next-Generation Sequencing (NGS)?

What is Comparative Genomic Hybridization (CGH)?

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