Target Name: MEF2D
NCBI ID: G4209
Review Report on MEF2D Target / Biomarker Content of Review Report on MEF2D Target / Biomarker
MEF2D
Other Name(s): MEF2D variant 2 | MADS box transcription enhancer factor 2, polypeptide D | Myocyte enhancer factor 2D/deleted in azoospermia associated protein 1 fusion protein | MEF2D/DAZAP1 fusion | MADS box transcription enhancer factor 2, polypeptide D (myocyte enhancer factor 2D) | DKFZp686I1536 | MEF2D variant 1 | MEF2D_HUMAN | Myocyte enhancer factor 2D, transcript variant 1 | Myocyte-specific enhancer factor 2D (isoform 2) | Myocyte-specific enhancer factor 2D | OTTHUMP00000031853 | Myocyte-specific enhancer factor 2D (isoform 1) | myocyte enhancer factor 2D | OTTHUMP00000031852 | Myocyte enhancer factor 2D, transcript variant 2

MEF2D Gene: A Drug Target for Neurological Disorders

MEF2D (MutL homolog 2D) is a gene that encodes a protein known as MEF2D. MEF2D is a key regulator of the microtubule network, which is a complex of filaments that organize and transport cells in various organisms. Mutations in the MEF2D gene have been linked to various neurological and developmental disorders, including cancer, neurodegenerative diseases, and developmental delays. As a result, MEF2D has emerged as a promising drug target for a variety of diseases.

TheMEF2D gene was first identified in the 1990s as a gene that encodes a protein with homology to the protein p180, which is a microtubule protein that is involved in the regulation of cell division and growth. Thep180 protein is a key component of the microtubule network and is thought to play a role in the assembly and disassembly of microtubules. Subsequently, researchers identified that theMEF2D gene encodes a protein that is highly conserved and similar to p180.

Following these findings, researchers began to investigate the functions of theMEF2D gene and its protein. They found that theMEF2D protein was involved in the regulation of microtubule dynamics and stability. Specifically, they found that theMEF2D protein was involved in the assembly and disassembly of microtubules and that it played a role in regulating the stability of microtubules. These findings suggested that theMEF2D protein could be a potential drug target for a variety of neurological and developmental disorders.

Since its initial identification, theMEF2D gene has been studied extensively in order to understand its functions and potential as a drug target. Researchers have found that theMEF2D gene is involved in the regulation of a variety of cellular processes, including cell division, cell migration, and neurotransmission. They have also found that theMEF2D protein is involved in the regulation of microtubule dynamics and stability, as well as in the regulation of cell survival and proliferation.

In addition to its functions in cell regulation, theMEF2D gene has also been shown to be involved in the development and progression of various diseases. For example, studies have found that mutations in theMEF2D gene are associated with a variety of neurological and developmental disorders, including cancer, neurodegenerative diseases, and developmental delays. These findings suggest that theMEF2D gene and its protein may be useful for the development of new treatments for a variety of diseases.

Given the potential for theMEF2D gene and its protein to be involved in the regulation of various cellular processes and the development of diseases, researchers have been actively exploring potential drug targets for theMEF2D gene. One approach that has been explored for theMEF2D gene is the use of small molecules, such as drugs that can modulate the activity of theMEF2D protein. Researchers have found that a variety of small molecules have been shown to be able to modulate the activity of theMEF2D protein, including inhibitors of microtubule assembly and inhibitors of microtubule disassembly. These findings suggest that theMEF2D gene and its protein may be a promising drug target for a variety of neurological and developmental disorders.

Another approach that has been explored for theMEF2D gene is the use of genetic modifiers, such as CRISPR/Cas9 technology. Researchers have used this technology to modify theMEF2D gene and create modified genes that can be used to study the functions of theMEF2D protein. For example, researchers have used CRISPR/Cas9 to

Protein Name: Myocyte Enhancer Factor 2D

Functions: Transcriptional activator which binds specifically to the MEF2 element, 5'-YTA[AT](4)TAR-3', found in numerous muscle-specific, growth factor- and stress-induced genes. Mediates cellular functions not only in skeletal and cardiac muscle development, but also in neuronal differentiation and survival. Plays diverse roles in the control of cell growth, survival and apoptosis via p38 MAPK signaling in muscle-specific and/or growth factor-related transcription. Plays a critical role in the regulation of neuronal apoptosis (By similarity)

The "MEF2D Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about MEF2D comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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