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Related Concept Videos

Genomics02:02

Genomics

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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Gene Therapy00:59

Gene Therapy

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Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be...
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Genome-wide Association Studies-GWAS01:11

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Combination Therapies and Personalized Medicine02:50

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Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
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Human Genetics01:28

Human Genetics

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Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
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Treatment Resistant Cancers02:56

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Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
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Genomics in Treatment Development.

Yogesh Dwivedi1, Richard C Shelton2

  • 1Department of Psychiatry and Behavioral Neurobiology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Advances in Neurobiology
|March 17, 2023
PubMed
Summary

Genomic medicine has advanced treatments in many fields, but neuroscience lags due to complex genetic links. Epigenetics offers a promising avenue for developing novel central nervous system (CNS) disorder treatments.

Keywords:
Cytochrome enzymesDrug metabolismDrug–drug interactionsEnrichment strategiesEpigeneticsGeneticsGenome-wide association studiesGenomicsPharmacogenomicsUridine 5′-diphospho-glucuronosyltransferases

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Area of Science:

  • Neuroscience
  • Genomics
  • Pharmacogenomics
  • Epigenetics

Background:

  • The Human Genome Project enabled genomically focused treatments, yet neuroscience has seen limited progress.
  • Neurological and mental health conditions are rarely linked to single-gene variants, hindering genomic treatment development.
  • Current pharmacogenomic applications primarily focus on drug metabolism and adverse reactions, not novel therapy creation.

Purpose of the Study:

  • To explore the limited translation of genomic information into novel therapies in neuroscience.
  • To highlight epigenetics as a promising area for understanding and treating CNS disorders.
  • To investigate the role of environmental factors in epigenetic modifications relevant to brain function.

Main Methods:

  • Review of current genomic and epigenomic research in neuroscience.
  • Analysis of the limitations in translating genetic findings into clinical treatments for CNS disorders.
  • Exploration of epigenetic mechanisms, such as DNA methylation, influenced by environmental factors.

Main Results:

  • Genomic-based treatments have been less successful in neuroscience compared to other fields.
  • Epigenetics, influenced by environmental factors, presents potential new therapeutic targets for CNS disorders.
  • Environmental factors can induce chemical DNA modifications, impacting gene expression relevant to brain function.

Conclusions:

  • Epigenetic modifications induced by environmental factors are crucial for understanding CNS disorders.
  • Epigenetics holds significant potential for identifying future treatment targets in neuroscience.
  • Further research into epigenetics is vital for advancing neurological and mental health therapies.