Genetic Variants

Coronaviruses are RNA viruses that belong to the family Coronavirus. They are known to cause respiratory and gastrointestinal infections in humans and many other animals. The COVID-19 pandemic has brought this family of viruses to the forefront of scientific research, with a focus on understanding the genetic variants of the virus that have emerged. Genetic variants are changes in the DNA sequence of the virus. These changes can occur naturally as part of the virus's replication process. Some mutations can be advantageous to the virus, allowing it to replicate and spread more efficiently. Other mutations can be detrimental, making it more difficult for the virus to survive. The emergence of new genetic variants of SARS-CoV-2, the virus that causes COVID-19, has raised concerns about the ability of the virus to spread more easily and cause more severe disease. The Delta variant, for example, is highly transmissible and has been associated with an increase in hospitalizations and deaths. Understanding the genetic variants of the virus is essential to developing effective treatments and vaccines. Scientists are studying the genetic makeup of the virus in order to identify potential targets for the development of new therapies. In addition, tracking the genetic variants of the virus is critical for understanding the spread of the virus globally. This information can be used to guide public health interventions and inform vaccine development efforts. The International Journal of Coronaviruses is committed to publishing the latest research on genetic variants of coronaviruses. By staying up-to-date on the latest findings, we can work together to better understand and combat this threat to global health.

Related Articles

30 article(s) found

Single Nucleotide Polymorphisms associated with alimentary fatty liver disease are not genetic risk factors for treatment-associated hepatic steatosis in HIV patients on HAART

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Genetic Polymorphisms in Patients with Epilepsy: A Mini Review.

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Molecular Cytogenetic Investigations in a Novel Chromosomal Abnormality of t(10;15)(q22;q22) in a Pediatric Precursor-B-Acute Lymphoblastic Leukemia Patient

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A Review of the Histologic, Genetic and Molecular Characteristics of Meningioma Pathogenesis and Progression

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Epigenetics and Nutrition

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Rice Epigenetic Pathways: Great Genetic Variation and Implication for Rapid Rice Breeding

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Scientific and Technological Interventions for Attaining Precision in Plant Genetics and Breeding

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Endocrine Disrupting Chemicals: Epigenetic Relevance and Mechanisms

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Genetic Diversity of Large Japanese Field Mouse Apodemus speciosus Populations and Identification of their Food Plant Resources using DNA Barcoding in an Industrial Green Space

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Genetic Diversity, Phylogenetic Tree and Principal Component Analysis Based on Morpho-Metric Traits of Assam Chilli

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Epigenetic Biomarkers in Head and Neck Cancer 

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Long Non-Coding RNAs Emerging as Potential Epigenetic Biomarkers for Tobacco and/or Alcohol-Induced Head and Neck Cancer

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Research Status and Application Prospect of Epigenetic Regulation of BDNF Gene Expression in Chronic Pain 

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Genetic-Mathematical Modelling of Mutational Processes in a Population

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Allele Based Inference on Evolution and Extinction; A Genetic Drift Approach

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Role of Tie2, CD14, Angiopoietin as Angiogenetic Markers in Hepatocellular Carcinoma Complicating Hepatitis C Virus Infection

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Natural Selection in a Population is a Problem of Nonlinear Genetics

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The Genetic Multiplicity- Multiple Endocrine Neoplasia type I

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Anatomical Variants of the Placenta in Sudanese and their Relation to the Neonatal Outcome

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Evaluations of phylogenetic proximity in a group of 67 dogs with osteosarcoma: a pilot study

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The Intersection of Cultural Characteristics and Genetics on the Prevalence of Delayed Sleep Phase Syndrome in Brazilian and Japanese Adults

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Genetic Algorithm Coupled with Neural Networks to Guesstimate the Subsurface Features of the Earth

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Genetic-Mathematical Modelling of the Populations Interaction

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Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryo during Organogenesis and their Role as Epigenetics Regulators able to Reverse Neurosensory Hearing Loss

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Tay-Sachs Disease: From Molecular Characterization to Ethical Quandaries and the Possibility of Genetic Medicine

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Detection of Smuggled Genetically Modified Crops and Assessment of its Environmental Impact in the Ethio -Sudan Trans Boundary Area, North West Ethiopia

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Interventional Programs for Genetically Disabled People Through Evidence-Based Advocacy

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Rbm45 Phylogenetics, Protein Domain Conservation, and Gene Architecture in Clade Metazoa

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Understanding Inherited Bleeding Disorders: Genetic Mutations in Blood Coagulation Factors and Regulatory Proteins

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Plasma TREM2 Levels, Alcohol Consumption, and Liver Enzymes in Patients with Alcohol use Disorder: A Sex-Dependent Relationship Involving MS4A6A Genetic Polymorphism

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