Track Categories

The track category is the heading under which your abstract will be reviewed and later published in the conference printed matters if accepted. During the submission process, you will be asked to select one track category for your abstract.

Technique that uses genes to treat or prevent human disease by normal Genes into cells in place of missing or defective ones in order to correct genetic disorders is commonly known as Gene therapy. To treat a disorder by inserting a gene into a patient's cells instead of using drugs or surgery. Gene therapy is designed to introduce genetic material into cells to compensate for abnormal genes or to make a beneficial protein. If a mutated gene causes a necessary protein to be faulty or missing, gene therapy may be able to introduce a normal copy of the Gene to restore the function of the protein.

  • Track 1-1Hepatitis
  • Track 1-2ZFNs
  • Track 1-3TALENs
  • Track 1-4Muscular dystropy
  • Track 1-5 cystic fibrosis
  • Track 1-6 Somatic gene therapy
  • Track 1-7Germline gene therapy
  • Track 1-8Gene augmentation therapy
  • Track 1-9Gene inhibition therapy
  • Track 1-10Prolotherapy

Researchers use this technique to carry virus of the genetic cargo into cells, viruses evolved to do with their own Genetic material repair or do missing replacement. Virus are obligate intracellular parasites Very efficient at transferring viral DNA into host cell Specific target cells depending on the viral attachment proteins (capsid or glycoproteins) non-essential Genes of virus are deleted and exogenous genes are inserted.

  • Track 2-1 Retroviruses
  • Track 2-2Adenoviruses
  • Track 2-3Envelope protein pseudo typing of viral vectors
  • Track 2-4Replication-competent vectors
  • Track 2-5Herpes simplex virus
  • Track 2-6Injection of naked DNA.

Regenerative medicine is a branch of research in tissue engineering and molecular biology which deals with the process of replacing, engineering or regenerating human cells, tissues or organs to restore or establish normal function". Treatment which cure diseases using novel therapies, such as stem cell therapy and bioengineering. In stem cell therapy, or regenerative medicine, researchers study how stem cells may be used to replace, repair, reprogram or renew your diseased cells.

  • Track 3-1Apligraf
  • Track 3-2 Osteogenic
  • Track 3-3Carticel
  • Track 3-4Derma graft
  • Track 3-5Plastic surgery

Stem Cell Therapy is a type of cell therapy in which therapeutic efficacy exclusively attributed to the potency of donor stem cells, presented in any quantity and purity. The treatment of various disorders, non-serious to life threatening, by using stem cells. The bone marrow and manifest with various systemic complications. Stem cells from a donor (either from cord blood or bone marrow) are known to reconstitute the defective bone marrow and permanently overcome the disorder. Degenerative disorders arise from degeneration or wear and tear of bone, cartilage, muscle, fat or any other tissue, cell or organ.

  • Track 4-1Osteoarthritis
  • Track 4-2Diabetes
  • Track 4-3Chronic renal failure
  • Track 4-4Congestive cardiac failure
  • Track 4-5Myocardial infarction
  • Track 4-6Hematopoietic disorders

Genomics is an area within genetics that concerns the sequencing and analysis of an organism's genome. The Genome is the entire DNA content that is present within one cell of an organism. Experts in genomics strive to determine complete DNA sequences and perform genetic mapping to help understand disease. The Human Genome Project is a global, long-term research effort to identify the estimated 30,000 genes in human DNA (deoxyribonucleic acid) and to figure out the sequences of the chemical bases that make up human DNA. 23 pair of genes make a human genome’s.

  • Track 5-1Fruit Fly Genome
  • Track 5-2Human Anatomy
  • Track 5-3Molecular Biology
  • Track 5-4Mouse Genome
  • Track 5-5 Lynch syndrome
  • Track 5-6 Epigenome

The study of  proteomics is about  proteins are responsible for both the structure and the functions of all living things. Genes are simply the instructions for making proteins. It is proteins that make life. Within an individual organism, the Genome is constant, but the proteome varies and is dynamic. Every cell in an individual organism has the same set of genes, but the set of proteins produced in different tissues differ from one another and are dependent on gene expression. Proteomics is the large-scale study of proteins. Proteins are vital parts of living organisms, with many functions. The proteome is the entire set of proteins that are produced or modified by an organism or system.

  • Track 6-1Protein micro array
  • Track 6-2iTRAQ
  • Track 6-3x-ray crystallography
  • Track 6-4NMR spectroscopy
  • Track 6-5X-ray Tomography
  • Track 6-6optical fluorescence microscopy
  • Track 6-7SILAC

Immunotherapy treats the cancer which  that helps  immune system fight cancer. The immune system helps your body fight infections and other diseases. It is made up of white blood cells and organs and tissues of the lymph system. Immunotherapy is a type of biological therapy. Due to rapidly pushing field of tumour immunology as of late, there has been age of a couple of new procedures for treating development called Immunotherapies.

  • Track 7-1 Checkpoint inhibitors
  • Track 7-2Adoptive cell transfer
  • Track 7-3Monoclonal antibodies
  • Track 7-4Cytokines
  • Track 7-5BCG

As an organism grows and develops, carefully orchestrated chemical reactions activate and deactivate parts of the genome at strategic times and in specific locations. Epigenetics is the study of these chemical reactions and the factors that influence them. The examination of changes in living creatures caused by alteration of quality verbalization instead of adjustment of the inherited code itself. Epigenetics are unfaltering heritable characteristics that can't be cleared up by changes in DNA progression.

  • Track 8-1Cancer Therapeutics
  • Track 8-2phenotypic traits
  • Track 8-3Treats organs
  • Track 8-4Treats organs
  • Track 8-5DNA methylation
  • Track 8-6DNA methylation
  • Track 8-7Histone acetylase (HAT) inhibitor

A cell culture is a group of cells that develops from a single original cell.   technique is the procedure of cell development under research facility conditions in a controlled way, where all the basic development necessities are being controlled in a particular sum. A portion of these components incorporate Oxygen prerequisites, Carbon dioxide necessities, Light necessities and some more. Cell cultures are of different kinds, for example, microbial cultures, Viral cultures, Animal cell culturing .cultures to test cell responses under controlled conditions, to study interactions between cells, and to select specific cells for further study.

  • Track 9-1Lineage specification
  • Track 9-2Cancer cell phenotype
  • Track 9-3Cancer cell phenotype
  • Track 9-4Fibrosis
  • Track 9-5Hepatocyte function
  • Track 9-6Hepatocyte function
  • Track 9-7Mechanosensin

Cellular pathology is the study of disease using the techniques of modern cell biology. The aim is to understand how cellular and molecular mechanisms interact during disease processes. Cell pathology is also an introduction to the world of  biomedical research. The Cellular Pathology department examines tissue specimens from patients, taken during either surgical operations or post-mortem examination. Examinations of the tissues and organs are made to determine a diagnosis and provide information on further treatment. Emerging discipline within pathology which is focused in the study and diagnosis of disease through the examination of molecules within organs, tissues or bodily fluids. It is multi-disciplinary in nature and focuses mainly on the sub-microscopic aspects of disease.

  • Track 10-1Histopathology
  • Track 10-2Dermatopathology
  • Track 10-3 Neuropathology
  • Track 10-4Non-gynaecological cytology
  • Track 10-5Immunohistochemistry
  • Track 10-6FISH testing
  • Track 10-7Frozen sections
  • Track 10-8Cytopathology

Gene Therapy has made important medical advances in less than two decades. Within this short time span, it has moved from the conceptual stage to technology development and laboratory research to clinical translational trials for a variety of deadly diseases. Gene therapy is the addition of particular Genes at some particular locales into a person's cells or tissues to treat an illness, in which the inadequate or non-working quality is then supplanted with the working quality.

  • Track 11-1Severe Combined Immune Deficiency (ADA-SCID)
  • Track 11-2Chronic Granulomatous Disorder (CGD)
  • Track 11-3Haemophilia
  • Track 11-4 Cancer
  • Track 11-5Neurodegenerative Diseases
  • Track 11-6HIV

The  ability to make highly specific changes in the DNA sequence of a living organism, essentially customizing its genetic makeup. Gene editing is performed using enzymes, particularly nucleases that have been engineered to target a specific DNA sequence, where they introduce cuts into the DNA strands, enabling the removal of existing DNA and the insertion of replacement DNA.

  • Track 12-1CRISPR-Cas9
  • Track 12-2ZFNs
  • Track 12-3TALENs
  • Track 12-4Hematological disease

Cell damage can happen as a result of cell harm, and cell harm can furthermore happen as a result of advancement in cell's condition on account of outside or inside stimuli. Exactly when a cell couldn't change and repair itself to this advancing condition, cell destruction happens. Cell end is of 2 forms Apoptosis ( Programmed Cell passing) and Necrosis (Cell destruction in view of harm).

  • Track 13-1Coagulation Necrosis
  • Track 13-2Liquefactive Necrosis
  • Track 13-3Mannosidosis

NHGRI  defines genomic medicine as an emerging medical discipline that involves using genomic information about an individual as part of their clinical care and the health outcomes and policy implications of that clinical use. Already, Genomic is making an impact in the fields of oncology, pharmacology, rare and undiagnosed diseases, and infectious disease. 

  • Track 14-1Pharmacogenomics
  • Track 14-2Genomic medicine
  • Track 14-3Conservation genomics
  • Track 14-4Conservation genomics
  • Track 14-5Synthetic biology
  • Track 14-6Epigenomics

Gene therapy could be targeted to egg and sperm cells (germ cells), which would allow the inserted gene to be passed to future generations. The  risks and benefits of the experimental use of animals; the risk of creating new diseases for which there is no treatment by combining animal DNA or human DNA with plant DNA. The  potential long-term risks to the environment; the potential for increased suffering of transgenic organisms. The immune system may respond to the working gene copy that has been inserted by causing inflammation. The working gene might be slotted into the wrong spot. The working gene might produce too much of the missing enzyme or protein, causing other health problems.

  • Track 15-1Somatic gene therapy
  • Track 15-2Germline gene therapy
  • Track 15-3pharmacogenomics
  • Track 15-4Ethical issues with gmos
  • Track 15-5 Eugenics