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.

Cell Science Research contemplates cells – their physiological properties, their structure, the organelles they contain, communications with their condition, their life cycle, division, demise and cell work.

 

 

  • Track 1-1Advances in Cell Sciences and Tissue Engineering
  • Track 1-2Molecular Biology of the Cell

Quality treatment is characterized as an arrangement of methodologies that adjust the statement of a person's qualities or repair anomalous qualities. Every system includes the organization of a particular nucleic corrosive (DNA or RNA). Nucleic acids are regularly not taken up by cells, hence uncommon transporters; purported 'vectors' are required. Vectors can be of either popular or non-viral nature though Cell treatment is characterized as the organization of living entire cells into the patient for the treatment of a malady. The beginning of the cells can be from a similar individual (autologous source) or from another individual (allogeneic source). Cells can be gotten from undifferentiated organisms, for example, bone marrow or incited pluripotent foundational microorganisms (iPSCs), reinvented from skin fibroblasts or adipocytes. Immature microorganisms are connected with regards to bone marrow transplantation specifically. Different procedures include the use of pretty much develop cells, separated in vitro (in a dish) from foundational microorganisms.

 

  • Track 2-1Cell therapy products
  • Track 2-2Skin cell therapy
  • Track 2-3Gene therapy products
  • Track 2-4Process of gene therapy
  • Track 2-5various types of gene therapy
  • Track 2-6Different vectors for gene therapy

Regenerative Medicine alludes to a gathering of biomedical ways to deal with look into and clinical applications which are gone for supplanting or "recovering" human cells, tissues or organs to reestablish or set up ordinary capacities which were upset because of ailments. The field of Regenerative drug has pulled in much consideration as it holds the guarantee of recovering harmed tissues and organs in the body by supplanting harmed tissue or by invigorating the body's own repair components to mend harmed tissues or organs. It likewise may empower researchers to develop tissues and organs in the lab and securely embed them inside the body. Regenerative arrangements therefore can be a progressive advance in the field of medicinal services

  • Track 3-1 Regeneration Manufacturing Challenges for Regenerative Medicine
  • Track 3-2Regenerative Medicine Market
  • Track 3-3Cellular Engineering
  • Track 3-4Nuclear Reprogramming
  • Track 3-5Progenitor Cell Injection
  • Track 3-6Invitro Grown Organ Transplantation
  • Track 3-7Genetic Engineering
  • Track 3-8Functional Restoration
  • Track 3-9Physical Therapy Modalities
  • Track 3-10Regeneration in Humans

Because of quickly propelling field of tumor immunology in recent years, there has been generation of a few new techniques for treating growth called Immunotherapies. Immunotherapy is a kind of treatment that expands the quality of safe reaction against tumors either by empowering the exercises of particular segments of safe framework or by checking signals delivered by disease cells that smother insusceptible reactions. A few kinds of immunotherapy are additionally called as biologic treatment or biotherapy. Late progressions in growth immunotherapies have given new helpful methodologies. These incorporate tumor-related macrophages as treatment focuses in oncology, in-situ initiation of platelets with checkpoint inhibitors for post-surgical growth immunotherapy, safe checkpoint barricade and related endocrinopathies and some more.

 

  • Track 4-1Monoclonal antibodies
  • Track 4-2Immune checkpoint inhibitors
  • Track 4-3Immune system modulators
  • Track 4-4Cancer Vaccines
  • Track 4-5Other, non-specific immunotherapies

An undifferentiated mass of cell in a multicellular creature which is equipped for offering ascend to inconclusive number of cells of a similar sort, and from which certain different sorts of cell emerge by separation. Undifferentiated organisms can separate into particular cell composes. The two characterizing qualities of an undifferentiated cell are never-ending self-reestablishment and the capacity to separate into a particular grown-up. There are two noteworthy classes of immature microorganisms: pluripotent that can turn out to be any cell in the grown-up body, and multipotent that is confined to turning into a more restricted populace of cells

  • Track 5-1Stem cell line
  • Track 5-2Cell potency
  • Track 5-3Gene knockout
  • Track 5-4stem cell genomics

The investigation of changes in living beings caused by adjustment of quality articulation as opposed to modification of the hereditary code itself. Epigenetics are steady heritable attributes that can't be clarified by changes in DNA succession

  • Track 6-1Bone Remodeling And Osteoporosis
  • Track 6-2Single-cell Technology In Cancer Research
  • Track 6-3Stem Cell Epigenetics And Disease

The Human Genome Project is a long haul venture by worldwide researcher to create itemized hereditary and physical maps of the human genome. Analysts are occupied with finding and distinguishing the greater part of its qualities and building up the grouping of the qualities and every single other segment of the genome.

 

  • Track 7-1Cellular and Molecular Genetics
  • Track 7-2Drug Discovery
  • Track 7-3Neurodevelopmental Disorders
  • Track 7-4 Transplantation
  • Track 7-5 Cytogenetics
  • Track 7-6Congenital Disorders
  • Track 7-7Diabetes and Obesity
  • Track 7-8Cancer and Genome Integrity
  • Track 7-9 Stem cells and Regenerative Medicine
  • Track 7-10Bioinformatics in Human Genetics

Deoxyribonucleic corrosive, generally known as DNA, contains the outlines of life. Inside its structures are the codes required for the get together of proteins and non-coding RNA – these sub-atomic apparatuses influence all the organic frameworks that make and look after life. By understanding the arrangement of DNA, analysts have possessed the capacity to illustrate the structure and capacity of proteins and in addition RNA and have picked up a comprehension of the basic reasons for malady. Cutting edge Sequencing (NGS) is a capable stage that has empowered the sequencing of thousands to a large number of DNA atoms at the same time. This effective apparatus is changing fields, for example, customized prescription, hereditary sicknesses, and clinical diagnostics by offering a high throughput alternative with the ability to succession numerous people in the meantime.

 

 

  • Track 8-1Exome sequencing
  • Track 8-2Hybrid sequencing approach
  • Track 8-3Sequencing Technologies
  • Track 8-4Cell and Gene Therapy
  • Track 8-5NGS Data Analysis
  • Track 8-6Role of NGS in Cancer Drug Development
  • Track 8-7Clinical Applications of NGS
  • Track 8-8 Advances of NGS in Therapeutics

CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) Technology is a standout amongst the most capable yet straightforward apparatus for genome altering. It encourages and enables analysts to effortlessly change DNA groupings and adjust quality capacities. It has numerous potential applications that incorporate remedying hereditary scatters, treating and keeping the spread of illnesses and enhancing crops. CRISPR famously utilized as CRISPR-Cas9 where CRISPRs are specific extends of DNA and Cas9 is the protein which is a compound that demonstrations like a couple of atomic scissors, fit for cutting DNA strands. The guarantee of CRISPR innovation however raises moral worries as it isn't 100% effective. In any case, the advancement of CRISPR-Cas9 has upset the engineered science industry in this day and age, being a straightforward and powerful quality altering apparatus.

 

  • Track 9-1Designer TALEN Technology Information
  • Track 9-2CRISPR-Cas9 Technology Information
  • Track 9-3High-throughput functional genomics using CRISPR–Cas9
  • Track 9-4Improving genome editing with drugs
  • Track 9-5CRISPR mRNA and protein

Proteomics is the expansive scale investigation of proteomes. A proteome is an arrangement of proteins created in a living being, framework, or natural setting. We may allude to, for example, the proteome of an animal types (for instance, Homo sapiens) or an organ (for instance, the liver). The proteome isn't steady; it varies from cell to cell and changes after some time. To some degree, the proteome mirrors the fundamental transcriptome. Notwithstanding, protein action (frequently surveyed by the response rate of the procedures in which the protein is included) is likewise tweaked by numerous elements notwithstanding the articulation level of the pertinent quality.

 

  • Track 10-1Protein Expression and Analysis
  • Track 10-2 Integrating Transcriptomics and Proteomics
  • Track 10-3 Neuroproteomics & Neurometabolomics
  • Track 10-4 Immunoproteomics
  • Track 10-5Cancer and Clinical proteomics
  • Track 10-6 Food and Nutritional Proteomics
  • Track 10-7 Plant Proteomics and Applications
  • Track 10-8Proteomics for Bioinformatics
  • Track 10-9Proteomics in Personalized Medicine

Traditional techniques for quality treatment incorporate transfection. It wound up plainly wasteful and restricted basically because of conveyance of quality into currently multiplying cells invitro. Quality treatment uses the conveyance of DNA into cells by methods for vectors, for example, organic nanoparticles or viral vectors and non-viral strategies. The Several sorts of infections vectors utilized as a part of quality treatment are retrovirus, adenovirus, adeno-related infection and herpes simplex infection. While other recombinant viral vector frameworks have been produced, retroviral vectors remain the most well known vector framework for quality treatment conventions and greatest application because of their verifiable noteworthiness as the primary vectors created for effective quality treatment application and the earliest stages of the field of quality treatment

 

  • Track 11-1Vectors for Gene Therapy
  • Track 11-2Retroviral and Other Viral Vector
  • Track 11-3Non -Viral Vectors in Gene Therapy
  • Track 11-4Calcium Phosphate Transfection
  • Track 11-5Electroporation
  • Track 11-6Targeted Vector Systems
  • Track 11-7Transductional Targeting
  • Track 11-8Fusion Protein Targeting
  • Track 11-9Targeting Cell Surface Molecules

Cardiovascular infections have turned into an expanding clinical issue all around. Another test in the treatment of the cardiovascular infection is cell transplantation or cell cardiomyoplasty. Intense ischaemic damage and incessant cardiomyopathies prompt perpetual loss of cardiovascular tissue and eventually heart disappointment. Momentum treatments wide mean to constrict the obsessive changes that happen when damage and to downsize chance components of vas illnesses. In any case, they don't enhance the patient's personal satisfaction or the guess more than direct. Distinctive sorts of undifferentiated organisms have been utilized for foundational microorganism treatment.

  • Track 12-1Heart arrhythmia
  • Track 12-2Venous thrombosis
  • Track 12-3Peripheral artery disease

Cell treatment items require an assortment of wellbeing contemplations. Undifferentiated organism and quality items are heterogeneous substances. There are a few zones that especially should be tended to as it is very not the same as that of pharmaceuticals. These range from making cluster consistency, item soundness to item wellbeing, quality and adequacy through pre-clinical, clinical investigations and showcasing approval. This audit outlines the current directions/rules in US, EU, India, and the related difficulties in creating SCBP with accentuation on clinical angle.

 

  • Track 13-1safety aspects
  • Track 13-2clinical studies
  • Track 13-3product stability

The huge number of organizations associated with cell treatment has expanded movement amazingly amid the previous couple of years. More than 500 organizations have been distinguished to be engaged with cell treatment and 305 of these are profiled 291 co-operations. Of these organizations, 170 are associated with foundational microorganisms. The Profiles of 72 scholarly foundations in the US associated with cell treatment alongside their business coordinated efforts. Allogeneic innovation with more than 350 clinical trials is ready to command the commercialization of cell treatments in advertise. Advance R&D in cell and quality treatment is relied upon to blossom given the naturally based points of interest.

  • Track 14-1Cell Therapy in Market
  • Track 14-2Allogenic Technology in Market
  • Track 14-3Cell and Gene Therapy Companies
  • Track 14-4Alliance Companies
  • Track 14-5Blooming Era of Gene Therapy

In biology, a gene is a unit of heredity transferred from a parent to offspring. Regions or groups of genes make up a plant or animal's DNA structure and are what determine some characteristics of the offspring. More simply put, a gene contains a particular set of instructions.

In horticulture, a plant's genes influence the development of the plant, as they are parts of its chromosomes and are inherited through sexual propagation.

Plant genes or genetics are what researchers aim to manipulate in their quest for genetically modified organisms (GMOs).

"Longevity" is here and there utilized as an equivalent word for "future" in demography. Notwithstanding, the term life span is once in a while intended to allude just to particularly seemingly perpetual individuals from a populace, though future is constantly characterized factually as the normal number of years staying at a given age. For instance, a populace's future during childbirth is the same as the normal age at death for all individuals conceived around the same time (on account of accomplices). Life span is best idea of as a term for general gatherings of people signifying 'run of the mill length of life' and particular measurable definitions ought to be elucidated when vital.There are numerous troubles in validating the longest human life expectancy ever by current confirmation benchmarks, inferable from erroneous or deficient birth measurements. Fiction, legend, and old stories have proposed or asserted life expectancies before or future tremendously longer than those checked by current principles, and life span accounts and unsubstantiated life span guarantees regularly discuss their reality in the present.

  • Track 16-1Long-lived individuals
  • Track 16-2Major factors
  • Track 16-3Change over time
  • Track 16-4Non-human biological longevity
  • Track 16-5Biological immortality
  • Track 16-6Future

Gene therapy is the insertion of specific genes at some specific sites into an individual's cells or tissues to treat a disease, in which the defective or non-working gene is then replaced with the working gene.

  • Track 17-1Genomics: Disease and Evolution
  • Track 17-2Gene therapy and Genetic Disease
  • Track 17-3Gene therapy for Cancer treatment
  • Track 17-4Gene therapy for Cystic Fibrosis
  • Track 17-5Gene therapy for Sickle Cell Anemia
  • Track 17-6Gene therapy for Muscular Dystrophy
  • Track 17-7Advancements in gene therapy

Stem Cell therapy is a kind of therapy wherein stem cell are used specifically to prevent a particular disease. Stem cells nowadays has been increasingly used for the treatment of neurological disorders, cardiovascular disorders, and many others. Recent studies are going on for the treatment of Spinal cord injury as well. Thus, Stem cell therapy has a great scope in future as well.

  • Track 18-1Stem Cell Therapies in Neurology
  • Track 18-2Stem Cell Therapies in Cardiology
  • Track 18-3Stem Cell Therapies in Orthopaedics
  • Track 18-4Stem cell therapy to treat diseases
  • Track 18-5Bone Marrow transplant
  • Track 18-6Stem cell treatment for neurological disorders
  • Track 18-7Stem cell treatment for heart disease
  • Track 18-8Embryonic Stem Cell Research

Gene Editing is a technique where the defective gene is being removed or replaced from the genome, so as to change the defective form of gene to an working form. Various techniques such as gene replacement, gene knock out, gene knock down are used for this purpose. Also, site directed mutagenesis has been widely used for gene editing purposes.

  • Track 19-1Genetic Engineering
  • Track 19-2Zinc Finger Nucleases
  • Track 19-3Genome engineering
  • Track 19-4Gene Editing Techniques
  • Track 19-5Functional Genomics
  • Track 19-6Gene Silencing
  • Track 19-7Use of Nucleases in Gene Editing
  • Track 19-8Mutagenesis

Various vectors are being used in the gene therapy so, as to deliver the gene of interest in the target cell. The DNA is directly targeted to the cell. Viral vectors are generally used for targeting the specific DNA to the target cell. Examples of viral vectors include, Retroviruses, Adenoviruses, Herpes Simplex viruses Apart from viral vectors, we also have non-viral vectors including physical and chemical methods for targeting.

  • Track 20-1Viral Vectors
  • Track 20-2Chemical methods
  • Track 20-3Physical methods
  • Track 20-4Hybrid methods
  • Track 20-5Cis and Trans acting element

Cell biology is the study of cell and how the cell functions. Cell consist of many organelles that perform specific functions and play an important role in the growth and development of an organism. Cells are of 2 types Prokaryotic Cell and Eukaryotic Cell. Example of a Prokaryotic Cell includes, Bacteria, on the other hand Animal Cell and Plant Cell are characterized as Eukaryotic Cells

  • Track 21-1Cellular Structures
  • Track 21-2Cell functions
  • Track 21-3Cell metabolism
  • Track 21-4Cell functioning
  • Track 21-5Cell growth and division
  • Track 21-6Advancements in Cell therapy

Gaining lot interest among the researchers, Gene therapy still has too many ethical issues. Some of which include the use of foreign gene insertion into the nonfunctional gene. Also using the animal models for the study of gene therapy and cell therapy experiments has created too many ethical issues amongst people. 

  • Track 22-1Using animal models for experimental studies
  • Track 22-2Germline gene therapy and ethical issues
  • Track 22-3Somatic gene therapy
  • Track 22-4Human genome and gene therapy
  • Track 22-5Ethics of human gene and gene therapy

Gene therapy have a lot of recent and future advancements, also has a high scope in tissue engineering as well. Tissue engineering is done by combining cells, Various engineering methods,  and suitable biochemical and physicochemical factors for improvement and it’s use in tissue. Tissue engineering involves generally the use of a scaffold which leads to formation of viable tissue for specific medical purpose. 

  • Track 23-1Advancements in tissue engineering
  • Track 23-2Advancements in tissue engineering
  • Track 23-3Gene therapy for bone engineering
  • Track 23-4Gene therapy, tissue engineering and sports medicine
  • Track 23-5Future aspects of tissue engineering with gene therapy
  • Track 23-6Use of Scaffold for tissue engineering

Genomic medicine is a recent and emerging field. It is also used in treatment of specific disorders. Areas included, not only are specifically limited to: precision medicine, novel methods and software, disease genomics but a wide range of understand the complex system and then using the personalized medicine for treatment of various diseases.

  • Track 24-1Genomic science and medicine
  • Track 24-2Pharmacogenomics
  • Track 24-3Disease treatment using genomic medicines
  • Track 24-4Personalized medicine
  • Track 24-5Epigenomics

Cell culture technique is the process of cell growth under laboratory conditions in a controlled manner, where all the essential growth requirements are being controlled in a specific amount. Some of these factors include Oxygen requirements, Carbon dioxide requirements, Light requirements and many more. Cell cultures are of various types, such as microbial cultures, Viral cultures, animal cell culturing.

  • Track 25-1Primary Cultures
  • Track 25-2Cell lines
  • Track 25-3Suspension Cultures
  • Track 25-4Microbiological Cultures
  • Track 25-5Viral Cultures
  • Track 25-6Bioprocess Engineering and cell cultures

Pathology, is the study of disease. Some diseases represent hinderance in the ability of a cell to develop and function normally, and in some cases disease may result when external stimuli produce a sudden change in the cell's environment that make it impossible for the cell to maintain homeostasis. 

  • Track 26-1Cytopathology
  • Track 26-2Histopathology
  • Track 26-3Coronial Autopsy
  • Track 26-4Dermatopathology
  • Track 26-5Non-gynecological cytology
  • Track 26-6Neuropathology

Cell damage can occur due to cell injury, and cell injury can further occur due to change in cell’s environment due to external or internal stimuli. When a cell could not adapt and repair itself to this changing environment, cell death occurs. Cell death is of 2 types Apoptosis ( Programmed Cell death) and Necrosis (Cell death due to injury).

  • Track 27-1Apoptosis
  • Track 27-2Necrosis
  • Track 27-3Cell injury
  • Track 27-4Cell swelling
  • Track 27-5Biochemical changes in Cell injury

In recent years, the inter crossing of nanotechnology in stem cell biology and biomedicine has led to an emerging new research field, known as stem cell nanotechnology. Stem cell nanotechnology is defined as the application of nanotechnology in stem cells research and development, and it is characterized as highly rapid in development, highly interdisciplinary, and highly controversial.