Call for Abstract
World Congress on Molecular Biology & Genetics, will be organized around the theme “”
Molecular Biology & Genetics 2019 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Molecular Biology & Genetics 2019
Submit your abstract to any of the mentioned tracks.
Register now for the conference by choosing an appropriate package suitable to you.
- Track 1-1Cell Biology, Immunology, Cancer Research, neurobiological signaling pathway, Biochemistry, Biostatistics, Cellular Neurobiology, Bioinformatics
Regenerative medicine is the branch of medicine that develops methods to regrow, repair or replace damaged or diseased cells, organs or tissues. Regenerative medicine includes the generation and use of therapeutic stem cells, tissue engineering and the production of artificial organs.
- Track 2-1Tissue Engineering and Biomaterials, Cellular Therapies, Medical Devices and Artificial Organs,
- Track 3-1Oncological, Regenerative Medicine, Molecular Basis of Disease Study Nutritional and Metabolic Mechanisms of Chronic Disease Study,Translational Pharmacology
Metabolomics is the large-scale study of small molecules, commonly known as metabolites, within cells, biofluids, tissues or organisms. Collectively, these small molecules and their interactions within a biological system are known as the metabolome.Just as genomics is the study of DNA and genetic information within a cell, and transcriptomics is the study of RNA and differences in mRNA expression; metabolomics is the study of substrates and products of metabolism, which are influenced by both genetic and environmental factors.
Metabolomics : Small molecules, Single cells
- Track 4-1 Metabolic Profiling,Therapeutic Metabolomics, Transcriptomics, Metabolic Modelling, Recent Advancements in Metabolomics, Analytical Metabolomics, Metabolomics & Pharmacology, Metabolic syndrome
Hormone Molecular Biology (HMB) is dedicated to the provision of basic data on molecular aspects of hormones in physiology and pathophysiology.
- Track 5-1 Progesterone Safety, Progesterone and Breast Health, Progesterone and Menstrual Health/PMS, Infertility, Pregnancy, Progesterone and Bone Health, Progesterone and Bone Health, Progesterone and the Nervous System/Brain
- Track 6-1Molecular Cloning, Gene Delivery, DNA Sequencing, Microarrays, DNA Sequencing
DNA fingerprinting, one of the great discoveries of the late 20th century, has revolutionized forensic investigations. This review briefly recapitulates 30 years of progress in forensic DNA analysis which helps to convict criminals, exonerate the wrongly accused, and identify victims of crime, disasters, and war. Current standard methods based on short tandem repeats (STRs) as well as lineage markers (Y chromosome, mitochondrial DNA) are covered and applications are illustrated by casework examples. Benefits and risks of expanding forensic DNA databases are discussed and we ask what the future holds for forensic DNA fingerprinting.
- DNA in a crime
- Molecular proofing
- Track 7-1DNA and forensic science, DNA profiling , DNA analysis in forensic science – short tandem repeats, DNA analysis in forensic science – Y chromosome DNA
Pharmacogenomics, genomic information is used to study individual responses to drugs. When a gene variant is associated with a particular drug response in a patient, there is the potential for making clinical decisions based on genetics by adjusting the dosage or choosing a different drug, for example. Scientists assess gene variants affecting an individual's drug response the same way they assess gene variants associated with diseases: by identifying genetic loci associated with known drug responses, and then testing individuals whose response is unknown. Modern approaches include multigene analysis or whole-genome single nucleotide polymorphism (SNP) profiles, and these approaches are just coming into clinical use for drug discovery and development.
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetic, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.Genes can be the common factor of the qualities of most human-inherited traits. Study of human genetics can be useful as it can answer questions about human nature, understand the diseases and development of effective disease treatment, and understand genetics of human life. This article describes only basic features of human genetics; for the genetics of disorders please see: medical genetics.
is a genetic problem caused by one or more abnormalities in the genome. Most genetic disorders are quite rare and affect one person in every several thousands or millions.Genetic disorders may be hereditary, passed down from the parents' genes. In other genetic disorders, defects may be caused by new mutations or changes to the DNA. In such cases, the defect will only be passed down if it occurs in the germ line.
- Track 9-1Genetic Epidemiology, Immunogenetics, Genetic Diseases, Medical genetics, DNA Sequencing, Human Evolutionary genetics, Cancer genetics, Pharmacogenomics and Pharmacogenetics, Bioinformatics and Computational Biology, Epigenetics
- Track 9-2Single gene inheritance, Multifactorial inheritance, Chromosome abnormalities, Mitochondrial inheritance
- Track 10-1Academic Subtracks: Antibodies, Cloning, Congenital Disorders, Cytogenetics & Karyotyping, Drug treatments, Germ line mutations
- Track 10-2Business subtracks : Cell biotechnology, Cloning, DNA technology, Gene expression, Gene isolation, Gene splicing, Genetic research
Plant genetics deals with heredity in plants, specifically mechanisms of hereditary transmission and variation of inherited characteristics. Plant genetics differs from animal genetics in a number of ways: somatic mutations can contribute to the germ line more easily as flowers develop at the end of branches composed of somatic cells; polyploidy is more common; and plants additionally contain chloroplastic DNA.
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.
- Track 11-1Plant Biochemistry and Biosystem, Plant Molecular Biology, Plant & Environment, Plant Physiology
- Track 11-2Human Genome Project, Gene structure and genome structure (DNA, chromatin, chromosomes, and nucleus), Genetic modification, Gene expression and control over it , Genetics of development processes, Population genetics, Application of genetics in medicine,
Bioorganic chemistry is a rapidly growing scientific discipline that combines organic chemistry and biochemistry. While biochemistry aims at understanding biological processes using chemistry, bioorganic chemistry attempts to expand organic-chemical researches (that is, structures, synthesis, and kinetics) toward biology. When investigating metalloenzymes and cofactors, bioorganic chemistry overlaps bioinorganic chemistry. Biophysical organic chemistry is a term used when attempting to describe intimate details of molecular recognition by bioorganic chemistry.