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14th International Conference on Genetic Disorders and Gene Therapy, will be organized around the theme “Synergy to Rehabilitate the Innovations in Genetics”
Genetics 2020 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Genetics 2020
Submit your abstract to any of the mentioned tracks.
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Genetics is the inheritance analysis. Heredity is a biological process in which the parent transmits those genes to their children or offspring. Each child inherits genes from both their biological parents and, in exchange, expresses specific traits. Some of these characteristics may be physical, e.g. hair and eye colour, skin colour, etc. On the other hand, certain genes may also carry the risk of certain diseases and disorders that can spread to their offspring from parents.
- Track 1-1Behavioural Genetics.
- Track 1-2Classical Genetics.
- Track 1-3Developmental Genetics.
- Track 1-4Conservation Genetics.
- Track 1-5Ecological Genetics.
- Track 1-6Epigenomics
- Track 1-7Genetic Engineering. Metagenics.
Genes are heredity form squares. They're transferred from one parent to another. We carry the DNA, the instructions to produce proteins. The proteins do the vast majority of cell function. We transfer particles from one place to the next, form structures, isolate toxins, and perform various other support tasks. At times there is a change, a value improvement, or gene modification. The conversion changes the criteria of the quality to make a protein, so the protein does not function properly or is completely missing.
- Track 2-1Multifactorial disorder
- Track 2-2Chromosomal disorder
Gene therapy requires the introduction into an organism of one or more foreign genes to treat inherited or acquired genetic defects. DNA encoding a remedial protein is packaged into a "vector" in gene therapy, which holds the DNA inside the body's cells. Gene therapy is a form of treatment for genetic disorders. Genetic counselling is a process for assessing and understanding the risk of an inherited medical condition from a family. A genetic counsellor is a health care professional with medical genetics and counselling specialized training.
- Track 3-1Detecting conditions
- Track 3-2Adult genetics
- Track 3-3ART/Infertility genetics
- Track 3-4Cardiovascular genetics
- Track 3-5Hereditary cancer genetics
- Track 3-6Neurogenetics
- Track 3-7Pediatric genetics
- Track 3-8Prenatal genetics
\r\n Immunogenetics is the branch of medical genetics which investigates the relationship between the immune system and genetics. Autoimmune disorders, such as diabetes type, are complex genetic traits that are caused by immune system defects. Identifying genes that define immune defects can identify new target genes for therapeutic approaches.
Genomics is genomics research, the whole arrangement of hereditary material within a form of life. Genomics involves the sequencing and analysis of genomes. Genomics is also concerned about the structure, ability, analysis and advancement of genomes. In contrast to the hereditary quality, which refers to the investigation of the individual qualities and their parts of the heritage, genome.
- Track 5-1Functional genomics
- Track 5-2Structural genomics
- Track 5-3Metagenomics
- Track 5-4Genomic medicine
- Track 5-5Synthetic biology and bioengineering
\r\n Human genetics, is study for Analysis of the parent's succession of characteristics. In human heritage as no fundamental way differs from that in other organisms. Human heredity research occupies a key genetic role. Much of this fascination derives from a deep desire to know who and why human beings are as they are. In a more practical way, Understanding human inheritance is critical in the prediction, diagnosis and treatment of genetic diseases. The quest to establish human health's genetic basis has given rise to the medical genetics industry. Medicine has generally given emphasis and purpose to human genetics, so it is often considered interchangeable with the terms of clinical genetics and human genetics.
Fortunately, with no medical problems or birth defects, most children are born healthy. Nevertheless, some children are born with differences in body structure, brain development, or body chemistry that may lead to problems with health, development, school performance, and/or social interaction. Pediatric geneticists were trained to identify the causes and history of these diseases. They may suggest tests and treatments that may help you understand and take care of the condition of your child. Pediatric geneticists can also help families understand whether certain disorders are inherited (from genes) and provide screening to family members who may be at risk of having children with similar problems.
- Track 7-1Birth defects
- Track 7-2Down syndrome
- Track 7-3Fetal alcohol syndrome
- Track 7-4Inborn errors of metabolism
- Track 7-5Familial or hereditary problems
- Track 7-6Short or tall stature
\r\n Clinical Genetics is the restorative claim to fame which offers suggestive administration and "inherited advice" to individuals or families with, or at risk of, diseases that may be hereditary. Hereditary scatters may affect any structure or age gathering. The purpose of the Hereditary Administrations is to enable those affected by, or at risk of, a hereditary issue to live.
- Track 8-1Metabolic/biochemical genetics
- Track 8-2Cytogenetic
- Track 8-3Molecular genetics
- Track 8-4Diagnostic evaluation
- Track 8-5Mitochondrial genetics
\r\n Neurogenetics studies the role of genetics in nervous system development and function. This recognizes neural features like phenotypes (i.e., observable or non-measurable manifestations of an individual's genetic make-up) and is mainly based on the fact. Individuals ' nervous systems are belonging to the same species, may not be the same. As the name implies, it draws elements from both neuroscience and genetics research, concentrating in particular on how its transmitted characteristics influence the genetic code that an organism bears. Mutations can have a wide range of effects on the individual's quality of life in this genetic sequence. In the context of neurogenetics, neurological diseases, behaviour and personality are all studied. In the mid to late 1900s, the field of neurogenetics emerged with developments and closely following advances made in the technologies available.
\r\n Nano therapy is a Nano medicine branch that involves using nanoparticles to deliver a drug to a specific target body position to treat the disease through a process called targeting. This technique has become more popular compared to conventional approaches because it provides high precision when it comes to the delivery of therapeutic formulations. There is no targeting for conventional chemotherapy, which means that the drug is merely carried by the circulatory system until it enters and works on the affected part of the body.
- Track 10-1Passive Targeting
- Track 10-2Active Targeting
\r\n Personalized medicine hopes to tailor therapies to your genetic make-up one day. Modern drugs save millions of lives a year. Even if it works for other people, any medication might not work for you. Or it might cause severe side effects for you but not for someone else. Your gender, lifestyle and nutrition all have an effect on your drug response. Pharmacogenomics is the study of how the unique genetic structure (genome) of a person influences his or her medication response.
\r\n The development of recombinant proteins and other secondary metabolites in plants is represented in plant molecular farming. Such technology relies on the genetic transformation of plants that can be achieved through methods of stable gene transfer, such as gene transfer to nucleus and chloroplasts, and unstable transfer methods such as viral vectors.
- Track 12-1The strategies of plant transformation
- Track 12-2The advantages of utilizing transgenic plants as bioreactors
- Track 12-3The advantages of utilizing transgenic plants as bioreactors
- Track 12-4The limitations and optimization of plant production systems
- Track 12-5Predicting the intracellular localization of the recombinant protein
- Track 12-6Proteins and biomedicines produced in plants
- Track 12-7Molecular farming and metabolic engineering
\r\n Fertilization and Embryogensis is the process of Fusion of sperm and ovum to form Zygote. Fertilization usually take place in oviduct. Ovum is in secondary oocyte stage during fertilization. Secondary oocyte is surrounded by two layer-zona pellucida and zona reticulate. Sperm move toward the secondary oocyte and bind to the receptor on zona pellucida. After sperm enter the oocyte, the zona pellucida become fertilization membrane preventing other sperm to enter. It is the entry of sperm that stimulate second meiotic division of Oocyte . Acrosome of sperm release proteolytic enzyme (Hyaluronidase) that digest the egg wall and then the pro-nucleuses fuse form zygote (2n). Zygote undergoes repeated cell division called cleavage. Cleavage starts as the zygote moves down from oviduct to uterus 3-5 days after fertilization, zygote develop into ball like structure of cell with central cavity; blastocyst (Blastula stage).Outer cell of blastocyst is known as trophoblastic cell while inner cell is known as embryonic cell. Trophoblastic cell secrete HCG (human chorionic gonadotropin) hormone; similar in function as LH. It Prevent degredation of corpus luteum, therefore corpus luteum continue to secrete progesterone and oestrogen, which help continuous growth of endometrium wall causing menstruation cycle to stop.
Cancer is a genetic problem where normal cell enhancement regulation is lost. Now, cancer biology is one of the fastest-growing cell differentiating abilities. At the nuclear level, a mutation(s) of DNA causes cancer, resulting in the development of twisted cells. The increasing dimension of these changes is guarded and occurs in external cells. In any case, the germ line is secured by a couple of individuals. The mutation(s) occurs in two cell characteristics classes on cogenes and the characteristics of the tumour silencer. Tumour silencer characteristics monitor cell division and extension camouflage under standard conditions. Changes in these characteristics lead to unregulated cell replication which results in tumours with odd cell cycles and growth of tumours. The features of the tumour silencer contribute to the disease by inactivating limit BiogenesiCancer cytogenetics
\r\n Developmental genetics is the study of how qualities control development and advancement of a living being for a mind-blowing duration cycle. A recently prepared egg cell or zygote contains a remarkable gathering of qualities that will control its improvement from a solitary cell into a fetus through examples of differential quality articulation during the time spent embryogenesis.