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4th International Conference on Molecular Medicine and Diagnostics, will be organized around the theme “Novel Insights in Molecular Medicine and Diagnosis for Leading a Better Life”

Molecular Medicine 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 Medicine 2019

Submit your abstract to any of the mentioned tracks.

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Molecular medicine is a broad field which deals with the development of diseases at a molecular level and identifies fundamental molecular and genetic errors of disease and to develop molecular interventions to correct them. Molecular structures and mechanisms are described by Physical, chemical, biological, bioinformatics and medical techniques. Disease pathogenesis at the molecular or physiological level may lead to the design of specific tools for disease diagnosis, treatment, or prevention.

By understanding the genes, proteins, and other cellular molecules work molecular medicine develops ways to diagnose and treat disease. Molecular Medicine develops knowledge and skills in cellular and molecular biology.

  • Track 1-1Molecular Medicine Cancer
  • Track 1-2Molecular Medicine Scope
  • Track 1-3Molecular Mechanisms
  • Track 1-4Molecular Surgery
  • Track 1-5Metabolomics
  • Track 1-6Molecular pathological epidemiology
  • Track 1-7Mutation

Molecular diagnostics is a collection of techniques used to analyse an individual's genetic code and to identify biological markers in the genome and proteome. Molecular diagnostics apply molecular biology to see how cell express their genes to medical testing. For any successful application of gene therapy or biologic response modifiers, molecular diagnostics offers a great tool. Molecular diagnostics now provides most laboratory tests in infectious diseases, genetics, and an increasing number in oncology. Molecular diagnostics analyse a person's health at a molecular level by detecting specific sequences in deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) that may be related to disease

  • Track 2-1Genetic Tests
  • Track 2-2Molecular Tests
  • Track 2-3Polymerase Chain Reaction
  • Track 2-4Molecular Diagnostics Market
  • Track 2-5Molecular Biology
  • Track 2-6Medical Testing
  • Track 2-7Genetic hybridization tests

Molecular genetics employs methods of both molecular biology and genetics to study the structure, function and interactions among genes at a molecular level.

The study of chromosomes and gene expression of an organism can give an accurate and deep understanding of heredity, genetic variation, and mutations. Molecular Genetics and Genomics cover all areas on the latest research innovations, population genetics, gene function and expression and molecular genetics. Molecular genetics is concerned with the study of your favourite gene, genomics is concerned with studying all the genes. Molecular genomics is a critical component of the expanding database linking alterations of DNA and RNA with the disease, disease prognosis and therapeutic response.

  • Track 3-1Genes and genomes
  • Track 3-2PCR and Real-Time PCR
  • Track 3-3Microarrays
  • Track 3-4Next-Generation Sequencing
  • Track 3-5Sanger Sequencing

Molecular oncology refers to the chemistry of cancer and tumours at the molecular scale and their development and application on molecularly targeted therapies.

Molecular Oncology studies especially the genetic alterations and their implications. Molecular Oncology focuses on new discoveries, approaches, as well as technical developments in basic, clinical and discovery-driven cancer research. It mainly focuses on advances in the understanding of disease processes leading to human tumour development. Molecular Oncology establishes novel concepts of clear clinical significance in diagnosis, prognosis and prevention strategies.

  • Track 4-1DNA repair
  • Track 4-2Apoptosis
  • Track 4-3Cancer genetics
  • Track 4-4Molecular pathology
  • Track 4-5Tumour immunology

A biomarker is used as an indicator of the biological state. In routine clinical use Oncology biomarkers actually, make their way. A biological marker points to the presence of a disease, a physiological change, response to treatment, or a psychological condition.

Molecular biomarkers are used for various purposes including disease diagnosis and prognosis and assessment of treatment response. Over the last decade, there has been a significant increase in the number of drug labels containing information on molecular biomarkers. In most of the chronic diseases, biomarkers can confirm a difficult diagnosis or even make it possible in the first place.

  • Track 5-1Genetic Testing and Molecular Biomarkers
  • Track 5-2Drug labelling
  • Track 5-3Cancer biomarkers
  • Track 5-4Disease-related biomarkers
  • Track 5-5Drug-related biomarkers
  • Track 5-6Biomarkers in Drug Development
  • Track 5-7Biomarker requirements

Molecular biology is the study of biological activity between biomolecules in the various systems of a cell. It also includes the interactions between DNA, RNA, proteins and their biosynthesis as well as the regulation of these interactions.

Cellular and Molecular Biology majorly study the processes that occur within and between the body's cells. This includes genes, the way cells carry nutrients throughout the body, and how diseases attack healthy cells. The process of replication, transcription and translation of the genetic material are studied under Molecular biology. Cellular biology study cells, including their function, systems, structure and interactions with living organisms. These typically work in medical fields and are often focused on the treatment of disease.

  • Track 6-1Genetics
  • Track 6-2Biochemistry
  • Track 6-3Immunology
  • Track 6-4Cytochemistry
  • Track 6-5Cell signalling
  • Track 6-6Transcription
  • Track 6-7Structural biology

Molecular pathology is the study of molecules within organs, tissues or bodily fluids. Molecular pathology is commonly used in the diagnosis of bone, soft tissue tumours, cancer and infectious diseases. The purpose of molecular pathology is to understand the mechanisms of disease by identifying molecular and pathway alterations. It is considered the heart of modern diagnostics and translational research. Molecular pathology studies and diagnose disease through the examination of genetic and molecular abnormalities. Molecular pathology and biomarkers are used to study molecular and genomic abnormalities in tissues for diagnostic and prognostic purposes. Molecular diagnosis is useful and sometimes necessary as an adjunct for diagnosis especially in morphologically or clinically unusual lesions.

  • Track 7-1Molecular diagnostics
  • Track 7-2Molecular Genetic Pathology
  • Track 7-3Medical Genetics
  • Track 7-4Molecular tests
  • Track 7-5Molecular pathological epidemiology
  • Track 7-6Pathology
  • Track 7-7Precision medicine

Living things all are alike at the cellular and molecular level. The fundamental similarities between living organisms are explained by evolutionary theory. Major topics in molecular evolution concern the rates and impacts of single nucleotide changes, origins of new genes, the evolution of development, and ways that evolutionary forces influence genomic and phenotypic changes. Some of the key advances are quantitative estimates of both the diversity in populations and of evolutionary relationships, as well as improvements in theoretical understanding. There is an improved understanding of the function of proteins and much better models of the common patterns of development.

  • Track 8-1Mechanisms of molecular evolution
  • Track 8-2Evolutionary biology
  • Track 8-3Population genetics
  • Track 8-4Genetic drift
  • Track 8-5Gene content and distribution
  • Track 8-6Molecular phylogenetics

Advances in cell and molecular biology studies have revolutionized the diagnosis and treatment of many different diseases. It is considered as a modern Biotechnology concerned with understanding the Genetic Diagnosis, Molecular Diagnosis, Molecular Forensics.

People at the present day are facing serious global challenges in healthcare from emerging and re-emerging diseases. The availability of new sequencing methods, microarrays, microfluidics, biosensors, and biomarker assayshas made a shift toward developing diagnostic platforms, which stimulates growth in the field regarding diagnosis, prognosis, and treatment, leading to improved outcomes and greater cost savings.

  • Track 9-1Genetic Marker
  • Track 9-2Screening
  • Track 9-3DNA-Profiling
  • Track 9-4Cytogenetics
  • Track 9-5Transcriptome
  • Track 9-6Cancer Biomarkers
  • Track 9-7Biomarker Toxicologies
  • Track 9-8Inherited Diseases

Much research is being done in foetal whole exome sequencing and is beginning to play a large role in miscarriage testing. With all this research and screening, clinicians and genetic counsellors need to keep abreast of these changes and guidelines in order to effectively care for patients.

The genetic cause of foetal abnormalities detected on ultrasound imaging and in high-risk families can be significantly identified and improved in Foetal diagnostic exome sequencing. Testing based on isolation of foetal cells from maternal blood would provide an attractive alternative to testing of cell-free DNA. An updated implementation of these different approaches will make lively discussion and insight into this field and is headed ways for researchers, test providers, clinicians and clinics to take these developments into consideration.

  • Track 10-1Advances in Prenatal Molecular Diagnostics
  • Track 10-2Cell-free DNA screening
  • Track 10-3Cell-based DNA testing
  • Track 10-4Biomarkers for preeclampsia and pre-term birth
  • Track 10-5Prenatal and Reproductive Diagnostics
  • Track 10-6Non-Invasive Prenatal Diagnosis

Point-of-care testing is medical diagnostic testing at the time and place of patient care.  In Recent years there are tremendous advances in POCD due to innovations lab-on-a-chip technologies, and complementary technologies. Critical advances in POCD provides directions for future research. Point-of-care allows physicians and medical staff to accurately achieve real-time, lab-quality diagnostic results within minutes rather than hours. The global Point of Care diagnostic tests renders immediate results providing improved patient care in rural areas too. This factor has significantly impacted the market growth.

  • Track 11-1Point-of-Care Testing by Clinical Setting
  • Track 11-2Point-of-Care Testing Patents
  • Track 11-3Chronic Disease Management at the Point of Care
  • Track 11-4POC Informatics
  • Track 11-5Increasing Global Access to Care
  • Track 11-6Portable Point-Of-Care Testing Systems
  • Track 11-7

Clinical diagnostics is defined as diagnosis and treatment of human disease. Clinical diagnostics for a disease can be done by patient's complaints based on signs, symptoms and medical history rather than on laboratory examination or medical imaging. Clinical diagnostics is considered as an ever-changing field of medicine and research. In recent years Clinical diagnostics has become more exciting as advances in new techniques aid in fulfilling the potential of personalized medicine. Clinical research determines the safety and effectiveness of medications, devices, diagnostic products and treatments.

  • Track 12-1Differential diagnosis
  • Track 12-2Diagnostic Test
  • Track 12-3Nursing diagnosis
  • Track 12-4Clinical diagnosis of ADHD
  • Track 12-5Clinical research ethics
  • Track 12-6Clinical Trial Management System
  • Track 12-7Clinical Biostatistics

Infectious diseases are caused by pathogenic organisms such as viruses, bacteria, or fungus. Normally harmless but under certain conditions, they can be fatal and can cause death too. They can be spread from one person to another directly or indirectly. Infectious diseases are caused by infection-causing organisms that use the human body for surviving, reproducing and colonizing. These organisms are known as pathogens.

Antibiotics are used to treat bacterial infections;

Antiviral agents treat viral infections;


Antifungal agents treat fungal infections.

  • Track 13-1Urinary Tract Infections
  • Track 13-2Neurodegenerative Diseases
  • Track 13-3Cryptococcal meningitis
  • Track 13-4Bacterial Infectious Diseases
  • Track 13-5Viral Infectious Diseases
  • Track 13-6Protozoal Infectious Diseases
  • Track 13-7Fungal Infectious Diseases
  • Track 13-8Zoonotic diseases

Next-generation sequencing (NGS) has revolutionised the study of genomics and molecular biology by allowing us to sequence DNA and RNA much more quickly and cheaply than the previously used Sanger sequencing. Next Generation Sequencing (NGS) relies on capillary electrophoresis. NGS although with shorter read lengths and less accuracy reduces the time that genome sequencing projects took with Sanger methods.

Thousands to millions of DNA molecules can be sequenced simultaneously by using Powerful Next Generation Sequencing (NGS) platform. By offering a high throughput option NGS is revolutionizing in fields such as personalized medicinegenetic diseases, and clinical diagnostics.

  • Track 14-1llumina (Solexa) sequencing
  • Track 14-2Roche 454 sequencing
  • Track 14-3Proton / PGM sequencing
  • Track 14-4SOLiD sequencing
  • Track 14-5Massive parallel sequencing
  • Track 14-6Sanger sequencing

Immunogenicity is the ability of a particular substance induce a humoral and/or cell-mediated immune responses. An immune response can be potentially elicited by administering any substance into the human body.

Products which increase the potential of anti-drug antibodies include :

Therapeutic antibodies, enzyme therapies, peptides and combination products.

An immune response may also impact a drug’s safety and efficacy. Assays should be designed in such a way that they provide sufficient sensitivity and are free from potential risks to the target patient population. By designing assays with these factors, it is possible to gather data about the strength and type of immune response that a drug may produce in humans.

  • Track 15-1Bridging ELISA
  • Track 15-2Type II hypersensitivity reaction
  • Track 15-3Clinical Trial Support
  • Track 15-4Total Antibody Assay
  • Track 15-5Enzyme Linked Immuno Sorbent Assay (ELISA)

Metagenomics is the study of genetic material recovered from environmental samples. Metagenomics could be an asset of analysis techniques comprising several connected approaches and ways. We tend to anticipate that metagenomics can complement and stimulate analysis on people and their genomes.

Metagenomics represents a brand-new approach in exceedingly genomic analysis. Metagenomic libraries can be screened for novel physiological, metabolic, and genetic options. Though long and labour-intensive, metagenomics is the most powerful environmental approach that provides prospects to get novel genes and novel biomoleculesthrough the expression of genes from an uncultivated and unknown bacterium in a recipient host cell. Metagenomic information ought to contain DNA sequences for all the genes within the microorganism community

  • Track 16-1Application of Genomics to Uncultured Microorganisms
  • Track 16-2Gene analysis by metagenomics
  • Track 16-3The Human Microbiome
  • Track 16-4Microbial Metagenomics
  • Track 16-5Metatranscriptomics
  • Track 16-6Metaproteomics

Cell therapies and regenerative medication boost the health of patients by repairing, replacing, or by creating broken cells within the body. Some elements of our bodies will repair themselves quite well when injured, while others don’t repair in any respect. We can’t develop an entire leg or arm; however, some animals will develop – or regenerate – whole body elements. Stem cells (SC) offer totally different. Despite the promise of embryonic stem cells, in several cases, adult or perhaps vertebrate stem cells give a lot of fascinating approach for clinical applications.  Clinical applications in regenerative medication have increased tremendously throughout the last ten years. Regenerative medication revolutionizes the method to improve the health and quality of life by restoring, maintaining or enhancing tissue and functions of organs.

  • Track 17-1Regenerative Medicine
  • Track 17-2Cord blood
  • Track 17-3Induced pluripotent stem cells
  • Track 17-4Stem cell treatments
  • Track 17-5Artificial organ
  • Track 17-6Cell therapies
  • Track 17-7Aesthetic medicine

Clinical chemistry is usually involved with analysis of bodily fluids for diagnostic and therapeutic functions. It's an applied style of organic chemistry. There are currently several blood tests and clinical tests with intensive diagnostic capabilities. These are performed on any bodily fluid or plasma. The foremost common specimens tested in clinical chemistry are blood and Serum. Many various tests exist to check glucose, electrolytes, enzymes, hormones, lipids (fats),  and proteins. By running tests on these samples, physicians will confirm patient conditions and potential diseases, and recommend a counselled treatment up. Clinical chemistry procedures create precise diagnoses, offer effective treatment choices and monitor a patient’s response to treatment.

  • Track 18-1Clinical Endocrinology
  • Track 18-2Toxicology
  • Track 18-3Therapeutic Drug Monitoring
  • Track 18-4Urinalysis
  • Track 18-5Panel tests
  • Track 18-6Clinical Biochemistry
  • Track 18-7Blood Tests

Pharmacogenomics is the study of the gene effect on a person’s response to medication. This comparatively new field combines pharmacological medicine and genetics to develop effective, safe medications and doses that may be tailored to a person’s genetic makeup. Several medications presently accessible do not work a similar manner for everybody. Adverse drug reactions are a unit of big trouble for hospitalizations. With the data gained from the HGP, researchers are learning variations in genes have an effect on the body’s response to medications.

The field of pharmacogenomics continues to be in its infancy. Its use is presently quite restricted, however new approaches are in clinical trials. In future, pharmacogenomics can permit the tailored medication to treat health issues, as well as disorders, Alzheimer sickness, cancer, HIV/AIDS, and asthma.

  • Track 19-1Drug-Gene Testing
  • Track 19-2Clinical Pharmacogenomics
  • Track 19-3Precision Pharmacotherapy
  • Track 19-4Pharmacogenetics
  • Track 19-5Personalized Medicine
  • Track 19-6Pharmacoproteomics

DNA sequencing is the method of sequencing the base pairs of a DNA (As, Ts, Cs, and Gs). Sequencing a whole organism’s DNA is a huge task. It needs breaking the DNA into several smaller items, sequencing the items, and collection of these sequences into one long "consensus."

These bases give the information on genotype and also the phenotype. Nucleotides aren't the sole determinants of phenotypes but are essential to their information. Every individual and organism feature a specific ester base sequence. DNA sequencing additionally underpins pharmacogenomics. This can be a comparatively new field that is leading to an individualized medication. Over a hundred and forty medication approved by the FDA currently by pharmacogenomic data in their labelling.

  • Track 20-1DNA extraction
  • Track 20-2DNA polymerase
  • Track 20-3Epigenetics
  • Track 20-4Recombinant DNA
  • Track 20-5Restriction enzymes
  • Track 20-6Sanger sequencing

Translational medicine is defined as an interdisciplinary branch of the biomedical field. By using a highly collaborative approach Translational medicine is growing in biomedical research discipline and aims to expedite the discovery of new diagnostic tools and treatments. Within public health, translational medicine is focused on ensuring proven strategies for disease treatment and prevention. Translational medicine aims to improve human health and longevity by determining the relevance to human disease of novel discoveries in the biological sciences. Translational medicine is enhancing the efficiency of biomedical discovery and application. There are many compelling reasons to find cost-effective solutions to health care delivery. 

  • Track 21-1Current Research in Translational Medicine
  • Track 21-2Clinical and Translational Medicine
  • Track 21-3Disease-targeted research
  • Track 21-4Evidence-based research
  • Track 21-5Preclinical research
  • Track 21-6Translational medical science

Integrative Molecular Medicine covers novel findings in molecular, biological, and biomedicine research. The broad spectrum of Integrative Molecular Medicine includes rare and common disorders from diagnosis to treatment.

Molecular drugs strive to know traditional body functioning and illness pathological process at the molecular level which can enable researchers and physician-scientists to use that information within the style of specific molecular tools for illness identification, treatment, and prognosis. Integrative Molecular drugs (imMed) offers a scientific setting, which mixes basic and clinical analysis and offers a broad vary of advanced opportunities.

  • Track 22-1Clinical Science
  • Track 22-2Integrative Molecular Biology & Biotechnology
  • Track 22-3Medical Microbiology
  • Track 22-4Nanotechnology