Online / Physical Event

EuroScicon Conference on

Cell and Gene Therapy

Theme: Advancements in Cell and Gene Therapy : Making a dead cell work

Event Date & Time

Event Location

Amsterdam, Netherlands

Brochure Program Abstract Registration ReaderBase Awards

20 Years Of Excellence in Scientific Events

Performers / Professionals From Around The Globe

Conference Speaker

Joel I. Osorio

Westhill University School of Medicine
Mexico

Conference Speaker

Rachel Knevel

Department of Rheumatology
Netherlands

Conference Speaker

Khalid Shah

Vice Chairman, Department of Neurosurgery, Brigham and Womens Hospital
USA

Conference Speaker

Hazem Barmada

M.D., FRCS Ed, FRCSEd (CTh), FRCS (CTH)CardioVascular & Thoracic Surgeon
Mississippi

Conference Speaker

Jun Dou

Department of Pathogenic Biology and Immunology, School of Medicine, Southeast University
China

Conference Speaker

Dawid Serafin

Doctor of aesthetic medicine
Poland

Conference Speaker

Huanxiang Zhang

Department of Cell Biology, Medical College of Soochow University
China

Conference Speaker

Xueguang Sun

UC Department of Pediatrics
USA

Conference Speaker

Gabrielle Bradshaw

Queensland University of Technology
Australia

Conference Speaker

Hassan El motawkel

Saudi German Hospital, Aseer
Egypt

Conference Speaker

Segundo Mesa

Psychiatric Hospital of Havana
Cuba

Conference Speaker

Esma S Yolcu

University of Louisville
USA

Tracks & Key Topics

Cell and Gene Therapy 2018

About Conference

The EuroSciCon will be holding the international Cell and Gene Therapy 2018 conference focusing on Advancements in Cell and Gene therapyAugust 20-21, 2018 in Amsterdam, Netherlands. The theme of this year’s meeting is Advancements in Cell and Gene Therapy : Making a dead cell work" that will provide an international platform for discussion of present and future challenges in Cell and Gene therapy and expertise meeting. World-leading health practitioners, clinicians, educators and researchers will present cutting-edge and practical clinical techniques based upon widely accepted evidence and will introduce new and emerging research.

What’s New

Cell and Gene Therapy 2018 includes international attendee workshops, lectures and symposia, including a designated registration area, a refreshment break and gala lunch. So come and join the leading expertise people in the field of Cell and Gene therapy and allied professionals from August 20-21, 2018, in Netherlands, to keep up with the rapidly accelerating pace of change that is already having an impact on the field of Cell and Gene Therapy and will continue to in the future.

About Venue

Amsterdam is the capital of Netherlands. Amsterdam is a city that's rich in the visitor sights. It has many ancient churches and many magnificent museums as well. As the commercial capital of the Netherlands and one of the top financial centers in Europe. Amsterdam offers a lot more, like the world-class Van Gogh Museum, the Rijksmuseum and shopping on Nine Little Streets. Families may enjoy a visit to the NEMO Science Museum and Vondelpark. So pack your bag, pick up a camera and get ready for an adventure in Amsterdam!!

Sessions & Tracks

Gene therapy for Diseases

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.

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Stem Cell 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.

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Gene Editing

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.

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Vectors Used in Gene Therapy

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.

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Cell Biology

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

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Ethical issues related to Gene 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.

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Gene therapy in tissue engineering

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.

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Genomic Medicine

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.

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Cell culture processes

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.

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Cellular Pathology

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.

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Cell damage and adaptation

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).

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Cell Science Research

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.

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Cell & Gene Therapy

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.

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Regenerative Medicine

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.

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Immunotherapy

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.

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Genetics and stem cell biology

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.

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Epigenetics

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.

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Human Genomics

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.

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Next Generation Sequencing

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.

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Gene Editing and CRISPR Based Technologies

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.

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Proteomics

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.

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Viral Gene Therapy

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.

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Cell Therapy of Cardiovascular Disorders

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.

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 Regulatory and Safety Aspects of Cell and Gene Therapy

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.

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Markets & Future Prospects for Cell & Gene Therapy

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.

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A huge thanks to all our amazing partners. We couldn’t have a conference without you!

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Sponsors/Exhibitors

A huge thanks to all our amazing partners. We couldn’t have a conference without you!

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EuroSciCon Events are produced by Euroscicon Ltd

EuroSciCon, founded in 2001 is a UK based independent life science Events Company with predominantly business and academic client base. The key strategic objective of EuroSciCon is to communicate science and medical research between academia, clinical practice and the pharmaceutical industry. Most of its events are in Europe and London or live streamed. EuroSciCon expanded its operations to international in association with Meetings International, Singapore. All major meetings of EuroSciCon and Meetings International will issue Continued Professional Education (CPD), Continued Education (CE), Continued Medical Education (CME) Credits.