Genetic Diseases Services For Clinical Medicine
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by BioVenicbased in USA
The proportion of cats suffering from genetic diseases is much higher than universal cognition. For most of these hereditary diseases, traditional detection means cannot accurately diagnose. However, the onset of these diseases is often accompanied by serious ever irretrievable consequences. Compared with treatment after the onset, anticipating and avoiding the risks from the beginning is much ...
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based in USA
As an institute, the NIEHS is uniquely positioned to investigate the interplay between environmental exposures, human biology, genetics, and common diseases that limit our longevity and quality of life. NIEHS research uses state-of-the-art science and technology to understand how environmental factors influence the development and progression of disease, so that we may prevent disease and improve ...
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Manufactured by CENTOGENE N.V.based in GERMANY
Carrier screening can determine if a healthy person carries a genetic disease, identify people at risk of developing a genetic disease, or help assess the risk of a couple passing a genetic disease onto their children. ...
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Manufactured by Creative Biolabsbased in CHINA
Genes are the basis of heredity. Sometimes, one or more genes mutated and changed can lead to a medical condition called a genetic disease. Antibodies to genetic diseases bind to proteins involved in genetic diseases and have a wide range of uses in basic research. https://neutab.creative-biolabs.com/category-genetic-disease-34.htm ...
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Manufactured by Creative Biolabsbased in CHINA
The nucleic acid drug, as a novel therapeutic modality, can achieve long-lasting or even curative effects via gene regulations, replacement or editing. They have great potential to treat human diseases such as viral infections, cancers, and genetic ...
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Manufactured by CENTOGENE N.V.based in GERMANY
Whole Exome Sequencing (WES) is a comprehensive genetic test that identifies changes in a patient's DNA that are causative or related to their medical concerns. By focusing on the entire protein-coding regions of the genome – the exome – WES offers you the coverage you need to diagnose patients rapidly and ...
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based in USA
Most disease-related variants are found in exons, exome sequencing is a method to understand genetic causes of diseases or conditions. Optimized workflow for FFPE samples. Expert scientific and project support. IDT, SureSelect, Twist Biosciences, Illumina capture options. Mature bioinformatics ...
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Manufactured by CENTOGENE N.V.based in GERMANY
The fastest and most comprehensive genetic testing available for newborns, infants and children less than 24 months old in intensive care. CentoICU – Genetic Testing When Every Moment Counts. Up to one-third of all babies and children admitted to the ICU have a genetic disease. For many patients, early identification can make a difference in their immediate and long-term ...
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Manufactured by Boster Biological Technologybased in USA
Gene therapy is a method of delivering therapeutic genes to cells or tissues using modified viruses or other technologies in order to address genetic disorders at their source. The understanding of how the adeno-associated virus (AAV) may be utilized as an efficient delivery mechanism for therapeutic genetic material into living tissue is one of the most exciting breakthroughs in contemporary ...
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Manufactured by Ozgene Pty Ltd.based in AUSTRALIA
Knock-in mice have an insertion in a specific locus in order to produce genetically modified mice for customised research purposes. Reporter genes, human genes, related genes from the same organism, or point mutations can be introduced into the protein-coding region of a gene to produce knock-in mice. The difference between the knock-in and knockout approach is that knock-in mouse models are ...
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Manufactured by BioMarinbased in USA
In alignment with our commitment to scientific innovation and areas of unmet medical need, we may provide product and funding support for independent research in rare diseases and genetic ...
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Manufactured by Deep Genomicsbased in CANADA
AI Drives Unprecedented Number of Valuable Medicines by Combining Prediction and Scale. Our proprietary AI Workbench is designed for data-driven prediction, positive feedback loops, and exponential growth. It enables us to identify leads for over 50% of the novel targets we select, and to do so quickly. This is a game changer. In 2018, our proprietary AI Workbench unlocked our first targets in ...
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based in USA
Expectant parents want to do everything they can before the birth of their baby. The Avero Carrier Test looks at a patient’s genes to see if they may carry a disease that they could pass on to their child. Knowing a patient’s genetic carrier status is one of the most important things you can do to help them prepare for ...
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Manufactured by Ozgene Pty Ltd.based in AUSTRALIA
Knockout mice are animal models that have been genetically modified to delete or inactivate a specific gene. The term ‘knockout’ refers to knocking out the functionality of the target gene. These mouse models allow researchers to gain insight into how the loss of the gene affects physiology, behavior and disease development. Observing the characteristics of a knockout phenotype can ...
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Manufactured by HemoShear Therapeutics, Inc.based in USA
Using our powerful REVEAL-TxTM drug discovery platform, our scientists are identifying and validating promising approaches to develop novel treatments aiming to extend and improve the quality of life of patients with rare diseases. In our most advanced program, the company is conducting a phase 2 clinical trial of HST5040, an oral small molecule investigational drug for the treatment of patients ...
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based in USA
Lovelace Biomedical is very much focused on gene therapy for genetic diseases testing in human clinical trials. Our ultimate aim is to give best gene therapy medicine. http://www.lovelacebiomedical.org/specialty-expertise/gene-therapy/ ...
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Manufactured by RareStone Groupbased in CHINA
Rare neurological diseases include developmental defects of the nervous system, genetic and metabolic diseases, neuroimmune diseases, neurological tumors, special types of infectious diseases of the nervous system, neurodegenerative diseases, and neuromuscular diseases. At present, more than 7,000 rare diseases have been found in humans, about 60% of which are neurological diseases. ...
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Manufactured by Creative Biolabsbased in CHINA
Creative Biolabs provides a comprehensive range of primary antibodies for genetic disorders. These antibodies show high specificity, activity, performance and repeatability in a variety of technologies, including: ...
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based in INDIA
How Our Gene Expression Analysis Services Can Help You ? Genes encode proteins and proteins dictate cell function. Therefore, the thousands of genes expressed in a particular cell determine what that cell can do. Moreover, each step in the flow of information from DNA to RNA to protein provides the cell with a potential control point for self-regulating its functions by adjusting the amount and ...
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based in ISRAEL
SIA's philanthropic research supports the Israeli Duchenne Parent Association. This is an eort to develop a cure for Duchenne Muscular Dystrophy (DMD). DMD is the most common, fatal genetic disorder diagnosed in childhood. It aects approximately 1 in every 3,500 male infants born. We invite you to read more about SIA’s Philanthropic DMD Research and Duchenne Animal ...
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