Hereditary Diseases Services For Clinical Medicine
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by iFyber, LLCbased in USA
iFyber provides a suite of biofilm tests to verify the efficacy of antimicrobial medical devices and drugs. Biofilms are complex communities of microbes protected within a matrix of sugars, proteins, and extracellular DNA. These characteristics, in addition to their tolerance to antibiotics, make biofilms significantly more difficult to prevent and remove. Research has shown that between 60 to ...
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Manufactured by Invitae Corporationbased in USA
The Invitae Comprehensive Carrier Screen checks your DNA for over 280 genetic conditions including cystic fibrosis, Tay-Sachs disease, fragile X syndrome, and spinal muscular atrophy. This is the same test your Ob-Gyn may offer at your 8-week appointment—but there’s no reason to wait. The sooner you know your results, the ...
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by ICON plcbased in IRELAND
Focused on the unique needs of device and diagnostics manufacturers, ICON has broad experience in supporting trials of respiratory disease and infectious disease affecting respiratory function. The prevalence of respiratory diseases will continue to rise as our global population ages and the incidence of chronic diseases, such as COPD and asthma, increases exponentially. ICON has considerable ...
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based in FRANCE
We offer a comprehensive solution for hereditary and rare disease data that detects both commonly accessible variants and relevant challenging variants such as mid-sized deletions, Alu elements and larger structural ...
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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 PhysioAssistbased in FRANCE
Simeox is the result of several years of research and development in partnership with CNRS and CRCM (Resources and competences center for cystic fibrosis) Hôpital Nord in Marseille (France). The PhysioAssist research program was devoted to the study of bronchial mucus and helped develop the technology present in the Simeox device. ...
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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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by BIO-CATbased in USA
BIO-CATs Research and Development provides customer support in many areas, including: Custom formulation of digestive blends for dietary supplements, based on nutritional efficiency, food sensitivities, al 1 ergenicity, and product stability Enzyme hydrolysis in food and ingredient processing based on processing conditions and desired products including taste, texture, solubility, and ...
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Manufactured by Creative Biolabsbased in CHINA
Autophagy is a key catabolic process that ensures the removal of excess or damaged cellular components under physiological and pathological conditions, and provides a metabolic supply in the absence of extracellular nutrients, thereby maintaining the proper balance of cells. Optimal autophagy activity plays an important protective role in several human diseases, such as neurodegenerative ...
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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 Destiny Pharma plcbased in UNITED KINGDOM
Work on earlier programmes investigating infections in areas such as respiratory, dermal, ocular and biofilms carries on as research projects, including academic and/or commercial collaborations and grant funded ...
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