Synonymer & Anagram | Engelska ordet AAV

Exempel på hur man kan använda AAV i en mening

• Because of this, the present value AAV is lower than the $70 million he'd otherwise earn if there were no deferrals.
• Marine Corps and SAIC officials unveiled the AAV SU prototype in January 2016, with survivability enhancements including replacing the angled EAAK with 49 advanced buoyant ceramic armor panels, a bonded spall liner, armor-protected external fuel tanks, an aluminum armor underbelly providing Mine Resistant Ambush Protected (MRAP)-equivalent blast protection, and blast mitigating seats as well as a more powerful engine, new suspension system, and increased reserve buoyancy.
• They are detected as a blood test in a number of autoimmune disorders, but are particularly associated with systemic vasculitis, so called ANCA-associated vasculitides (AAV).
• Gene therapy vectors using AAV can infect both dividing and quiescent cells and persist in an extrachromosomal state without integrating into the genome of the host cell.
• The carburettor up to Chassis number SFC100 was a single double downdraught Stromberg type AAV 26 until 1952 when it was replaced by a Zenith DBVC42.
• The main difference between Visa and Mastercard implementations lies in the method to generate the UCAF (Universal Cardholder Authentication Field): Mastercard uses AAV (Accountholder Authentication Value) and Visa uses CAVV (Cardholder Authentication Verification Value).
• The research was published in Science Translational Medicine in 2021 and showed the possibility of a less immunogenic gene therapy with the new TLR9-edited Adeno-associated viruses (AAV) as a safer viral vector.
• The most widely known dependovirus is adeno-associated virus (AAV) which was originally discovered as a contaminant in a sample of simian adenovirus.
• This protein correlates strongly with adeno-associated virus type 2 vectors (AAV) resulting in a significant increase in AAV-mediated transgene expression in human cell lines.
• In 2008, three independent research groups reported that patients with the rare genetic retinal disease Leber's congenital amaurosis had been successfully treated using gene therapy with adeno-associated virus (AAV).
• AAV also presents very low immunogenicity, mainly restricted to generating neutralising antibodies, and little well defined cytotoxic response.
• One disadvantage that scAAV faces is that due to robust gene expression, transgene products delivered via scAAV elicit a stronger immune response than those same transgenes delivered via a single-stranded AAV vector.
• This work began with the discovery in his laboratory of a new family of primate AAVs; over 120 new AAV capsids were rescued as latent genomes from primate tissues and studied for their biology and potential as vectors.
• Gene therapy has been proven effective at treating a variety of disorders, including neurodegenerative disorders such as Parkinson's disease (PD) and Alzheimer's disease (AD), in rodent and non-human primate models, and in humans, via the application of neurotrophic factors, such as nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and glial cell line-derived neurotrophic factor (GDNF), and via the application of enzymes such as glutamic acid decarboxylase (GAD), which commonly use adeno-associated viruses (AAV) as a vector.
• Alpine Astrovillage (AAV) is a center for astrophotography and stargazing in the eastern Swiss Alps, high above the valley floor of the Val Müstair in the canton Graubünden.
• On 24 November 2011, Jonathan Wyatt, a Bristol barrister, received a 'good copy' of the REP1 gene, administered through an adeno-associated virus (AAV) – serotype 2 (AAV2) – as a vector, in fluid under the retina.
• She has been recognized for her distinguished contributions to the field, having designed, sponsored, and conducted the first clinical trial of an adeno-associated viral vector (AAV) gene therapy injected into the skeletal muscle (1999), the first trial of AAV gene therapy introduced into the liver (2001), and the first trial in the US of an AAV gene therapy injected into the subretinal space (2007).
• Typically employed options include but are not limited to plasmids and viral vectors such as adeno-associated virus (AAV) vector or lentivirus vector.
• Adeno-associated virus (AAV) has been researched as a viral vector in gene therapy for cancer treatment as an oncolytic virus.
• Samulski's research has focused on the study of the human non-pathogenic parvovirus adeno-associated virus (AAV) and its use in gene therapies.

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