Results 1 to 10 of about 123,260 (289)

Genetic Variation in Insect Vectors: Death of Typology? [PDF]

open access: yesInsects, 2018
The issue of typological versus population thinking in biology is briefly introduced and defined. It is then emphasized how population thinking is most relevant and useful in vector biology.
Jeffrey R. Powell
doaj   +4 more sources

Genetic Targeting of Adenoviral Vectors [PDF]

open access: hybridMolecular Therapy, 2000
Victor Krasnykh   +2 more
openalex   +5 more sources

Genetic control of vectors [PDF]

open access: yesPests and vector-borne diseases in the livestock industry, 2018
In a context of tighter regulations on approved insecticide molecules, the spread of insecticide resistance in insect vectors of human and animal diseases and the introduction of exotic vectors to new territories call for the development of new pest control methods and strategies.
Bouyer, Jérémy, Marois, Eric
openaire   +5 more sources

Biomimetic Peptides: A New Generation of Gene Transfer Vectors [PDF]

open access: yesمجله دانشکده پزشکی اصفهان, 2022
Gene therapy is a new approach that aims to modify defective genes or intracellular expression of therapeutic proteins, and this depends on the use of high-efficiency gene transfer systems.
Hooman Mahmoudi Aznaveh, Maryam Nikkhah
doaj   +1 more source

Differentiation of Human Adipose-Derived Mesenchymal Stromal/Stem Cells into Insulin-Producing Cells with A Single Tet-Off Lentiviral Vector System [PDF]

open access: yesCell Journal, 2022
Objective: Human adipose-derived mesenchymal stromal/stem cells (hASC) constitute an attractive source of stemcells for cell-based therapies in regenerative medicine and tissue engineering as they are easy to acquire fromlipoaspirate, expansion, and ...
Hiroyuki Moriyama   +4 more
doaj   +1 more source

A Biosafety Study of Human Umbilical Cord Blood Mononuclear Cells Transduced with Adenoviral Vector Carrying Human Vascular Endothelial Growth Factor cDNA In Vitro

open access: yesBiomedicines, 2023
The biosafety of gene therapy remains a crucial issue for both the direct and cell-mediated delivery of recombinant cDNA encoding biologically active molecules for the pathogenetic correction of congenital or acquired disorders.
Ilnur I. Salafutdinov   +10 more
doaj   +1 more source

Evaluation of the Autologous Genetically Enriched Leucoconcentrate on the Lumbar Spinal Cord Morpho-Functional Recovery in a Mini Pig with Thoracic Spine Contusion Injury

open access: yesBiomedicines, 2023
Background: Pathological changes associated with spinal cord injury (SCI) can be observed distant, rostral, or caudal to the epicenter of injury. These remote areas represent important therapeutic targets for post-traumatic spinal cord repair.
Ravil Garifulin   +9 more
doaj   +1 more source

Integrase deficient lentiviral vector: prospects for safe clinical applications [PDF]

open access: yesPeerJ, 2022
HIV-1 derived lentiviral vector is an efficient transporter for delivering desired genetic materials into the targeted cells among many viral vectors. Genetic material transduced by lentiviral vector is integrated into the cell genome to introduce new ...
Chee-Hong Takahiro Yew   +6 more
doaj   +2 more sources

A Multifaceted Approach to Optimizing AAV Delivery to the Brain for the Treatment of Neurodegenerative Diseases

open access: yesFrontiers in Neuroscience, 2021
Despite major advancements in gene therapy technologies, there are no approved gene therapies for diseases which predominantly effect the brain. Adeno-associated virus (AAV) vectors have emerged as the most effective delivery vector for gene therapy ...
Jonathan M. Fischell, Paul S. Fishman
doaj   +1 more source

Home - About - Disclaimer - Privacy