Viral Vector News and Research

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Viral Vector is a type of virus used in cancer therapy. The virus is changed in the laboratory and cannot cause disease. Viral vectors may produce tumor antigens (proteins found on a tumor cell) to stimulate an antitumor immune response in the body. Viral vectors may also be used to carry genes that can change cancer cells back to normal cells.
UC Davis researchers awarded $1.5 million NIH grant for CRISPR cancer treatment

UC Davis researchers awarded $1.5 million NIH grant for CRISPR cancer treatment

Novel viral vector improves gene therapy for sickle cell disease

Novel viral vector improves gene therapy for sickle cell disease

Researchers make breakthrough in gene therapy for sickle cell disease

Researchers make breakthrough in gene therapy for sickle cell disease

New study shows response to HIV vaccine in 6 weeks

New study shows response to HIV vaccine in 6 weeks

New study shows response to HIV vaccine in 6 weeks

New study shows response to HIV vaccine in 6 weeks

New gene therapy helps stroke patients develop new neurons

New gene therapy helps stroke patients develop new neurons

Protein implicated in neuron growth and cell adhesion appears crucial for pain sensitization

Protein implicated in neuron growth and cell adhesion appears crucial for pain sensitization

Researchers use genetically manipulated virus to combat prostate cancer

Researchers use genetically manipulated virus to combat prostate cancer

Sartorius Stedim Biotech introduces new ambr 15 cell culture microbioreactor system

Sartorius Stedim Biotech introduces new ambr 15 cell culture microbioreactor system

Yposkesi chairman to speak on ‘Manufacturing and the CDMO Perspective’ at Cell and Gene Meeting

Yposkesi chairman to speak on ‘Manufacturing and the CDMO Perspective’ at Cell and Gene Meeting

Merck to collaborate with GenScript for plasmid and virus manufacturing in China

Merck to collaborate with GenScript for plasmid and virus manufacturing in China

Single CRISPR treatment can safely and stably correct genetic disease

Single CRISPR treatment can safely and stably correct genetic disease

Scientists develop new gene therapy that prevents axon destruction in mice

Scientists develop new gene therapy that prevents axon destruction in mice

Cobra Biologics announces appointment of Dr Darrell Sleep as Director of Innovation

Cobra Biologics announces appointment of Dr Darrell Sleep as Director of Innovation

New method modifies blood stem cells to reverse genetic mutation that causes IPEX

New method modifies blood stem cells to reverse genetic mutation that causes IPEX

New technology based on moths and magnets could help treat genetic diseases

New technology based on moths and magnets could help treat genetic diseases

NEC and Transgene sign MOU for strategic collaboration aimed at treating solid cancers

NEC and Transgene sign MOU for strategic collaboration aimed at treating solid cancers

Findings offer new insight into early changes that occur during AD pathology

Findings offer new insight into early changes that occur during AD pathology

Scientists reprogram mature inhibitory neurons into dopaminergic cells

Scientists reprogram mature inhibitory neurons into dopaminergic cells

Study: Brain's neurons are more changeable in adulthood than previously thought

Study: Brain's neurons are more changeable in adulthood than previously thought