Animal models are important for understanding the pathogenesis of human diseases and for developing and testing new drugs. Pigs have been widely used in the research on the cardiovascular, skin barrier, gastrointestinal, and central nervous systems as well as organ transplantation. Recently, pigs also become an attractive large animal model for the study of neurodegenerative diseases because their brains are very similar to human brains in terms of mass, gully pattern, vascularization, and the proportions of the gray and white matters. Although adeno-associated virus type 9 (AAV9) has been widely used to deliver transgenes in the brain, its utilization in large animal models remains to be fully characterized. Here, we report that intravenou...
Adeno-associated virus (AAV) vectors have become an attractive tool for efficient gene transfer into...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Intrathecal (IT) gene transfer using adeno-associated virus (AAV) may be clinically promising as a t...
Animal models are important for understanding the pathogenesis of human diseases and for developing ...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Within the last decade there have been several severe combined immunodeficient (SCID) pig models dis...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Genetically modified animal models are commonly used for in vivo studies of human diseases. Mice are...
Genetically modified animal models are commonly used for in vivo studies of human diseases. Mice are...
Mucopolysaccharidosis type I is a recessive genetic disease caused by deficiency of the lysosomal en...
Large animal models are vital in the validation of gene therapies, acting in a translational capacit...
Hunter syndrome is an X-linked recessive disease caused by deficiency of the lysosomal enzyme iduron...
Gene therapy is being explored for its potential to treat neurodegenerative diseases such as Alzheim...
Adeno-associated virus (AAV) vectors have become an attractive tool for efficient gene transfer into...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Intrathecal (IT) gene transfer using adeno-associated virus (AAV) may be clinically promising as a t...
Animal models are important for understanding the pathogenesis of human diseases and for developing ...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Within the last decade there have been several severe combined immunodeficient (SCID) pig models dis...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Genetically modified animal models are commonly used for in vivo studies of human diseases. Mice are...
Genetically modified animal models are commonly used for in vivo studies of human diseases. Mice are...
Mucopolysaccharidosis type I is a recessive genetic disease caused by deficiency of the lysosomal en...
Large animal models are vital in the validation of gene therapies, acting in a translational capacit...
Hunter syndrome is an X-linked recessive disease caused by deficiency of the lysosomal enzyme iduron...
Gene therapy is being explored for its potential to treat neurodegenerative diseases such as Alzheim...
Adeno-associated virus (AAV) vectors have become an attractive tool for efficient gene transfer into...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Intrathecal (IT) gene transfer using adeno-associated virus (AAV) may be clinically promising as a t...