Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Melisa Vance"'
Autor:
Joana S Boura, Melisa Vance, Weihong Yin, Catarina Madeira, Cláudia Lobato da Silva, Christopher D Porada, Graça Almeida-Porada
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 1, Iss C (2014)
Mesenchymal stromal cells (MSC) constitutively express low levels of human leukocyte antigen-G (HLA-G), which has been shown to contribute to their immunomodulatory and anti-inflammatory properties. Here, we hypothesized that overexpression of HLA-G
Externí odkaz:
https://doaj.org/article/1a4674f592854288b2ca80ff049638c1
Autor:
Aravind Asokan, Telmo Llanga, Giridhar Murlidharan, Brian C. Gilger, Neil C Chungfat, Joanne Kurtzberg, R. Jude Samulski, William D. Bennett, Kenton T. Woodard, Matthew L. Hirsch, Melisa Vance
Publikováno v:
Scientific Reports
Although cord blood transplantation has significantly extended the lifespan of mucopolysaccharidosis type 1 (MPS1) patients, over 95% manifest cornea clouding with about 50% progressing to blindness. As corneal transplants are met with high rejection
Publikováno v:
Molecular Therapy. 24:S40-S41
Mucopolysaccharidosis type 1 (MPS1), also known as Hurler syndrome, is a genetic lysosomal storage disease that results from the loss-of-function mutations present on the L-iduronidase (IDUA) gene. As a consequence, glycosaminoglycans accumulate aber
Publikováno v:
Molecular Therapy. 24:S217-S218
AAV gene therapy has demonstrated success for the treatment of several ocular diseases with the tropism and efficiency of AAV retinal transduction being a function of the route of administration. Subretinal injection has been the primary route to del
Autor:
Laurie R. Goodrich, Joanne Kurtzberg, Llanga Telmo, Richard Jude Samulski, Matthew L. Hirsch, Melisa Vance
Publikováno v:
Blood. 126:2041-2041
Mucopolysaccharidosis type 1 (MPS1), also known as Hurler syndrome, is a genetic lysosomal storage disease that results from the loss-of-function mutations present on the L-iduronidase (IDUA) gene. As a consequence, glycosaminoglycans accumulate aber
Autor:
Melisa Vance, Joana S. Boura, Christopher D. Porada, Cláudia Lobato da Silva, Graça Almeida-Porada, Catarina Madeira, Weihong Yin
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 1, Iss C (2014)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Mesenchymal stromal cells (MSC) constitutively express low levels of human leukocyte antigen-G (HLA-G), which has been shown to contribute to their immunomodulatory and anti-inflammatory properties. Here, we hypothesized that overexpression of HLA-G