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Blood
|
January 8, 2003
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
Catherine S Manno, Amy J Chew, Sylvia Hutchison, et al.
Science Translational Medicine
|
November 28, 2014
Human COL7A1-corrected induced pluripotent stem cells for the treatment of recessive dystrophic epidermolysis bullosa
Vittorio Sebastiano, Hanson Hui Zhen, Bahareh Haddad, et al.
Science Translational Medicine
|
December 1, 2017
Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase
Francesco Puzzo, Pasqualina Colella, Maria G Biferi, et al.
Stem Cells (Dayton, Ohio)
|
October 14, 2006
Sarcoma derived from cultured mesenchymal stem cells
Jakub Tolar, Alma J Nauta, Mark J Osborn, et al.
Nature Medicine
|
February 14, 2006
Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
Catherine S Manno, Glenn F Pierce, Valder R Arruda, et al.
The New England Journal of Medicine
|
November 20, 2014
Long-term safety and efficacy of factor IX gene therapy in hemophilia B
Amit C Nathwani, Ulreke M Reiss, Edward G D Tuddenham, et al.
The New England Journal of Medicine
|
December 14, 2011
Adenovirus-associated virus vector-mediated gene transfer in hemophilia B
Amit C Nathwani, Edward G D Tuddenham, Savita Rangarajan, et al.
Page
of 20
Search research articles
Search
Showing results (191-200 of 197) with videos related to
Sort By:
Page
of 20
You have reached the last page of results.
This site can display upto 197 results.
Blood
|
January 8, 2003
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
Catherine S Manno, Amy J Chew, Sylvia Hutchison, et al.
Science Translational Medicine
|
November 28, 2014
Human COL7A1-corrected induced pluripotent stem cells for the treatment of recessive dystrophic epidermolysis bullosa
Vittorio Sebastiano, Hanson Hui Zhen, Bahareh Haddad, et al.
Science Translational Medicine
|
December 1, 2017
Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase
Francesco Puzzo, Pasqualina Colella, Maria G Biferi, et al.
Stem Cells (Dayton, Ohio)
|
October 14, 2006
Sarcoma derived from cultured mesenchymal stem cells
Jakub Tolar, Alma J Nauta, Mark J Osborn, et al.
Nature Medicine
|
February 14, 2006
Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
Catherine S Manno, Glenn F Pierce, Valder R Arruda, et al.
The New England Journal of Medicine
|
November 20, 2014
Long-term safety and efficacy of factor IX gene therapy in hemophilia B
Amit C Nathwani, Ulreke M Reiss, Edward G D Tuddenham, et al.
The New England Journal of Medicine
|
December 14, 2011
Adenovirus-associated virus vector-mediated gene transfer in hemophilia B
Amit C Nathwani, Edward G D Tuddenham, Savita Rangarajan, et al.
Page
of 20