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pro vyhledávání: '"Alexandra M. Highet"'
Autor:
Yanling Liao, Munenari Itoh, Albert Yang, Hongwen Zhu, Samantha Roberts, Alexandra M. Highet, Shaun Latshaw, Kelly Mitchell, Carmella Van De Ven, Angela Christiano, Mitchell S. Cairo
Publikováno v:
Cell Transplantation, Vol 23 (2014)
Human umbilical cord blood (CB)-derived unrestricted somatic stem cells (USSCs) have previously been demonstrated to have a broad differentiation potential and regenerative beneficial effects when administered in animal models of multiple degenerativ
Externí odkaz:
https://doaj.org/article/274792e175fd40fd983438dfa9b075cf
Autor:
Alexandra M Highet, Yanling Liao, Mitchell S. Cairo, Munenari Itoh, Shaun Latshaw, Hongwen Zhu, Angela M. Christiano, Albert Yang, Samantha Roberts, Carmella van de Ven, Kelly Mitchell
Publikováno v:
Cell Transplantation, Vol 23 (2014)
Human umbilical cord blood (CB)-derived unrestricted somatic stem cells (USSCs) have previously been demonstrated to have a broad differentiation potential and regenerative beneficial effects when administered in animal models of multiple degenerativ
Autor:
Munenari Itoh, Samantha Roberts, Alexandra M Highet, Albert Yang, Angela M. Christiano, Mitchell S. Cairo, Yanling Liao
Publikováno v:
Biology of Blood and Marrow Transplantation. 18:S373-S374
Autor:
Munenari Itoh, Yanling Liao, Alexandra M Highet, Samantha Roberts, Angela M. Christiano, Mitchell S. Cairo, Albert Yang
Publikováno v:
Blood. 118:4824-4824
Abstract 4824 Background: Recessive dystrophic epidermolysis bullosa (RDEB) is a severe inherited skin blistering disease caused by mutations in the type VII collagen (COL7A1) gene that encodes a major component in anchoring fibrils (Christiano et.al
Autor:
Albert Yang, Yanling Liao, Munenari Itoh, Carmella van de Ven, Shaun Latshaw, Mitchell S. Cairo, Angela M. Christiano, Alexandra M Highet, Samantha Roberts
Publikováno v:
Biology of Blood and Marrow Transplantation. (2):S349
s / Biol Blood Marrow Transplant 19 (2013) S342eS354 S349 than targeting either alone. Erythropoietin-producing hepatocellular carcinoma-A2 (EphA2)-specific CAR T cells were used to target the A549 tumor cells. EphA2-specific T cells when administere