Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gilly Martin"'
Autor:
Joanna D. Davies, Sara E. Marshall, Stephen P. Cobbold, Jenny M. Phillips, Gilly Martin, Herman Waldmann
Publikováno v:
Transplantation. 62:1614-1621
The induction of tolerance in a primed immune system would be valuable therapeutically, but has been difficult to achieve. Mice primed to multiple minor histoincompatible antigens (minors) are able to rapidly reject secondary grafts using either thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ffdf4710799c81e9c20df18dd837daf
https://doi.org/10.1097/00007890-199612150-00015
https://doi.org/10.1097/00007890-199612150-00015
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::524efc0773c2846c31335a18c0b6a331
https://doi.org/10.1111/j.1600-065x.1992.tb01423.x
https://doi.org/10.1111/j.1600-065x.1992.tb01423.x
Autor:
Els M. E. Verdegaal, Conny Hoogstraten, Cornelia S. McLean, Susanne Osanto, M. Leigh Shaw, Jayne Curry, Gilly Martin, Peter T. Loudon
Publikováno v:
The journal of gene medicine. 5(5)
Background DISC-hGMCSF is a gH-deleted HSV-2 based vector expressing human GM-CSF that has entered clinical trials for the therapy of metastatic melanoma. To determine whether this product also has potential to treat breast carcinoma, a series of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a192a512a4470478b8c579533ea51665
https://pubmed.ncbi.nlm.nih.gov/12731089
https://pubmed.ncbi.nlm.nih.gov/12731089
Autor:
Jayne C. Miller, M. Leigh Shaw, Mike Boursnell, Debbie A. Day, Diane M. Blakeley, Richard C. Lowden, Cornelia S. McLean, Peter T. Loudon, Imogen A. Duncan, Gilly Martin
Publikováno v:
The journal of gene medicine. 3(5)
Background DISC-hGMCSF is a gH-deleted HSV-2 based vector expressing human GM-CSF that is being developed for cancer immunotherapy. To support first clinical use, a range of preclinical safety studies were performed using DISC-hGMCSF in addition to D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25410ca332efe5ef0746af99648e8c2e
https://pubmed.ncbi.nlm.nih.gov/11601759
https://pubmed.ncbi.nlm.nih.gov/11601759
Autor:
Terry Ulrich, Stephen J. Thompson, Glen Leesman, Gilly Martin, Clare Varley, Alison Mann, Marie Davies, Stephen Thompson, Finn Holding, Maria J. Watts, Jonathan T Beech, Terry O'neill
Publikováno v:
Biochemical Society transactions. 25(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ae90eb5980eb0a31cb103342dfe4f9f
https://pubmed.ncbi.nlm.nih.gov/9191318
https://pubmed.ncbi.nlm.nih.gov/9191318
Publikováno v:
European journal of immunology. 20(12)
Mice given short courses of anti-CD4 and anti-CD8 monoclonal antibodies became tolerant of allogeneic skin grafted at the same time. Tolerance could be obtained without T cell depletion across multiple minor antigen mismatches, both in naive and prim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f3fde92aed46669791fd60862f7173e
https://pubmed.ncbi.nlm.nih.gov/1980112
https://pubmed.ncbi.nlm.nih.gov/1980112
Publikováno v:
Transplantation. 42:239-247
One of the major complications of allogeneic bone marrow transplantation is graft-versus-host disease. This can be avoided by removing the mature T cells from the marrow, most conveniently by the use of monoclonal antibodies. However, T cell purging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7d4be7df2a5d6f47ae681a6fa0839c2
https://doi.org/10.1097/00007890-198609000-00003
https://doi.org/10.1097/00007890-198609000-00003
Publikováno v:
Scopus-Elsevier
Allogeneic reactions are the major limitation to organ transplantation. These are manifested as rejection of the grafted tissue, and also, in the case of bone marrow transplantation (BMT), graft-versus-host disease (GVHD). Recent methods of avoiding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::406d421825de484257321e7f2400edb2
https://doi.org/10.1038/323164a0
https://doi.org/10.1038/323164a0