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1 ay provide an alternative to donor lungs for transplantation therapy.
2 and targeted injection of MSCs can optimize transplantation therapy.
3 ction represents a promising new approach to transplantation therapy.
4 ecome a prominent and pervasive influence on transplantation therapy.
5 that is crucial to the effectiveness of the transplantation therapy.
6 l pulp tissues, are potential tools for cell transplantation therapy.
7 beneficial to improve the outcomes for islet transplantation therapy.
8 ntial for clinical application of liver cell transplantation therapy.
9 possibilities for in vitro research and cell transplantation therapy.
10 permeability and immune-protection for islet transplantation therapy.
11 derlie beta cell failure and/or hamper islet transplantation therapy.
12 ood should make them valuable candidates for transplantation therapy.
13 , may impose two major barriers in LCAs cell transplantation therapy.
14 of ex vivo expanded hematopoietic cells for transplantation therapy.
15 fering with BTLA signaling in post-stem cell transplantation therapies.
16 afe source of endodermal-derived tissues for transplantation therapies.
17 , providing an unlimited source of cells for transplantation therapies.
18 otropic liver transplantation and hepatocyte transplantation therapies.
19 creen and toxicity testing, and for cellular transplantation therapies.
20 ns ranging from in vitro diagnostics to cell transplantation therapies.
21 em (hES) cells offer the opportunity for new transplantation therapies.
22 n and suggest a potential role for stem cell transplantation therapies.
23 , as a source of human DA neurons for use in transplantation therapies.
24 a novel source of cells for transfusion and transplantation therapies.
25 ifferentiation and may play a role in future transplantation therapies.
26 unlimited supply of specific cell types for transplantation therapies.
27 in vitro that are needed for autologous HSC transplantation therapies.
29 logies, is a promising approach for cellular transplantation therapy and for in vitro disease modelin
31 s to create patient-specific donor cells for transplantation therapy, avoiding immunorejection, a maj
32 e development of future dopamine neuron cell transplantation therapy-based approaches, indicating tha
33 ion about the use of totipotent ESCs in cell transplantation therapy, because they may act as an unan
34 unlimited source of cells suitable for such transplantation therapy can be derived from embryonic st
35 n this review we examine how stem cell-based transplantation therapies compare with these novel and e
38 new avenues for basic research and potential transplantation therapies for neurological diseases.
42 ells will need to be identified if effective transplantation therapy for chronic pain is to be develo
44 R-HLA mismatching in hematopoietic stem cell transplantation therapy for leukemia and new, more speci
46 to successful allogeneic hematopoietic cell transplantation therapy for the treatment of hematologic
48 y mAb has been used for immunosuppression in transplantation, therapy for leukemia, and autoimmune di
49 great success including those awaiting liver transplantation, therapy has been extended to patients w
50 hematopoietic cell culture technologies for transplantation therapies have progressed significantly
52 l role of human embryonic stem (ES) cells in transplantation therapy have often overshadowed their po
53 opments in the application of stem cells for transplantation therapies in neurodegenerative diseases.
54 e for the future application of hES cells in transplantation therapies in which the use of aneuploid
59 Noonan syndrome and for improving stem cell transplantation therapy in Noonan-syndrome-associated le
60 tial hinderance to the use of such cells for transplantation therapy of insulin-dependent diabetes me
63 a strategy for extending the availability of transplantation therapy, particularly for older patients
67 may also improve the chances for successful transplantation therapy via earlier reinduction therapy,
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