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R F Wynn

Showing results (11-20 of 26) with videos related to

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Molecular Genetics and Metabolism|December 11, 2012
Developmental outcome post allogenic bone marrow transplant for Niemann Pick Type C2C Breen, R F Wynn, A O'Meara, et al.
Pediatric Blood & Cancer|July 17, 2009
Inflammatory BCG adenitis associated with immune reconstitution following allogeneic haematopoietic stem cell transplant in infancyE Searle, H Patel, F J Vilar, et al.
Bone Marrow Transplantation|May 16, 2000
Donor bone marrow from a sibling with inborn error of metabolism for treatment of acute leukaemia - clinical and biochemical consequences in the non-affected recipientS Meyer, M Thornley, R F Wynn, et al.
Bone Marrow Transplantation|October 12, 1999
Failure of allogeneic bone marrow transplantation to correct Diamond-Blackfan anaemia despite haemopoietic stem cell engraftmentR F Wynn, J D Grainger, T F Carr, et al.
British Journal of Haematology|June 10, 2000
Dynamics of telomere shortening in neutrophils and T lymphocytes during ageing and the relationship to skewed X chromosome inactivation patternsJ D Robertson, R E Gale, R F Wynn, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Marrow stromal cells from patients affected by MPS I differentially support haematopoietic progenitor cell developmentM A Baxter, R F Wynn, L Schyma, et al.
Bone Marrow Transplantation|January 16, 2007
Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic diseaseH Church, K Tylee, A Cooper, et al.
Lancet (London, England)|February 5, 1998
Accelerated telomere shortening in young recipients of allogeneic bone-marrow transplantsR F Wynn, M A Cross, C Hatton, et al.
Bone Marrow Transplantation|May 23, 2006
Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndromeJ Cox-Brinkman, J-J Boelens, J E Wraith, et al.
Pediatric Transplantation|December 30, 2014
In vivo T-cell depletion using alemtuzumab in family and unrelated donor transplantation for pediatric non-malignant disease achieves engraftment with low incidence of graft vs. host diseaseM A Saif, R Borrill, B W Bigger, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|December 11, 2012
Developmental outcome post allogenic bone marrow transplant for Niemann Pick Type C2C Breen, R F Wynn, A O'Meara, et al.
Pediatric Blood & Cancer|July 17, 2009
Inflammatory BCG adenitis associated with immune reconstitution following allogeneic haematopoietic stem cell transplant in infancyE Searle, H Patel, F J Vilar, et al.
Bone Marrow Transplantation|May 16, 2000
Donor bone marrow from a sibling with inborn error of metabolism for treatment of acute leukaemia - clinical and biochemical consequences in the non-affected recipientS Meyer, M Thornley, R F Wynn, et al.
Bone Marrow Transplantation|October 12, 1999
Failure of allogeneic bone marrow transplantation to correct Diamond-Blackfan anaemia despite haemopoietic stem cell engraftmentR F Wynn, J D Grainger, T F Carr, et al.
British Journal of Haematology|June 10, 2000
Dynamics of telomere shortening in neutrophils and T lymphocytes during ageing and the relationship to skewed X chromosome inactivation patternsJ D Robertson, R E Gale, R F Wynn, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Marrow stromal cells from patients affected by MPS I differentially support haematopoietic progenitor cell developmentM A Baxter, R F Wynn, L Schyma, et al.
Bone Marrow Transplantation|January 16, 2007
Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic diseaseH Church, K Tylee, A Cooper, et al.
Lancet (London, England)|February 5, 1998
Accelerated telomere shortening in young recipients of allogeneic bone-marrow transplantsR F Wynn, M A Cross, C Hatton, et al.
Bone Marrow Transplantation|May 23, 2006
Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndromeJ Cox-Brinkman, J-J Boelens, J E Wraith, et al.
Pediatric Transplantation|December 30, 2014
In vivo T-cell depletion using alemtuzumab in family and unrelated donor transplantation for pediatric non-malignant disease achieves engraftment with low incidence of graft vs. host diseaseM A Saif, R Borrill, B W Bigger, et al.
Pageof 3