Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Leena Karnik"'
Autor:
Eden Biltibo, Reena Jayani, Leena Karnik, Adam Gassas, Farah O'Boyle, Daniel Dexter, Karina Wilkerson, Katie S. Gatwood, Lindsay Orton, Bhagirathbhai Dholaria, Bipin N. Savani, Brian G. Engelhardt, Salyka M. Sengsayadeth, Carrie Lynn Kitko, James P Connelly, Adetola A. Kassim, Josu de la Fuente
Publikováno v:
Blood. 140:7613-7615
Autor:
Eden Biltibo, Reena V Jayani, Leena Karnik, Adam Gassas, Farah O’Boyle, Karina Wilkerson, Katie S. Gatwood, Lindsay Orton, Bhagirathbhai Dholaria, Bipin Savani, Brian G. Engelhardt, Salyka Sengsayadeth, Carrie L. Kitko, James A Connelly, Adetola A. Kassim, Josu de la Fuente
Publikováno v:
Transplantation and Cellular Therapy. 29:S295-S296
Autor:
C Christodoulidou, H Ren, M H Zaidi, Adam J. Mead, Anindita Roy, Alexia Katsarou, Bethan Psaila, Leena Karnik, Q Al-Oqaily, Deena Iskander, Valentina S. Caputo, Yvonne Harrington, Kanagaraju Ponnusamy, David M. Bodine, Pritesh Trivedi, Aristeidis Chaidos, Nikolaos Trasanidis, Supat Thongjuea, Mark Robinson, J de la Fuente, Marjorie Brand, Zeinab Mokhtari, Kikkeri N. Naresh, Guanlin Wang, C G Palii, Elisabeth F. Heuston, Irene Roberts, Richard Szydlo, Anastasios Karadimitris
Ribosome dysfunction underlies the pathogenesis of many cancers and heritable ribosomopathies. Here, we investigate how mutations in either ribosomal protein large (RPL) or ribosomal protein small (RPS) subunit genes selectively affect erythroid prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d7beb80b780f8923efa20f1cd028371
https://ora.ox.ac.uk/objects/uuid:8537a5fd-eb59-46b0-80f7-b19bd5159ab7
https://ora.ox.ac.uk/objects/uuid:8537a5fd-eb59-46b0-80f7-b19bd5159ab7
Autor:
Kathryn A. Culos, Françoise Bernaudin, Mathieu Kuentz, Josu de la Fuente, Adetola A. Kassim, Michael R. DeBaun, Robert A. Brodsky, Nathalie Dhedin, Gérard Socié, Tatsuki Koyama, Leena Karnik
Publikováno v:
Biology of Blood and Marrow Transplantation. 25:1197-1209
Curative therapy for individuals with severe sickle cell disease (SCD) who lack an HLA-identical sibling donor has been frustratingly elusive. In with the goal of improving engraftment while minimizing transplantation-related morbidity, a multi-insti
Autor:
Leena Karnik, Adam Gassas, Kirstin Lund, Farah O'Boyle, Josu de la Fuente, Shahzya Chaudhury, Toni Petterson
Publikováno v:
Blood. 138:2906-2906
Haemopoietic stem cell transplantation (HSCT) is a well-established treatment modality for the cure of transfusion dependent thalassaemia (TDT) and sickle cell disease (SCD). Clonal evolution has recently been identified as a concerning event in the
Autor:
Michael R. DeBaun, Hemalatha G. Rangarajan, Ali Al-Ahmari, Satya Prakash Yadav, James A. Connelly, Erfan Nur, Carrie L. Kitko, Thalita Cristina de Mello Costa, Adeseye Michael Akinsete, Rabi Hanna, Maria Isabel, William Tse, Roberto Luiz da Silva, Mohsen Alzahrani, Vandy Black, Josu de la Fuente, Michael Kent, Belinda Pinto Simões, Nathalie Dhedin, Nelson Hamerschlak, Karina L Wilkerson, Tatsuki Koyama, Jennifer Andrews, Renato L. Guerino-Cunha, Courtney D. Fitzhugh, Leena Karnik, RV Gouveia, Robert A. Brodsky, Adriana Seber, Juliana Folloni Fernandes, Ben Carpenter, Biljana Horn, Michael J. Eckrich, Carmem Bonfim, Kathryn A. Culos, Adetola A. Kassim, Ibrahim Ahmed
Publikováno v:
Blood. 136:8-9
Introduction: HLA-Haploidentical bone marrow transplant (haplo-BMT) is a curative approach for individuals with severe sickle cell disease (SCD) who lack an HLA-identical sibling donor. Haplo-BMT expands the donor pool among adults and children with
Autor:
Deena Iskander, Guanlin Wang, Elisabeth F Heuston, Chrysi Christodoulidou, Bethan Psaila, Mark E Robinson, Aristeidis Chaidos, Pritesh Trivedi, Nikolaos Trasanidis, Alexia Katsarou, Richard Szydlo, NISC Comparative SequencingProgram, Qais Al-Oqaily, Valentina S Caputo, Kanagaraju Ponnusamy, Anindita Roy, Leena Karnik, Kikkeri Naresh, Adam J. Mead, Supat Thongjuea, Marjorie Brand, Josu de la Fuente, David M. Bodine, Irene Roberts, Anastasios Karadimitris
Publikováno v:
Blood. 136:1-2
Background: Diamond- Blackfan Anemia (DBA) is a rare, heritable ribosomopathy caused by mutations in ribosomal protein large (RPL) and small (RPS) subunit genes. The diagnostic criteria of DBA include presentation in infancy with virtually no mature
Autor:
Rabi Hanna, Dilan A Patel, Adetola A. Kassim, Carrie L. Kitko, Leena Karnik, Josu de la Fuente, James A. Connelly
Publikováno v:
Biology of Blood and Marrow Transplantation. 26:S221-S222
Background Post-transplant cyclophosphamide (PTCy) enables allogeneic hematopoietic cell transplant (Allo-HCT) across the human leukocyte antigen barrier. Allo-HCT for severe transfusion dependent thalassemia is restricted in its application due to l
Autor:
Becky Armstrong, Dilan A Patel, Josu de la Fuente, Karina Wilkerson, Kemar V Prussien, Leena Karnik, Adetola A. Kassim
Publikováno v:
Pediatric Blood & Cancer. 67
Autor:
Madan Jagasia, Adetola A. Kassim, Dilan A Patel, Katie S. Gatwood, Nathalie Dhedin, Jim Connelly, Gowri Satyanarayana, Josu de la Fuente, Carrie L. Kitko, Katie Culos, Leena Karnik, Sanjay R. Mohan, Heidi Chen, Brian G. Engelhardt
Publikováno v:
Transpl Infect Dis
Background Haploidentical bone marrow transplant (haplo-BMT) offers near universal donor availability as a curative modality for individuals with severe sickle cell disease (SCD). However, the required intense immunodepletion is associated with incre