Zobrazeno 1 - 10
of 250
pro vyhledávání: '"Andrew J. Cant"'
Autor:
Juliana M. F. Silva, Fani Ladomenou, Ben Carpenter, Sharat Chandra, Petr Sedlacek, Renata Formankova, Vicky Grandage, Mark Friswell, Andrew J. Cant, Zohreh Nademi, Mary A. Slatter, Andrew R. Gennery, Sophie Hambleton, Terence J. Flood, Giovanna Lucchini, Robert Chiesa, Kanchan Rao, Persis J. Amrolia, Paul Brogan, Lucy R. Wedderburn, Julie M. Glanville, Rachael Hough, Rebecca Marsh, Mario Abinun, Paul Veys
Publikováno v:
Blood Advances, Vol 2, Iss 7, Pp 777-786 (2018)
Abstract: Patients with juvenile idiopathic arthritis (JIA) can experience a severe disease course, with progressive destructive polyarthritis refractory to conventional therapy with disease-modifying antirheumatic drugs including biologics, as well
Externí odkaz:
https://doaj.org/article/be03c5eb281f42709fcd3eaff75a70fb
Autor:
David J. Swan, Dominik Aschenbrenner, Christopher A. Lamb, Krishnendu Chakraborty, Jonathan Clark, Sumeet Pandey, Karin R. Engelhardt, Rui Chen, Athena Cavounidis, Yuchun Ding, Natalio Krasnogor, Christopher D. Carey, Meghan Acres, Stephanie Needham, Andrew J. Cant, Peter D. Arkwright, Anita Chandra, Klaus Okkenhaug, Holm H. Uhlig, Sophie Hambleton
Publikováno v:
Haematologica, Vol 104, Iss 10 (2019)
Externí odkaz:
https://doaj.org/article/4f6e2df160434dd095e8d7ffcfc30910
Autor:
Tanya I. Coulter, Andrew J. Cant
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Activated phosphoinositide 3-kinase δ syndrome (APDS), also known as PASLI disease (p110d-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency) are combined immunodeficiencies resulting from gain-of-function mutations
Externí odkaz:
https://doaj.org/article/5bb9fb2629cc429fbb4aa159b2c8891b
Autor:
Christo Tsilifis, Su Han Lum, Zohreh Nademi, Sophie Hambleton, Terence J. Flood, Eleri J. Williams, Stephen Owens, Mario Abinun, Andrew J. Cant, Mary A. Slatter, Andrew R. Gennery
Publikováno v:
Journal of Clinical Immunology. 42:851-858
Hematopoietic stem cell transplantation and gene therapy are the only curative therapies for severe combined immunodeficiency (SCID). In patients lacking a matched donor, TCRαβ/CD19-depleted haploidentical family donor transplant (TCRαβ-HaploSCT)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7472f5cdb7d0ae6d3e256f52237de87
https://doi.org/10.1007/s10875-022-01239-z
https://doi.org/10.1007/s10875-022-01239-z
Autor:
Hidenori Ohnishi, Hirokazu Kanegane, Andrew J. Cant, Kazushi Izawa, Eleri Williams, Mayuka Shiraki, Kunihiro Shinoda, Hiroshi Nihira, Andrew R. Gennery, Zohreh Nademi, Yoshitaka Honda, Mary Slatter, Kana Matsumoto, Norifumi Yokoyama, Ryuta Nishikomori
Publikováno v:
Journal of Clinical Immunology. 41:1954-1956
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b597a04a3236df79934f16a2da49c9d
https://doi.org/10.1007/s10875-021-01124-1
https://doi.org/10.1007/s10875-021-01124-1
Autor:
Terry Flood, Sabeena Selvarajah, Sophie Hambleton, Andrew J. Cant, Andrew R. Gennery, Kay Carruthers, Peter McNaughton, Angela Deyà-Martínez, Mary Slatter, Zohreh Nademi, Helen Watson, Su Han Lum, Mario Abinun, Ali Sobh
Publikováno v:
Bone Marrow Transplantation. 56:1200-1204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97659beb01d1f196eeffe143a6a054cd
https://doi.org/10.1038/s41409-020-01152-2
https://doi.org/10.1038/s41409-020-01152-2
Autor:
Sinisa Savic, James A. Poulter, Andrew J. Cant, Eamonn Sheridan, Helen Griffin, Dylan Lawless, Sophie Hambleton, Neil V. Morgan, Stefan Przyborski, Siti Mardhiana Mohamad, Rashida Anwar, Jennifer Shrimpton, Clive Carter, Gina M. Doody, Karin R. Engelhardt, Kevin Windebank, Meghan Acres, Catherine Cargo, Stephan Ehl, Frédéric Rieux-Laucat, Chris M. Bacon, Sean O’Riordan, Anne Rensing-Ehl, Jarmila Stremenova Spegarova, Majlinda Lako, Philip Chetcuti, Aneta Mikulasova
Publikováno v:
Blood. 136:1055-1066
Molecular dissection of inborn errors of immunity can help to elucidate the nonredundant functions of individual genes. We studied 3 children with an immune dysregulation syndrome of susceptibility to infection, lymphadenopathy, hepatosplenomegaly, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90025e03a10adb11ab54564e2391eb9
https://doi.org/10.1182/blood.2020005844
https://doi.org/10.1182/blood.2020005844
Outcome of autoimmune cytopenia after hematopoietic cell transplantation in primary immunodeficiency
Autor:
Andrew J. Cant, Mary Slatter, Andrew R. Gennery, Shirelle Burton-Fanning, Sophie Hambleton, Sabeena Selvarajah, Terry Flood, Eleri Williams, Marieke Emonts, Stephen Owens, Peter McNaughton, Lisa Newton, Julie Gandy, Angela Deyà-Martínez, Ali Sobh, Sheila Waugh, Su Han Lum, Mario Abinun, Zohreh Nademi
Publikováno v:
Journal of Allergy and Clinical Immunology. 146:406-416
Background Post hematopoietic cell transplantation (HCT) autoimmune cytopenia (AIC) is a potentially life-threatening complication, but studies focusing on large cohorts of patients transplanted for primary immunodeficiency are lacking. Objectives Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10c402bed6e6a065f3cfa6696405735
https://doi.org/10.1016/j.jaci.2020.04.053
https://doi.org/10.1016/j.jaci.2020.04.053
Autor:
Christo, Tsilifis, Su Han, Lum, Zohreh, Nademi, Sophie, Hambleton, Terence J, Flood, Eleri J, Williams, Stephen, Owens, Mario, Abinun, Andrew J, Cant, Mary A, Slatter, Andrew R, Gennery
Publikováno v:
Journal of clinical immunology. 42(4)
Hematopoietic stem cell transplantation and gene therapy are the only curative therapies for severe combined immunodeficiency (SCID). In patients lacking a matched donor, TCRαβ/CD19-depleted haploidentical family donor transplant (TCRαβ-HaploSCT)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c12f9b7e94914fdedd46f69add81dc09
https://pubmed.ncbi.nlm.nih.gov/35305204
https://pubmed.ncbi.nlm.nih.gov/35305204
Autor:
Stephanie C. Harrison, Jennifer Heimall, Ásgeir Haraldsson, Ben Carpenter, Austen Worth, Rainer Doffinger, Christo Tsilifis, Paul Veys, Bodo Grimbacher, Andrew J. Cant, Terence J. Flood, Zohreh Nademi, Gabriela Barcenas-Morales, Rachael Hough, Mario Abinun, Mary Slatter, Stephen Jolles, Waleed Al-Herz, Mark J. Ponsford, Andrew R. Gennery
Publikováno v:
Journal of Clinical Immunology
Autosomal dominant hyper-IgE syndrome caused by dominant-negative loss-of-function mutations in signal transducer and activator of transcription factor 3 (STAT3) (STAT3-HIES) is a rare primary immunodeficiency with multisystem pathology. The quality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5961c6244e316ae633d909f404ff2a2e
https://orca.cardiff.ac.uk/id/eprint/138444/1/Harrison2021_Article_HematopoieticStemCellTransplan.pdf
https://orca.cardiff.ac.uk/id/eprint/138444/1/Harrison2021_Article_HematopoieticStemCellTransplan.pdf
