Immunology, Immunodeficiency, Transplantation, Internal medicine and Hematopoietic stem cell transplantation are his primary areas of study. His work is dedicated to discovering how Immunology, Virology are connected with Gene and other disciplines. His Immunodeficiency research integrates issues from P110δ, Mutation, T cell, Autoimmune disease and Allergy.
Andrew J. Cant combines subjects such as Survival analysis, Pediatrics, Severe combined immunodeficiency and Chronic granulomatous disease with his study of Transplantation. In his study, Busulfan and Transplantation Conditioning is strongly linked to Gastroenterology, which falls under the umbrella field of Internal medicine. His Hematopoietic stem cell transplantation research is multidisciplinary, incorporating perspectives in Survival rate, Hematology, DOCK8 Deficiency and Progressive multifocal leukoencephalopathy.
His main research concerns Immunology, Transplantation, Primary immunodeficiency, Internal medicine and Immunodeficiency. The concepts of his Immunology study are interwoven with issues in Hematopoietic stem cell transplantation and Severe combined immunodeficiency. His studies deal with areas such as Stem cell and Chronic granulomatous disease as well as Transplantation.
The various areas that Andrew J. Cant examines in his Primary immunodeficiency study include Intensive care medicine, Pediatrics and Virology. His research integrates issues of Gastroenterology, Transplantation Conditioning and Oncology in his study of Internal medicine. His studies in Immunodeficiency integrate themes in fields like Mutation, Cancer research and Pathology.
Andrew J. Cant focuses on Immunology, Hematopoietic stem cell transplantation, Primary immunodeficiency, Transplantation and Immunodeficiency. Andrew J. Cant has included themes like Exome sequencing and Stem cell in his Immunology study. The study incorporates disciplines such as Total body irradiation, Severe combined immunodeficiency and Lymphocyte in addition to Hematopoietic stem cell transplantation.
Internal medicine and Surgery are inextricably linked to his Transplantation research. His Internal medicine research is multidisciplinary, incorporating elements of Gastroenterology and Oncology. His Immunodeficiency research includes elements of Phenotype, Cancer research and Chemotaxis.
Andrew J. Cant mainly focuses on Immunology, Transplantation, Immunodeficiency, Primary immunodeficiency and Hematopoietic stem cell transplantation. His Immunology study combines topics in areas such as Biallelic Mutation and IRF8. His Transplantation study deals with the bigger picture of Surgery.
Andrew J. Cant has researched Immunodeficiency in several fields, including Phenotype, Chemotaxis, Cell adhesion, Nonsense mutation and Intercellular Adhesion Molecule-1. His work carried out in the field of Primary immunodeficiency brings together such families of science as Exome sequencing, Autoimmune disease, Prednisolone, Tacrolimus and Rituximab. His Hematopoietic stem cell transplantation study is associated with Internal medicine.
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Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99
Corinne Antoine;Susanna Müller;Andrew Cant;Marina Cavazzana-Calvo.
The Lancet (2003)
IRF8 mutations and human dendritic-cell immunodeficiency.
Sophie Hambleton;Sandra Salem;Jacinta Bustamante;Venetia Bigley.
The New England Journal of Medicine (2011)
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
Anne Puel;Anne Puel;Rainer Döffinger;Angels Natividad;Angels Natividad;Maya Chrabieh;Maya Chrabieh.
Journal of Experimental Medicine (2010)
Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage
Ivan Angulo;Oscar Vadas;Fabien Garçon;Edward Banham-Hall.
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations
Joshua D. Milner;Tiphanie P. Vogel;Lisa Forbes;Chi A. Ma.
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
Rachel Emma Dickinson;Helen Griffin;Venetia Bigley;Louise N. Reynard.
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL
Cristina Sobacchi;Annalisa Frattini;Matteo M Guerrini;Mario Abinun.
Nature Genetics (2007)
Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: Entering a new century, do we do better?
Andrew R. Gennery;Andrew R. Gennery;Mary A. Slatter;Mary A. Slatter;Laure Grandin;Pierre Taupin.
The Journal of Allergy and Clinical Immunology (2010)
The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency
Venetia Bigley;Muzlifah Haniffa;Sergei Doulatov;Xiao-Nong Wang.
Journal of Experimental Medicine (2011)
Long-Term Immune Reconstitution and Outcome After HLA-Nonidentical T-Cell–Depleted Bone Marrow Transplantation for Severe Combined Immunodeficiency: A European Retrospective Study of 116 Patients
Elie Haddad;Paul Landais;Wilhelm Friedrich;Bert Gerritsen.
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