A Rheinländer, B Schraven, U Bommhardt - Immunology letters, 2018 - Elsevier
CD45 is an evolutionary highly conserved receptor protein tyrosine phosphatase exclusively expressed on all nucleated cells of the hematopoietic system. It is characterized by the …
N Wellhausen, RP O'Connell, S Lesch… - Science translational …, 2023 - science.org
In the absence of cell surface cancer-specific antigens, immunotherapies such as chimeric antigen receptor (CAR) T cells, monoclonal antibodies, or bispecific T cell engagers typically …
ML Hermiston, Z Xu, A Weiss - Annual review of immunology, 2003 - annualreviews.org
▪ Abstract Regulation of tyrosine phosphorylation is a critical control point for integration of environmental signals into cellular responses. This regulation is mediated by the reciprocal …
FA Bonilla, DA Khan, ZK Ballas, J Chinen… - Journal of Allergy and …, 2015 - Elsevier
The American Academy of Allergy, Asthma & Immunology (AAAAI) and the American College of Allergy, Asthma & Immunology (ACAAI) have jointly accepted responsibility for …
LD Notarangelo - Journal of Allergy and Clinical Immunology, 2010 - Elsevier
In the last years, advances in molecular genetics and immunology have resulted in the identification of a growing number of genes causing primary immunodeficiencies (PIDs) in …
S Hacein-Bey-Abina, F Le Deist, F Carlier… - New england journal …, 2002 - Mass Medical Soc
Background X-linked severe combined immunodeficiency due to a mutation in the gene encoding the common γ (γc) chain is a lethal condition that can be cured by allogeneic stem …
WT Shearer, E Dunn, LD Notarangelo… - Journal of allergy and …, 2014 - Elsevier
Background The approach to the diagnosis of severe combined immunodeficiency disease (SCID) and related disorders varies among institutions and countries. Objectives The …
A Fischer, LD Notarangelo, B Neven… - Nature reviews Disease …, 2015 - nature.com
Severe combined immunodeficiencies (SCIDs) comprise a group of rare, monogenic diseases that are characterized by an early onset and a profound block in the development …
Can genetic and clinical findings made in a single patient be considered sufficient to establish a causal relationship between genotype and phenotype? We report that up to 49 of …