2015 - Distinguished Service Award, Clinical Immunology Society
2015 - AAI-Steinman Award for Human Immunology Research, American Association of Immunologists
Immunology, B cell, Molecular biology, Bruton's tyrosine kinase and Genetics are his primary areas of study. Mary Ellen Conley focuses mostly in the field of Immunology, narrowing it down to matters related to Gene rearrangement and, in some cases, Gene mutation, Severe combined immunodeficiency and B-1 cell. His Molecular biology study integrates concerns from other disciplines, such as Immunoglobulin light chain, Antibody and Cellular differentiation.
His study in Bruton's tyrosine kinase focuses on X-linked agammaglobulinemia in particular. He usually deals with X-linked agammaglobulinemia and limits it to topics linked to Cell culture and SH3 domain, Tyrosine, Kinase and Kinase activity. A large part of his Genetics studies is devoted to Mutation.
His primary areas of investigation include Immunology, Genetics, Bruton's tyrosine kinase, Molecular biology and X-linked agammaglobulinemia. Mary Ellen Conley has included themes like Severe combined immunodeficiency and Family history in his Immunology study. His Bruton's tyrosine kinase research integrates issues from Genotype, Kinase, B cell and Intron.
His work deals with themes such as Cell and Cellular differentiation, which intersect with B cell. In his research, Transcription factor is intimately related to Transcription, which falls under the overarching field of Molecular biology. His X-linked agammaglobulinemia study combines topics in areas such as Cell culture, Neutropenia, Pediatrics and Lymphocyte.
Mary Ellen Conley mainly investigates Immunology, Primary immunodeficiency, B cell, CD19 and B-cell receptor. The concepts of his Immunology study are interwoven with issues in X-linked agammaglobulinemia, Retrospective cohort study and MEDLINE. His study in Mutation extends to B cell with its themes.
His CD19 research is included under the broader classification of Molecular biology. His work in Molecular biology tackles topics such as Antibody which are related to areas like Ex vivo. His studies in B-cell receptor integrate themes in fields like Cell, Cancer research and Bruton's tyrosine kinase.
His scientific interests lie mostly in Primary immunodeficiency, Expert committee, Immunology, B cell and Family medicine. His Primary immunodeficiency research is mostly focused on the topic Combined immunodeficiencies. The Immunology study combines topics in areas such as Hyper IgM syndrome and Intensive care medicine.
He interconnects Mast cell, Molecular biology, Mutation and CD19 in the investigation of issues within B cell. His Molecular biology research incorporates elements of Missense mutation and Frameshift mutation. His Family medicine study incorporates themes from Alternative medicine, Disease, Bioinformatics and Immunodeficiency.
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Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia
Satoshi Tsukada;Douglas C. Saffran;David J. Rawlings;Ornella Parolini;Ornella Parolini.
Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies).
Mary Ellen Conley;Luigi D. Notarangelo;Amos Etzioni.
Clinical Immunology (1999)
CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome
R. Cutler Allen;Richard J. Armitage;Mary Ellen Conley;Howard Rosenblatt.
Human blood IgM “memory” B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire
Sandra Weller;Moritz C. Braun;Bruce K. Tan;Andreas Rosenwald.
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
Rainer Döffinger;Asma Smahi;Christine Bessia;Frédéric Geissmann.
Nature Genetics (2001)
Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel.
Frontiers in Immunology (2014)
Primary immunodeficiencies: 2009 update
Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova.
The Journal of Allergy and Clinical Immunology (2009)
The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.
Jerry A. Winkelstein;Mary C. Marino;Hans Ochs;Ramsey Fuleihan.
Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel.
The Journal of Allergy and Clinical Immunology (2007)
X-linked agammaglobulinemia: report on a United States registry of 201 patients.
Jerry A. Winkelstein;Mary C. Marino;Howard M. Lederman;Stacie M. Jones.
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