A. K. Dobbs

发表

Cutting Edge: A Hypomorphic Mutation in Igβ (CD79b) in a Patient with Immunodeficiency and a Leaky Defect in B Cell Development1

M. Conley, A. K. Dobbs, Tianyu Yang, 2007, The Journal of Immunology.

A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical disease

S. Shurtleff, T. Kurosaki, M. Conley, 2008, Clinical and experimental immunology.

Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function.

L. Notarangelo, İ. Reisli, L. Henderson, 2018, Blood.

Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K

E. Coustan-Smith, M. Conley, Yong-Dong Wang, 2012, The Journal of experimental medicine.

Disseminated and Congenital Toxoplasmosis in a Mother and Child With Activated PI3-Kinase δ Syndrome Type 2 (APDS2): Case Report and a Literature Review of Toxoplasma Infections in Primary Immunodeficiencies

S. Pittaluga, L. Notarangelo, S. Rosenzweig, 2019, Front. Immunol..

Complete Absence of CD3γ Protein Expression Is Responsible for Combined Immunodeficiency with Autoimmunity Rather than SCID

L. Notarangelo, A. K. Dobbs, R. Castagnoli, 2020, Journal of Clinical Immunology.

PAX1 is essential for development and function of the human thymus

T. Myers, J. Casanova, L. Notarangelo, 2020, Science Immunology.

Primary B cell immunodeficiencies: comparisons and contrasts.

D. Campana, E. Coustan-Smith, M. Conley, 2009, Annual review of immunology.

Immunodeficiencies: Comparisons and Contrasts

D. Campana, E. Coustan-Smith, M. Conley, 2009 .

Agammaglobulinemia associated with BCR⁻ B cells and enhanced expression of CD19.

E. Coustan-Smith, M. Conley, A. K. Dobbs, 2011, Blood.

Refractory, fatal autoimmune hemolytic anemia due to ineffective thymic‐derived T‐cell reconstitution following allogeneic hematopoietic cell transplantation for hypomorphic RAG1 deficiency

L. Notarangelo, A. K. Dobbs, A. Basu, 2022, Pediatric blood & cancer.

Membranous glomerulopathy in an adult patient with X-linked agammaglobulinemia receiving intravenous gammaglobulin.

D. Warnock, W. Cook, M. Conley, 2011, Journal of investigational allergology & clinical immunology.

A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X‐linked gene WAS

T. Yang, M. Conley, A. K. Dobbs, 2007, Clinical genetics.

Agammaglobulinemia associated with BCR⁻ B cells and enhanced expression of CD19.

E. Coustan-Smith, A. K. Dobbs, F. Saulsbury, 2011, Blood.

A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical disease

S. Shurtleff, A. K. Dobbs, D. Farmer, 2008, Clinical and experimental immunology.