H. Dadi

发表

Successful hematopoietic stem cell transplantation in a patient with a novel mutation in coronin 1A

A. Ovadia, V. H. Kim, B. Reid, 2019, LymphoSign Journal.

Effect of CD3δ Deficiency on Maturation of α/β and γ/δ T-Cell Lineages in Severe Combined Immunodeficiency

A. Simon, H. Dadi, C. Roifman, 2003 .

Chronic mucocutaneous candidiasis associated with a novel frameshift mutation in IL-17 receptor alpha

H. Dadi, A. Aujnarain, Amarilla B. Mandola, 2019, LymphoSign Journal.

The biological significance of TLR3 variant, L412F, in conferring susceptibility to cutaneous candidiasis, CMV and autoimmunity.

A. Nahum, H. Dadi, C. Roifman, 2012, Autoimmunity reviews.

Human immune disorder arising from mutation of the alpha chain of the interleukin-2 receptor.

H. Dadi, C. Roifman, N. Sharfe, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Activation of phosphatidylinositol-3 kinase by ligation of the interleukin-7 receptor is dependent on protein tyrosine kinase activity.

H. Dadi, C. Roifman, S. Ke, 1994, Blood.

Muscarinic cholinergic receptor of rat brain

H. Dadi, R. Morris, 1984 .

A monoclonal antibody to human insulin-like growth factor-I: characterization, use in radioimmunoassay and effect on the biological activities of the growth factor.

M. Preece, H. Dadi, A. Taylor, 1989, Journal of molecular endocrinology.

Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain (IL6R) immunodeficiency.

A. Nahum, H. Dadi, C. Roifman, 2019, The Journal of allergy and clinical immunology.

Cloning and Characterization of the Human Homolog of Mouse Jak 2

H. Dadi, C. Roifman, I. Dalal, 1998 .

Cloning and characterization of the human homolog of mouse Jak2.

H. Dadi, C. Roifman, I. Dalal, 1998, Blood.

HUMAN INTERLEUKIN-2 RECEPTOR α DEFICIENCY

H. Dadi, C. Roifman, 2000, Radiologic Clinics of North America.

CD10 and CD44 genes of leukemic cells and malignant cell lines show no evidence of transformation‐related alterations

I. Andrulis, B. Kee, M. Letarte, 1991, Journal of cellular physiology.

Fatal combined immunodeficiency associated with heterozygous mutation in STAT1.

S. Pereira, A. Nahum, H. Dadi, 2014, The Journal of allergy and clinical immunology.

Purine metabolism, immune reconstitution, and abdominal adipose tumor after gene therapy for adenosine deaminase deficiency.

A. Aiuti, H. Dadi, C. Roifman, 2011, The Journal of allergy and clinical immunology.

Characterization of ζ-associated protein, 70 kd (ZAP70)-deficient human lymphocytes.

A. Nahum, R. Somech, H. Dadi, 2010, The Journal of allergy and clinical immunology.

Immune deficiencies , infection , and systemic immune disorders Characterization of z-associated protein , 70 kd ( ZAP 70 ) – deficient human lymphocytes

A. Nahum, R. Somech, H. Dadi, 2010 .

Activation of phosphatidylinositol-3 kinase by ligation of the interleukin-7 receptor on human thymocytes.

H. Dadi, C. Roifman, 1993, The Journal of clinical investigation.

Effect of CD3delta deficiency on maturation of alpha/beta and gamma/delta T-cell lineages in severe combined immunodeficiency.

A. Simon, H. Dadi, C. Roifman, 2003, The New England journal of medicine.

Time-dependent decline of T cell receptor excision circle levels in ZAP-70 deficiency.

D. Bulman, Sneha Suresh, B. Reid, 2020, The journal of allergy and clinical immunology. In practice.

NFκB pathway dysregulation due to reduced RelB expression leads to severe autoimmune disorders and declining immunity.

D. Lefaudeux, A. Ovadia, H. Dadi, 2022, Journal of autoimmunity.

Inhibition of acute lymphoblastic leukaemia by a Jak-2 inhibitor

A. Levitzki, M. Freedman, A. Gazit, 1996, Nature.

The effects of RelB deficiency on lymphocyte development and function.

D. Merico, H. Dadi, C. Roifman, 2015, Journal of autoimmunity.

Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant

A. Nahum, H. Dadi, C. Roifman, 2022, Frontiers in Immunology.

Cloning and characterization of a lymphoid-specific, inducible human protein tyrosine phosphatase, Lyp.

E. Shaoul, S. Cohen, H. Dadi, 1999, Blood.

CD44 in human placenta: localization and binding to hyaluronic acid.

M. Letarte, H. Dadi, S. St Jacques, 1993, Placenta.

Novel heterozygous PIK3CD mutation presenting with only laboratory markers of combined immunodeficiency

B. Reid, H. Dadi, C. Roifman, 2020 .

Dual loss of p110&dgr; PI3‐kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic features

D. Merico, S. Grinstein, D. Chitayat, 2017, Journal of Allergy and Clinical Immunology.

IL-21 signalling via STAT3 primes human naive B cells to respond to IL-2 to enhance their differentiation into plasmablasts.

J. Casanova, J. Ziegler, Joanne M. Smart, 2013, Blood.

Defective T cell receptor signaling and CD8+ thymic selection in humans lacking Zap-70 kinase

A. Cohen, H. Dadi, M. Shahar, 1994, Cell.

Diffuse large B-cell lymphoma as presenting feature of Zap-70 deficiency.

H. Dadi, C. Roifman, E. Grunebaum, 2011, The Journal of allergy and clinical immunology.

Combined immunodeficiency caused by a novel homozygous NFKB1 mutation.

D. Merico, B. Reid, H. Dadi, 2020, The Journal of allergy and clinical immunology.

Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)

D. Merico, J. Pomerantz, Mark G. F. Sun, 2017, The Journal of allergy and clinical immunology.

Haemophagocytic lymphohistiocytosis in X‐linked severe combined immunodeficiency

H. Dadi, E. Grunebaum, J. Zhang, 2000, British journal of haematology.

Ephrin stimulation modulates T cell chemotaxis

A. Freywald, H. Dadi, C. Roifman, 2002, European journal of immunology.

Inhibition of acute lymphoblastic and myeloid leukemias by a novel kinase inhibitor.

Z. Estrov, A. Freywald, H. Dadi, 2003, Blood.

Establishing reference ranges for lymphocyte proliferation responses to phytohemagglutinin in patients with T cell dysfunction

H. Dadi, L. Vong, Mohammad Alsalamah, 2019, LymphoSign Journal.

Human immune disorder arising from mutation of the α chain of the interleukin-2 receptor

H. Dadi, C. Roifman, N. Sharfe, 1997 .

Jak3 activation in human lymphocyte precursor cells

H. Dadi, C. Roifman, N. Sharfe, 1997, Clinical and experimental immunology.

JAK3 protein tyrosine kinase mediates interleukin-7-induced activation of phosphatidylinositol-3' kinase.

H. Dadi, C. Roifman, N. Sharfe, 1995, Blood.

DNA‐Binding domain mutations confer severe outcome at an early age among STAT1 gain‐of‐function patients

A. Nahum, H. Dadi, C. Roifman, 2021, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in ZAP70 and RNF168

J. Lupski, J. Orange, Z. Coban-Akdemir, 2017, Front. Immunol..

Interleukin 7 receptor mediates the activation of phosphatidylinositol-3 kinase in human B-cell precursors.

H. Dadi, C. Roifman, S. Ke, 1993, Biochemical and biophysical research communications.

The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity.

A. Nahum, H. Dadi, C. Roifman, 2011, The Journal of allergy and clinical immunology.

inhibitor Inhibition of acute lymphoblastic and myeloid leukemias by a novel kinase

Z. Estrov, H. Dadi, C. Roifman, 2013 .

Purification of the muscarinic acetylcholine receptor from rat forebrain.

N. Birdsall, E. Hulme, M. Wheatley, 1985, Biochemical Society Transactions.

A novel mutation in LIG4 in an infant presenting with severe combined immunodeficiency with thymic medullary dysplasia

D. Merico, H. Dadi, C. Roifman, 2017 .

Identification of a polymorphism in human CD44.

D. Cox, M. Letarte, H. Dadi, 1991, Nucleic acids research.