M. Adriani

发表

Activation of the liver X receptors alters CD4+ T cell membrane lipids and signalling through direct regulation of glycosphingolipid synthesis

E. Havrdová, D. Owen, G. Robinson, 2019 .

Monocyte NOTCH 2 expression predicts IFN-b immunogenicity in multiple sclerosis patients

P. Dönnes, B. Hemmer, E. Havrdová, 2018 .

Using Serum Metabolomics to Predict Development of Anti-drug Antibodies in Multiple Sclerosis Patients Treated With IFNβ

P. Dönnes, A. Fogdell-Hahn, K. Waddington, 2020, Frontiers in Immunology.

Sex differences in autoimmunity could be associated with altered regulatory T cell phenotype and lipoprotein metabolism

D. Isenberg, H. Peckham, A. Radziszewska, 2019, bioRxiv.

To the editor : A 91 V is a polymorphism in the perforin gene not causative of an FHLH phenotype

V. Poggi, C. Pignata, L. Racioppi, 2022 .

Cutaneous Manifestations as Presenting Sign of Autoimmune Lymphoproliferative Syndrome in Childhood

A. Chiocchetti, U. Dianzani, C. Pignata, 2005, Dermatology.

Impaired in vitro regulatory T cell function associated with Wiskott-Aldrich syndrome.

R. Siegel, P. Schwartzberg, F. Candotti, 2007, Clinical immunology.

The Cellular Amount of the Common γ-Chain Influences Spontaneous or Induced Cell Proliferation1

C. Pignata, L. Palamaro, S. Amorosi, 2009, The Journal of Immunology.

Low Percentage of Signal Regulatory Protein α/β+ Memory B Cells in Blood Predicts Development of Anti-drug Antibodies (ADA) in Adalimumab-Treated Rheumatoid Arthritis Patients

D. Isenberg, X. Mariette, M. Pallardy, 2018, Front. Immunol..

Foamy virus vector-mediated gene correction of a mouse model of Wiskott-Aldrich syndrome.

F. Candotti, M. Adriani, G. Jagadeesh, 2012, Molecular therapy : the journal of the American Society of Gene Therapy.

Allogeneic bone marrow transplantation restores IGF-I production and linear growth in a γ-SCID patient with abnormal growth hormone receptor signaling

C. Pignata, M. Salerno, B. Rotoli, 2004, Bone Marrow Transplantation.

Nail dystrophy associated with a heterozygous mutation of the nude/SCID human FOXN1 (WHN) gene.

C. Pignata, A. Christiano, J. Frank, 2005, Archives of dermatology.

Ancestral Founder Mutation of the Nude (FOXN1) Gene in Congenital Severe Combined Immunodeficiency Associated with Alopecia in Southern Italy Population

F. Fusco, C. Pignata, M. Ursini, 2004, Annals of human genetics.

Exacerbated experimental arthritis in Wiskott–Aldrich syndrome protein deficiency: Modulatory role of regulatory B cells

L. Notarangelo, S. Burns, A. Thrasher, 2014, European journal of immunology.

Defective inhibition of B-cell proliferation by Wiskott-Aldrich syndrome protein-deficient regulatory T cells.

Krysten A Jones, F. Candotti, S. Anderson, 2011, Blood.

Atypical features of familial hemophagocytic lymphohistiocytosis.

R. Clementi, C. Pignata, L. Racioppi, 2004, Blood.

Monocyte NOTCH2 expression predicts IFN-β immunogenicity in multiple sclerosis patients.

P. Dönnes, B. Hemmer, Karel Medek, 2018, JCI insight.

Functional Interaction of Common γ-Chain and Growth Hormone Receptor Signaling Apparatus1

C. Pignata, S. Amorosi, F. Candotti, 2006, The Journal of Immunology.

Brief report Atypical features of familial hemophagocytic lymphohistiocytosis

R. Clementi, L. Racioppi, F. Locatelli, 2004 .

FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetus

C. Pignata, S. Amorosi, M. D'armiento, 2008, Clinical genetics.

Advances in understanding regulatory myeloid cells

C. Vetro, A. Romano, M. Adriani, 2011, Cancer Biology & Therapy.