A. Pianta

发表

A deletion 3' to the PAX6 gene in familial aniridia cases.

G. Damante, D. Fabbro, P. Grammatico, 2007, Molecular vision.

Two rheumatoid arthritis–specific autoantigens correlate microbial immunity with autoimmune responses in joints

A. Steere, C. Costello, K. Strle, 2017, The Journal of clinical investigation.

Molecular analysis of a human PAX6 homeobox mutant

G. Tell, F. Fogolari, Elisa Bregant, 2006, European Journal of Human Genetics.

Effects of histone acetylation on sodium iodide symporter promoter and expression of thyroid-specific transcription factors.

G. Tell, S. Filetti, D. Russo, 2005, Endocrinology.

Mesomelia‐synostoses syndrome: Description of a patient presenting a monoallelic expression of SULF1 without alterations in the SLCOA1 gene

B. Bembi, Elisa Bregant, G. Damante, 2018, Clinical genetics.

Evidence of the Immune Relevance of Prevotella copri, a Gut Microbe, in Patients With Rheumatoid Arthritis

A. Steere, C. Costello, Elise E. Drouin, 2017, Arthritis & rheumatology.

T-Helper 17 Cell Cytokine Responses in Lyme Disease Correlate With Borrelia burgdorferi Antibodies During Early Infection and With Autoantibodies Late in the Illness in Patients With Antibiotic-Refractory Lyme Arthritis

A. Steere, R. Sadreyev, A. Anselmo, 2017, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

SMPD1 Mutation Update: Database and Comprehensive Analysis of Published and Novel Variants

B. Bembi, M. Filocamo, R. Sinnott, 2016, Human mutation.

Annexin A2 is a target of autoimmune T and B cell responses associated with synovial fibroblast proliferation in patients with antibiotic-refractory Lyme arthritis.

A. Steere, C. Costello, K. Strle, 2015, Clinical immunology.

A Highly Expressed Human Protein, Apolipoprotein B-100, Serves as an Autoantigen in a Subgroup of Patients With Lyme Disease.

A. Steere, C. Costello, K. Strle, 2015, The Journal of infectious diseases.

Identification of Novel, Immunogenic HLA–DR‐Presented Prevotella copri Peptides in Patients With Rheumatoid Arthritis

A. Steere, C. Costello, K. Strle, 2021, Arthritis & rheumatology.

Two novel NPM1 mutations in a therapy‐responder AML patient

R. Fanin, G. Tell, C. di Loreto, 2009, Hematological oncology.

Nucleophosmin Delocalization in Thyroid Tumour Cells

G. Tell, D. Russo, Nadia Passon, 2011, Endocrine pathology.

Nucleophosmin is overexpressed in thyroid tumors.

G. Tell, I. Paron, C. di Loreto, 2010, Biochemical and biophysical research communications.

Unexpected phenotype of a typical NPM1 mutant

R. Fanin, G. Tell, G. Damante, 2009, British journal of haematology.

Matrix metalloproteinase-10 is a target of T and B cell responses that correlate with synovial pathology in patients with antibiotic-refractory Lyme arthritis.

A. Steere, C. Costello, K. Strle, 2016, Journal of autoimmunity.

Functional characterization of the common c.-32-13T>G mutation of GAA gene: identification of potential therapeutic agents

B. Bembi, E. Buratti, F. Baralle, 2013, Nucleic acids research.

GENETIC STUDIES OF HEREDITARY THROMBOCYTHEMIA

A. Pianta, 2013 .

Concomitant ABCG2 overexpression and FLT3‐ITD mutation identify a subset of acute myeloid leukemia patients at high risk of relapse

R. Fanin, G. Damante, D. Fabbro, 2011, Cancer.

Fludarabine-based induction therapy does not overcome the negative effect of ABCG2 (BCRP) over-expression in adult acute myeloid leukemia patients.

R. Fanin, G. Damante, D. Fabbro, 2010, Leukemia research.

Autoimmunity to synovial extracellular matrix proteins in patients with postinfectious Lyme arthritis

A. Steere, A. Barbour, J. Moon, 2023, The Journal of clinical investigation.