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CD20-Mimotope Peptides: A Model to Define the Molecular Basis of Epitope Spreading

International journal of molecular sciences, 2019-04, Vol.20 (8), p.1920

2019

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Sleep disturbances and behavioral symptoms in pediatric Sotos syndrome

Frontiers in neurology, 2024, Vol.15, p.1360055-1360055

2024

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Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion

Stem cell research, 2023-02, Vol.66, p.103007-103007, Article 103007

2023

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Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5

Stem cell research, 2024-04, Vol.76, p.103324-103324, Article 103324

2024

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Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome

Genes, 2023-01, Vol.14 (2), p.295

2023

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NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint

Life (Basel, Switzerland), 2022-07, Vol.12 (7), p.988

2022

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Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome

Genes, 2023-03, Vol.14 (4), p.810

2023

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Azacytidine mitigates experimental sclerodermic chronic graft-versus-host disease

Journal of hematology and oncology, 2016-07, Vol.9 (1), p.53-53, Article 53

2016

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Comparative analysis of cancer vaccine settings for the selection of an effective protocol in mice

Journal of translational medicine, 2013-05, Vol.11 (1), p.120-120, Article 120

2013

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Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects

Gene, 2023-01, Vol.851, p.146970-146970, Article 146970

2023

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Beyond APECED: An update on the role of the autoimmune regulator gene (AIRE) in physiology and disease

Autoimmunity reviews, 2018-04, Vol.17 (4), p.325-330

2018

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A longitudinal characterization of the adaptive and behavioral profile in Sotos syndrome

American journal of medical genetics. Part A, 2024-06, Vol.194 (6), p.e63553-n/a

2024

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Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants

American journal of medical genetics. Part A, 2023-07, Vol.191 (7), p.1836-1848

2023

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Alteration of Th17 and Treg cell subpopulations co-exist in patients affected with systemic sclerosis

Clinical immunology (Orlando, Fla.), 2011-06, Vol.139 (3), p.249-257

2011

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Exome Analysis Reveals Novel Missense and Deletion Variants in the ICC2D2A/I Gene as Causative of Joubert Syndrome

Genes, 2023-03, Vol.14 (4)

2023

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CD39 is highly involved in mediating the suppression activity of tumor-infiltrating CD8+ T regulatory lymphocytes

Cancer Immunology, Immunotherapy, 2013-05, Vol.62 (5), p.851-862

2013

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Residual tumor micro-foci and overwhelming regulatory T lymphocyte infiltration are the causes of bladder cancer recurrence

Oncotarget, 2016-02, Vol.7 (6), p.6424-6435

2016

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Indoleamine 2,3 dioxygenase gene polymorphisms correlate with CD8+ Treg impairment in systemic sclerosis

Human immunology, 2013-02, Vol.74 (2), p.166-169

2013

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Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia Areata

Clinical and experimental medicine, 2014-02, Vol.14 (1), p.91-97

2014

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Cyclophosphamide inhibits the generation and function of CD8+ regulatory T cells

Human immunology, 2012-03, Vol.73 (3), p.207-213

2012

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AIRE polymorphism, melanoma antigen-specific T cell immunity, and susceptibility to melanoma

Oncotarget, 2016-09, Vol.7 (38), p.60872-60884

2016

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The role of AIRE polymorphisms in melanoma

Clinical immunology (Orlando, Fla.), 2010-07, Vol.136 (1), p.96-104

2010

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Abstract A020: The analyses of immune infiltrate and gene expression of MAGE antigens in bladder cancer allow to explain and predict recurrence

Cancer immunology research, 2016-01, Vol.4 (1_Supplement), p.A020-A020

2016

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Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata

Conteduca, Giuseppina

2012

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Androgen receptor, PARP signaling, and tumor microenvironment: the ‘perfect triad’ in prostate cancer?

Therapeutic advances in medical oncology, 2024-01, Vol.16, p.17588359241258443

2024

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CD20-Mimotope Peptides: A Model to Define the Molecular Basis of Epitope Spreading

Sleep disturbances and behavioral symptoms in pediatric Sotos syndrome

Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion

Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5

Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome

NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint

Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome

Azacytidine mitigates experimental sclerodermic chronic graft-versus-host disease

Comparative analysis of cancer vaccine settings for the selection of an effective protocol in mice

Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects

Beyond APECED: An update on the role of the autoimmune regulator gene (AIRE) in physiology and disease

A longitudinal characterization of the adaptive and behavioral profile in Sotos syndrome

Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants

Alteration of Th17 and Treg cell subpopulations co-exist in patients affected with systemic sclerosis

Exome Analysis Reveals Novel Missense and Deletion Variants in the ICC2D2A/I Gene as Causative of Joubert Syndrome

CD39 is highly involved in mediating the suppression activity of tumor-infiltrating CD8+ T regulatory lymphocytes

Residual tumor micro-foci and overwhelming regulatory T lymphocyte infiltration are the causes of bladder cancer recurrence

Indoleamine 2,3 dioxygenase gene polymorphisms correlate with CD8+ Treg impairment in systemic sclerosis

Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia Areata

Cyclophosphamide inhibits the generation and function of CD8+ regulatory T cells

AIRE polymorphism, melanoma antigen-specific T cell immunity, and susceptibility to melanoma

The role of AIRE polymorphisms in melanoma

Abstract A020: The analyses of immune infiltrate and gene expression of MAGE antigens in bladder cancer allow to explain and predict recurrence

Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata

Androgen receptor, PARP signaling, and tumor microenvironment: the ‘perfect triad’ in prostate cancer?

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