(Q34380329)

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Altered B cell homeostasis and toll-like receptor 9-driven response in type 1 diabetes carriers of the C1858T PTPN22 allelic variant: implications in the disease pathogenesis

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25333705%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Altered B cell homeostasis and toll-like receptor 9-driven response in type 1 diabetes carriers of the C1858T PTPN22 allelic variant: implications in the disease pathogenesis (English)

1 reference

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21 February 2020

type-1 diabetes

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toll-like receptor

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Antonino Crinò

2

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21 February 2020

3

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21 February 2020

7

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21 February 2020

Alessandra Fierabracci

9

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21 February 2020

author name string

Elena Gianchecchi

1

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21 February 2020

Rosa Luciano

4

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21 February 2020

Valentina Perri

5

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21 February 2020

Anna Lo Russo

6

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21 February 2020

M Manuela Rosado

8

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21 February 2020

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21 October 2014

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21 February 2020

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21 February 2020

9

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21 February 2020

10

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21 February 2020

e110755

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21 February 2020

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Creative Commons Attribution 4.0 International

21 October 2014

1 reference

April 2022 Public Data File from Crossref

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0 references

Regulation of type I interferon responses

1 reference

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B-lymphocyte depletion with rituximab and β-cell function: two-year results

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TLR9 deficiency promotes CD73 expression in T cells and diabetes protection in nonobese diabetic mice.

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6 July 2018

The autoimmunity-associated gene PTPN22 potentiates toll-like receptor-driven, type 1 interferon-dependent immunity

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Why do we need IgM memory B cells?

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6 July 2018

The putative role of the C1858T polymorphism of protein tyrosine phosphatase PTPN22 gene in autoimmunity.

1 reference

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6 July 2018

Association of the PTPN22 gene (+1858C/T, -1123G/C) polymorphisms with type 1 diabetes mellitus: a systematic review and meta-analysis

1 reference

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6 July 2018

PTPN22 alters the development of regulatory T cells in the thymus

1 reference

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6 July 2018

Protein tyrosine phosphatases in lymphocyte activation and autoimmunity

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6 July 2018

Making progress: preserving beta cells in type 1 diabetes

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6 July 2018

Altered B cell homeostasis is associated with type I diabetes and carriers of the PTPN22 allelic variant

1 reference

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6 July 2018

Rituximab selectively suppresses specific islet antibodies

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6 July 2018

The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans

1 reference

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6 July 2018

Increased T cell proliferative responses to islet antigens identify clinical responders to anti-CD20 monoclonal antibody (rituximab) therapy in type 1 diabetes

1 reference

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6 July 2018

Why is PTPN22 a good candidate susceptibility gene for autoimmune disease?

1 reference

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6 July 2018

Peptide immunotherapies in Type 1 diabetes: lessons from animal models

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6 July 2018

Identification of a variant form of tyrosine phosphatase LYP

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6 July 2018

Genetics of the autoimmune polyglandular syndrome type 3 variant

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6 July 2018

Unravelling autoimmune pathogenesis by screening random peptide libraries with human sera

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6 July 2018

Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling

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B-cell tolerance checkpoints in health and autoimmunity

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Protein tyrosine phosphatases in autoimmunity.

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6 July 2018

Reduced CD4+T cell activation in children with type 1 diabetes carrying the PTPN22/Lyp 620Trp variant

1 reference

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6 July 2018

Sites and stages of autoreactive B cell activation and regulation.

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6 July 2018

Linkage proof for PTPN22, a rheumatoid arthritis susceptibility gene and a human autoimmunity gene

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Role of PTPN22 in type 1 diabetes and other autoimmune diseases

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6 July 2018

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

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6 July 2018

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Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

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6 July 2018

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

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6 July 2018

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

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Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis.

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Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease

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21 January 2018

The PTPN22 620W allele is a risk factor for Wegener's granulomatosis

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Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes

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21 January 2018

Tissue-type plasminogen activator promotes murine myofibroblast activation through LDL receptor-related protein 1-mediated integrin signaling

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Innate stimulation of B1a cells enhances the autoreactive IgM repertoire in the NOD mouse: implications for type 1 diabetes.

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The Role of Toll-Like Receptors 3 and 9 in the Development of Autoimmune Diabetes in NOD Mice

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12 December 2020

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21 February 2020

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Europe PubMed Central

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21 February 2020

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21 February 2020

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