WorldCat Identities

Villa, Anna

Overview
Works: 15 works in 18 publications in 2 languages and 25 library holdings
Roles: Author, Illustrator, Other
Publication Timeline
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Most widely held works by Anna Villa
I due regnanti : una fiaba nella vita by Flora Bresciani Nicassio( Book )

2 editions published in 1989 in Italian and held by 4 WorldCat member libraries worldwide

Il mondo a quadretti : ovvero, il fascino dell'aritmetica by Flora Bresciani Nicassio( Book )

2 editions published in 1991 in Italian and held by 2 WorldCat member libraries worldwide

Genetics of Osteopetrosis by Eleonora Palagano( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

Come si vive in Italia? : Indice di qualità regionale dello sviluppo : QUARS 2008 by Anna Villa( Book )

2 editions published in 2008 in Italian and held by 2 WorldCat member libraries worldwide

Omenn Syndrome: A Disorder of Rag1 and Rag2 Genes by Anna Villa( )

1 edition published in 1999 in English and held by 2 WorldCat member libraries worldwide

Come si vive in Trentino? : Il QUARS, la qualità sociale e ambientale dello sviluppo nella Provincia di Trento by Anna Villa( Book )

1 edition published in 2008 in Italian and held by 2 WorldCat member libraries worldwide

Establishment and characterization of a new mammary adenocarcinoma cell line derived from MMTV neu transgenic mice by Maria Grazia Sacco( )

1 edition published in 1998 in English and held by 2 WorldCat member libraries worldwide

Tutti i numeri dell'equo : il commercio equo e solidale in Italia by Elena Viganò( Book )

1 edition published in 2008 in Italian and held by 2 WorldCat member libraries worldwide

Omenn Syndrome: inflammation and autoimmunity by Anna Villa( )

1 edition published in 2011 in English and held by 2 WorldCat member libraries worldwide

Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration( )

1 edition published in 2013 in English and held by 1 WorldCat member library worldwide

Abstract : In Omenn syndrome, altered dendritic cell distribution and impaired migration represent an additional level of immune dysregulation, contributing to the pathogenesis of autoimmunity. Abstract : OS is a severe combined immunodeficiency characterized by erythrodermia and protracted diarrhea as a result of infiltration of oligoclonal-activated T cells, caused by hypomorphic mutations in RAGs. The RAG2 R229Q mouse model fully recapitulates the clinical OS phenotype. We evaluated whether T and B cell defects, together with the abnormal lymphoid structure, could affect DC homeostasis and function. High density of LCs was observed in skin biopsies of Omenn patients and in the derma of RAG2 R229Q mice, correlating with the presence of erythrodermia. In vivo models of cutaneous skin painting and CHS demonstrated a decreased migration of RAG2 R229Q DCs--in particular, LCs--into draining LNs. Interestingly, at steady state, RAG2 R229Q mice showed a reduction in DC number in all hematopoietic organs except LNs. Analysis of the MHCII marker revealed a diminished expression also upon the LPS-driven inflammatory condition. Despite the decreased number of peripheral DCs, BM pre-cDCs were present in normal number compared with RAG2 +/+ controls, whereas pDCs and monocytes were reduced significantly. Overall, these results point to a secondary defect in the DC compartment, which contributes to clinical manifestations and autoimmunity in OS
Indicatori di benessere e politiche pubbliche : quattro proposte by Giulio Marcon( )

1 edition published in 2011 in Italian and held by 1 WorldCat member library worldwide

Platelets in Wiskott-Aldrich syndrome: Victims or executioners?( )

1 edition published in 2017 in English and held by 1 WorldCat member library worldwide

Abstract: Microthrombocytopenia is the clinical hallmark of WAS, a rare X-linked immunodeficiency that is characterized by eczema, autoimmunity, and cancer susceptibility. This disease is caused by mutations in the WAS gene, which is expressed in hematopoietic cells and regulates actin cytoskeleton remodeling thereby modulating various cellular functions, including motility, immunologic synapse assembly, and signaling. Despite extensive studies that have provided great insight into the relevance of this molecule to innate and cellular immunity, the exact mechanisms of microthrombocytopenia in WAS are still unknown. This review focuses on the recent progress made in dissecting the pathogenesis of platelet defects in patients with WAS and their murine counterparts. In parallel, we will provide an overview of the state-of-the art platelets as immune modulators at the interface between hemostasis and the immune system, which suggests that these cells may have a direct role in the pathogenesis of immune dysregulation in WAS
Un viaggio nel cervello : le avventure di Curiosone e Cellulina by Bresciani Nicassio Flora( Book )

1 edition published in 1988 in Italian and held by 1 WorldCat member library worldwide

WASP regulates suppressor activity of human and murine CD4+CD25+FOXP3+ natural regulatory T cells by Francesco Marangoni( )

1 edition published in 2007 in English and held by 0 WorldCat member libraries worldwide

 
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Audience level: 0.93 (from 0.63 for Clonazione ... to 1.00 for I due regn ...)

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