نتایج جستجو برای: nod2 protein

تعداد نتایج: 1236028  

2015
Gao Tan Run-hua Li Chen Li Fang Wu Xin-mei Zhao Jia-yi Ma Shan Lei Wen-di Zhang Fa-chao Zhi

Ileal Crohn's disease (CD) arising from the alteration of intestinal homeostasis is characterized by two features, namely a decrease in Paneth cell-produced antimicrobial peptides that play a key role in maintaining this balance and an increase in NOD2, an intracellular sensor. Although mutations in NOD2 are highly correlated with the incidence of CD, the physiological role of NOD2 in intestina...

2015
Emmanuel Denou Karine Lolmède Lucile Garidou Celine Pomie Chantal Chabo Trevor C Lau Morgan D Fullerton Giulia Nigro Alexia Zakaroff-Girard Elodie Luche Céline Garret Matteo Serino Jacques Amar Michael Courtney Joseph F Cavallari Brandyn D Henriksbo Nicole G Barra Kevin P Foley Joseph B McPhee Brittany M Duggan Hayley M O'Neill Amanda J Lee Philippe Sansonetti Ali A Ashkar Waliul I Khan Michael G Surette Anne Bouloumié Gregory R Steinberg Rémy Burcelin Jonathan D Schertzer

Pattern recognition receptors link metabolite and bacteria-derived inflammation to insulin resistance during obesity. We demonstrate that NOD2 detection of bacterial cell wall peptidoglycan (PGN) regulates metabolic inflammation and insulin sensitivity. An obesity-promoting high-fat diet (HFD) increased NOD2 in hepatocytes and adipocytes, and NOD2(-/-) mice have increased adipose tissue and liv...

Journal: :Inflammatory bowel diseases 2012
Oloruntosin Adeyanju David T Okou Clifton Huang Archana Kumar Cary Sauer Courtney Galloway Mahadev Prasad Jon Waters David J Cutler Michael E Zwick Tanvi Dhere Subra Kugathasan

BACKGROUND Crohn's disease (CD) is highly heritable. NOD2 has emerged as the main susceptibility gene among individuals of European ancestry; however, NOD2 does not appear to contribute to CD susceptibility among many non-European populations. Today's African American (AA) population represents an admixture of West African (80%) and European (20%) ancestry. Since genotype-based tools are becomi...

2013
M Pardeo E Cortis C Bracaglia R Nicolai F De Benedetti A Insalaco

Introduction Blau syndrome (BS) is a rare autosomal dominant, autoinflammatory syndrome characterized by the clinical triad of granulomatous, recurrent uveitis, dermatitis and symmetric arthritis. The arthritis is usually a polyarticular exuberant synovitis and tenosynovitis and represents the characteristic phenotypic feature. Uveitis occurs in most patients and commonly evolves to a panuveiti...

2015
Manon Le Bel Jean Gosselin Rui Lu

Leukotriene B4 (LTB4), a central mediator of inflammation, is well known for its chemoattractant properties on effectors cells of the immune system. LTB4 also has the ability to control microbial infection by improving host innate defenses through the release of antimicrobial peptides and modulation of intracellular Toll-like receptors (TLRs) expression in response to agonist challenge. In this...

Journal: :Ginekologia polska 2008
Piotr Magnowski Krzysztof Medrek Magdalena Magnowska Małgorzata Stawicka Helena Kedzia Bohdan Górski Jan Lubiński Marek Spaczyński

OBJECTIVE There is an increasing evidence that genetic factors play a role in the etiology of malignant tumors. Mutations of BRCA1 and BRCA2 genes are responsible for an increased risk of ovarian cancer. The role of mutations in NOD2 gene in this type of neoplasm is still under investigation. THE AIM The aim of this study was to determine: 1. incidence of NOD 2 3020insC constitutional mutatio...

Journal: :Journal of clinical microbiology 2009
Béatrice Bercot Caroline Kannengiesser Claire Oudin Bernard Grandchamp Marie-José Sanson-le Pors Stéphane Mouly Carole Elbim

We report the first case of granulomatous mastitis due to Corynebacterium kroppenstedtii linked to strongly impaired neutrophil responses to Nod2 agonist and a single nucleotide polymorphism within the NOD2 gene (SNP13 [Leu1007fsinsC]) in a heterozygous state. These findings provided the first demonstration of impaired Nod2 function associated with corynebacterial infection.

Journal: :Haematologica 2006
Miquel Granell Alvaro Urbano-Ispizua Juan Ignacio Aróstegui Francesc Fernández-Avilés Carmen Martínez Montserrat Rovira Josefa Rius Susana Plaza Anna Gaya Alfons Navarro Carme Talarn Enric Carreras Mariano Monzó Emili Montserrat Jordi Yagüe

BACKGROUND AND OBJECTIVES Three single nucleotide polymorphisms (SNP) in the NOD2/CARD15 gene have been associated with the incidence and the severity of acute graft-versus-host disease (GVHD) following allogeneic stem cell transplantation (SCT). We hypothesized that the clinical effect of SNP in NOD2/CARD15 might be different in patients submitted to T-cell-depleted allogeneic SCT, in which do...

2015
Fabian Schnitzler Matthias Friedrich Christiane Wolf Johannes Stallhofer Marianne Angelberger Julia Diegelmann Torsten Olszak Cornelia Tillack Florian Beigel Burkhard Göke Jürgen Glas Peter Lohse Stephan Brand David L Boone

BACKGROUND A previous study suggested an association of the single nucleotide polymorphism (SNP) rs72796353 (IVS4+10 A>C) in the NOD2 gene with susceptibility to Crohn's disease (CD). However, this finding has not been confirmed. Given that NOD2 variants still represent the most important predictors for CD susceptibility and phenotype, we evaluated the association of rs72796353 with inflammator...

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