نتایج جستجو برای: tnfaip3

تعداد نتایج: 403  

2015
Jiyang Yu Preeti Putcha Jose M. Silva

The Connectivity Map (CMAP) project profiled human cancer cell lines exposed to a library of anticancer compounds with the goal of connecting cancer with underlying genes and potential treatments. Since the therapeutic goal of most anticancer drugs is to induce tumor-selective apoptosis, it is critical to understand the specific cell death pathways triggered by drugs. This can help to better un...

2017
Ye Sun Zhiqiang Lin Chi-Hsiu Liu Yan Gong Raffael Liegl Thomas W Fredrick Steven S Meng Samuel B Burnim Zhongxiao Wang James D Akula William T Pu Jing Chen Lois E H Smith

Pathological neovessels growing into the normally avascular photoreceptors cause vision loss in many eye diseases, such as age-related macular degeneration and macular telangiectasia. Ocular neovascularization is strongly associated with inflammation, but the source of inflammatory signals and the mechanisms by which these signals regulate the disruption of avascular privilege in photoreceptors...

2014
Hwa Chia Chai Kek Heng Chua Soo Kun Lim Maude Elvira Phipps

Polymorphisms in genes involved in toll-like receptor/interferon signalling pathways have been reported previously to be associated with SLE in many populations. This study aimed to investigate the role of seven single nucleotide polymorphisms within TNFAIP3, STAT4, and IRF5, which are involved in upstream and downstream pathways of type I interferon production, in SLE in the South East Asian p...

Journal: :Blood 2011
Yuanyuan Chu J Christoph Vahl Dilip Kumar Klaus Heger Arianna Bertossi Edyta Wójtowicz Valeria Soberon Dominik Schenten Brigitte Mack Miriam Reutelshöfer Rudi Beyaert Kerstin Amann Geert van Loo Marc Schmidt-Supprian

The ubiquitin-editing enzyme A20/TNFAIP3 is essential for controlling signals inducing the activation of nuclear factor-κB transcription factors. Polymorphisms and mutations in the TNFAIP3 gene are linked to various human autoimmune conditions, and inactivation of A20 is a frequent event in human B-cell lymphomas characterized by constitutive nuclear factor-κB activity. Through B cell-specific ...

Journal: :Egyptian Journal of Medical Human Genetics 2021

Abstract Background Primary immune thrombocytopenia (PIT) is an acquired auto-immune disease characterized by decreased platelet count with increased bleeding tendency. The tumor necrosis factor associated induced protein-3 (TNFAIP3) codes for the ubiquitin-modifying enzyme that indispensable limiting inflammation. TNFAIP3 single-nucleotide polymorphisms (SNP) has been implicated in susceptibil...

Journal: :Histopathology 2017
Michiel van den Brand Jos Rijntjes Konnie M Hebeda Laura Menting Carolyn V Bregitha Wendy B C Stevens Walter J F M van der Velden Bastiaan B J Tops J Han J M van Krieken Patricia J T A Groenen

AIMS To investigate the spectrum of mutations in 20 genes involved in B-cell receptor and/or Toll-like receptor signalling resulting in activation of nuclear factor-κB (NF-κB) in 20 nodal marginal zone lymphomas (NMZLs), 20 follicular lymphomas (FLs), and 11 cases of B-cell lymphoma, unclassifiable (BCL-u). METHODS AND RESULTS Nodal marginal zone lymphomas were diagnosed according to strict c...

Journal: :Diabetes 2007
Watip Boonyasrisawat Delphine Eberle Simonetta Bacci Yuan-Yuan Zhang David Nolan Ernest V Gervino Michael T Johnstone Vincenzo Trischitta Steven E Shoelson Alessandro Doria

A20 or tumor necrosis factor (TNF)-induced protein 3 (TNFAIP3) is a negative regulator of nuclear factor-kappaB (NF-kappaB). We have investigated whether polymorphisms in this gene are associated with increased atherosclerosis in diabetic patients. Five tag single nucleotide polymorphisms (SNPs) were typed in 479 type 2 diabetic patients from Boston, including 239 coronary artery disease (CAD)-...

2011
John Bowes Gisela Orozco Edward Flynn Pauline Ho Rasha Brier Helena Marzo-Ortega Laura Coates Ross McManus Anthony W Ryan David Kane Eleanor Korendowych Neil McHugh Oliver FitzGerald Jonathan Packham Ann W Morgan Ian N Bruce Anne Barton

OBJECTIVES To investigate a shared genetic aetiology for skin involvement in psoriasis and psoriatic arthritis (PsA) by genotyping single-nucleotide polymorphisms (SNPs), reported to be associated in genome-wide association studies of psoriasis, in patients with PsA. METHODS SNPs with reported evidence for association with psoriasis were genotyped in a PsA case and control collection from the...

2016
Karthik A. Ganapathi Vaidehi Jobanputra Fabio Iwamoto Preti Jain Jinli Chen Luciano Cascione Odelia Nahum Brynn Levy Yi Xie Pallavi Khattar Daniela Hoehn Francesco Bertoni Vundavalli V. Murty Stefania Pittaluga Elaine S. Jaffe Bachir Alobeid Mahesh M. Mansukhani Govind Bhagat

The dura is a rare site of involvement by marginal zone lymphoma (MZL) and the biology of dural MZL is not well understood. We performed genome-wide DNA copy number and targeted mutational analysis of 14 dural MZL to determine the genetic landscape of this entity. Monoallelic and biallelic inactivation of TNFAIP3 by mutation (n=5) or loss (n=1) was observed in 6/9 (67%) dural MZL exhibiting pla...

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