نتایج جستجو برای: il7r

تعداد نتایج: 206  

2007
Frida Lundmark

Multiple sclerosis is a chronic neurological disease, where both genetic and environmental factors are influencing the susceptibility and pathogenesis. Epidemiological studies have clearly demonstrated the existence of a genetic component by comparing the degree of shared genetic material and the risk of MS, where the degree of shared genetic material clearly correlates with the risk of MS. Unt...

2011
Chen Shochat Noa Tal Obul R. Bandapalli Chiara Palmi Ithamar Ganmore Geertruy te Kronnie Gunnar Cario Giovanni Cazzaniga Andreas E. Kulozik Martin Stanulla Martin Schrappe Andrea Biondi Giuseppe Basso Dani Bercovich Martina U. Muckenthaler Shai Izraeli

Gain-of-function mutations in interleukin-7 receptor-a (IL7R) in childhood acute lymphoblastic leukemias Chen Shochat, Noa Tal, Obul R. Bandapalli, Chiara Palmi, Ithamar Ganmore, Geertruy te Kronnie, Gunnar Cario, Giovanni Cazzaniga, Andreas E. Kulozik, Martin Stanulla, Martin Schrappe, Andrea Biondi, Giuseppe Basso, Dani Bercovich, Martina U. Muckenthaler, and Shai Izraeli Vol. 208, No. 5, May...

Journal: :Proceedings of the National Academy of Sciences 2013

2015
Sandrine Degryse Jan Cools

Recent studies of acute lymphoblastic leukemia have identified activating mutations in components of the interleukin-7 receptor complex (IL7R, JAK1, and JAK3). It will be of interest to investigate both JAK1 and JAK3 kinase inhibitors as targeted agents for these leukemias.

2012
Willemijn M. Passtoors Judith M. Boer Jelle J. Goeman Erik B. van den Akker Joris Deelen Bas J. Zwaan Ann Scarborough Ruud van der Breggen Rolf H. A. M. Vossen Jeanine J. Houwing-Duistermaat Gert Jan B. van Ommen Rudi G. J. Westendorp Diana van Heemst Anton J. M. de Craen Andrew J. White David A. Gunn Marian Beekman P. Eline Slagboom

The Leiden Longevity Study consists of families that express extended survival across generations, decreased morbidity in middle-age, and beneficial metabolic profiles. To identify which pathways drive this complex phenotype of familial longevity and healthy aging, we performed a genome-wide gene expression study within this cohort to screen for mRNAs whose expression changes with age and assoc...

Journal: :Frontiers in Molecular Biosciences 2021

We aimed to explore the tumor mutational burden (TMB) and immune infiltration in HCC investigate new biomarkers for immunotherapy. Transcriptome gene mutation data were downloaded from GDC portal, including 374 samples 50 matched normal samples. Furthermore, we divided into high low TMB groups, analyzed differential genes between them with GO, KEGG, GSEA. Cibersort was used assess cell Finally,...

Journal: :Journal of Investigative Dermatology 2022

Systemic lupus erythematosus (SLE) is a female-biased multisystem inflammatory disease with substantial morbidity and mortality limited treatment options. Our lab previously found that VGLL3, putative transcription co-factor increased activity in female cells, can drive lupus-like systemic inflammation when overexpressed mouse epidermis under the K5 promoter. IL-7 signaling was to be elevated s...

2011
Supinda Bunyavanich Erik Melen Jemma B Wilk Mark Granada Manuel E Soto-Quiros Lydiana Avila Jessica Lasky-Su Gary M Hunninghake Magnus Wickman Göran Pershagen George T O'Connor Scott T Weiss Juan C Celedόn

BACKGROUND Allergic rhinitis (AR) affects up to 80% of children with asthma and increases asthma severity. Thymic stromal lymphopoietin (TSLP) is a key mediator of allergic inflammation. The role of the TSLP gene (TSLP) in the pathogenesis of AR has not been studied. OBJECTIVE To test for associations between variants in TSLP, TSLP-related genes, and AR in children with asthma. METHODS We g...

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