نتایج جستجو برای: ada2

تعداد نتایج: 189  

Journal: :Journal of Immunology 2023

Abstract Acute respiratory distress syndrome (ARDS) is a severe complication of COVID-19 characterized by immune dysregulation. The pathogenesis for this, particularly the involvement infiltrative monocytes, poorly understood. Extracellular ATP released during inflammation and hypoxia rapidly scavenged into adenosine, which further converted inosine adenosine deaminase (ADA). ADA2 an extracellu...

انصاری, هانی, خسروانی, دنیا, ذاکر بستان آباد, سعید, رحیمی, محمد کریم, فلاح, ایمان , قلمی, مصطفی,

سابقه و هدف : پلورال افیوژن، در زمینه کثیری از بیماری ها رویت می گردد که دو گروه عمده آن، بد خیمی ها و سل می باشند . در مطالعه حاضر به منظور بررسی سودمندی تشخیص اندازه گیری ایزو آدنوزین دی آمیناز (ADA) و آنزیم های آن و اینترفرون گاما آزمون در مایع پلور با توجه به علل مختلف در جامعه ایران روی بیماران پلورال افیوژن انجام شد و مقایسه آن روی سه گروه بیماران سل افیوژنی، بدخیمی ها و بیماران غیر سلی ا...

Journal: :Arquivos De Neuro-psiquiatria 2023

Case presentation: A 8-year-old girl, born in southeast Brazil, was taken to the neurologist by her parents investigate repeated unexplained neurological deficits. When she 4 years old, presented with livedo reticularis, abdominal pain, fever, and lower digestive hemorrhage. She extensively investigated, showing increased ESR RCP, negative tests for ANA, rheumatoid factor, ANCA, cryoglobulin, a...

2016
Sari Kassem Zoltan Villanyi Martine A. Collart

Acetylation of histones regulates gene expression in eukaryotes. In the yeast Saccharomyces cerevisiae it depends mainly upon the ADA and SAGA histone acetyltransferase complexes for which Gcn5 is the catalytic subunit. Previous screens have determined that global acetylation is reduced in cells lacking subunits of the Ccr4–Not complex, a global regulator of eukaryotic gene expression. In this ...

2015
H Ozdogan S Ugurlu A Hacioglu E Tahir Turanli A Kirectepe Aydin

Case A patient with juvenile onset recurrent febrile attacks associated with familial polyarteritis nodosa (PAN) and who carries CECR1 and MEFVgene mutations is described. The index case, a 23 year old male patient with recurrent attacks of fever and arthritis since the age of 7 was diagnosed initially as Familial Mediterranean Fever (FMF). A beneficial response to treatment with colchicine was...

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