نتایج جستجو برای: hla phenotyping

تعداد نتایج: 46994  

Journal: :Journal of medical genetics 1997
M C Bittencourt M A Morris J Chabod A Gos B Lamy F Fellmann S E Antonarakis E Plouvier P Herve P Tiberghien

Uniparental isodisomy is defined as the inheritance of two copies of the same parental chromosome and can result in defects when it produces homozygosity for a recessive mutation or in the presence of imprinting. We describe the detection of a chromosome 6 uniparental isodisomy in a 9 year old girl, discovered during a search for an HLA identical sib. HLA typing, erythrocyte phenotyping, and ge...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1388

یکی از مولکولهای غیرکلاسیک از آنتی ژنهای سازگاری نسجی کلاس یک hla-g : مقدمه hla- تا hla-g انسان است که دارای هفت ایزوفرم پروتئینی شامل چهار پروتئین متصل به غشا ( 1 hla- می باشد.ایزوفرم های غشایی و محلول (hla-g تا 7 hla-g و سه پروتئین محلول ( 5 (g4 خصوصیات تولرژنیک که به نفع فرار تومور از نظارت سیستم ایمنی است را نشان می دهند. g مواد و روشها: این مطالعه روی 30 بیمار مبتلا به آدنوکارسینوم معد...

Journal: :Leukemia research 2007
Martin Schwonzen Volker Diehl Mario Dellanna Peter Staib

Immunophenotyping of acute leukemia using flow cytometry after density gradient separation (dg-sep) of mononuclear cells is the international gold standard. But destroying red cells by whole blood lysis (wb-lysis) after direct staining has found a broad usage. Both methods revealed congruent results in phenotyping of 26 cases of acute myeloid leukemias by testing CD4, CD7, CD11b, CD11c, CD13, C...

2016
Valérie Faivre Anne-Claire Lukaszewicz Didier Payen

BACKGROUND The downregulation of blood monocyte HLA-DR expression also occurs in tissue infiltrative cells in a context of acute clinical inflammation, especially sepsis. This context favors the development of secondary infections and results from various mechanisms. Little is known about HLA-DR expression on bone marrow (BM) cells of the monocyte lineage, the source of circulating monocytes. T...

اونق, عبدالغفار, دلیرژ, نوروز, لقمانی, علیرضا, محب علیان, هادی,

Background: Multiple Sclerosis (MS) is an autoimmune disease with impairment in function of central nervous system. Macrophages and dendritic cells play important roles in alleviating or progression of the disease. These cells can cause inflammation and damage to the myelin of nerve cells by realizing of harmful substances when these cells get matured. We studied the effect of Alternaria altern...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1389

مقدمه :یکی از انواع شایع آلرژی رینیت آلرژی است .عامل اصلی این نوع آلرژی گرده گل ها، درختان و علف های هرز است .این گیاهان به طور عمده در بهار و تابستان گرده افشانی می کنند . یکی از این گیاهان آرتمیسیا ولگاریس است که در اواخر تابستان گرده افشانی می کند و از شیوع با?یی در سراسر جهان از جمله ایران برخوردار است . ارتباط مهمی بین آلل های hla-drb1 و آلرژی به گیاه آرتمیسیا ولگاریس در شهرستان سبزوار واق...

2011
Robert C. Kaplan Elizabeth Sinclair Alan L. Landay Nell Lurain A. Richey Sharrett Stephen J. Gange Xiaonan Xue Peter Hunt Roksana Karim David M. Kern Howard N. Hodis Steven G. Deeks

BACKGROUND Individuals infected with human immunodeficiency virus (HIV) have increased risk of cardiovascular events. It is unknown whether T cell activation and senescence, 2 immunologic sequelae of HIV infection, are associated with vascular disease among HIV-infected adults. METHODS T cell phenotyping and carotid ultrasound were assessed among 115 HIV-infected women and 43 age- and race/et...

2016
Tom van Gils Tine van de Donk Gerd Bouma Foke van Delft E Andra Neefjes-Borst Chris J J Mulder

OBJECTIVE Collagenous sprue (CS) is a rare form of small bowel enteropathy characterised by a thickened basement membrane and is, in most of the literature, reported as part of coeliac disease. Multiple treatment strategies are suggested in CS, but there is no standardised therapy. The aim of this series is to describe 4 cases of CS and to propose thioguanine (6-TG) treatment. DESIGN We revie...

Journal: :Human molecular genetics 2010
Hiroe Sato Felix A Woodhead Tariq Ahmad Jan C Grutters Paolo Spagnolo Jules M M van den Bosch Lisa A Maier Lee S Newman Sonoko Nagai Takateru Izumi Athol U Wells Roland M du Bois Kenneth I Welsh

The HLA class II (DRB1 and DQB1) associations with sarcoidosis have been studied by several groups but often without consistent results. In this paper, we consider the hypothesis that observed inconsistencies relate to distinct, genetically encoded disease phenotypes which differ in prevalence between centres. We therefore typed HLA-DRB1 and DQB1 in 340 UK, 139 Dutch and 163 Japanese sarcoidosi...

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