نتایج جستجو برای: فاکتور xiii

تعداد نتایج: 20849  

Factor XIII deficiency is a bleeding disorder that its prevalence in the general population is about 1 in 2 million people around the world. In Iran, the high rate of consanguineous marriages lead to high rate of disorder with 473 factor XIII deficient patients that is about 12 times higher than the global Prevalence of disorder. The study, is a comprehensive review of all aspects of factor XII...

شهره زارع کاریزی فاطمه اسکندری, محمد تقی اکبری

مقدمه: سقط خود به خودی مکرر جنین، یکی از معضلاتی است که تقریباً 5% زوجین با آن رو به رو هستند. با توجه به این موضوع و با توجه به ارتباط سقط ها با ترومبوفیلیاها، مطالعه حاضر با هدف بررسی چند شکلی G103T فاکتور XIII به عنوان یک عامل مؤثر در روند انعقاد و ارتباط آن با سقط مکرر جنین انجام شد. روش‌کار: این مطالعه مورد- شاهدی طی سال های 91-1389 انجام شد. 105 زن که حداقل 2 یا بیشتر از 2 سقط قبل از هفته ...

Journal: :journal of cellular and molecular anesthesia 0
majid naderi shadi tabibian shaban alizadeh zahra sadat abtahi akbar dorgalaleh department of hematology and blood transfusion, school of allied medical sciences, iran university of medical sciences, tehran, iran.

background: factor xiii (fxiii) is a heterotetramer composing two subunits including fxiii-a and fxiii-b. several common gene variations were observed in fxiii-a gene with obvious ethnic difference. this study assessed pattern of tyr204phe as a common fxiii-a gene variation among iranian population. materials and methods: this study was conducted on eighty iranian unrelated individuals. genotyp...

Journal: :The Journal of clinical investigation 1969
J McDonagh R P McDonagh J M Delâge R H Wagner

Plasma and platelet factor XIII levels were measured in normal human donors and in a patient congenitally deficient in factor XIII. The purpose of these experiments was to study the role of platelet factor XIII in blood coagulation. On polyacrylamide disc electrophoresis, factor XIII activity in extracts of washed normal platelets appeared as a single peak. This peak was missing or very low whe...

Journal: :journal of cell and molecular research 0
dor mohammad kordi-tamandani zohreh rezaei akbar dorgalaleh-mail

congenital factor xiii deficiency is a very rare bleeding disorder, but because of the high rate of consanguineous marriages, it is common in sistan and baluchestan province of iran. the discovery of promoter hypermethylation of numerous mirnas in human diseases has demonstrated an epigenetic mechanism for aberrant mirna expression. the present study has analyzed methylation and expression stat...

2013
Sho Mokuda Yosuke Murata Naoya Sawada Kenichiro Matoba Akihiro Yamada Makoto Onishi Yasuaki Okuda Kazuo Jouyama Eiji Sugiyama Kiyoshi Takasugi

Factor XIII is one of the twelve coagulation factors and also known as a fibrin-stabilizing factor. In 2012, we encountered a male RA patient with hemorrhagic factor XIII deficiency who had been treated with tocilizumab for two years. There are few reports regarding the relationship between tocilizumab (a humanized monoclonal antibody against the interleukin-6 receptor (IL-6R)) and factor XIII....

2005
TIMO VÄISÄNEN Taina Pihlajaniemi Asta Pirskanen

Type XIII collagen belongs to the group of transmembrane collagens. In this thesis the plasma membrane localisation and function of type XIII collagen have been studied using cell biological methods. Type XIII collagen was found to reside in focal adhesions. It appeared in these structures at a very early stage of their assembly and disappeared from them concurrently with focal adhesion protein...

2017
MEHMET SERDAR YILDIRIM ORHAN AYYILDIZ

Factor XIII (Fibrin-stabilizing factor) is a tetrameric structural pro-transglutaminase from the transglutaminase family. Factor XIII activity is associated with the structure of fibrin clot. Factor XIII turns into XIII-A, which is an active transglutaminase, in the result phase of coagulation cascade together with Ca and thrombin activation. The main aim of Factor XIIIA is to connect ε(δ-gluta...

Journal: :IACR Cryptology ePrint Archive 2013
Masao Kasahara

In this paper, we present a new class of public key cryptosystems by modifying K(XII)SE(1)PKC [1], referred to as K(XIII)SE(1)PKC, and a particular class of K(XIII)SE(1)PKC, Kp(XIII)SE(1)PKC. We show that K(XIII)SE(1)PKC would improve both the coding rate and the security, compared with K(XII)SE(1)PKC. We also show that Kp(XIII)SE(1)PKC realizes the coding rate of exactly 1.0. In a sharp contra...

Journal: :journal of comprehensive pediatrics 0
mojtaba vahid golpayegani department of pediatric dentistry, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iran hossein behnia department of oral & maxillofacial surgery, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mahvareh akhgar araghi pedodontist, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) ghassem ansari department of pediatric dentistry, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iran; department of pediatric dentistry, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-21 22255537

conclusions the case was fully investigated and diagnosed as a case with factor xiii deficiency causing such uncontrolled bleeding after extraction of a tooth. introduction factor xiii deficiency is a relatively rare hereditary bleeding disorder, which is usually found during infancy or early childhood. this condition may involve both genders within different races in an equal manner. its incid...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید