نتایج جستجو برای: fh protein

تعداد نتایج: 1237776  

Journal: :Arquivos brasileiros de cardiologia 2009
Sônia Silva Prado Mário Luiz Ribeiro Gilberto Perez Cardoso Kelb Bousquet-Santos Luis Guillermo Coca Velarde Antônio Cláudio Lucas da Nóbrega

BACKGROUND In Western countries type 2 diabetes mellitus (DM2) is the leading cause of morbidity and mortality, particularly from cardiovascular causes. Since a family history of diabetes, even in non-diabetic subjects, is regarded as an increased risk of coronary heart disease, the use of approved surrogate markers of early atherosclerosis, specially of ultrasonic measurements of the carotid a...

Journal: :Developmental Cognitive Neuroscience 2015
Julia E. Cohen-Gilbert Jennifer T. Sneider David J. Crowley Isabelle M. Rosso J. Eric Jensen Marisa M. Silveri

Neuroimaging studies of individuals with family histories of alcoholism provide evidence suggesting neurobiological risk factors for alcoholism. Youth family history positive (FH+) for alcoholism exhibit increased impulsivity compared to family history negative (FH-) peers in conjunction with altered functional activation in prefrontal cortex, including anterior cingulate cortex (ACC). This stu...

ژورنال: :مجله دانشگاه علوم پزشکی شهرکرد 0
سمیه اسدی somayeh asadi کیهان قطره سامانی keyhan gatreh samani مهدی بنی طالبی mehdi banitalebi غلامرضا مبینی gholamreza mobini جواد صفاری چالشتری javad saffari chaleshtori مریم طاهرزاده قهفرخی maryam taherzadeh ghahfarrokhi فاطمه شایسته

چکیده: زمینه و هدف: هایپرکلسترولمی فامیلی (fh) بیماری غالب اتوزومال است که عمدتاً بدلیل جهش در ژن گیرنده لیپوپروتئین با دانسیته کم (ldlr) ایجاد می شود. این مطالعه با هدف بررسی تغییرات ژن ldlr بیماران مبتلا به کلسترول بالای خانوادگی در استان چهارمحال و بختیاری انجام شد. روش بررسی: در این مطالعه توصیفی- آزمایشگاهی، 57 بیمار مشکوک به fh غربالگری و با استفاده از روش pcr-sscp جهش در پروموتر و اگزون ه...

2017
Eszter Trojnár Mihály Józsi Katalin Uray Dorottya Csuka Ágnes Szilágyi Danko Milosevic Vesna D. Stojanović Brankica Spasojević Krisztina Rusai Thomas Müller Klaus Arbeiter Kata Kelen Attila J. Szabó György S. Reusz Satu Hyvärinen T. Sakari Jokiranta Zoltán Prohászka

INTRODUCTION In autoimmune atypical hemolytic uremic syndrome (aHUS), the complement regulator factor H (FH) is blocked by FH autoantibodies, while 90% of the patients carry a homozygous deletion of its homolog complement FH-related protein 1 (CFHR1). The functional consequence of FH-blockade is widely established; however, the molecular basis of autoantibody binding and the role of CFHR1 defic...

Mohhammad Taghikhani, Cyrus Zeinali, Pejman Fard-Esfahani, Shohreh Khatami, Soghra Rouhi Dehboneh,

Familial hypercholesterolemia (FH) is an autosomal co-dominant disorder of lipid metabolism, caused by mutations in LDL receptor gene. The penetrance of FH is almost 100%, meaning that half of the offspring of affected parents born with disease. The patients are at risk of premature coronary heart disease (CHD). There is no report about the molecular basis of FH in Iran. Identification of mutat...

Journal: :Life 2023

Background: Familial Hypercholesterolemia (FH) is a hereditary condition that causes rise in blood cholesterol throughout person’s life. FH can result myocardial infarction and even sudden death if not treated. thought to be caused mainly by variants the gene for low-density lipoprotein receptor (LDLR). This study aimed investigate genetic patients, verify their pathogenicity, comprehend relati...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1998
R Kinders T Jones R Root C Bruce H Murchison M Corey L Williams D Enfield G M Hass

The BTAstat and BTA TRAK tests are new immunoassays that detect and measure an antigen in the urine of individuals diagnosed with bladder cancer. As described in this report, the monoclonal antibodies used in these kits were developed by immunizing mice with partially purified protein preparations derived from the urine of patients with bladder cancer. The antigen that is recognized by the mono...

2011
Sunil Sudarshan Karthigayan Shanmugasundaram Susan L. Naylor Shu Lin Carolina B. Livi Christine F. O'Neill Dipen J. Parekh I-Tien Yeh Lu-Zhe Sun Karen Block

Germline mutations of FH, the gene that encodes for the tricarboxylic acid TCA (TCA) cycle enzyme fumarate hydratase, are associated with an inherited form of cancer referred to as Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC). Individuals with HLRCC are predisposed to the development of highly malignant and lethal renal cell carcinoma (RCC). The mechanisms of tumorigenesis proposed h...

Journal: :The Biochemical journal 1997
J Hellwage S Kühn P F Zipfel

Complement factor H (FH) and factor-H-like protein 1 (FHL-1) are human plasma proteins with regulatory functions in the alternative pathway of complement activation. FH and FHL-1 are organized in repetitive elements termed short consensus repeats (SCRs) and the seven SCRs of FHL-1 are identical with the N-terminal domain of the 20 SCRs of FH. The fourth SCR of both proteins (SCR 4) includes the...

Journal: :Infection and immunity 2016
Daniel P Miller Lee D Oliver Brittney K Tegels Lucas A Reed Nathaniel S O'Bier Kurni Kurniyati Lindsay A Faust Christine K Lawson Anna M Allard Melissa J Caimano Richard T Marconi

The Treponema denticola FhbB protein contributes to immune evasion by binding factor H (FH). Cleavage of FH by the T. denticola protease, dentilisin, may contribute to the local immune dysregulation that is characteristic of periodontal disease (PD). Although three FhbB phyletic types have been defined (FhbB1, FhbB2, and FhbB3), the in vivo expression patterns and antigenic heterogeneity of Fhb...

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