نتایج جستجو برای: fluctuation hypothesis fh

تعداد نتایج: 247227  

ژورنال: :مجله دانشگاه علوم پزشکی شهرکرد 0
فاطمه شایسته fatemeh shayesteh cellular and molecular research center, shahrekord university of med sci. iran کیهان قطره سامانی kyehan ghatreh samani cellular and molecular research center, shahrekord university of med sci. iran منوچهر شیرانی manoochehr shirani medical entomologis, zabol univ. of med. sci. iran. ندا پروین nada parvin medical plants research center, shahrekord univ. of med. sci. iran جواد صفاری چالشتری javad saffari chaleshtori msc student, biochemistry dept., payamnoor univ. tehran. iran مریم طاهرزاده فر رخشهری mariam taherzadeh farokhshahri msc student, biochemistry dept., payamnoor univ. tehran. iran غلامرضا مبینی

چکیده: زمینه و هدف: کلسترول بالای خانوادگی (fh) یک اختلال اتوزوم غالب است که عمدتاً به علت جهش های ژن ldlr و apob-100ایجاد می شود. تاکنون اساس مولکولی fh بطور مفصل در بسیاری از جمعیت ها تشریح شده است ولی هنوز اطلاعات مولکولی اندکی در ارتباط با fh در ایران موجود است. هدف از این مطالعه بررسی فراوانی 3 جهش شایع ژنی آپولیپوپروتئین b-100 ((apob-100 در یک جمعیت ایرانی است. روش بررسی: در این مطالعه توص...

Journal: :Sozial Extra 2020

2015
Morten Hjuler Nielsen Helle Irvine Simon Vedel Bent Raungaard Henning Beck-Nielsen Aase Handberg

OBJECTIVE Animal and in vitro studies have suggested that hypercholesterolemia and increased oxidative stress predisposes to monocyte activation and enhanced accumulation of oxidized LDL cholesterol (oxLDL-C) through a CD36-dependent mechanism. The aim of this study was to investigate the hypothesis that elevated oxLDL-C induce proinflammatory monocytes and increased release of monocyte-derived...

Journal: :iranian biomedical journal 0
پژمان فرداصفهانی pejman fard-esfahani سیروس زینلی cyrus zeinali صغری روحی دهنبه soghra rouhi dehboneh محمد تقی خانی mohhammad taghikhani شهره خاتمی shohreh khatami

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...

Ehsan Farashahi Yazd, Elaheh Asadi, Mohammad Hassan Sheikhha, Nasrin Ghasemi, Razieh Zarifian Yeganeh,

Familial hypercholesterolemia (FH) is an inherited common autosomal Mendelian disorder of lipoprotein metabolism with a population prevalence of 1 in 500. FH is characterized by severely elevated levels of low-density lipoprotein cholesterol (LDL-C), which result in surplus deposition of cholesterol in tissues. This condition leads to premature at hero sclerosis and early-onset of coronary hear...

Journal: :The Journal of antibiotics 1993
K Saitoh T Tsuno M Kakushima M Hatori T Furumai T Oki

Pradimicin S was isolated from the culture filtrate of Actinomadura spinosa AA0851. NMR and MS analyses proved that pradimicin S is the 3'-O-(3''-O-sulfo-beta-D-glucopyranosyl) analog of pradimicin A, a new member of the pradimicin family of antibiotics. Stereochemical assignment was made by correlating pradimicin S with pradimicin L.

Journal: :The Journal of experimental biology 2015
Zhongqi Chen Michael Snow Craig S Lawrence Anthony R Church Shawn R Narum Robert H Devlin Anthony P Farrell

Rainbow trout (Oncorhynchus mykiss Walbaum) in southern Western Australia have undergone passive selection for over 19 generations to survive high water temperatures. Based on the conceptual model of 'oxygen- and capacity-limited thermal tolerance', we measured critical thermal maximum (CTmax), maximum heart rate (fH,max) and aerobic scope to test the hypothesis that these rainbow trout can mai...

Journal: :Arteriosclerosis and thrombosis : a journal of vascular biology 1994
W R Fisher L A Zech P W Stacpoole

The biology of the low-density lipoprotein (LDL) receptor has been examined in detail, and a paradigm for LDL metabolism has evolved from comparative studies of cholesterol metabolism in a variety of cells cultured from normal individuals and subjects with familial hypercholesterolemia (FH). Cultured cells from patients with homozygous FH lack a functional LDL receptor and show diminished LDL c...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

2008
Jianxiang Tian

In this paper, an argon-like canonical system is studied. We introduce five hypothesis to deal with the total potential of the system. Then the balanced liquid-gas coexistence phenomenon is analyzed. Good equations of state and phase diagram are given. PACS Codes: 05.20.Jj; 05.70.-a; 05.70.Ce; 05.70.Fh.

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