نتایج جستجو برای: minor β

تعداد نتایج: 258041  

Journal: :international journal of hematology-oncology and stem cell research 0
ebrahim miri-moghaddam genetics of non-communicable disease research centre, zahedan university of medical sciences, zahedan, iran ; department of genetics, zahedan university of medical sciences, zahedan, iran. narjes sargolzaie department of community medicine, zahedan university of medical sciences, zahedan, iran.

objective: the two most frequent hypochromic microcytic anemias are β- thalassemia minor (btm) and iron deficiency anemia (ida). several discrimination indices have been proposed to quickly discriminate these similar entities via parameters obtained from automated blood count analyzers. the aim of this study to evaluate the diagnostic reliability of ten discrimination indices in the differentia...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1393

همان طور که رایج است، ifn-β به عنوان یک عامل تعدیل کننده سیستم ایمنی در درمان بیماری مولتیپل اسکلروزیس استفاده می شود. اگرچه بعد از مدتی اثر بخشی درمانی آن به واسطه تولید آنتی بادی های خنثی کننده در بدن فرد بیمار محدود می شود. اخیراً سلول های مزانکایمال حاصل از بافت چربی(ad-mscs) به عنوان یک روش درمانی امید بخش در درمان بیماری های خود ایمن مخصوصاً مولتیپل اسکلروزیس و مدل حیوانی آن یعنی انسفالومیل...

Journal: :Circulation. Cardiovascular genetics 2016
Bing Yu Sara L Pulit Shih-Jen Hwang Jennifer A Brody Najaf Amin Paul L Auer Joshua C Bis Eric Boerwinkle Gregory L Burke Aravinda Chakravarti Adolfo Correa Albert W Dreisbach Oscar H Franco Georg B Ehret Nora Franceschini Albert Hofman Dan-Yu Lin Ginger A Metcalf Solomon K Musani Donna Muzny Walter Palmas Leslie Raffel Alex Reiner Ken Rice Jerome I Rotter Narayanan Veeraraghavan Ervin Fox Xiuqing Guo Kari E North Richard A Gibbs Cornelia M van Duijn Bruce M Psaty Daniel Levy Christopher Newton-Cheh Alanna C Morrison

BACKGROUND Rare genetic variants influence blood pressure (BP). METHODS AND RESULTS Whole-exome sequencing was performed on DNA samples from 17 956 individuals of European ancestry and African ancestry (14 497, first-stage discovery and 3459, second-stage discovery) to examine the effect of rare variants on hypertension and 4 BP traits: systolic BP, diastolic BP, pulse pressure, and mean arte...

Journal: :Journal of Multivariate Analysis 2023

This paper considers the asymptotic behavior in β-Hölder spaces, and under Lp losses, of a Dirichlet kernel density estimator proposed by Aitchison Lauder (1985) for analysis compositional data. In recent work, Ouimet Tolosana-Delgado (2022) established uniform strong consistency normality this estimator. As complement, it is shown here that Aitchison–Lauder can achieve minimax rate asymptotica...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2012
Thomas J Kunicki Shirley A Williams Diane J Nugent Mark Yeager

OBJECTIVE The interindividual variation in platelet α(2)β(1) exceeds a 2-fold variance in platelet α(IIb)β(3) level. Our objective was to parse the contribution of mean platelet volume (MPV) and integrin gene alleles to this variation in large cohorts of patients with acute coronary syndrome (ACS) and normal subjects. METHODS AND RESULTS Platelet α(IIb)β(3) and α(2)β(1) levels were measured b...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علامه طباطبایی 1388

عاملهای شناختی، شخصیتی و موقعیتی متعددی یافت شده است که می توانند با پرخاشگری ارتباط داشته باشند. فهم چگونگی ارتباط درونی این عاملها برای پیش بینی، سنجش، و درمان پرخاشگری زندانیانی که سابقه رفتارهای پرخاشگرانه را دارند، بسیار اساسی است. پژوهشهای قبلی نقش بالقوه ای را برای توانایی حل مساله اجتماعی بعنوان یک میانجیگر بین تکانشگری و پرخاشگری پیشنهاد کرده اند. ( موران و همکاران، 2002). علاوه بر این...

Journal: :international journal of hematology-oncology and stem cell research 0
z rahimi medical biology research center, kermanshah university of medical sciences, kermanshah, iran. biochemistry department, medical school, kermanshah university of medical sciences, kermanshah, iran a merat biochemistry department, medical school, shiraz university of medical sciences, shiraz, iran m akhzari biochemistry department, medical school, shiraz university of medical sciences, shiraz, iran m haghshenass hematology research center, shiraz university of medical sciences, shiraz, iran nagel ronald l department of medicine, division of hematology; department of physiology and biophysics, albert einstein college of medicine, bronx, ny, usa gerard nathalie nserm u763, hôpital robert debrè, paris, france

introduction: β-globin gene cluster haplotypes are useful in diagnosis of particular molecular defects in β-thalassemia, prenatal diagnosis of β-thalassemia, and elucidating population affinities. methods: β-globin gene cluster haplotypes were studied in 150 β-thalassemia minor and 52 healthy in-dividuals from the fars province of iran. dna was extracted from leukocytes of whole blood by phe-no...

2012
Christopher M. O'Connor Mona Fiuzat Peter E. Carson Inder S. Anand Jonathan F. Plehn Stephen S. Gottlieb Marc A. Silver JoAnn Lindenfeld Alan B. Miller Michel White Ryan Walsh Penny Nelson Allen Medway Gordon Davis Alastair D. Robertson J. David Port James Carr Guinevere A. Murphy Laura C. Lazzeroni William T. Abraham Stephen B. Liggett Michael R. Bristow

BACKGROUND Pharmacogenetics involves complex interactions of gene products affecting pharmacodynamics and pharmacokinetics, but there is little information on the interaction of multiple genetic modifiers of drug response. Bucindolol is a β-blocker/sympatholytic agent whose efficacy is modulated by polymorphisms in the primary target (β(1) adrenergic receptor [AR] Arg389 Gly on cardiac myocytes...

2016
Yasemin Işık Balcı Şule Ünal Fatma Gümrük

Conflict of Interest: The authors of this paper have no conflicts of interest, including specific financial interests, relationships, and/or affiliations relevant to the subject matter or materials included. References 1. Harteveld CL, Higgs DR. Alpha-thalassaemia. Orphanet J Rare Dis 2010;5:13. 2. Blackwell RQ, Jim RT, Tan TG, Weng MI, Liu CS, Wang CL. Hemoglobin G Waimanalo: alpha-64 Asp lead...

2014
Mehrdad Payandeh Zohreh Rahimi Mohammad Erfan Zare Atefeh Nasir Kansestani Farzad Gohardehi Amir Hossein Hashemian

Hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency in certain area particularly Mediterranean and Middle Eastern countries. Hemoglobinopathies include structural variants of hemoglobin (Hb S, Hb C, HbE,…) and thalassaemias which are inherited defects in the globin chains synthesis. The present study was conducted to determine the prevalence of h...

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