نتایج جستجو برای: minor β

تعداد نتایج: 258041  

Journal: :Combinatorica 2021

Gerards and Seymour conjectured that every graph with no odd Kt minor is (t − 1)-colorable. This a strengthening of the famous Hadwiger’s Conjecture. Geelen et al. proved $$O(t\sqrt {\log t} )$$ -colorable. Using methods present authors Postle recently developed for coloring graphs minor, we make first improvement on this bound by showing O(t(logt)β)-colorable β > 1/4.

حسینی , سیدحمزه, سلجوقیان , آناهیتا, ضرغامی , مهران, غفاری ساروی , وجیهه,

Background and purpose: Previous studies indicate an important genetic factor in the etiology of β-Thalassemia and bipolar mood disorder. There has been several case reports implicating a possible association between the two conditions. But the results of a cross sectional study was not reconfirming. Regarding different patterns of mutations in different geographical areas, this study was per...

2007
M. Reza KERAMATI N. Tayyebi

The most common hypochrom microcytic anemia are iron deficiency anemia (IDA) and thalassemia minor (TM). The results of some studies have shown that IDA can cause misdiagnosis of heterozygote β-thalassemia due to decrease in HbA2 level. Our aim in this study was evaluating the effect of IDA on HbA2 levels; Furthermore hematolagic values in CBC of these two diseases will be compared. In this stu...

2018
Mohammad Zamani Amin Vahedi Ahmad Tamaddoni Ali Bijani Mojgan Bagherzade Javad Shokri-Shirvani

Background Until now, no study has been reported investigating the association between β-thalassemia minor and Helicobacter pylori (H. pylori) infection. This study was designed to compare H. pylori infection rate between β-thalassemia minor patients and healthy controls. Methods A number of 100 β-thalassemia minor patients (50 males, 50 females) and 100 gender-matched healthy controls were p...

2011
Sedigheh Amooee Alamtaj Samsami Jamileh Jahanbakhsh Mehran Karimi

BACKGROUND β-thalassemia is the most common hereditary disease in Iran and more than 2 million carriers of the β-thalassemia mutant gene are living in this country. OBJECTIVE To determine pregnancy outcome of women with β-thalassemia minor. MATERIALS AND METHODS In this retrospective, case-control study in two universities affiliated hospitals in Shiraz, all pregnancies occurred between 200...

Journal: :Discrete Mathematics 2004
Manoel Lemos James G. Oxley

Let H be a graph with κ1 components and κ2 blocks, and let G be a minor-minimal 2-connected graph having H as a minor. This paper proves that |E(G)| − |E(H)| ≤ α(κ1 − 1) + β(κ2 − 1) for all (α, β) such that α + β ≥ 5, 2α + 5β ≥ 20, and β ≥ 3. Moreover, if one of the last three inequalities fails, then there are graphs G and H for which the first inequality

2017
Wolfgang J Schnedl Michael Schenk Sonja Lackner Sandra J Holasek Harald Mangge

Background: β-thalassemia minor is characterized by reduced β-haemoglobin chain synthesis and sometimes mild anaemia, although carriers of β-thalassemia minorare usually clinically asymptomatic.Nonspecific abdominal complaints may be caused by gastrointestinal carbohydrate malabsorption (lactose and fructose) and/or malabsorption of biogenic amines (histamine), or proteins (gluten). Objectives:...

Journal: :Journal of Community Hospital Internal Medicine Perspectives 2017

2015
Takao Kuge Hiroki Nagoya Theodora Tryfona Tsunemi Kurokawa Yoshihisa Yoshimi Naoshi Dohmae Kazufumi Tsubaki Paul Dupree Yoichi Tsumuraya Toshihisa Kotake

β-1,3:1,4-Glucan is a major cell wall component accumulating in endosperm and young tissues in grasses. The mixed linkage glucan is a linear polysaccharide mainly consisting of cellotriosyl and cellotetraosyl units linked through single β-1,3-glucosidic linkages, but it also contains minor structures such as cellobiosyl units. In this study, we examined the action of an endo-β-1,3(4)-glucanase ...

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