Results 291 to 300 of about 586,911 (331)
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Journal of Computational Chemistry, 2019
This work studies the underlying nature of H‐bonds (HBs) of different types and strengths and tries to predict binding energies (BEs) based on the properties derived from wave function analysis.
S. Emamian +3 more
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This work studies the underlying nature of H‐bonds (HBs) of different types and strengths and tries to predict binding energies (BEs) based on the properties derived from wave function analysis.
S. Emamian +3 more
semanticscholar +1 more source
European Journal of Haematology, 1995
Abstract: The hemoglobin (Hb) lepore‐Boston is a β‐globin structural variant, produced in a reduced amount and formed from the fusion of N‐terminus δ‐(residues 1–87) and C‐terminus β‐chains (residues 116–146). This type of fusion protein is quite common in Southern Italy (Campania, Calabria, and Sicily). We report here the hematological and hemoglobin
E, Mirabile +4 more
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Abstract: The hemoglobin (Hb) lepore‐Boston is a β‐globin structural variant, produced in a reduced amount and formed from the fusion of N‐terminus δ‐(residues 1–87) and C‐terminus β‐chains (residues 116–146). This type of fusion protein is quite common in Southern Italy (Campania, Calabria, and Sicily). We report here the hematological and hemoglobin
E, Mirabile +4 more
openaire +2 more sources
Cell, 1980
Abstract We have taken advantage of the preferential digestion of active genes by DNAase I to investigate the chromosomal structure of embryonic and adult β-globin genes during erythropoiesis in chick embryos, and in particular to examine the question of hemoglobin switching during development.
J, Stalder +4 more
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Abstract We have taken advantage of the preferential digestion of active genes by DNAase I to investigate the chromosomal structure of embryonic and adult β-globin genes during erythropoiesis in chick embryos, and in particular to examine the question of hemoglobin switching during development.
J, Stalder +4 more
openaire +2 more sources
Association of Hb Q‐Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy
European Journal of Haematology, 2005Abstract: Hemoglobin (Hb) Q‐Thailand [α74(EF3): Asp→His] is an abnormal Hb found mainly in China and South‐east Asian countries. Association of the αQ‐Thailand allele with α‐thalassemia has important implications in diagnosis. We report the hitherto undescribed conditions of this variant in two unrelated pregnant Thai women.
Kanokwan, Sanchaisuriya +5 more
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The Journal of Applied Laboratory Medicine
Abstract Background The quantitation of glycated hemoglobin (Hb A1c) represents an average blood glucose level for a period of 2 to 3 months for diagnosing, monitoring, and managing diabetes mellitus. Unreliable results are reported when hemoglobin (Hb) variants are present in the sample. Patients are
Ankitha K Puthiyaveettil +3 more
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Abstract Background The quantitation of glycated hemoglobin (Hb A1c) represents an average blood glucose level for a period of 2 to 3 months for diagnosing, monitoring, and managing diabetes mellitus. Unreliable results are reported when hemoglobin (Hb) variants are present in the sample. Patients are
Ankitha K Puthiyaveettil +3 more
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HB − MAC: Improving the Random − HB # Authentication Protocol
2009The Random - HB # protocol is a significant improvement of the HB + protocol introduced by Juels and Weis for the authentication of low-cost RFID tags. Random - HB # improves HB + in terms of both security and practicality. It is provably resistant against man-in-the-middle attacks, where the adversary can modify messages send from the reader to the ...
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Seminars in Hematology, 2018
The mutation of β6 from glu to val in hemoglobin is responsible for the polymer formation that leads to vaso-occlusion, and a range of severe consequences in sickle cell disease. The treatment of the disease can be addressed in many ways, but the prevention of polymer formation is one of the most fundamental approaches one can take.
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The mutation of β6 from glu to val in hemoglobin is responsible for the polymer formation that leads to vaso-occlusion, and a range of severe consequences in sickle cell disease. The treatment of the disease can be addressed in many ways, but the prevention of polymer formation is one of the most fundamental approaches one can take.
openaire +2 more sources