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  1. 川崎医学会機関誌
  2. Kawasaki Medical Journal
  3. Vol.12(1986)
  4. No.1

Hemoglobinopathies Due to Abnormal Functional Properties of Hemoglobin Molecule Part I. Stable Abnormal Hemoglobins with High Oxygen Affinity and Erythrocytosis

https://kwmed.repo.nii.ac.jp/records/172
https://kwmed.repo.nii.ac.jp/records/172
26c382fa-241e-4b8f-b3d1-1cd70c36daac
名前 / ファイル ライセンス アクション
KJ00010221339.pdf KJ00010221339.pdf (1.5 MB)
Item type [ELS]学術雑誌論文 / Journal Article(1)
公開日 2017-01-23
タイトル
タイトル Hemoglobinopathies Due to Abnormal Functional Properties of Hemoglobin Molecule Part I. Stable Abnormal Hemoglobins with High Oxygen Affinity and Erythrocytosis
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Gulzar, A. NIAZI

× Gulzar, A. NIAZI

en Gulzar, A. NIAZI

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SHIBATA, Susumu

× SHIBATA, Susumu

en SHIBATA, Susumu

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著者所属(英)
en
Departament of Pathology, King Faisal University, College of Medicine and Medical Sciences
著者所属(英)
en
Department of Medicine, Kawasaki Medical School
キーワード
言語 en
主題Scheme Other
主題 Hemoglobinopathies
キーワード
言語 en
主題Scheme Other
主題 Hemoglobins with altered oxygen affinity
キーワード
言語 en
主題Scheme Other
主題 Erythrocytosis
キーワード
言語 en
主題Scheme Other
主題 Cysnosis
記事種別(英)
内容記述タイプ Other
内容記述 Original Article
言語 en
抄録(英)
en
The hemoglobin (Hb) tetramer exists in equilibrium between two quaternary conformations R and T and any alteration that will affect this equilibrium will have a marked effect on the function of hemoglobin. As a rule, it can be stated that any amino acid substitution that would stabilize the Hb tetramer in the oxy conformation will result in a hemoglobin variant with an increased oxygen affinity. Conversely, any amino acid substitution that would favour the deoxy configuration will produce a hemoglobin mutant with decreased oxygen affinity. Since the discovery of Hb Chesapeake in 1966, more than 130 ab normal hemoglobins with an altered oxygen affinity have been reported. Out of these 77 are stable variants and the rest being unstable hemo globins. The present review describes the molecular basis of 77 stable variants with an altered oxygen affinity and a comprehensive hematological data which should be of great interest to clinicians has been presented. In many cases, these abnormal hemoglobins manifest their presence either by familial erythrocytosis or clinical cyanosis. The molecular abnormality has been caused by substitution in α1β2 contact, carboxy terminal of globin chains or 2,3 DPG binding site. Stable abnormal hemoglobins of mutation at α1β2 and α1β1 contacts with high oxygen affinity only are dealt with in the present part of this review.
書誌情報 en : Kawasaki medical journal

巻 12, 号 1, p. 1-14, 発行日 1986
URL
識別子 http://igakkai.kms-igakkai.com/wp/wp-content/uploads/1986en/12(1)1-14.1986.pdf
識別子タイプ URI
DOI
識別子タイプ DOI
関連識別子 https://doi.org/10.11482/KMJ-E12(1)1
ISSN
収録物識別子タイプ PISSN
収録物識別子 0385-0234
ISSN
収録物識別子タイプ EISSN
収録物識別子 2434-3404
雑誌書誌ID
収録物識別子タイプ NCID
収録物識別子 AA00710169
雑誌書誌ID
収録物識別子タイプ NCID
収録物識別子 AA12029005
著者版フラグ
出版タイプ VoR
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