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THE METABOLISM OF THE INDIVIDUAL C14 LABELED HEMOGLOBINS IN PATIENTS WITH H-THALASSEMIA, WITH OBSERVATIONS ON RADIOCHROMATE BINDING TO THE HEMOGLOBINS DURING RED CELL SURVIVAL.

作者信息

GABUZDA T G, NATHAN D G, GARDNER F H

出版信息

J Clin Invest. 1965 Feb;44(2):315-25. doi: 10.1172/JCI105145.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77d/292479/7595296ae10f/jcinvest00250-0168-a.jpg

引用本文的文献

1
Haemoglobin E and alpha-Thalassaemia.
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2
Hemoglobin Hasharon (alpha-2-47 his(CD5)beta-2): a hemoglobin found in low concentration.
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5
[Alpha-thalassemia with HbH and Hb Bart's in a German family].
Klin Wochenschr. 1967 Dec 1;45(23):1193-200. doi: 10.1007/BF01727633.
7
Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.
Proc Natl Acad Sci U S A. 1977 Sep;74(9):3960-4. doi: 10.1073/pnas.74.9.3960.

本文引用的文献

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Nature. 1959 Sep 19;184:872-3. doi: 10.1038/184872a0.
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ALPHA-CHAIN OF HUMAN HEMOGLOBIN: OCCURRENCE IN VIVO.
Science. 1964 Feb 7;143(3606):590-1. doi: 10.1126/science.143.3606.590.
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The abnormal haemoglobins in haemoglobin-H disease.
Biochem J. 1963 May;87(2):240-8. doi: 10.1042/bj0870240.
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The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion.
Proc Natl Acad Sci U S A. 1962 Nov 15;48(11):1880-6. doi: 10.1073/pnas.48.11.1880.
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Comparative metabolism of haemoglobins A and F in thalassaemia.
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