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Literature DB >> 13105702

Studies on abnormal hemoglobins. VIII. The gelling phenomenon of sickle cell hemoglobin: its biologic and diagnostic significance.

K SINGER, L SINGER.

Abstract

Entities: Gene

Keywords: HEMOGLOBIN

Mesh：

Substances：

Year: 1953 PMID： 13105702

Source DB: PubMed Journal: Blood ISSN： 0006-4971 Impact factor: 22.113

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28 in total

1. Thermodynamic studies of polymerization of deoxygenated sickle cell hemoglobin.

Authors: B Magdoff-Fairchild; W N Poillon; T Li; J F Bertles
Journal: Proc Natl Acad Sci U S A Date: 1976-04 Impact factor: 11.205

2. Supersaturation in sickle cell hemoglobin solutions.

Authors: J Hofrichter; P D Ross; W A Eaton
Journal: Proc Natl Acad Sci U S A Date: 1976-09 Impact factor: 11.205

3. Arterialization of peripheral venous blood in sickle cell disease.

Authors: Masoud Nahavandi; Richard M Millis; Fatemeh Tavakkoli; Meville Q Wyche; Elliott Perlin; William P Winter; Oswaldo Castro
Journal: J Natl Med Assoc Date: 2002-05 Impact factor: 1.798

4. A critical review of human haemoglobin variants. II. Individual haemoglobins.

Authors: G H BEAVEN; W B GRATZER
Journal: J Clin Pathol Date: 1959-03 Impact factor: 3.411

5. The effect of methemoglobin formation in sickle cell disease.

Authors: E BEUTLER
Journal: J Clin Invest Date: 1961-10 Impact factor: 14.808

6. Studies on the destruction of red blood cells. XII. Factors influencing the role of S hemoglobin in the pathologic physiology of sickle cell anemia and related disorders.

Authors: M S GREENBERG; E H KASS; W B CASTLE
Journal: J Clin Invest Date: 1957-06 Impact factor: 14.808

Studies on abnormal hemoglobins. VIII. The gelling phenomenon of sickle cell hemoglobin: its biologic and diagnostic significance.

1. Thermodynamic studies of polymerization of deoxygenated sickle cell hemoglobin.

2. Supersaturation in sickle cell hemoglobin solutions.

3. Arterialization of peripheral venous blood in sickle cell disease.

4. A critical review of human haemoglobin variants. II. Individual haemoglobins.

5. The effect of methemoglobin formation in sickle cell disease.

6. Studies on the destruction of red blood cells. XII. Factors influencing the role of S hemoglobin in the pathologic physiology of sickle cell anemia and related disorders.

7. Properties of sickle-cell haemoglobin.

8. Hyposthenuria in sickle cell anemia: a reversible renal defect.

9. [Abnormal human hemoglobin].

10. [Studies on the biological and physical-chemical properties of sickle-cell hemoglobin].