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Dive into the research topics where Robert B. Thompson is active.

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Featured researches published by Robert B. Thompson.


Experimental and Molecular Pathology | 1966

Electron microscopic studies on blood smears and hemoglobin in sickle cell disease

Paul J. Rau; Robert B. Thompson

Abstract A replication method for the electron microscopic examination of blood cell surfaces and purified hemoglobin is described. Significant structural alterations were observed in erythrocytes and serum in blood smears from patients with sickle cell disease. Examination of hemoglobin by this method revealed rod-shaped crystals containing four internal electron-dense strands with dimensions which were in striking agreement with the length of the peptide chain and distance between iron atoms reported by other workers from X-ray diffraction studies. Therefore, it is believed that the crystals observed in this study represent molecular aggregates of hemoglobin. Although three dimensional crystals were present along cell surfaces and in close proximity to erythrocytes in blood smears from patients with sickle cell disease, they were not present within cells. It is suggested that an interface effect between hemoglobin and the cell membranes may be the mechanism by which sickling occurs. Studies of dilute solutions of hemoglobin which were dried on formvar films and examined in the electron microscope without further preparation showed structures containing four electrondense globules. These latter units were considered to represent hemoglobin molecules which had expanded by dissociation.


American Journal of Physiology | 1965

PHYSIOLOGIC DIFFERENCES IN HEMOGLOBIN VARIANTS.

Robert B. Thompson; Richard L. Warrington; W.N. Bell


Human Heredity | 1965

Hb-S, Beta Thalassemia and Hb-A21 (B2) in a Family with Evidence of a Crossover Between Beta and Delta Loci

Robert B. Thompson; J. Odom; W.N. Bell


Acta Haematologica | 1965

THALASSEMIA WITH COMPLETE ABSENCE OF HEMOGLOBIN A2 IN AN ADULT.

Robert B. Thompson; J. Odom; R. Warrington; W.N. Bell


Nature | 1966

Haemoglobin variants in a species of wild mice-Peromyscus maniculatus.

Robert B. Thompson; H. B. Hewett; S. S. Kilgore; A. P. Shepherd; W.N. Bell


Human Heredity | 1965

Interaction Between Genes for Delta Thalassemia and Hereditary Persistence of Foetal Hemoglobin

Robert B. Thompson; R. Warrington; J. Odom; W.N. Bell


The American Journal of the Medical Sciences | 1965

Splenomegaly, anemia and thalassemia intermedia.

Robert B. Thompson; J. Odom; W.N. Bell


Acta Haematologica | 1965

The sickling phenomenon in a white male without Hb-S.

Robert B. Thompson; P.J. Rau; J. Odom; W.N. Bell


Acta Haematologica | 1964

Three Inherited Intra-Erythrocytic Defects: Hereditary Spherocytosis, Hb S and Hb C

Robert B. Thompson; Mason G. Robertson


Acta Haematologica | 1966

A New Thalassemic Syndrome: Homozygous Hemoglobin S Disease Delta Thalassemia

Robert B. Thompson; B.H. Hewett; E. Ard; J. Odom; W.N. Bell

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W.N. Bell

University of Mississippi Medical Center

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J. Odom

University of Mississippi Medical Center

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E. Ard

University of Mississippi Medical Center

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R. Warrington

University of Mississippi Medical Center

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B.H. Hewett

University of Mississippi Medical Center

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C.G. Jenkins

University of Mississippi Medical Center

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Mason G. Robertson

University of Mississippi Medical Center

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P.J. Rau

University of Mississippi Medical Center

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Paul J. Rau

University of Mississippi Medical Center

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Robert W. Mayo

University of Mississippi Medical Center

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