(Q47732892)

English

Haemoglobin Constant Spring--a chain termination mutant?

scientific article published in December 1971

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

Haemoglobin Constant Spring--a chain termination mutant? (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

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Milner PF

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

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Clegg JB

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

Weatherall DJ

2

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

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publication date

1 December 1971

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

234

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

5328

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

337-340

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Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

Abnormal Haemoglobins and the Genetic Code

1 reference

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Hemoglobin Gun Hill: deletion of five amino acid residues and impaired heme-globin binding

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Hemoglobin Freiburg: abnormal hemoglobin due to deletion of a single amino acid residue

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The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion

1 reference

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New hemoglobin possessing a higher electrophoretic mobility than normal adult hemoglobin

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Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)

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Hæmoglobin H Disease in Thailand: a Genetical Study

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The haemoglobin constitution of infants with the haemoglobin Bart's hydrops foetalis syndrome

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Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain

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The pattern of disordered haemoglobin synthesis in homozygous and heterozygous beta-thalassaemia

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Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok)

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Preparation of polymeric protein markers and an investigation of their behavior in sodium dodecyl sulfate-polyacrylamide gel electrophoresis

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STUDIES ON HEMOGLOBIN BIOSYNTHESIS: ASYNCHRONOUS SYNTHESIS OF HEMOGLOBIN A AND HEMOGLOBIN A2 BY ERYTHROCYTE PRECURSORS

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Haemoglobin Synthesis in β-Thalassaemia

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Unbalanced globin chain synthesis in alpha-thalassemia heterozygotes

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Silent hemoglobin alpha genes in apes: potential source of thalassemia

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Haemoglobin Tak: a variant with additional residues at the end of the beta-chains

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Unexpectedly large size of globin messenger ribonucleic acid

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Release, identification, and isolation of messenger RNA from mammalian ribosomes

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Homozygous Hb J Tongariki: Evidence for Only One Alpha Chain Structural Locus in Melanesians

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Alpha- and beta-thalassemia in Thailand

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Identifiers

10.1038/234337A0

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/4944483

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