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Hemoglobin M

A group of abnormal hemoglobins in which amino acid substitutions take place in either the alpha or beta chains but near the heme iron. This results in facilitated oxidation of the hemoglobin to yield excess methemoglobin which leads to cyanosis.
Also Known As:
M, Hemoglobin
Networked: 18 relevant articles (2 outcomes, 1 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Magalhães Maia, Tabita: 1 article (03/2013)
2. Bento, Celeste: 1 article (03/2013)
3. Relvas, Luis: 1 article (03/2013)
4. Carvalhais, Ines: 1 article (03/2013)
5. Pereira, Alexandra: 1 article (03/2013)
6. Farela Neves, José: 1 article (03/2013)
7. Moita, Filipa: 1 article (03/2013)
8. Ribeiro, Maria L: 1 article (03/2013)
9. Abreu, Gabriela: 1 article (03/2013)
10. Banerjee, Arnab: 1 article (06/2008)

Related Diseases

1. Methemoglobinemia
2. Cyanosis
3. Anoxia (Hypoxia)

Related Drugs and Biologics

1. Methylene Blue (Methylthioninium Chloride)
2. Cytochrome-B(5) Reductase (Methemoglobin Reductase)
3. Methemoglobin
4. Hemoglobins (Hemoglobin)
5. beta-Globins (beta Globin)
6. Cytochromes b5 (Cytochrome b5)
7. Dinoprost
8. Oxidoreductases
9. Globins