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Hemoglobin is a peer-reviewed journal published by Taylor & Francis, covering Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Hemoglobin structure and function.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Hemoglobin 12 (3): 45–58.
Formats any DOI in Hemoglobin style. No sign-up. |
| Publishes research in | Hemoglobinopathies and Related Disorders Iron Metabolism and Disorders Hemoglobin structure and function Blood groups and transfusion Erythrocyte Function and Pathophysiology |
| ISSN | 0363-0269 |
| Citation impact (2-yr) | 0.76 |
| h-index | 60 |
| i10-index | 1,226 |
| Total citations | 37,492 |
| Top institutions publishing here | Augusta University |
| Journal website | www.tandfonline.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
We describe a rapid procedure for constructing cloned human genomic libraries from small amounts of peripheral blood. High molecular weight DNA is isolated from 5-20 ml peripheral blood, partially cleaved with Eco R1, and 8-22 kb fragments are cloned using bacteriophage Charon 4A and suitable E. coli host. Using the approach we have isolated and…
Cet article etudie successivement la frequence de la thalassemie α, de la thalassemie β, des variants genetiques de la chaine α et de la chaine β, de l'hemoglobine constant spring et de l'HbE
This chromatographic procedure uses DEAE-cellulose as ion exchanger and glycine-KCN-NaC1 solutions as developers. Blood samples from several adults and newborn infants with alpha, beta, delta, or gamma chains variants have been analysed. The hemoglobins are eluted as compact and symmetrical zones, and the separation of many hemoglobin types is greatly improved. The procedure is relatively…
Zinc (Zn), copper (Cu) and iron (Fe) are essential minerals that are required for a variety of biomolecules to maintain the normal structure, function, and proliferation of cells. These metals can be toxic in excessive amounts, especially in certain genetic disorders. The homeostasis of these trace elements results from a tightly coordinated regulation by different…
AbstractThalassemia (thal) and hemoglobinopathies are widespread, recessive inherited diseases. Approximately 250 million people (4.5% of the world population) carry abnormal hemoglobin (Hb) genes. Southeast Asia consists of 10 countries, i.e. Brunei, Cambodia, Indonesia, Laos, Malaysia, Myanmar, the Philippines, Singapore, Thailand, and Vietnam, with a total population of more than 400 million. In most of these…
