The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Sickle-Cell Anemia: Molecular and Cellular Bases of Therapeutic Approaches: (First of Three Parts)
Abstract
THE term "molecular disease" was coined almost 30 years ago by Linus Pauling and his associates to describe their analysis of the abnormality in sickle-cell anemia.1 Since that time tremendous progress has been made in the understanding of the structure and function of this mutant hemoglobin molecule and the conditions under which it aggregates when deoxygenated to form a gel. Indeed, in the last decade, particularly in the last few years, there has been an explosive growth in knowledge of the structure of the gel of sickle hemoglobin and the mechanism of its formation. The exact relations among gelation, sickling . . .
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Citations
Cites
Sickle Cell Anemia, a Molecular Disease
Pauling, L., Itano, H. A., Singer, S. J., & Wells, I. C. (1949) · Science · doi:10.1126/science.110.2865.543 · Cited by 2,319
A Specific Chemical Difference Between the Globins of Normal Human and Sickle-Cell Anæmia Hæmoglobin
INGRAM, V. M. (1956) · Nature · doi:10.1038/178792a0 · Cited by 896
Analysis of non-ideal behavior in concentrated hemoglobin solutions
Ross, P. D., & Minton, A. P. (1977) · Journal of Molecular Biology · doi:10.1016/s0022-2836(77)80191-5 · Cited by 275
Cited by
Riess, J. G. (2001) · Chemical Reviews · doi:10.1021/cr970143c · Cited by 773
Hemoglobin S gelation and sickle cell disease
Eaton, W., & Hofrichter, J. (1987) · Blood · doi:10.1182/blood.v70.5.1245.1245 · Cited by 425
Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?
Powars, D., Weiss, J., Chan, L., & Schroeder, W. (1984) · Blood · doi:10.1182/blood.v63.4.921.921 · Cited by 314
Brittenham, G., Schechter, A., & Noguchi, C. (1985) · Blood · doi:10.1182/blood.v65.1.183.183 · Cited by 197
Self-citation
Metadata
- Authors
- Dean, J., & Schechter, A. N.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1978-10-05
- Volume
- 299
- Issue
- 14
- Pages
- 752-763
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2072295347
- Cited by
- 237
- References
- 3
- FWCI
- 13.04
- Type
- journal article
- Language
- en
- Open access
- closed
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- Dean, J., & Schechter, A. N. (1978). Sickle-Cell Anemia: Molecular and Cellular Bases of Therapeutic Approaches: (First of Three Parts). New England Journal of Medicine. https://doi.org/10.1056/nejm197810052991405
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
