The DOI matches its Crossref record; 142 of the 143 references it cites were found in a registry or an index.
Hemoglobin S gelation and sickle cell disease
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“The rate and extent of polymerization is modified by the erythrocyte HbF concentration. 2”
From Fetal hemoglobin in sickle cell anemia (2020) · cites this paper as [2]
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Citations
Cites
ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL.
Monod, J., Wyman, J., & Changeux, J. (1965) · Journal of Molecular Biology · doi:10.1016/s0022-2836(65)80285-6 · Cited by 7,681
Krogh, A. (1919) · The Journal of Physiology · doi:10.1113/jphysiol.1919.sp001839 · Cited by 1,433
Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.
Platt, O., Orkin, S. H., Dover, G., Beardsley, G. P., Miller, B. A., & Nathan, D. G. (1984) · Journal of Clinical Investigation · doi:10.1172/jci111464 · Cited by 532
Hofrichter, J., Ross, P. D., & Eaton, W. A. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.12.4864 · Cited by 520
Self-citationErythrocyte Adherence to Endothelium in Sickle-Cell Anemia
Hebbel, R. P., Boogaerts, M., Eaton, J. W., & Steinberg, M. H. (1980) · New England Journal of Medicine · doi:10.1056/nejm198005013021803 · Cited by 518
Kinetics of sickle hemoglobin polymerization
Ferrone, F. A., Hofrichter, J., & Eaton, W. A. (1985) · Journal of Molecular Biology · doi:10.1016/0022-2836(85)90175-5 · Cited by 505
Self-citationAbnormal Adherence of Sickle Erythrocytes to Cultured Vascular Endothelium
Hebbel, R. P., Yamada, O., Moldow, C. F., Jacob, H. S., White, J. G., & Eaton, J. W. (1980) · Journal of Clinical Investigation · doi:10.1172/jci109646 · Cited by 421
Abnormal rheology of oxygenated blood in sickle cell anemia
Chien, S., Usami, S., & Bertles, J. F. (1970) · Journal of Clinical Investigation · doi:10.1172/jci106273 · Cited by 358
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
Hemoglobin as a receptor of drugs and peptides: x-ray studies of the stereochemistry of binding
Perutz, M. F., Fermi, G., Abraham, D. J., Poyart, C., & Bursaux, E. (1986) · Journal of the American Chemical Society · doi:10.1021/ja00265a036 · Cited by 299
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Effects of Inhaled Nitric Oxide on Blood Elements: A Novel Therapy for Sickle Cell Disease
Head, C. A. (1999) · Respiratory Care · doi:10.1177/002013249904400306
New therapeutic strategies for the treatment of β-hemoglobinopathies
Weber, L. (2018) · theses.fr (ABES) · doi:10.70675/09314463zdfd1z46b4z9c0cz32c6c2c5ccc2
Lalanne‐Mistrih, M. (2019) · theses.fr (ABES) · doi:10.70675/aa735006z75a2z4c63zaa8cz82d11d170a47
Immunogénétique en drépanocytose
Tozatto‐Maio, K. (2019) · theses.fr (ABES) · doi:10.70675/92d0b87bz2afdz446dza5bdze7321b6555d7
Modulation et rôle des paramètres hémorhéologiques dans la physiopathologie de la drépanocytose
Griffon, C. (2018) · theses.fr (ABES) · doi:10.70675/ad2b1266zad9fz4070z9fd7z1abcbdd2b38f
Stauffer, É. (2021) · doi:10.70675/65143700zc6e4z45e0z8273z3a91bb022450
Cellular pathogenesis of HbSC disease
Gibson, J. S., Wadud, R., Ding, P., Rees, D. C., Brewin, J. N., & CONNOLLY, K. M. (2026) · Seminars in Hematology · doi:10.1053/j.seminhematol.2026.05.002
The Journey of Gene Therapy in Sickle Cell Disease: How Molecular Advances Meet Clinical Care
Tardif, M., Saby, M., Forté, S., & Pincez, T. (2026) · Cells · doi:10.3390/cells15100939
Perspective Chapter: Fetal Hemoglobin Modulators
Walke, V. A. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1017037
Gene therapy for hereditary hematological disorders: From clinical breakthroughs to future horizons
Chen, Z., Wang, W., Wu, Y., Qiang, Y., Cheng, W., & Liu, F. (2026) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2026.103075
Endothelin receptor antagonism in sickle cell disease: Is the time now?
Kane, B. J., Derebail, V. K., & Kasztan, M. (2026) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2026-0168
OKONJI, K. S., Daramola, A. O., Folaranmi, O. E., & Alade, O. T. (2026) · World Scientific News · doi:10.65770/fpyd6165
BindingDB (2012) · UC San Diego · doi:10.7270/q23f4qgh
Metadata
- Authors
- Eaton, W., & Hofrichter, J.
- Affiliations
- National Institutes of Health (US)
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 1987-11-01
- Volume
- 70
- Issue
- 5
- Pages
- 1245-1266
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1919238100
- Cited by
- 425
- References
- 143
- Citations by year
- 2026: 10 · 2025: 2 · 2024: 9 · 2023: 13 · 2022: 12 · 2021: 16 · 2020: 11 · 2019: 23 · 2018: 18 · 2017: 16 · 2016: 15 · 2015: 8 · 2014: 8 · 2013: 18 · 2012: 14
- FWCI
- 12.91
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Hemoglobin structure and function
- Health Sciences › Medicine › Hematology › Blood properties and coagulation
- Keywords
- hemoglobin S, sickle cell disease, hemoglobin polymerization, vaso-occlusive crisis
- MeSH terms
- Anemia, Sickle Cell, Gels, Hemoglobin, Sickle, Humans, Oxyhemoglobins, Protein Conformation
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