The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Paroxysmal Nocturnal Hemoglobinuria: Evidence for Monoclonal Origin of Abnormal Red Cells
Open accessAbstract
Paroxysmal nocturnal hemoglobinuria (PNH) was diagnosed in a 26-year-old Nigerian woman who subsequently died of amebic colitis. The patient’s red cells exhibited mosaicism with respect to glucose 6-phosphate dehydrogenase, in that some of them had the A, and some of them had the B variant of this enzyme (as expected in female subjects heterozygous at this sex-linked locus). The red cells bearing the PNH abnormality only had the B variant, suggesting that they all belonged to a single abnormal clone.
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Citations
Cites
Gene Action in the X-chromosome of the Mouse (Mus musculus L.)
LYON, M. F. (1961) · Nature · doi:10.1038/190372a0 · Cited by 3,978
Beutler, E., Yeh, M., & Fairbanks, V. F. (1962) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.48.1.9 · Cited by 503
Glucose-6-Phosphate Dehydrogenase Mosaicism: Utilization as a Cell Marker in the Study of Leiomyomas
Linder, D., & Gartler, S. M. (1965) · Science · doi:10.1126/science.150.3692.67 · Cited by 395
Davidson, R. G., Nitowsky, H. M., & Childs, B. (1963) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.50.3.481 · Cited by 364
Hereditary Disorders of Erythrocyte Metabolism.
Necheles, T. F. (1968) · Archives of Internal Medicine · doi:10.1001/archinte.1968.00300090087024 · Cited by 193
Paroxysmal Nocturnal Hemoglobinuria
CROSBY, W. H. (1953) · Blood · doi:10.1182/blood.v8.9.769.769 · Cited by 189
Dameshek, W. (1967) · Blood · doi:10.1182/blood.v30.2.251.251 · Cited by 181
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Genetic Tests with a Sex-Linked Marker: Glucose-6-Phosphate DehydrogenasePreprint
Nance, W. E. (1964) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1964.029.01.043 · Cited by 96
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Cited by
Rother, R. P., Rollins, S. A., Mojcik, C. F., Brodsky, R. A., & Bell, L. (2007) · Nature Biotechnology · doi:10.1038/nbt1344 · Cited by 778
Paroxysmal nocturnal hemoglobinuria
Brodsky, R. A. (2014) · Blood · doi:10.1182/blood-2014-02-522128 · Cited by 648
Diseases of complement dysregulation-an overview
Wong, E. K. S., & Kavanagh, D. (2018) · Seminars in Immunopathology · doi:10.1007/s00281-017-0663-8 · Cited by 115
Gargiulo, L., Lastraioli, S., Cerruti, G., Serra, M., Loiacono, F., Zupo, S., Luzzatto, L., & Notaro, R. (2007) · Blood · doi:10.1182/blood-2006-10-052381 · Cited by 56
Self-citation
Metadata
- Authors
- ONI, S. B., OSUNKOYA, B. O., & LUZZATTO, L.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 1970-08-01
- Volume
- 36
- Issue
- 2
- Pages
- 145-152
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1957167758
- Cited by
- 275
- References
- 11
- FWCI
- 2.25
- Type
- journal article
- Language
- en
- Open access
- bronze
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- ONI, S. B., OSUNKOYA, B. O., & LUZZATTO, L. (1970). Paroxysmal Nocturnal Hemoglobinuria: Evidence for Monoclonal Origin of Abnormal Red Cells. Blood. https://doi.org/10.1182/blood.v36.2.145.145
Data sources
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.