The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Telomeres in T and B cells
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Citations
Cites
Specific Association of Human Telomerase Activity with Immortal Cells and Cancer
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“It was proposed initially that telomerase is expressed in germ-line cells — for which the maintenance of telomeres is crucial to fertility — and in transformed cells that are immortalized or have unlimited growth capacity, but not in normal somatic cell”
BackgroundTelomeres shorten during ageing of human fibroblasts
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Extension of Life-Span by Introduction of Telomerase into Normal Human Cells
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The RNA Component of Human Telomerase
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Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
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Essential role of mouse telomerase in highly proliferative organs
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“However, the breeding of successive generations of telomerase-deficient mice results in the progressive shortening of telomeres and, eventually (after ∼5–6 generations), both males and females are sterile, apparently owing to replicative failure and the increased apoptosis of germ-line cell”
BackgroundHemann, M. T., Strong, M. A., Hao, L.-Y., & Greider, C. W. (2001) · Cell · doi:10.1016/s0092-8674(01)00504-9 · Cited by 1,219
Control of telomere length by the human telomeric protein TRF1
van Steensel, B., & de Lange, T. (1997) · Nature · doi:10.1038/385740a0 · Cited by 1,219
Evidence for a mitotic clock in human hematopoietic stem cells: loss of telomeric DNA with age.
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p53- and ATM-Dependent Apoptosis Induced by Telomeres Lacking TRF2
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Pot1, the Putative Telomere End-Binding Protein in Fission Yeast and Humans
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The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
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Protection of mammalian telomeres
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Activation of telomerase in human lymphocytes and hematopoietic progenitor cells
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“This has been shown most extensively for lymphocyte”
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Telomerase Activity in Hematopoietic Cells Is Associated with Self-Renewal Potential
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T Cell Telomere Length in HIV-1 Infection: No Evidence for Increased CD4 + T Cell Turnover
Wolthers, K. C., Bea, G., Wisman, A., Otto, S. A., de Roda Husman, A.-M., Schaft, N., de Wolf, F., Goudsmit, J., Coutinho, R. A., van der Zee, A. G. J., et al. (1996) · Science · doi:10.1126/science.274.5292.1543 · Cited by 286
Impaired germinal center reaction in mice with short telomeres
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Self-citationDifferential regulation of CD8+ T cell senescence in mice and men
Akbar, A. N., Soares, M. V. D., Plunkett, F. J., & Salmon, M. (2001) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(00)00198-6 · Cited by 46
Cited by
Accelerated telomere shortening in response to life stress
Epel, E. S., Blackburn, E. H., Lin, J., Dhabhar, F. S., Adler, N. E., Morrow, J. D., & Cawthon, R. M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407162101 · Cited by 3,002
Aubert, G., & Lansdorp, P. M. (2008) · Physiological Reviews · doi:10.1152/physrev.00026.2007 · Cited by 1,188
Chan, S. R. W. L., & Blackburn, E. H. (2004) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2003.1370 · Cited by 595
Are senescence and exhaustion intertwined or unrelated processes that compromise immunity?
Akbar, A. N., & Henson, S. M. (2011) · Nature Reviews Immunology · doi:10.1038/nri2959 · Cited by 474
Human immunosenescence: is it infectious?
Pawelec, G., Akbar, A., Caruso, C., Solana, R., Grubeck‐Loebenstein, B., & Wikby, A. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00271.x · Cited by 405
Metadata
- Authors
- Hodes, R. J., Hathcock, K. S., & Weng, N.-P.
- Venue
- Nature Reviews Immunology
- Published
- 2002-09
- Volume
- 2
- Issue
- 9
- Pages
- 699-706
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W2093808264
- Cited by
- 309
- References
- 26
- FWCI
- 1.16
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
