The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Permanent correction of an inherited ectodermal dysplasia with recombinant EDA
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Gene defect in ectodermal dysplasia implicates a death domain adapter in development
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Clinical aspects of X-linked hypohidrotic ectodermal dysplasia.
Clarke, A., Phillips, D. I., Brown, R., & Harper, P. S. (1987) · Archives of Disease in Childhood · doi:10.1136/adc.62.10.989 · Cited by 274
Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis.
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Cited by
The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond
Dostert, C., Grusdat, M., Letellier, E., & Brenner, D. (2019) · Physiological Reviews · doi:10.1152/physrev.00045.2017 · Cited by 498
Making a tooth: growth factors, transcription factors, and stem cells
ZHANG, Y. D., CHEN, Z., SONG, Y. Q., LIU, C., & CHEN, Y. P. (2005) · Cell Research · doi:10.1038/sj.cr.7290299 · Cited by 313
Ectodysplasin signaling in development.
Mikkola, M. L., & Thesleff, I. (2003) · Cytokine & Growth Factor Reviews · doi:10.1016/s1359-6101(03)00020-0 · Cited by 217
Generation of the primary hair follicle pattern.
Mou, C., Jackson, B., Schneider, P., Overbeek, P. A., & Headon, D. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600825103 · Cited by 206
Self-citationEctodermal dysplasias: Clinical and molecular review
Visinoni, Á. F., Lisboa‐Costa, T., Pagnan, N. A. B., & Chautard‐Freire‐Maia, E. A. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32864 · Cited by 181
Metadata
- Authors
- Gaide, O., & Schneider, P.
- Venue
- Nature Medicine
- Published
- 2003-04-07
- Volume
- 9
- Issue
- 5
- Pages
- 614-618
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W2058225094
- Cited by
- 211
- References
- 5
- FWCI
- 3.86
- Type
- journal article
- Language
- en
- Open access
- green
- Licence
- www.springer.com/tdm (tdm)
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