The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
The RET Proto-Oncogene in Multiple Endocrine Neoplasia Type 2 and Hirschsprung's Disease
Abstract
Recent years have brought major advances in our understanding of the molecular genetic basis of both types of multiple endocrine neoplasia (MEN), an autosomal dominant cancer syndrome. MEN type 1 (MEN-1 [designated “MEN 1” by the Second International MEN Workshop]) is the triad of parathyroid, pancreatic islet-cell, and anterior pituitary tumors.1 Carcinoid, adrenal cortical, and lipoid tumors may also occur in MEN-1. Its susceptibility gene has been mapped but not isolated, and in some kindreds polymorphic markers that flank the gene can be used for predictive DNA testing.2 MEN type 2 (MEN-2) is a syndrome of medullary thyroid carcinoma, pheochromocytoma, . . .
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Cites
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Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene
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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
Mulligan, L. M., Kwok, J. B. J., Healey, C. S., Elsdon, M. J., Eng, C., Gardner, E., Love, D. R., Mole, S. E., Moore, J. K., Papi, L., et al. (1993) · Nature · doi:10.1038/363458a0 · Cited by 1,966
Self-citationDefects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
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Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
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Self-citationA missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's disease
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Cited by
The diagnosis and medical management of advanced neuroendocrine tumors.
Kaltsas, G. A., Besser, G. M., & Grossman, A. B. (2004) · Endocrine Reviews · doi:10.1210/er.2003-0014 · Cited by 674
Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma
Pacak, K., Linehan, W. M., Eisenhofer, G., Walther, M. M., & Goldstein, D. S. (2001) · Annals of Internal Medicine · doi:10.7326/0003-4819-134-4-200102200-00016 · Cited by 618
AACE/AAES MEDICAL/SURGICAL Guidelines for Clinical Practice: Management of Thyroid Carcinoma
Cobin, R. H., Gharib, H., Bergman, D. A., Clark, O. H., Cooper, D. S., Daniels, G. H., Dickey, R. A., Duick, D. S., Garber, J. R., Hay, I. D., et al. (2001) · Endocrine Practice · doi:10.4158/ep.7.3.202 · Cited by 365
Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma
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Metadata
- Authors
- Eng, C.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1996-09-26
- Volume
- 335
- Issue
- 13
- Pages
- 943-951
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2341242206
- Cited by
- 328
- References
- 53
- FWCI
- 30.00
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
