Similar articles for PMID: 16979782

Year	Number of Results
1996	1
1997	2
2002	1
2003	2
2004	1
2005	5
2006	11
2007	6
2008	4
2010	2
2011	1
2013	2
2014	3
2016	1
2017	1
2018	4
2019	2
2020	7
2024	0

1

Current concepts in RET-related genetics, signaling and therapeutics.

Plaza-Menacho I, Burzynski GM, de Groot JW, Eggen BJ, Hofstra RM. Plaza-Menacho I, et al. Trends Genet. 2006 Nov;22(11):627-36. doi: 10.1016/j.tig.2006.09.005. Epub 2006 Sep 18. Trends Genet. 2006. PMID: 16979782 Review.

2

RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors.

de Groot JW, Links TP, Plukker JT, Lips CJ, Hofstra RM. de Groot JW, et al. Endocr Rev. 2006 Aug;27(5):535-60. doi: 10.1210/er.2006-0017. Epub 2006 Jul 18. Endocr Rev. 2006. PMID: 16849421 Review.

3

RET receptor signaling: dysfunction in thyroid cancer and Hirschsprung's disease.

Asai N, Jijiwa M, Enomoto A, Kawai K, Maeda K, Ichiahara M, Murakumo Y, Takahashi M. Asai N, et al. Pathol Int. 2006 Apr;56(4):164-72. doi: 10.1111/j.1440-1827.2006.01942.x. Pathol Int. 2006. PMID: 16634961 Review.

4

[Thyroid carcinomas and Hirschsprung's disease--10-year experience with molecular genetic testing of the RET proto-oncogene].

Bendlová B, Dvoráková S, Václavíková E, Sýkorová V, Vlcek P, Skába R. Bendlová B, et al. Vnitr Lek. 2006 Oct;52(10):926-34. Vnitr Lek. 2006. PMID: 17063805 Review. Czech.

5

[Neural crest and multiple endocrinopathies].

Pasini A, Michiels FM, Chappuis-Flament S, Geneste O, Rossel M, Fournier L, Feunteun J, Lenoir G, Schuffenecker I, Billaud M. Pasini A, et al. C R Seances Soc Biol Fil. 1996;190(5-6):557-67. C R Seances Soc Biol Fil. 1996. PMID: 9074721 Review. French.

6

Neurotrophic factor receptor RET: structure, cell biology, and inherited diseases.

Runeberg-Roos P, Saarma M. Runeberg-Roos P, et al. Ann Med. 2007;39(8):572-80. doi: 10.1080/07853890701646256. Ann Med. 2007. PMID: 17934909 Review.

7

A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease.

Dvoráková S, Dvoráková K, Malíková M, Skába R, Vlcek P, Bendlová B. Dvoráková S, et al. J Pediatr Surg. 2005 Jun;40(6):e1-6. doi: 10.1016/j.jpedsurg.2005.03.031. J Pediatr Surg. 2005. PMID: 15991157

8

RET proto-oncogene testing in infants presenting with Hirschsprung disease identifies 2 new multiple endocrine neoplasia 2A kindreds.

Fialkowski EA, DeBenedetti MK, Moley JF, Bachrach B. Fialkowski EA, et al. J Pediatr Surg. 2008 Jan;43(1):188-90. doi: 10.1016/j.jpedsurg.2007.09.043. J Pediatr Surg. 2008. PMID: 18206480

9

Evaluation of the role of RET polymorphisms/haplotypes as modifier loci for MEN 2, and analysis of the correlation with the type of RET mutation in a series of Spanish patients.

Fernández RM, Navarro E, Antiñolo G, Ruiz-Ferrer M, Borrego S. Fernández RM, et al. Int J Mol Med. 2006 Apr;17(4):575-81. Int J Mol Med. 2006. PMID: 16525712

10

The Y606C RET mutation causes a receptor gain of function.

Ercolino T, Lombardi A, Becherini L, Piscitelli E, Cantini G, Gaglianò MS, Serio M, Luconi M, Mannelli M. Ercolino T, et al. Clin Endocrinol (Oxf). 2008 Aug;69(2):253-8. doi: 10.1111/j.1365-2265.2008.03197.x. Epub 2008 Jan 31. Clin Endocrinol (Oxf). 2008. PMID: 18248647

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