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Results: 1 to 20 of 171

1.

Detection of mutations in RET proto-oncogene codon 634 through double tandem hybridization.

Maldonado-Rodríguez R, Espinosa-Lara M, Barrera-León O, Colin-Tovar C, González-Yebra B, Salcedo-Vargas M, Santiago-Hernández JC, Méndez-Tenorio A, Beattie KL.

Mol Biotechnol. 2003 Oct;25(2):113-29.

PMID:
14526122
[PubMed - indexed for MEDLINE]
2.

Hybridization of glass-tethered oligonucleotide probes to target strands preannealed with labeled auxiliary oligonucleotides.

Maldonado-Rodriguez R, Espinosa-Lara M, Calixto-Suárez A, Beattie WG, Beattie KL.

Mol Biotechnol. 1999 Feb;11(1):1-12.

PMID:
10367278
[PubMed - indexed for MEDLINE]
3.

Occurrence of the Cys611Tyr mutation and a novel Arg886Trp substitution in the RET proto-oncogene in multiple endocrine neoplasia type 2 families and sporadic medullary thyroid carcinoma cases originating from the central region of Portugal.

Prazeres HJ, Rodrigues F, Figueiredo P, Naidenov P, Soares P, Bugalho MJ, Lacerda M, Campos B, Martins TC.

Clin Endocrinol (Oxf). 2006 Jun;64(6):659-66.

PMID:
16712668
[PubMed - indexed for MEDLINE]
4.

Low density DNA microarray for detection of most frequent TP53 missense point mutations.

Rangel-López A, Maldonado-Rodríguez R, Salcedo-Vargas M, Espinosa-Lara JM, Méndez-Tenorio A, Beattie KL.

BMC Biotechnol. 2005 Feb 15;5:8.

PMID:
15713227
[PubMed - indexed for MEDLINE]
Free PMC Article
5.
6.

Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung's disease.

Nishikawa M, Murakumo Y, Imai T, Kawai K, Nagaya M, Funahashi H, Nakao A, Takahashi M.

Eur J Hum Genet. 2003 May;11(5):364-8.

PMID:
12734540
[PubMed - indexed for MEDLINE]
Free Article
7.

[Management of multiple endocrine neoplasia syndrome type 2 families in association with rare germline mutations of the RET proto-oncogene].

Fitze G, Saeger HD, Roesner D, Schackert HK.

Klin Padiatr. 2004 Sep-Oct;216(5):270-6. German.

PMID:
15455293
[PubMed - indexed for MEDLINE]
8.

Somatic trinucleotide change encompassing codons 882 and 883 of the RET proto-oncogene in a patient with sporadic medullary thyroid carcinoma.

Bugalho MJ, Coelho I, Sobrinho LG.

Eur J Endocrinol. 2000 Jun;142(6):573-5.

PMID:
10822219
[PubMed - indexed for MEDLINE]
Free Article
9.

[Association of deletions of the RET proto-oncogene wtih aggressive course of sporatic C-cell carcinoma].

Musholt PB, Musholt TJ, Moley JF, Scheumann GF.

Langenbecks Arch Chir Suppl Kongressbd. 1998;115(Suppl I):261-5. German.

PMID:
14518256
[PubMed - indexed for MEDLINE]
10.

Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.

Moore SW, Appfelstaedt J, Zaahl MG.

J Pediatr Surg. 2007 Feb;42(2):326-32.

PMID:
17270543
[PubMed - indexed for MEDLINE]
11.

New presentation of familial medullary thyroid carcinoma in 87-year-old patient with high-risk RET proto-oncogene codon 620 mutation.

Jaggard MK, MacRae C, Ifeacho S, Robinson S, Tolley NS.

J Laryngol Otol. 2009 Jul;123(7):796-800. doi: 10.1017/S0022215108003472. Epub 2008 Sep 4. Review.

PMID:
18771606
[PubMed - indexed for MEDLINE]
12.

Study of the RET gene and his implication in thyroid cancer: Morocco case family.

Ainahi A, Kebbou M, Timinouni M, Benabdeljalil N, Fechtali T, Oufara S, El Antri S.

Indian J Cancer. 2006 Jul-Sep;43(3):122-6.

PMID:
17065770
[PubMed - indexed for MEDLINE]
Free Article
13.

Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations.

Machens A, Holzhausen HJ, Thanh PN, Dralle H.

Surgery. 2003 Sep;134(3):425-31.

PMID:
14555929
[PubMed - indexed for MEDLINE]
14.

An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma.

Cordella D, Muzza M, Alberti L, Colombo P, Travaglini P, Beck-Peccoz P, Fugazzola L, Persani L.

Endocr Relat Cancer. 2006 Sep;13(3):945-53.

PMID:
16954442
[PubMed - indexed for MEDLINE]
Free Article
15.

Hereditary medullary thyroid cancer in Slovenia--genotype-phenotype correlations.

Bergant D, Hocevar M, Besic N, Glavac D, Korosec B, Caserman S.

Wien Klin Wochenschr. 2006 Jul;118(13-14):411-6.

PMID:
16865646
[PubMed - indexed for MEDLINE]
16.

Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR.

Feriotto G, Ferlini A, Ravani A, Calzolari E, Mischiati C, Bianchi N, Gambari R.

Hum Mutat. 2001;18(1):70-81.

PMID:
11438995
[PubMed - indexed for MEDLINE]
17.

A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening.

Kaldrymides P, Mytakidis N, Anagnostopoulos T, Vassiliou M, Tertipi A, Zahariou M, Rampias T, Koutsodontis G, Konstantopoulou I, Ladopoulou A, Bei T, Yannoukakos D.

Clin Endocrinol (Oxf). 2006 May;64(5):561-6.

PMID:
16649977
[PubMed - indexed for MEDLINE]
18.

Ret proto-oncogene mutations in apparently sporadic Turkish medullary thyroid carcinoma patients: Turkmen study.

Erdogan MF, Gürsoy A, Ozgen G, Cakir M, Bayram F, Ersoy R, Algün E, Cetinarslan B, Cömlekçi A, Kadioglu P, Balci MK, Yetkin I, Kabalak T, Erdogan G.

J Endocrinol Invest. 2005 Oct;28(9):806-9.

PMID:
16370559
[PubMed - indexed for MEDLINE]
19.

RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B.

Zhou Y, Zhao Y, Cui B, Gu L, Zhu S, Li J, Liu J, Yin M, Zhao T, Yin Z, Yu C, Chen C, Wang L, Xiao B, Hong J, Zhang Y, Tang Z, Wang S, Li X, Ning G.

Clin Endocrinol (Oxf). 2007 Oct;67(4):570-6. Epub 2007 Jun 15.

PMID:
17573899
[PubMed - indexed for MEDLINE]
20.

Occurrence of medullary thyroid carcinoma, bronchial carcinoid tumor, and papillary thyroid carcinoma in a family bearing the RET G691S polymorphism.

Rotondi M, Ercolino T, Fonte R, Lagonigro MS, Leporati P, Villani L, La Manna L, Mannelli M, Chiovato L.

J Endocrinol Invest. 2009 Feb;32(2):115-8.

PMID:
19411807
[PubMed - indexed for MEDLINE]

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