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Items: 1 to 20 of 104

1.

Association of SNP rs1867277 in FOXE1 Gene and Cleft Lip with or without Cleft Palate in a Han Chinese Population.

Xie L, Deng Y, Yuan Y, Tan X, Liu L, Li N, Deng C, Liu H, Dai L.

Fetal Pediatr Pathol. 2018 Apr;37(2):89-94. doi: 10.1080/15513815.2018.1424278. Epub 2018 Mar 6.

PMID:
29509083
2.

WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion.

Huynh MT, Boudry-Labis E, Duban B, Andrieux J, Tran CT, Tampere H, Ceraso D, Manouvrier S, Tachdjian G, Roche-Lestienne C, Vincent-Delorme C.

Am J Med Genet A. 2017 Jun;173(6):1690-1693. doi: 10.1002/ajmg.a.38206. Epub 2017 Apr 11.

PMID:
28398607
3.

Genotype Analyses in the Japanese and Belarusian Populations Reveal Independent Effects of rs965513 and rs1867277 but Do Not Support the Role of FOXE1 Polyalanine Tract Length in Conferring Risk for Papillary Thyroid Carcinoma.

Nikitski AV, Rogounovitch TI, Bychkov A, Takahashi M, Yoshiura KI, Mitsutake N, Kawaguchi T, Matsuse M, Drozd VM, Demidchik Y, Nishihara E, Hirokawa M, Miyauchi A, Rubanovich AV, Matsuda F, Yamashita S, Saenko VA.

Thyroid. 2017 Feb;27(2):224-235. doi: 10.1089/thy.2015.0541. Epub 2016 Dec 15.

PMID:
27824288
4.

Profiling analysis of FOX gene family members identified FOXE1 as potential regulator of NSCLC development.

Ji GH, Cui Y, Yu H, Cui XB.

Cell Mol Biol (Noisy-le-grand). 2016 Sep 30;62(11):57-62.

PMID:
27755953
5.

FOXE1 Polymorphism Interacts with Dietary Iodine Intake in Differentiated Thyroid Cancer Risk in the Cuban Population.

Ren Y, Lence-Anta JJ, Pereda CM, Chappe M, Velasco M, Infante I, Bustillo M, Turcios S, Leufroy A, Guérin T, Noël L, Lesueur F, Maillard S, Cléro E, Xhaard C, Allodji RS, Rubino C, Rodriguez R, Ortiz RM, de Vathaire F.

Thyroid. 2016 Dec;26(12):1752-1760. Epub 2016 Oct 27.

PMID:
27610545
6.

Genetic variation of FOXE1 and risk for orofacial clefts in a California population.

Lammer EJ, Mohammed N, Iovannisci DM, Ma C, Lidral AC, Shaw GM.

Am J Med Genet A. 2016 Nov;170(11):2770-2776. doi: 10.1002/ajmg.a.37871. Epub 2016 Sep 8.

PMID:
27604706
7.

Association of FOXE1 polyalanine repeat region with thyroid cancer is dependent on tumour size.

Raimundo J, Alvelos MI, Azevedo T, Martins T, Rodrigues FJ, Lemos MC.

Clin Endocrinol (Oxf). 2017 Feb;86(2):243-246. doi: 10.1111/cen.13166. Epub 2016 Aug 22.

PMID:
27474100
8.

Aberrant Methylation of FOXE1 Contributes to a Poor Prognosis for Patients with Colorectal Cancer.

Sugimachi K, Matsumura T, Shimamura T, Hirata H, Uchi R, Ueda M, Sakimura S, Iguchi T, Eguchi H, Masuda T, Morita K, Takenaka K, Maehara Y, Mori M, Mimori K.

Ann Surg Oncol. 2016 Nov;23(12):3948-3955. Epub 2016 Jun 6.

PMID:
27271927
9.

rs965513 polymorphism as a common risk marker is associated with papillary thyroid cancer.

Wang F, Yan D, Ji X, Han J, Chen M, Qiao H, Zhang S.

Oncotarget. 2016 Jul 5;7(27):41336-41345. doi: 10.18632/oncotarget.9324.

10.

FOXE1 polymorphisms and non-syndromic orofacial cleft susceptibility in a Chinese Han population.

Yin X, Zhang H, Zhu Z, Wang H, Du Y, Li S, Zhang Z, Fan W, Pan Y.

Oral Dis. 2016 May;22(4):274-9. doi: 10.1111/odi.12435. Epub 2016 Jan 20.

PMID:
26728781
11.

The investigation of foxe1 variations in papillary thyroid carcinoma.

Somuncu E, Karatas A, Ferahman S, Saygili N, Yilmaz E, Ozturk O, Kapan M.

Int J Clin Exp Pathol. 2015 Oct 1;8(10):13458-64. eCollection 2015.

12.

Association between FOXE1 and non-syndromic orofacial clefts in a northeastern Chinese population.

Liu K, Lu Y, Ai L, Jiao B, Yu J, Zhang B, Liu Q.

Br J Oral Maxillofac Surg. 2015 Oct;53(8):705-10. doi: 10.1016/j.bjoms.2015.05.021. Epub 2015 Jun 19.

PMID:
26100861
13.

Somatic Mutations of FOXE1 in Papillary Thyroid Cancer.

Mond M, Bullock M, Yao Y, Clifton-Bligh RJ, Gilfillan C, Fuller PJ.

Thyroid. 2015 Aug;25(8):904-10. doi: 10.1089/thy.2015.0030. Epub 2015 Jun 19.

PMID:
25950909
14.

Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC).

Pereira JS, da Silva JG, Tomaz RA, Pinto AE, Bugalho MJ, Leite V, Cavaco BM.

Endocrine. 2015 May;49(1):204-14. doi: 10.1007/s12020-014-0470-0. Epub 2014 Nov 9.

PMID:
25381600
15.

Common genetic variants on FOXE1 contributes to thyroid cancer susceptibility: evidence based on 16 studies.

Zhuang Y, Wu W, Liu H, Shen W.

Tumour Biol. 2014 Jun;35(6):6159-66. doi: 10.1007/s13277-014-1896-y. Epub 2014 Apr 18.

PMID:
24744143
16.

Role for tissue-dependent methylation differences in the expression of FOXE1 in nontumoral thyroid glands.

Abu-Khudir R, Magne F, Chanoine JP, Deal C, Van Vliet G, Deladoëy J.

J Clin Endocrinol Metab. 2014 Jun;99(6):E1120-9. doi: 10.1210/jc.2013-4414. Epub 2014 Mar 19.

17.

Strong association of variants around FOXE1 and orofacial clefting.

Ludwig KU, Böhmer AC, Rubini M, Mossey PA, Herms S, Nowak S, Reutter H, Alblas MA, Lippke B, Barth S, Paredes-Zenteno M, Muñoz-Jimenez SG, Ortiz-Lopez R, Kreusch T, Hemprich A, Martini M, Braumann B, Jäger A, Pötzsch B, Molloy A, Peterlin B, Hoffmann P, Nöthen MM, Rojas-Martinez A, Knapp M, Steegers-Theunissen RP, Mangold E.

J Dent Res. 2014 Apr;93(4):376-81. doi: 10.1177/0022034514523987. Epub 2014 Feb 21.

PMID:
24563486
18.

Quantitative assessment of common genetic variants on FOXE1 and differentiated thyroid cancer risk.

Zhu H, Xi Q, Liu L, Wang J, Gu M.

PLoS One. 2014 Jan 29;9(1):e87332. doi: 10.1371/journal.pone.0087332. eCollection 2014.

19.

FOXE1 association with differentiated thyroid cancer and its progression.

Penna-Martinez M, Epp F, Kahles H, Ramos-Lopez E, Hinsch N, Hansmann ML, Selkinski I, Grünwald F, Holzer K, Bechstein WO, Zeuzem S, Vorländer C, Badenhoop K.

Thyroid. 2014 May;24(5):845-51. doi: 10.1089/thy.2013.0274. Epub 2014 Jan 29.

20.

FOXE1 mutations in Thai patients with oral clefts.

Srichomthong C, Ittiwut R, Siriwan P, Suphapeetiporn K, Shotelersuk V.

Genet Res (Camb). 2013 Oct;95(5):133-7. doi: 10.1017/S0016672313000177. Epub 2013 Nov 20.

PMID:
24252547

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