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Items: 1 to 20 of 69

1.

PDGFRa mutations in humans with isolated cleft palate.

Rattanasopha S, Tongkobpetch S, Srichomthong C, Siriwan P, Suphapeetiporn K, Shotelersuk V.

Eur J Hum Genet. 2012 Oct;20(10):1058-62. doi: 10.1038/ejhg.2012.55. Epub 2012 Apr 4.

2.

Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site.

Brewster BL, Rossiello F, French JD, Edwards SL, Wong M, Wronski A, Whiley P, Waddell N, Chen X, Bove B; kConFab, Hopper JL, John EM, Andrulis I, Daly M, Volorio S, Bernard L, Peissel B, Manoukian S, Barile M, Pizzamiglio S, Verderio P, Spurdle AB, Radice P, Godwin AK, Southey MC, Brown MA, Peterlongo P.

Hum Mutat. 2012 Dec;33(12):1665-75. doi: 10.1002/humu.22159. Epub 2012 Aug 2.

PMID:
22753153
3.

MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.

Coutinho AM, Oliveira G, Katz C, Feng J, Yan J, Yang C, Marques C, AtaĆ­de A, Miguel TS, Borges L, Almeida J, Correia C, Currais A, Bento C, Mota-Vieira L, Temudo T, Santos M, Maciel P, Sommer SS, Vicente AM.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):475-83.

PMID:
17427193
4.

A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate.

Watanabe A, Akita S, Tin NT, Natsume N, Nakano Y, Niikawa N, Uchiyama T, Yoshiura K.

Cleft Palate Craniofac J. 2006 May;43(3):310-6.

PMID:
16681403
5.

MiR-196a binding-site SNP regulates RAP1A expression contributing to esophageal squamous cell carcinoma risk and metastasis.

Wang K, Li J, Guo H, Xu X, Xiong G, Guan X, Liu B, Li J, Chen X, Yang K, Bai Y.

Carcinogenesis. 2012 Nov;33(11):2147-54. doi: 10.1093/carcin/bgs259. Epub 2012 Aug 1.

PMID:
22859270
6.

Biological and epidemiological evidence of interaction of infant genotypes at Rs7205289 and maternal passive smoking in cleft palate.

Li L, Zhu GQ, Meng T, Shi JY, Wu J, Xu X, Shi B.

Am J Med Genet A. 2011 Dec;155A(12):2940-8. doi: 10.1002/ajmg.a.34254. Epub 2011 Oct 19.

PMID:
22012839
7.

A systematic analysis of the 3'UTR of HNF4A mRNA reveals an interplay of regulatory elements including miRNA target sites.

Wirsing A, Senkel S, Klein-Hitpass L, Ryffel GU.

PLoS One. 2011;6(11):e27438. doi: 10.1371/journal.pone.0027438. Epub 2011 Nov 30.

8.

Post-transcriptional regulation of Transforming Growth Factor Beta-1 by microRNA-744.

Martin J, Jenkins RH, Bennagi R, Krupa A, Phillips AO, Bowen T, Fraser DJ.

PLoS One. 2011;6(10):e25044. doi: 10.1371/journal.pone.0025044. Epub 2011 Oct 4.

9.

The chicken miR-150 targets the avian orthologue of the functional zebrafish MYB 3'UTR target site.

Guillon-Munos A, Dambrine G, Richerioux N, Coupeau D, Muylkens B, Rasschaert D.

BMC Mol Biol. 2010 Sep 2;11:67. doi: 10.1186/1471-2199-11-67.

10.

An miR-502-binding site single-nucleotide polymorphism in the 3'-untranslated region of the SET8 gene is associated with early age of breast cancer onset.

Song F, Zheng H, Liu B, Wei S, Dai H, Zhang L, Calin GA, Hao X, Wei Q, Zhang W, Chen K.

Clin Cancer Res. 2009 Oct 1;15(19):6292-300. doi: 10.1158/1078-0432.CCR-09-0826. Epub 2009 Sep 29.

11.

Molecular cloning, expression and variation analyses of the dopamine D2 receptor gene in pig breeds in China.

Xu HP, He XM, Fang MX, Hu YS, Jia XZ, Nie QH, Zhang XQ.

Genet Mol Res. 2011 Dec 5;10(4):3371-84. doi: 10.4238/2011.December.5.6.

12.

SDHA loss-of-function mutations in KIT-PDGFRA wild-type gastrointestinal stromal tumors identified by massively parallel sequencing.

Pantaleo MA, Astolfi A, Indio V, Moore R, Thiessen N, Heinrich MC, Gnocchi C, Santini D, Catena F, Formica S, Martelli PL, Casadio R, Pession A, Biasco G.

J Natl Cancer Inst. 2011 Jun 22;103(12):983-7. doi: 10.1093/jnci/djr130. Epub 2011 Apr 19.

PMID:
21505157
13.

Mechanistic insights into the link between a polymorphism of the 3'UTR of the SLC7A1 gene and hypertension.

Yang Z, Kaye DM.

Hum Mutat. 2009 Mar;30(3):328-33. doi: 10.1002/humu.20891.

PMID:
19067360
14.

[Sequence analyses of HIRA gene 3'UTR region and related microRNA].

Wang X, Zhang J, Cao Y, Diao L, Wang H, Ma X, Ma D, Huang G.

Zhonghua Yi Xue Za Zhi. 2014 Apr 29;94(16):1223-6. Chinese.

PMID:
24924885
15.

Identification of SATB2 as the cleft palate gene on 2q32-q33.

FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT.

Hum Mol Genet. 2003 Oct 1;12(19):2491-501. Epub 2003 Jul 29.

PMID:
12915443
16.

TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.

Suphapeetiporn K, Tongkobpetch S, Siriwan P, Shotelersuk V.

Clin Genet. 2007 Nov;72(5):478-83. Epub 2007 Sep 14.

PMID:
17868388
17.

Single nucleotide polymorphism associated with nonsyndromic cleft palate influences the processing of miR-140.

Li L, Meng T, Jia Z, Zhu G, Shi B.

Am J Med Genet A. 2010 Apr;152A(4):856-62. doi: 10.1002/ajmg.a.33236.

PMID:
20358594
18.

Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.

Tongkobpetch S, Suphapeetiporn K, Siriwan P, Shotelersuk V.

Int J Oral Maxillofac Surg. 2008 Jun;37(6):550-3. doi: 10.1016/j.ijom.2008.01.024. Epub 2008 Mar 19.

PMID:
18356023
19.

Susceptibility to chronic thromboembolic pulmonary hypertension may be conferred by miR-759 via its targeted interaction with polymorphic fibrinogen alpha gene.

Chen Z, Nakajima T, Tanabe N, Hinohara K, Sakao S, Kasahara Y, Tatsumi K, Inoue Y, Kimura A.

Hum Genet. 2010 Oct;128(4):443-52. doi: 10.1007/s00439-010-0866-8. Epub 2010 Jul 31.

PMID:
20677013
20.

Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGE-associated cleft palate.

Venza M, Visalli M, Venza I, Torino C, Tripodo B, Melita R, Teti D.

J Oral Pathol Med. 2009 Jan;38(1):18-23. doi: 10.1111/j.1600-0714.2008.00726.x.

PMID:
19192046

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