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Items: 7


Epigenomic profiling of newborns with isolated orofacial clefts reveals widespread DNA methylation changes and implicates metastable epiallele regions in disease risk.

Gonseth S, Shaw GM, Roy R, Segal MR, Asrani K, Rine J, Wiemels J, Marini NJ.

Epigenetics. 2019 Feb;14(2):198-213. doi: 10.1080/15592294.2019.1581591. Epub 2019 Mar 14.


Browning of Pig White Preadipocytes by Co-Overexpressing Pig PGC-1α and Mice UCP1.

Hou L, Xie M, Cao L, Shi J, Xu G, Hu C, Wang C.

Cell Physiol Biochem. 2018;48(2):556-568. doi: 10.1159/000491885. Epub 2018 Jul 18.


Lhx6 and Lhx8 promote palate development through negative regulation of a cell cycle inhibitor gene, p57Kip2.

Cesario JM, Landin Malt A, Deacon LJ, Sandberg M, Vogt D, Tang Z, Zhao Y, Brown S, Rubenstein JL, Jeong J.

Hum Mol Genet. 2015 Sep 1;24(17):5024-39. doi: 10.1093/hmg/ddv223. Epub 2015 Jun 12.


A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family.

Yıldırım Y, Kerem M, Köroğlu Ç, Tolun A.

Eur J Hum Genet. 2014 Mar;22(3):333-7. doi: 10.1038/ejhg.2013.138. Epub 2013 Jul 17.


Implications of TGFβ on Transcriptome and Cellular Biofunctions of Palatal Mesenchyme.

Zhu X, Ozturk F, Pandey S, Guda CB, Nawshad A.

Front Physiol. 2012 Apr 10;3:85. doi: 10.3389/fphys.2012.00085. eCollection 2012.


Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.

Nikopensius T, Kempa I, Ambrozaitytė L, Jagomägi T, Saag M, Matulevičienė A, Utkus A, Krjutškov K, Tammekivi V, Piekuse L, Akota I, Barkane B, Krumina A, Klovins J, Lace B, Kučinskas V, Metspalu A.

Birth Defects Res A Clin Mol Teratol. 2011 Apr;91(4):218-25. doi: 10.1002/bdra.20791. Epub 2011 Apr 1.


Isolated cleft palate in mice with a targeted mutation of the LIM homeobox gene lhx8.

Zhao Y, Guo YJ, Tomac AC, Taylor NR, Grinberg A, Lee EJ, Huang S, Westphal H.

Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15002-6.

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