Year |
Citation |
Score |
2023 |
Casasnovas-Nieves JJ, Rodríguez Y, Franco HL, Cadilla CL. Mechanisms of Regulation of the Gene by the TWIST2 and ADD1/SREBP1c Transcription Factors. Genes. 14. PMID 37761873 DOI: 10.3390/genes14091733 |
0.743 |
|
2021 |
Regner MJ, Wisniewska K, Garcia-Recio S, Thennavan A, Mendez-Giraldez R, Malladi VS, Hawkins G, Parker JS, Perou CM, Bae-Jump VL, Franco HL. A multi-omic single-cell landscape of human gynecologic malignancies. Molecular Cell. 81: 4924-4941.e10. PMID 34739872 DOI: 10.1016/j.molcel.2021.10.013 |
0.3 |
|
2021 |
Li S, Garay JP, Tubbs CA, Franco HL. CRISPR-based knockin mutagenesis of the pioneer transcription factor FOXA1: optimization of strategies for multi-allelic proteins in cancer cells. Febs Open Bio. PMID 33666335 DOI: 10.1002/2211-5463.13139 |
0.336 |
|
2019 |
Lewis MW, Li S, Franco HL. Transcriptional control by enhancers and enhancer RNAs. Transcription. 1-16. PMID 31791217 DOI: 10.1080/21541264.2019.1695492 |
0.379 |
|
2016 |
Franco HL, Nagari A, Xi Y, Li W, Richardson D, Tanaka K, Li J, Barton MC, Shi X, Keyomarsi K, Bedford MT, Li W, Dent SYR, Kraus WL. Abstract PR06: Analysis of enhancer transcription reveals novel gene regulatory networks in breast cancer Cancer Research. 76. DOI: 10.1158/1538-7445.Chromepi15-Pr06 |
0.373 |
|
2011 |
Franco HL, Casasnovas JJ, Leon RG, Friesel R, Ge Y, Desnick RJ, Cadilla CL. Nonsense mutations of the bHLH transcription factor TWIST2 found in Setleis Syndrome patients cause dysregulation of periostin. The International Journal of Biochemistry & Cell Biology. 43: 1523-31. PMID 21801849 DOI: 10.1016/J.Biocel.2011.07.003 |
0.52 |
|
2011 |
Franco HL, Casasnovas J, Rodríguez-Medina JR, Cadilla CL. Redundant or separate entities?--roles of Twist1 and Twist2 as molecular switches during gene transcription. Nucleic Acids Research. 39: 1177-86. PMID 20935057 DOI: 10.1093/nar/gkq890 |
0.626 |
|
2010 |
Tukel T, Šošić D, Al-Gazali LI, Erazo M, Casasnovas J, Franco HL, Richardson JA, Olson EN, Cadilla CL, Desnick RJ. Homozygous nonsense mutations in TWIST2 cause setleis syndrome American Journal of Human Genetics. 87: 289-296. PMID 20691403 DOI: 10.1016/J.Ajhg.2010.07.009 |
0.653 |
|
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