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PRRX1 gene

Known as: PAIRED-RELATED HOMEOBOX GENE 1, PRRX1, PAIRED MESODERM HOMEOBOX 1 
This gene plays a role in both transcriptional regulation and muscle cell development.
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Significance Heterotopic ossification (HO) is a debilitating condition in which bone forms inappropriately within soft tissues… Expand
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Highly Cited
2014
Highly Cited
2014
Carcinoma cells hijack the epithelial–mesenchymal transition (EMT) for tumor dissemination. Paired-related homeobox 1 (PRRX1) has… Expand
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Highly Cited
2014
Highly Cited
2014
One of the challenges in the treatment of colorectal cancer patients is that these tumors show resistance to radiation. MicroRNAs… Expand
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2013
2013
Agnathia-otocephaly is a rare craniofacial malformation complex that is caused by de novo heterozygous and biallelic mutations in… Expand
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2010
2010
Nilotinib-mediated inhibition of ABCB1 increases intracellular concentration of dasatinib in CML cells: implications for… Expand
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2008
2008
Angiogenesis is fundamental to normal placental development and aberrant angiogenesis contributes substantially to placental… Expand
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2008
2008
PMX1 is a member of a non-clustered homeobox gene family, not normally expressed in hematopoietic cells, and first identified for… Expand
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Highly Cited
2007
Highly Cited
2007
Human peroxiredoxins 1 and 2, also known as Prx1 and Prx2, are more than 90% homologous in their amino acid sequences. Prx1 and… Expand
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2000
2000
Abstract. In this study, we extend our examination of the function of the Prrx1 (a.k.a. Mhox, Prx1, K-2, and Pmx1) as well as… Expand
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1997
1997
In the promoters of many immediate early genes, including c-fos, CArG DNA regulatory elements mediate basal constituitive… Expand
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