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PubMed (cited) for id: 611211
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Mutations in RELT cause autosomal recessive amelogenesis imperfecta.
Clin Genet. 2019 Mar;95(3):375-383. doi: 10.1111/cge.13487. Epub 2018 Dec 21.
Clin Genet. 2019.
PMID: 30506946
Free PMC article.
Identification of RELT homologues that associate with RELT and are phosphorylated by OSR1.
Cusick JK, Xu LG, Bin LH, Han KJ, Shu HB.
Cusick JK, et al.
Biochem Biophys Res Commun. 2006 Feb 10;340(2):535-43. doi: 10.1016/j.bbrc.2005.12.033. Epub 2005 Dec 19.
Biochem Biophys Res Commun. 2006.
PMID: 16389068
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RELT, a new member of the tumor necrosis factor receptor superfamily, is selectively expressed in hematopoietic tissues and activates transcription factor NF-kappaB.
Sica GL, Zhu G, Tamada K, Liu D, Ni J, Chen L.
Sica GL, et al.
Blood. 2001 May 1;97(9):2702-7. doi: 10.1182/blood.v97.9.2702.
Blood. 2001.
PMID: 11313261
Free article.
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