DLX3

Distal-less homeobox 3
المعرفات
الأسماء المستعارة	DLX3, homeobox protein DLX-3
معرفات خارجية
أورثولوج
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	ويكي بيانات
اعرض/عدّل إنسان

DLX3‏ (Distal-less homeobox 3) هوَ بروتين يُشَفر بواسطة جين DLX3 في الإنسان.[1][2]

المراجع

Scherer SW, Heng HH, Robinson GW, Mahon KA, Evans JP, Tsui LC (أغسطس 1995)، "Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization"، Mamm Genome، 6 (4): 310–1، doi:10.1007/BF00352432، PMID 7613049.
"Entrez Gene: DLX3 distal-less homeobox 3"، مؤرشف من الأصل في 05 ديسمبر 2010.

قراءة متعمقة

Morasso MI, Radoja N (2005)، "Dlx Genes, p63, and Ectodermal Dysplasias"، Birth Defects Res. C Embryo Today، 75 (3): 163–71، doi:10.1002/bdrc.20047، PMC 1317295، PMID 16187309.
Bonaldo MF, Lennon G, Soares MB (1997)، "Normalization and subtraction: two approaches to facilitate gene discovery"، Genome Res.، 6 (9): 791–806، doi:10.1101/gr.6.9.791، PMID 8889548.
Nakamura S؛ Stock DW؛ Wydner KL؛ وآخرون (1997)، "Genomic analysis of a new mammalian distal-less gene: Dlx7"، Genomics، 38 (3): 314–24، doi:10.1006/geno.1996.0634، PMID 8975708.
Price JA؛ Bowden DW؛ Wright JT؛ وآخرون (1998)، "Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome"، Hum. Mol. Genet.، 7 (3): 563–9، doi:10.1093/hmg/7.3.563، PMID 9467018.
Roberson MS؛ Meermann S؛ Morasso MI؛ وآخرون (2001)، "A role for the homeobox protein Distal-less 3 in the activation of the glycoprotein hormone alpha subunit gene in choriocarcinoma cells"، J. Biol. Chem.، 276 (13): 10016–24، doi:10.1074/jbc.M007481200، PMID 11113121.
Park GT, Denning MF, Morasso MI (2001)، "Phosphorylation of murine homeodomain protein Dlx3 by protein kinase C"، FEBS Lett.، 496 (1): 60–5، doi:10.1016/S0014-5793(01)02398-5، PMC 1283141، PMID 11343707.
Peng L, Payne AH (2002)، "AP-2 gamma and the homeodomain protein distal-less 3 are required for placental-specific expression of the murine 3 beta-hydroxysteroid dehydrogenase VI gene, Hsd3b6"، J. Biol. Chem.، 277 (10): 7945–54، doi:10.1074/jbc.M106765200، PMID 11773066.
Sumiyama K؛ Irvine SQ؛ Stock DW؛ وآخرون (2002)، "Genomic structure and functional control of the Dlx3-7 bigene cluster"، Proc. Natl. Acad. Sci. U.S.A.، 99 (2): 780–5، doi:10.1073/pnas.012584999، PMC 117382، PMID 11792834.
Strausberg RL؛ Feingold EA؛ Grouse LH؛ وآخرون (2003)، "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
Imabayashi H؛ Mori T؛ Gojo S؛ وآخرون (2003)، "Redifferentiation of dedifferentiated chondrocytes and chondrogenesis of human bone marrow stromal cells via chondrosphere formation with expression profiling by large-scale cDNA analysis"، Exp. Cell Res.، 288 (1): 35–50، doi:10.1016/S0014-4827(03)00130-7، PMID 12878157.
Holland MP, Bliss SP, Berghorn KA, Roberson MS (2004)، "A role for CCAAT/enhancer-binding protein beta in the basal regulation of the distal-less 3 gene promoter in placental cells"، Endocrinology، 145 (3): 1096–105، doi:10.1210/en.2003-0777، PMID 14670999.
Haldeman RJ؛ Cooper LF؛ Hart TC؛ وآخرون (2005)، "Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome"، Bone، 35 (4): 988–97، doi:10.1016/j.bone.2004.06.003، PMID 15454107.
Gerhard DS؛ Wagner L؛ Feingold EA؛ وآخرون (2004)، "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)"، Genome Res.، 14 (10B): 2121–7، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
Dong J؛ Amor D؛ Aldred MJ؛ وآخرون (2005)، "DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism"، Am. J. Med. Genet. A، 133 (2): 138–41، doi:10.1002/ajmg.a.30521، PMID 15666299.
Islam M, Lurie AG, Reichenberger E (2006)، "Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity"، Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics، 100 (6): 736–42، doi:10.1016/j.tripleo.2005.04.017، PMID 16301156.
Otsuki T؛ Ota T؛ Nishikawa T؛ وآخرون (2007)، "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries"، DNA Res.، 12 (2): 117–26، doi:10.1093/dnares/12.2.117، PMID 16303743.
Morsczeck C (2006)، "Gene expression of runx2, Osterix, c-fos, DLX-3, DLX-5, and MSX-2 in dental follicle cells during osteogenic differentiation in vitro"، Calcif. Tissue Int.، 78 (2): 98–102، doi:10.1007/s00223-005-0146-0، PMID 16467978.
Berghorn KA؛ Clark-Campbell PA؛ Han L؛ وآخرون (2006)، "Smad6 represses Dlx3 transcriptional activity through inhibition of DNA binding"، J. Biol. Chem.، 281 (29): 20357–67، doi:10.1074/jbc.M603049200، PMID 16687405.

بوابة طب
بوابة علم الأحياء الخلوي والجزيئي
بوابة الكيمياء الحيوية

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[pmid7613049-1] Scherer SW, Heng HH, Robinson GW, Mahon KA, Evans JP, Tsui LC (أغسطس 1995)، "Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization"، Mamm Genome، 6 (4): 310–1، doi:10.1007/BF00352432، PMID 7613049.

[entrez-2] "Entrez Gene: DLX3 distal-less homeobox 3"، مؤرشف من الأصل في 05 ديسمبر 2010.