Homeobox A cluster is aprotein that in humans is encoded by the HOXA@gene.[2]
| HOXA@ | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | HOXA@, HOX1@, homeobox A cluster | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards:HOXA@;OMA:HOXA@ - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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References
edit- ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^"Entrez Gene: Homeobox A cluster". Retrieved2017-10-05.
Further reading
edit- Soulier J, Clappier E, Cayuela JM, Regnault A, García-Peydró M, Dombret H, Baruchel A, Toribio ML, Sigaux F (2005)."HOXA genes are included in genetic and biologic networks defining human acute T-cell leukemia (T-ALL)".Blood.106 (1):274–86.doi:10.1182/blood-2004-10-3900.PMID 15774621.
- Dik WA, Brahim W, Braun C, Asnafi V, Dastugue N, Bernard OA, van Dongen JJ, Langerak AW, Macintyre EA, Delabesse E (2005)."CALM-AF10+ T-ALL expression profiles are characterized by overexpression of HOXA and BMI1 oncogenes".Leukemia.19 (11):1948–57.doi:10.1038/sj.leu.2403891.PMID 16107895.
- Sessa L, Breiling A, Lavorgna G, Silvestri L, Casari G, Orlando V (2007)."Noncoding RNA synthesis and loss of Polycomb group repression accompanies the colinear activation of the human HOXA cluster".RNA.13 (2):223–39.doi:10.1261/rna.266707.PMC 1781374.PMID 17185360.
- Caudell D, Aplan PD (2008)."The role of CALM-AF10 gene fusion in acute leukemia".Leukemia.22 (4):678–85.doi:10.1038/sj.leu.2405074.PMC 2366104.PMID 18094714.
- Van Vlierberghe P, van Grotel M, Tchinda J, Lee C, Beverloo HB, van der Spek PJ, Stubbs A, Cools J, Nagata K, Fornerod M, Buijs-Gladdines J, Horstmann M, van Wering ER, Soulier J, Pieters R, Meijerink JP (2008)."The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia".Blood.111 (9):4668–80.doi:10.1182/blood-2007-09-111872.PMC 2343598.PMID 18299449.
- Yerges LM, Klei L, Cauley JA, Roeder K, Kammerer CM, Moffett SP, Ensrud KE, Nestlerode CS, Marshall LM, Hoffman AR, Lewis C, Lang TF, Barrett-Connor E, Ferrell RE, Orwoll ES, Zmuda JM (2009)."High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men".J. Bone Miner. Res.24 (12):2039–49.doi:10.1359/jbmr.090524.PMC 2791518.PMID 19453261.
- Lodder EM, Eussen BH, van Hassel DA, Hoogeboom AJ, Poddighe PJ, Coert JH, Oostra BA, de Klein A, de Graaff E (2009)."Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly".Chromosome Res.17 (6):737–44.doi:10.1007/s10577-009-9059-5.PMC 2759026.PMID 19672683.
- Ester AR, Weymouth KS, Burt A, Wise CA, Scott A, Gurnett CA, Dobbs MB, Blanton SH, Hecht JT (2009)."Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot".Am. J. Med. Genet. A.149A (12):2745–52.doi:10.1002/ajmg.a.33130.PMC 2795347.PMID 19938081.
- Ester AR, Weymouth KS, Burt A, Wise CA, Scott A, Gurnett CA, Dobbs MB, Blanton SH, Hecht JT (2009)."Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot".Am. J. Med. Genet. A.149A (12):2745–52.doi:10.1002/ajmg.a.33130.PMC 2795347.PMID 19938081.
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