MNX1
From Wikipedia, the free encyclopedia
Motor neuron and pancreas homeobox 1 (MNX1) also known as Homeobox HB9 (HLXB9), is a human gene.[1]
It can be associated with Currarino syndrome.
References
Further reading
- Catala M (2002). "Genetic control of caudal development.". Clin. Genet. 61 (2): 89–96. doi:10.1034/j.1399-0004.2002.610202.x. PMID 11940082.
- Deguchi Y, Kehrl JH (1991). "Nucleotide sequence of a novel diverged human homeobox gene encodes a DNA binding protein.". Nucleic Acids Res. 19 (13): 3742. doi:10.1093/nar/19.13.3742. PMC 328407. PMID 1677181.
- Deguchi Y, Kehrl JH (1991). "Selective expression of two homeobox genes in CD34-positive cells from human bone marrow.". Blood 78 (2): 323–8. PMID 1712647.
- Lynch SA, Bond PM, Copp AJ, et al. (1995). "A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.". Nat. Genet. 11 (1): 93–5. doi:10.1038/ng0995-93. PMID 7550324.
- Harrison KA, Druey KM, Deguchi Y, et al. (1994). "A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues.". J. Biol. Chem. 269 (31): 19968–75. PMID 7914194.
- Ross AJ, Ruiz-Perez V, Wang Y, et al. (1998). "A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.". Nat. Genet. 20 (4): 358–61. doi:10.1038/3828. PMID 9843207.
- Heus HC, Hing A, van Baren MJ, et al. (1999). "A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.". Genomics 57 (3): 342–51. doi:10.1006/geno.1999.5796. PMID 10329000.
- Belloni E, Martucciello G, Verderio D, et al. (2000). "Involvement of the HLXB9 homeobox gene in Currarino syndrome.". Am. J. Hum. Genet. 66 (1): 312–9. doi:10.1086/302723. PMC 1288336. PMID 10631160.
- Hagan DM, Ross AJ, Strachan T, et al. (2000). "Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.". Am. J. Hum. Genet. 66 (5): 1504–15. doi:10.1086/302899. PMC 1378009. PMID 10749657.
- Köchling J, Karbasiyan M, Reis A (2001). "Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.". Eur. J. Hum. Genet. 9 (8): 599–605. doi:10.1038/sj.ejhg.5200683. PMID 11528505.
- Nagel S, Scherr M, Quentmeier H, et al. (2005). "HLXB9 activates IL6 in Hodgkin lymphoma cell lines and is regulated by PI3K signalling involving E2F3.". Leukemia 19 (5): 841–6. doi:10.1038/sj.leu.2403716. PMID 15772702.
- Cheng J, Kapranov P, Drenkow J, et al. (2005). "Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution.". Science 308 (5725): 1149–54. doi:10.1126/science.1108625. PMID 15790807.
- Hori Y, Gu X, Xie X, Kim SK (2006). "Differentiation of insulin-producing cells from human neural progenitor cells.". PLoS Med. 2 (4): e103. doi:10.1371/journal.pmed.0020103. PMC 1087208. PMID 15839736.
- Kapranov P, Drenkow J, Cheng J, et al. (2005). "Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arrays.". Genome Res. 15 (7): 987–97. doi:10.1101/gr.3455305. PMC 1172043. PMID 15998911.
- von Bergh AR, van Drunen E, van Wering ER, et al. (2006). "High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.". Genes Chromosomes Cancer 45 (8): 731–9. doi:10.1002/gcc.20335. PMID 16646086.
- Kim IS, Oh SY, Choi SJ, et al. (2007). "Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.". J. Hum. Genet. 52 (8): 698–701. doi:10.1007/s10038-007-0173-y. PMID 17612791.
External links
- MNX1 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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