Motor neuron and pancreas homeobox 1 (MNX1) also known as Homeobox HB9 (HLXB9), is a human gene.cite web | title = Entrez Gene: HLXB9 homeobox HB9| url =| accessdate = ]

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Further reading

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*cite journal | author=Catala M |title=Genetic control of caudal development. |journal=Clin. Genet. |volume=61 |issue= 2 |pages= 89–96 |year= 2002 |pmid= 11940082 |doi=
*cite journal | author=Deguchi Y, Kehrl JH |title=Nucleotide sequence of a novel diverged human homeobox gene encodes a DNA binding protein. |journal=Nucleic Acids Res. |volume=19 |issue= 13 |pages= 3742 |year= 1991 |pmid= 1677181 |doi=
*cite journal | author=Deguchi Y, Kehrl JH |title=Selective expression of two homeobox genes in CD34-positive cells from human bone marrow. |journal=Blood |volume=78 |issue= 2 |pages= 323–8 |year= 1991 |pmid= 1712647 |doi=
*cite journal | author=Lynch SA, Bond PM, Copp AJ, "et al." |title=A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36. |journal=Nat. Genet. |volume=11 |issue= 1 |pages= 93–5 |year= 1995 |pmid= 7550324 |doi= 10.1038/ng0995-93
*cite journal | author=Harrison KA, Druey KM, Deguchi Y, "et al." |title=A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues. |journal=J. Biol. Chem. |volume=269 |issue= 31 |pages= 19968–75 |year= 1994 |pmid= 7914194 |doi=
*cite journal | author=Ross AJ, Ruiz-Perez V, Wang Y, "et al." |title=A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis. |journal=Nat. Genet. |volume=20 |issue= 4 |pages= 358–61 |year= 1998 |pmid= 9843207 |doi= 10.1038/3828
*cite journal | author=Heus HC, Hing A, van Baren MJ, "et al." |title=A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36. |journal=Genomics |volume=57 |issue= 3 |pages= 342–51 |year= 1999 |pmid= 10329000 |doi= 10.1006/geno.1999.5796
*cite journal | author=Belloni E, Martucciello G, Verderio D, "et al." |title=Involvement of the HLXB9 homeobox gene in Currarino syndrome. |journal=Am. J. Hum. Genet. |volume=66 |issue= 1 |pages= 312–9 |year= 2000 |pmid= 10631160 |doi=
*cite journal | author=Hagan DM, Ross AJ, Strachan T, "et al." |title=Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene. |journal=Am. J. Hum. Genet. |volume=66 |issue= 5 |pages= 1504–15 |year= 2000 |pmid= 10749657 |doi=
*cite journal | author=Köchling J, Karbasiyan M, Reis A |title=Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome. |journal=Eur. J. Hum. Genet. |volume=9 |issue= 8 |pages= 599–605 |year= 2001 |pmid= 11528505 |doi= 10.1038/sj.ejhg.5200683
*cite journal | author=Nagel S, Scherr M, Quentmeier H, "et al." |title=HLXB9 activates IL6 in Hodgkin lymphoma cell lines and is regulated by PI3K signalling involving E2F3. |journal=Leukemia |volume=19 |issue= 5 |pages= 841–6 |year= 2005 |pmid= 15772702 |doi= 10.1038/sj.leu.2403716
*cite journal | author=Cheng J, Kapranov P, Drenkow J, "et al." |title=Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution. |journal=Science |volume=308 |issue= 5725 |pages= 1149–54 |year= 2005 |pmid= 15790807 |doi= 10.1126/science.1108625
*cite journal | author=Hori Y, Gu X, Xie X, Kim SK |title=Differentiation of insulin-producing cells from human neural progenitor cells. |journal=PLoS Med. |volume=2 |issue= 4 |pages= e103 |year= 2006 |pmid= 15839736 |doi= 10.1371/journal.pmed.0020103
*cite journal | author=Kapranov P, Drenkow J, Cheng J, "et al." |title=Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arrays. |journal=Genome Res. |volume=15 |issue= 7 |pages= 987–97 |year= 2005 |pmid= 15998911 |doi= 10.1101/gr.3455305
*cite journal | author=von Bergh AR, van Drunen E, van Wering ER, "et al." |title=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. |journal=Genes Chromosomes Cancer |volume=45 |issue= 8 |pages= 731–9 |year= 2006 |pmid= 16646086 |doi= 10.1002/gcc.20335
*cite journal | author=Kim IS, Oh SY, Choi SJ, "et al." |title=Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome. |journal=J. Hum. Genet. |volume=52 |issue= 8 |pages= 698–701 |year= 2007 |pmid= 17612791 |doi= 10.1007/s10038-007-0173-y

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