“MNX1”的意思、由来-开放百科全书

References

1. ^{{cite web | title = Entrez Gene: HLXB9 homeobox HB9| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3110| accessdate = }}
2. ^{{cite journal | vauthors = Merello E, De Marco P, Ravegnani M, Riccipetitoni G, Cama A, Capra V | title = Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases | journal = Eur J Med Genet | volume = 56 | issue = 12 | pages = 648–54 | year = 2013 | pmid = 24095820 | doi = 10.1016/j.ejmg.2013.09.011 | url = }}

Further reading

{{cite journal | vauthors = Catala M | title = Genetic control of caudal development | journal = Clin. Genet. | volume = 61 | issue = 2 | pages = 89–96 | year = 2002 | pmid = 11940082 | doi = 10.1034/j.1399-0004.2002.610202.x }}

{{cite journal | vauthors = 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 | pmc = 328407 | doi = 10.1093/nar/19.13.3742 }}

{{cite journal | vauthors = 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 | vauthors = Lynch SA, Bond PM, Copp AJ, Kirwan WO, Nour S, Balling R, Mariman E, Burn J, Strachan T | 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 | vauthors = Harrison KA, Druey KM, Deguchi Y, Tuscano JM, Kehrl JH | 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 | vauthors = Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, Lynch SA, Lindsay S, Custard E, Belloni E, Wilson DI, Wadey R, Goodman F, Orstavik KH, Monclair T, Robson S, Reardon W, Burn J, Scambler P, Strachan T | 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 | vauthors = Heus HC, Hing A, van Baren MJ, Joosse M, Breedveld GJ, Wang JC, Burgess A, Donnis-Keller H, Berglund C, Zguricas J, Scherer SW, Rommens JM, Oostra BA, Heutink P | 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 | vauthors = Belloni E, Martucciello G, Verderio D, Ponti E, Seri M, Jasonni V, Torre M, Ferrari M, Tsui LC, Scherer SW | 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 | pmc = 1288336 | doi = 10.1086/302723 }}

{{cite journal | vauthors = Hagan DM, Ross AJ, Strachan T, Lynch SA, Ruiz-Perez V, Wang YM, Scambler P, Custard E, Reardon W, Hassan S, Nixon P, Papapetrou C, Winter RM, Edwards Y, Morrison K, Barrow M, Cordier-Alex MP, Correia P, Galvin-Parton PA, Gaskill S, Gaskin KJ, Garcia-Minaur S, Gereige R, Hayward R, Homfray T | 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 | pmc = 1378009 | doi = 10.1086/302899 }}

{{cite journal | vauthors = 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 | vauthors = Nagel S, Scherr M, Quentmeier H, Kaufmann M, Zaborski M, Drexler HG, MacLeod RA | 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 | vauthors = Cheng J, Kapranov P, Drenkow J, Dike S, Brubaker S, Patel S, Long J, Stern D, Tammana H, Helt G, Sementchenko V, Piccolboni A, Bekiranov S, Bailey DK, Ganesh M, Ghosh S, Bell I, Gerhard DS, Gingeras TR | 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 | vauthors = 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 = 2005 | pmid = 15839736 | pmc = 1087208 | doi = 10.1371/journal.pmed.0020103 }}

{{cite journal | vauthors = Kapranov P, Drenkow J, Cheng J, Long J, Helt G, Dike S, Gingeras TR | 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 | pmc = 1172043 | doi = 10.1101/gr.3455305 }}

{{cite journal | vauthors = von Bergh AR, van Drunen E, van Wering ER, van Zutven LJ, Hainmann I, Lönnerholm G, Meijerink JP, Pieters R, Beverloo HB | 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 | vauthors = Kim IS, Oh SY, Choi SJ, Kim JH, Park KH, Park HK, Kim JW, Ki CS | 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 }}

Clinical significance

References

Further reading

External links