脑特异性POU盒基因Brn4是一种位于人类和小鼠X染色体上的性连锁转录因子。 - Suppr

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超能文献

The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes.

作者信息

Douville P J, Atanasoski S, Tobler A, Fontana A, Schwab M E

机构信息

Brain Research Institute, University of Zurich, Switzerland.

出版信息

Mamm Genome. 1994 Mar;5(3):180-2. doi: 10.1007/BF00352353.

DOI:10.1007/BF00352353

PMID:7911044

Abstract

摘要

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The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes.脑特异性POU盒基因Brn4是一种位于人类和小鼠X染色体上的性连锁转录因子。

Mamm Genome. 1994 Mar;5(3):180-2. doi: 10.1007/BF00352353.

The gene for the ubiquitous octamer-binding protein Oct-1 is on human chromosome 1, region cen-q32, and near Ly-22 and Ltw-4 on mouse chromosome 1.普遍存在的八聚体结合蛋白Oct-1的基因位于人类1号染色体的cen-q32区域，在小鼠1号染色体上靠近Ly-22和Ltw-4。

Genomics. 1990 Apr;6(4):666-72. doi: 10.1016/0888-7543(90)90502-l.

The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear.性连锁坐立不安突变消除了胚胎内耳中Brn4/Pou3f4基因的表达。

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Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice.无晶状体小鼠中Pitx3同源框基因启动子区域的缺失及表达改变

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A human POU domain gene, mPOU, is expressed in developing brain and specific adult tissues.一种人类POU结构域基因，即mPOU，在发育中的大脑和特定的成年组织中表达。

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Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.X连锁混合性耳聋与POU结构域基因POU3F4突变之间的关联。

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Characterization of chicken octamer-binding proteins demonstrates that POU domain-containing homeobox transcription factors have been highly conserved during vertebrate evolution.鸡八聚体结合蛋白的特性表明，含POU结构域的同源框转录因子在脊椎动物进化过程中一直高度保守。

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The rapidly evolving Pem homeobox gene and Agtr2, Ant2, and Lamp2 are closely linked in the proximal region of the mouse X chromosome.快速进化的Pem同源框基因与Agtr2、Ant2和Lamp2在小鼠X染色体的近端区域紧密相连。

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Examination of POU homeobox gene expression in human breast cancer cells.

Int J Cancer. 1999 Mar 31;81(1):104-12. doi: 10.1002/(sici)1097-0215(19990331)81:1<104::aid-ijc18>3.0.co;2-q.

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本文引用的文献

A novel class of murine POU gene predominantly expressed in central nervous system.一类主要在中枢神经系统中表达的新型小鼠POU基因。

J Biol Chem. 1993 Apr 5;268(10):7449-57.

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.与X连锁无丙种球蛋白血症相关的基因是蛋白质酪氨酸激酶src家族的成员。

Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0.

Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes.X连锁无丙种球蛋白血症与X连锁免疫缺陷基因的共定位。

Science. 1993 Jul 16;261(5119):355-8. doi: 10.1126/science.8332900.

Repressor structure and the mechanism of positive control.阻遏物结构与正调控机制。

Cell. 1983 Feb;32(2):319-25. doi: 10.1016/0092-8674(83)90451-8.

X-linked recessive hypopituitarism.

Birth Defects Orig Artic Ser. 1971 May;7(6):24-7.

X-linked congenital panhypopituitarism.X连锁先天性全垂体功能减退症

Birth Defects Orig Artic Ser. 1971 May;7(6):21-3.

The information content of phase-known matings for ordering genetic loci.用于基因座排序的已知相位交配的信息内容。

Genet Epidemiol. 1985;2(4):349-61. doi: 10.1002/gepi.1370020404.

Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders.髓磷脂蛋白脂蛋白基因定位于X染色体：对X连锁髓鞘疾病的意义。

Science. 1985 Nov 22;230(4728):940-2. doi: 10.1126/science.3840606.

Etiological heterogeneity in X-linked spastic paraplegia.X连锁痉挛性截瘫的病因异质性。

Am J Hum Genet. 1987 Nov;41(5):933-43.

The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products.POU结构域：存在于哺乳动物的Pit-1、Oct-1、Oct-2以及秀丽隐杆线虫unc-86基因产物中的一个高度保守的区域。

Genes Dev. 1988 Dec;2(12A):1513-6. doi: 10.1101/gad.2.12a.1513.

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