No milk today (my Hox have gone away).
作者信息
Duboule D
机构信息
Department of Zoology and Animal Biology, University of Geneva, Sciences III, Quai Ernest Ansermet 30, 1211 Geneva 4, Switzerland.
出版信息
Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):322-3. doi: 10.1073/pnas.96.2.322.
Abstract
摘要
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本文引用的文献
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Paralogous mouse Hox genes, Hoxa9, Hoxb9, and Hoxd9, function together to control development of the mammary gland in response to pregnancy.同源的小鼠Hox基因Hoxa9、Hoxb9和Hoxd9共同发挥作用，以控制乳腺在妊娠反应中的发育。
Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):541-6. doi: 10.1073/pnas.96.2.541.
2
Genetic analysis of a conserved sequence in the HoxD complex: regulatory redundancy or limitations of the transgenic approach?HoxD复合体中保守序列的遗传分析：调控冗余还是转基因方法的局限性？
Dev Dyn. 1998 Sep;213(1):1-11. doi: 10.1002/(SICI)1097-0177(199809)213:1<1::AID-AJA1>3.0.CO;2-L.
3
The evolution of 'bricolage'.
Trends Genet. 1998 Feb;14(2):54-9. doi: 10.1016/s0168-9525(97)01358-9.
4
Hoxc13 mutant mice lack external hair.Hoxc13基因敲除小鼠没有体表毛发。
Genes Dev. 1998 Jan 1;12(1):11-20. doi: 10.1101/gad.12.1.11.
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Abnormal uterine stromal and glandular function associated with maternal reproductive defects in Hoxa-11 null mice.Hoxa-11基因敲除小鼠中与母体生殖缺陷相关的子宫基质和腺体功能异常。
Biol Reprod. 1997 May;56(5):1097-105. doi: 10.1095/biolreprod56.5.1097.
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Branchial HOX gene expression and human craniofacial development.鳃HOX基因表达与人类颅面发育
Dev Biol. 1997 Mar 1;183(1):49-60. doi: 10.1006/dbio.1996.8450.
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Male accessory sex organ morphogenesis is altered by loss of function of Hoxd-13.雄性附属性器官的形态发生因Hoxd - 13功能丧失而改变。
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Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia.人类髓系白血病中，核孔蛋白基因NUP98通过染色体易位t(7;11)(p15;p15)与HOXA9融合。
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