关于成年小鼠大脑中ATP10a印记状态的相互矛盾的报道：品系背景依赖性印记？ - Suppr | 超能文献

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On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?关于成年小鼠大脑中ATP10a印记状态的相互矛盾的报道：品系背景依赖性印记？

J Hum Genet. 2003;48(9):492-493. doi: 10.1007/s10038-003-0061-z. Epub 2003 Sep 4.

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Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting.Atp10a是人类印迹基因ATP10A在小鼠中的同源基因，它逃避了基因组印迹。

Genomics. 2003 Jun;81(6):644-7. doi: 10.1016/s0888-7543(03)00077-6.

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Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?关于人类GRB10在发育中的大脑中印迹状态的相互矛盾的报道：体细胞杂种用于预测表达等位基因起源的可靠性如何？

Am J Hum Genet. 2001 Feb;68(2):543-5. doi: 10.1086/318192.

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ES cell differentiation system recapitulates the establishment of imprinted gene expression in a cell-type-specific manner.胚胎干细胞分化系统以细胞类型特异性的方式再现印迹基因表达的建立。

Hum Mol Genet. 2012 Mar 15;21(6):1391-401. doi: 10.1093/hmg/ddr577. Epub 2011 Dec 9.

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Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells.利用诱导多能干细胞模拟基因组印记疾病

Methods Mol Biol. 2016;1353:45-64. doi: 10.1007/7651_2014_169.

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Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.人类GRB10基因在发育中的中枢神经系统中的母体抑制；GRB10在Silver-Russell综合征中的作用评估。

Eur J Hum Genet. 2001 Feb;9(2):82-90. doi: 10.1038/sj.ejhg.5200583.

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A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.在一个针对天使综合征印记缺陷的小鼠模型中，一个人类印记中心显示出印记的保守获得但维持出现分歧。

Hum Mol Genet. 2006 Feb 1;15(3):393-404. doi: 10.1093/hmg/ddi456. Epub 2005 Dec 20.

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[Angelman syndrome--diagnosis and therapy of genomic imprinting disorders].[天使综合征——基因组印记障碍的诊断与治疗]

No To Hattatsu. 2009 May;41(3):208-13.

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Control elements within the PWS/AS imprinting box and their function in the imprinting process.普拉德-威利综合征/安吉尔曼综合征印记框内的调控元件及其在印记过程中的功能。

Hum Mol Genet. 2004 Apr 1;13(7):751-62. doi: 10.1093/hmg/ddh085. Epub 2004 Feb 12.

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Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a.经验依赖型皮质可塑性的泛素连接酶基因 Ube3a 的基因组印记。

Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5611-6. doi: 10.1073/pnas.1001281107. Epub 2010 Mar 8.

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Deficiency of the lipid flippase ATP10A causes diet-induced dyslipidemia in female mice.脂质翻转酶 ATP10A 的缺乏导致雌性小鼠饮食诱导的血脂异常。

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Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1.携带15号染色体q11-q13.1拷贝数变异的人诱导多能干细胞衍生神经元的基因表达分析。

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Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation.

本文引用的文献

1

Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting.Atp10a是人类印迹基因ATP10A在小鼠中的同源基因，它逃避了基因组印迹。

Genomics. 2003 Jun;81(6):644-7. doi: 10.1016/s0888-7543(03)00077-6.

2

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb.小鼠Atp10c在海马体和嗅球中主要由母体表达。

J Hum Genet. 2003;48(4):194-8. doi: 10.1007/s10038-003-0009-3. Epub 2003 Mar 12.

3

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.