编码腺病毒E1A调控转录因子E4F的基因在人和小鼠中的染色体定位及组织表达 - Suppr

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超能文献

Chromosomal location and tissue expression of the gene encoding the adenovirus E1A-regulated transcription factor E4F in humans and mice.

作者信息

Rooney R J, Daniels R R, Jenkins N A, Gilbert D J, Rothammer K, Morris S W, Higgs D R, Copeland N G

机构信息

Department of Biochemistry, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Mamm Genome. 1998 Apr;9(4):320-3. doi: 10.1007/s003359900758.

DOI:10.1007/s003359900758

PMID:9530632

Abstract

摘要

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Chromosomal location and tissue expression of the gene encoding the adenovirus E1A-regulated transcription factor E4F in humans and mice.编码腺病毒E1A调控转录因子E4F的基因在人和小鼠中的染色体定位及组织表达

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Assignment of the E1A-regulated transcription factor E4F gene (E4F1) to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids.通过原位杂交和体细胞杂种将E1A调节的转录因子E4F基因（E4F1）定位于人类染色体带16p13.3。

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The adenovirus E1A-regulated transcription factor E4F is generated from the human homolog of nuclear factor phiAP3.腺病毒E1A调节的转录因子E4F由核因子phiAP3的人类同源物产生。

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本文引用的文献

Adenovirus E1A-regulated transcription factor p120E4F inhibits cell growth and induces the stabilization of the cdk inhibitor p21WAF1.腺病毒E1A调控转录因子p120E4F抑制细胞生长并诱导细胞周期蛋白依赖性激酶抑制剂p21WAF1的稳定性。

Mol Cell Biol. 1998 Jan;18(1):459-67. doi: 10.1128/MCB.18.1.459.

The adenovirus E1A-regulated transcription factor E4F is generated from the human homolog of nuclear factor phiAP3.腺病毒E1A调节的转录因子E4F由核因子phiAP3的人类同源物产生。

Mol Cell Biol. 1997 Apr;17(4):1890-903. doi: 10.1128/MCB.17.4.1890.

Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3.绘制人类16号染色体p3.3上围绕多囊肾病1型（PKD1）和结节性硬化症2型（TSC2）疾病基因的700千碱基区域的转录图谱。

Genome Res. 1996 Jun;6(6):525-37. doi: 10.1101/gr.6.6.525.

The mouse homologue of the polycystic kidney disease gene (Pkd1) is a single-copy gene.多囊肾病基因（Pkd1）的小鼠同源基因是一个单拷贝基因。

Genomics. 1996 Jun 1;34(2):233-5. doi: 10.1006/geno.1996.0273.

The peculiar journey of a selfish chromosome: mouse t haplotypes and meiotic drive.一条自私染色体的奇特旅程：小鼠t单倍型与减数分裂驱动

Trends Genet. 1993 Jul;9(7):250-4. doi: 10.1016/0168-9525(93)90090-5.

Identification and characterization of the tuberous sclerosis gene on chromosome 16.16号染色体上结节性硬化症基因的鉴定与特征分析

Cell. 1993 Dec 31;75(7):1305-15. doi: 10.1016/0092-8674(93)90618-z.

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EMBO J. 1993 Dec 15;12(13):4985-92. doi: 10.1002/j.1460-2075.1993.tb06192.x.

High-resolution genetic analysis of a deletion on mouse chromosome 17 extending over the fused, tufted, and homeobox Nkx2-5 loci.

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Report and abstracts of the third international workshop on human chromosome 16 mapping 1994. Pittsburgh, Pennsylvania, May 7-9, 1994.1994年第三届人类16号染色体图谱绘制国际研讨会报告及摘要。宾夕法尼亚州匹兹堡，1994年5月7日至9日。

Cytogenet Cell Genet. 1995;68(3-4):165-84. doi: 10.1159/000133909.

Human mitochondrial 3,2-trans-enoyl-CoA isomerase (DCI): gene structure and localization to chromosome 16p13.3.人线粒体3,2-反式烯酰辅酶A异构酶（DCI）：基因结构及定位于染色体16p13.3

Genomics. 1994 Sep 1;23(1):223-8. doi: 10.1006/geno.1994.1480.

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