Assignment of human myocyte-specific enhancer binding factor 2C (hMEF2C) to human chromosome 5q14 and evidence that MEF2C is evolutionarily conserved. - Suppr | 超能文献

Assignment of human myocyte-specific enhancer binding factor 2C (hMEF2C) to human chromosome 5q14 and evidence that MEF2C is evolutionarily conserved.

作者信息

Krainc D, Haas M, Ward D C, Lipton S A, Bruns G, Leifer D

机构信息

Department of Neurology, Children's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Genomics. 1995 Oct 10;29(3):809-11. doi: 10.1006/geno.1995.9927.

DOI:10.1006/geno.1995.9927

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Assignment of human myocyte-specific enhancer binding factor 2C (hMEF2C) to human chromosome 5q14 and evidence that MEF2C is evolutionarily conserved.

Genomics. 1995 Oct 10;29(3):809-11. doi: 10.1006/geno.1995.9927.

2

Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23.MADS结构域转录增强因子2（MEF2）基因家族的四个成员在人类染色体15q26、19p12、5q14和1q12-q23上的区域染色体定位。

Genomics. 1995 Oct 10;29(3):704-11. doi: 10.1006/geno.1995.9007.

3

Cloning, chromosomal localization, physical mapping, and genomic characterization of HKR3.HKR3的克隆、染色体定位、物理图谱构建及基因组特征分析

Genomics. 1996 Jul 15;35(2):289-98. doi: 10.1006/geno.1996.0359.

4

Mef2c is activated directly by Ets transcription factors through an evolutionarily conserved endothelial cell-specific enhancer.Mef2c通过一个进化上保守的内皮细胞特异性增强子被Ets转录因子直接激活。

Dev Biol. 2004 Nov 15;275(2):424-34. doi: 10.1016/j.ydbio.2004.08.016.

5

MEF2C DNA-binding activity is inhibited through its interaction with the regulatory protein Ki-1/57.MEF2C的DNA结合活性通过其与调节蛋白Ki-1/57的相互作用而受到抑制。

FEBS Lett. 2005 May 9;579(12):2615-22. doi: 10.1016/j.febslet.2005.03.078. Epub 2005 Apr 8.

6

Cooperative activation of atrial naturetic peptide promoter by dHAND and MEF2C.dHAND和MEF2C对心房利钠肽启动子的协同激活作用。

J Cell Biochem. 2004 Dec 15;93(6):1255-66. doi: 10.1002/jcb.20225.

7

Genomic structure of the human D-site binding protein (DBP) gene.人类D位点结合蛋白（DBP）基因的基因组结构。

Genomics. 1996 Jun 15;34(3):334-9. doi: 10.1006/geno.1996.0295.

8

Genomic structure and chromosomal localization of the novel ETS factor, PE-2 (ERF).新型ETS因子PE-2（ERF）的基因组结构与染色体定位

Genomics. 1997 Jun 1;42(2):227-35. doi: 10.1006/geno.1997.4730.

9

Organization of the human gene for nucleobindin (NUC) and its chromosomal assignment to 19q13.2-q13.4.人核结合蛋白（NUC）基因的组织及其在染色体上定位于19q13.2 - q13.4。

Genomics. 1996 Jun 1;34(2):181-6. doi: 10.1006/geno.1996.0263.

10

Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively.

Genomics. 1996 Jun 1;34(2):263-5. doi: 10.1006/geno.1996.0283.

引用本文的文献

1

Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study.对与骨密度（BMD）相关的全基因组显著位点进行靶向测序，发现了重要的新型和罕见变异：基因组流行病学心脏与衰老研究队列（CHARGE）靶向测序研究。

Hum Mol Genet. 2016 Dec 1;25(23):5234-5243. doi: 10.1093/hmg/ddw289.

2

Stem cell-mediated natural tissue engineering.干细胞介导的天然组织工程。

J Cell Mol Med. 2011 Jan;15(1):52-62. doi: 10.1111/j.1582-4934.2009.00972.x.