{"title":"发育中的人类黄斑的差异基因表达:使用罕见组织样本的微阵列分析。","authors":"Peter Kozulin, Jan M Provis","doi":"10.1007/s12177-009-9039-1","DOIUrl":null,"url":null,"abstract":"<p><p>The macula is a unique and important region in the primate retina that achieves high resolution and color vision in the central visual field. We recently reported data obtained from microarray analysis of gene expression in the macula of the human fetal retina (Kozulin et al., Mol Vis 15:45-59, 1). In this paper, we describe the preliminary analyses undertaken to visualize differences and verify comparability of the replicates used in that study, report the differential expression of other gene families obtained from the analysis, and show the reproducibility of our findings in several gene families by quantitative real-time PCR.</p>","PeriodicalId":73873,"journal":{"name":"Journal of ocular biology, diseases, and informatics","volume":" ","pages":"176-189"},"PeriodicalIF":0.0000,"publicationDate":"2009-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12177-009-9039-1","citationCount":"12","resultStr":"{\"title\":\"Differential gene expression in the developing human macula: microarray analysis using rare tissue samples.\",\"authors\":\"Peter Kozulin, Jan M Provis\",\"doi\":\"10.1007/s12177-009-9039-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The macula is a unique and important region in the primate retina that achieves high resolution and color vision in the central visual field. We recently reported data obtained from microarray analysis of gene expression in the macula of the human fetal retina (Kozulin et al., Mol Vis 15:45-59, 1). In this paper, we describe the preliminary analyses undertaken to visualize differences and verify comparability of the replicates used in that study, report the differential expression of other gene families obtained from the analysis, and show the reproducibility of our findings in several gene families by quantitative real-time PCR.</p>\",\"PeriodicalId\":73873,\"journal\":{\"name\":\"Journal of ocular biology, diseases, and informatics\",\"volume\":\" \",\"pages\":\"176-189\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-11-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s12177-009-9039-1\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of ocular biology, diseases, and informatics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s12177-009-9039-1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of ocular biology, diseases, and informatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12177-009-9039-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
摘要
黄斑是灵长类动物视网膜上一个独特而重要的区域,在中央视野中实现高分辨率和彩色视觉。我们最近报道了人类胎儿视网膜黄斑基因表达的微阵列分析获得的数据(Kozulin等人,Mol Vis 15:45-59, 1)。在本文中,我们描述了用于可视化差异和验证该研究中使用的重复的可比性的初步分析,报告了从分析中获得的其他基因家族的差异表达,并通过定量实时PCR显示了我们的发现在几个基因家族中的可重复性。
Differential gene expression in the developing human macula: microarray analysis using rare tissue samples.
The macula is a unique and important region in the primate retina that achieves high resolution and color vision in the central visual field. We recently reported data obtained from microarray analysis of gene expression in the macula of the human fetal retina (Kozulin et al., Mol Vis 15:45-59, 1). In this paper, we describe the preliminary analyses undertaken to visualize differences and verify comparability of the replicates used in that study, report the differential expression of other gene families obtained from the analysis, and show the reproducibility of our findings in several gene families by quantitative real-time PCR.