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囊性纤维化基因在人类胰腺发育中的表达定位

Localization of expression of the cystic fibrosis gene in human pancreatic development.

作者信息

Foulkes A G, Harris A

机构信息

Division of Medical and Molecular Genetics, UMDS, London, England.

出版信息

Pancreas. 1993 Jan;8(1):3-6. doi: 10.1097/00006676-199301000-00003.

DOI:10.1097/00006676-199301000-00003
PMID:7678325
Abstract

Cystic fibrosis (CF) is a disease that affects the function of specialized epithelial cells within the lungs, gut, pancreas, sweat glands, and male genital ducts. Following the cloning of the CF gene, it is possible to examine tissue-specific expression of this gene. To investigate the onset of the CF disease process, expression of the CF gene in midtrimester human fetal tissues has been analyzed by in situ hybridization using antisense RNA probes. The major site of CF gene expression at this stage of development is in the pancreas. Within the pancreas, CF mRNA is seen to be largely restricted to the epithelium of intralobular and small interlobular ducts.

摘要

囊性纤维化(CF)是一种影响肺、肠道、胰腺、汗腺和男性生殖管道内特殊上皮细胞功能的疾病。CF基因克隆后,就有可能检测该基因的组织特异性表达。为了研究CF疾病进程的起始,已使用反义RNA探针通过原位杂交分析了妊娠中期人胎儿组织中CF基因的表达。在这个发育阶段,CF基因表达的主要部位是胰腺。在胰腺内,CF mRNA在很大程度上局限于小叶内和小叶间小导管的上皮。

相似文献

1
Localization of expression of the cystic fibrosis gene in human pancreatic development.囊性纤维化基因在人类胰腺发育中的表达定位
Pancreas. 1993 Jan;8(1):3-6. doi: 10.1097/00006676-199301000-00003.
2
Expression of the cystic fibrosis gene in human foetal tissues.囊性纤维化基因在人胎儿组织中的表达。
Hum Mol Genet. 1993 Mar;2(3):213-8. doi: 10.1093/hmg/2.3.213.
3
Cell-specific localization of CFTR mRNA shows developmentally regulated expression in human fetal tissues.CFTR mRNA的细胞特异性定位显示其在人胎儿组织中的表达受发育调控。
Hum Mol Genet. 1993 Mar;2(3):219-24. doi: 10.1093/hmg/2.3.219.
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Regional expression of CFTR in developing human respiratory tissues.囊性纤维化跨膜传导调节因子(CFTR)在发育中的人类呼吸组织中的区域表达。
Am J Respir Cell Mol Biol. 1994 Apr;10(4):355-62. doi: 10.1165/ajrcmb.10.4.7510983.
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Expression of the cystic fibrosis gene in human development.囊性纤维化基因在人类发育中的表达。
Development. 1991 Sep;113(1):305-10. doi: 10.1242/dev.113.1.305.
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Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.通过原位杂交对人胃肠道中囊性纤维化跨膜传导调节因子mRNA进行定位。
J Clin Invest. 1994 Jan;93(1):347-54. doi: 10.1172/JCI116966.
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Skipping of exon 9 in CFTR mRNA of human adult and fetal pancreas from non-CF individuals.来自非囊性纤维化个体的成人和胎儿胰腺CFTR mRNA中外显子9的跳跃。
Hum Mol Genet. 1993 Dec;2(12):2141-2. doi: 10.1093/hmg/2.12.2141.
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Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue.囊性纤维化跨膜传导调节因子基因的无义突变R1162X不会降低鼻上皮组织中的信使核糖核酸表达。
J Clin Invest. 1993 Dec;92(6):2683-7. doi: 10.1172/JCI116885.
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Submucosal glands are the predominant site of CFTR expression in the human bronchus.
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Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice.人囊性纤维化跨膜传导调节因子定向至转基因小鼠的呼吸道上皮细胞。
Nat Genet. 1992 Sep;2(1):13-20. doi: 10.1038/ng0992-13.

引用本文的文献

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Stellate cells are in utero markers of pancreatic disease in cystic fibrosis.星状细胞是囊性纤维化中胰腺疾病的宫内标志物。
Mol Med. 2024 Aug 7;30(1):115. doi: 10.1186/s10020-024-00871-2.
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Analysis of DNase-I-hypersensitive sites at the 3' end of the cystic fibrosis transmembrane conductance regulator gene (CFTR).囊性纤维化跨膜传导调节因子基因(CFTR)3'端的脱氧核糖核酸酶I超敏位点分析。
Biochem J. 1999 Aug 1;341 ( Pt 3)(Pt 3):601-11.
3
Mouse pancreatic acinar/ductular tissue gives rise to epithelial cultures that are morphologically, biochemically, and functionally indistinguishable from interlobular duct cell cultures.
小鼠胰腺腺泡/导管组织产生的上皮细胞培养物在形态、生化和功能上与小叶间导管细胞培养物无法区分。
In Vitro Cell Dev Biol Anim. 1994 Sep;30A(9):622-35. doi: 10.1007/BF02631262.