人类家族性14号染色体p臂增加标记染色体中rRNA基因表达的调控 - Suppr

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Regulation of rRNA gene expression in a human familial 14p+ marker chromosome.

作者信息

Miller D A, Breg W R, Warburton D, Dev V G, Miller O J

出版信息

Hum Genet. 1978 Sep 19;43(3):289-97. doi: 10.1007/BF00278836.

DOI:10.1007/BF00278836

PMID:700703

Abstract

摘要

相似文献

Regulation of rRNA gene expression in a human familial 14p+ marker chromosome.人类家族性14号染色体p臂增加标记染色体中rRNA基因表达的调控

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Evidence for methylation of inactive human rRNA genes in amplified regions.扩增区域中失活的人类核糖体RNA基因甲基化的证据。

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[Molecular cytogenetic study on the case with 14p+ marker chromosome].

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Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.通过银染和原位杂交研究家族性相互易位t(9;13)(p11;p12)

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引用本文的文献

NO38 expression and nucleolar counts are correlated with cellular DNA content but not with proliferation parameters in colorectal carcinomas.NO38表达和核仁计数与结直肠癌中的细胞DNA含量相关，但与增殖参数无关。

Mol Pathol. 1997 Aug;50(4):201-8. doi: 10.1136/mp.50.4.201.

Extreme variant of the short arm of chromosome 15.15号染色体短臂的极端变异型。

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Amplification of (GACA)n simple repeats in an exceptional 14p+ marker chromosome.一条异常的14p+标记染色体中(GACA)n简单重复序列的扩增。

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NORs and satellite associations in a family with 13/14 translocation.一个患有13/14易位的家族中的核仁组织区和随体联合

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Polymorphism of 5-methylcytosine-rich DNA in human acrocentric chromosomes.人类近端着丝粒染色体中富含5-甲基胞嘧啶的DNA的多态性

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Human inherited marker chromosome 22 short-arm enlargement: investigation of rDNA gene multiplicity, Ag-band size, and acrocentric association.人类遗传性标记染色体22短臂增大：核糖体DNA基因多样性、银染带大小及近端着丝粒关联的研究

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Variability of the nucleolar organizer activity in human lymphocytes via Ag-staining.通过银染法检测人类淋巴细胞核仁组织区活性的变异性

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Amplified ribosomal RNA genes in a rat hepatoma cell line are enriched in 5-methylcytosine.大鼠肝癌细胞系中扩增的核糖体RNA基因富含5-甲基胞嘧啶。

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本文引用的文献

THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES.人类粗线期染色体上核仁形成的位点

Cytogenetics. 1964;3:124-34. doi: 10.1159/000129803.

[A case with balanced (14p+; 15p minus)-translocation].[一例平衡型（14号染色体短臂增加；15号染色体短臂缺失）易位病例]

Humangenetik. 1970;8(4):312-20. doi: 10.1007/BF00280330.

Double satellites: autoradiographic study of a chromosomal marker observed in two generations.双卫星：对两代中观察到的一种染色体标记的放射自显影研究。

Humangenetik. 1971;14(1):6-12. doi: 10.1007/BF00273026.

Localization of rDNA in the chimpanzee (Pan troglodytes) chromosome complement.黑猩猩（Pan troglodytes）染色体组中核糖体DNA的定位

Chromosoma. 1974;46(4):435-41. doi: 10.1007/BF00331631.

Frequency of satellite association in individuals with structural abnormalities of nucleolus organiser region.核仁组织区结构异常个体中卫星联合的频率。

Humangenetik. 1973 Apr 16;18(2):111-5. doi: 10.1007/BF00291477.

Location of ribosomal DNA in the human chromosome complement.核糖体DNA在人类染色体组中的定位。

Proc Natl Acad Sci U S A. 1972 Nov;69(11):3394-8. doi: 10.1073/pnas.69.11.3394.

Quinacrine fluorescence for identifying metaphase chromosomes, with special reference to photomicrography.用于鉴定中期染色体的喹吖因荧光法，特别涉及显微摄影术。

Stain Technol. 1972 Mar;47(2):87-93. doi: 10.3109/10520297209116456.

Expression of human and suppression of mouse nucleolus organizer activity in mouse-human somatic cell hybrids.人核仁组织区活性在小鼠 - 人类体细胞杂种中的表达及小鼠核仁组织区活性的抑制

Proc Natl Acad Sci U S A. 1976 Dec;73(12):4531-5. doi: 10.1073/pnas.73.12.4531.

Variation in the number of genes for rRNA among human acrocentric chromosomes: correlation with frequency of satellite association.人类近端着丝粒染色体中核糖体RNA基因数量的变异：与随体联合频率的相关性。

Cytogenet Cell Genet. 1976;17(4):221-30. doi: 10.1159/000130715.

Quantitative application RNA-DNA hybridization in situ.

Cytogenet Cell Genet. 1976;17(3):137-43. doi: 10.1159/000130705.

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