将D8S7和D8S11定位到8号染色体短臂的8p23.1带。 - Suppr

Suppr

超能文献

Physical mapping of D8S7 and D8S11 to the band 8p23.1 of the short arm of chromosome 8.

作者信息

Alkan M, Wood S, Borer U, Hofmann S, Bühler E

机构信息

Molecular Genetics and Cytogenetics Department, University Children's Hospital, Basel, Switzerland.

出版信息

Nucleic Acids Res. 1989 Oct 25;17(20):8395. doi: 10.1093/nar/17.20.8395.

DOI:10.1093/nar/17.20.8395

PMID:2813077

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC335000/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43d1/335000/13cd12cdf0d2/nar00137-0364-a.jpg

相似文献

Physical mapping of D8S7 and D8S11 to the band 8p23.1 of the short arm of chromosome 8.将D8S7和D8S11定位到8号染色体短臂的8p23.1带。

Nucleic Acids Res. 1989 Oct 25;17(20):8395. doi: 10.1093/nar/17.20.8395.

The human erg gene maps to chromosome 21, band q22: relationship to the 8; 21 translocation of acute myelogenous leukemia.人类erg基因定位于21号染色体q22带：与急性髓性白血病的8；21易位的关系。

Oncogene. 1988 Nov;3(5):497-500.

The human neurofilament gene (NEFL) is located on the short arm of chromosome 8.人类神经丝基因（NEFL）位于8号染色体的短臂上。

Cytogenet Cell Genet. 1987;45(1):30-2. doi: 10.1159/000132421.

A somatic cell hybrid mapping panel for regional assignment of human chromosome 13 DNA sequences.用于人类13号染色体DNA序列区域定位的体细胞杂交定位板。

Cytogenet Cell Genet. 1989;52(1-2):1-6. doi: 10.1159/000132827.

Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization.利用荧光原位杂交技术对前列腺癌8号染色体短臂进行缺失图谱分析。

Oncogene. 1994 Oct;9(10):3071-6.

Isolation of a yeast artificial chromosome spanning the 8;21 translocation breakpoint t(8;21)(q22;q22.3) in acute myelogenous leukemia.在急性髓性白血病中分离出跨越8;21易位断点t(8;21)(q22;q22.3)的酵母人工染色体。

Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4882-6. doi: 10.1073/pnas.88.11.4882.

Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomas.B细胞淋巴瘤中与复发性染色体易位t(3;14)(q27;q32)和t(3;22)(q27;q11)相关基因的鉴定。

Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5262-6. doi: 10.1073/pnas.90.11.5262.

MASL1, a candidate oncogene found in amplification at 8p23.1, is translocated in immunoblastic B-cell lymphoma cell line OCI-LY8.MASL1是一种在8p23.1扩增中发现的候选癌基因，在免疫母细胞性B细胞淋巴瘤细胞系OCI-LY8中发生易位。

Oncogene. 2004 Apr 1;23(14):2576-81. doi: 10.1038/sj.onc.1207352.

Assignment of IkappaB kinase beta (IKBKB) to human chromosome band 8p12-->p11 by in situ hybridization.

Cytogenet Cell Genet. 1998;82(1-2):32-3. doi: 10.1159/000015058.

Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint.遗传性肾癌3;8号染色体易位断点的定位克隆

Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8509-13. doi: 10.1073/pnas.90.18.8509.

引用本文的文献

D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).D8S7在8号染色体短臂的反向重复（inv dup 8p）中持续缺失。

Hum Genet. 1993 Oct;92(4):391-6. doi: 10.1007/BF01247342.

本文引用的文献

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。附录

Anal Biochem. 1984 Feb;137(1):266-7. doi: 10.1016/0003-2697(84)90381-6.

A DNA marker for human chromosome 8 that detects alleles of differing sizes.

Cytogenet Cell Genet. 1986;42(3):113-8. doi: 10.1159/000132262.

Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).从一个经流式细胞分选的人类8号染色体文库中分离并鉴定出可检测限制性片段长度多态性（RFLP）的DNA探针。

Am J Hum Genet. 1986 Dec;39(6):744-50.

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。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验