D22S15--a fetal brain cDNA with BanII and SacI RFLP.
作者信息
Rouleau G A, Kurnit D M, Neve R L, Bazanowsky A, Patterson D, Gusella J F
机构信息
Massachusetts General Hospital, Neurogenetics Department, Boston 02114.
出版信息
Nucleic Acids Res. 1988 Feb 25;16(4):1646. doi: 10.1093/nar/16.4.1646.
Abstract
摘要
相似文献
1
D22S15--a fetal brain cDNA with BanII and SacI RFLP.D22S15——一种具有BanII和SacI限制性片段长度多态性的胎儿脑互补DNA。
Nucleic Acids Res. 1988 Feb 25;16(4):1646. doi: 10.1093/nar/16.4.1646.
2
A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11-17q22).在人类（17q11 - 17q22）中，由来自HOX2基因座的探针经SacI和BanII鉴定出的一种中度常见的限制性片段长度多态性。
Nucleic Acids Res. 1987 Aug 11;15(15):6311. doi: 10.1093/nar/15.15.6311.
3
SacI RFLP in the human von Willebrand factor gene.人类血管性血友病因子基因中的SacI限制性片段长度多态性
Nucleic Acids Res. 1987 Aug 25;15(16):6766. doi: 10.1093/nar/15.16.6766.
4
An MPO cDNA clone identifies an RFLP with PstI.一个髓过氧化物酶（MPO）cDNA克隆鉴定出一个与PstI相关的限制性片段长度多态性（RFLP）。
Nucleic Acids Res. 1988 Feb 25;16(4):1649. doi: 10.1093/nar/16.4.1649.
5
Styl RFLP recognised by a human IRBP cDNA localised to chromosome 10.由定位于10号染色体的人IRBP cDNA识别的Styl RFLP。
Nucleic Acids Res. 1988 Feb 25;16(4):1645. doi: 10.1093/nar/16.4.1645.
6
SacI RFLP recognized by a human immunoglobulin kappa light chain constant region probe.由人免疫球蛋白κ轻链恒定区探针识别的SacI限制性片段长度多态性
Nucleic Acids Res. 1987 May 11;15(9):3942. doi: 10.1093/nar/15.9.3942.
7
A BanII dimorphic site located in the third intron of the human apolipoprotein AI (APOA1) gene.一个位于人类载脂蛋白AI（APOA1）基因第三个内含子中的BanII二态性位点。
Nucleic Acids Res. 1988 Feb 11;16(3):1221. doi: 10.1093/nar/16.3.1221.
8
XmnI RFLP at 5q13 detected by a 0.49 kb Xmn I fragment of human hexosaminidase (HEXB) cDNA.通过人己糖胺酶（HEXB）cDNA的0.49 kb XmnI片段检测到5q13处的XmnI限制性片段长度多态性。
Nucleic Acids Res. 1988 Aug 25;16(16):8198. doi: 10.1093/nar/16.16.8198.
9
Bgl II RFLP recognized by a human IRBP cDNA localized to chromosome 10.由定位于10号染色体的人视网膜间质视黄醇结合蛋白cDNA识别的Bgl II限制性片段长度多态性。
Nucleic Acids Res. 1987 Apr 10;15(7):3196. doi: 10.1093/nar/15.7.3196.
10
Human natriuretic peptides (ANP) gene locus: BsmI RFLP.人利钠肽（ANP）基因位点：BsmI限制性片段长度多态性
Nucleic Acids Res. 1987 Sep 25;15(18):7656. doi: 10.1093/nar/15.18.7656.
引用本文的文献
1
Comparative mapping of the constitutional and tumor-associated 11;22 translocations.先天性和肿瘤相关的11；22易位的比较图谱分析
Am J Hum Genet. 1989 Jul;45(1):128-39.
2
A t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene.脑膜瘤中的t(4;22)指向一个假定的肿瘤抑制基因的定位。
Am J Hum Genet. 1991 Apr;48(4):783-90.
本文引用的文献
1
A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.一个带有单条人类22号染色体的体细胞杂种纠正了缺乏腺苷琥珀酸酶活性的CHO突变体（Ade-I）中的缺陷。
Cytogenet Cell Genet. 1987;44(2-3):142-7. doi: 10.1159/000132358.
Zotero 插件