A strategy for the rapid isolation of new PCR based DNA polymorphisms.
作者信息
Hoban P R, Santibanez-Koref M F, Heighway J
机构信息
CRC Department of Cancer Genetics, Paterson Institute for Cancer Research, Manchester.
出版信息
J Med Genet. 1992 Apr;29(4):249-50. doi: 10.1136/jmg.29.4.249.
Abstract
摘要
相似文献
1
A strategy for the rapid isolation of new PCR based DNA polymorphisms.一种基于聚合酶链反应快速分离新的DNA多态性的策略。
J Med Genet. 1992 Apr;29(4):249-50. doi: 10.1136/jmg.29.4.249.
2
[A new method for detection of DNA polymorphisms using the polymerase chain reaction].
Tanpakushitsu Kakusan Koso. 1990 Dec;35(17):3085-90.
3
Mitochondrial DNA polymorphisms in Phytophthora infestans: new haplotypes are identified and re-defined by PCR.马铃薯晚疫病菌线粒体 DNA 多态性：通过 PCR 鉴定和重新定义新的单倍型。
J Microbiol Methods. 2013 Nov;95(2):117-21. doi: 10.1016/j.mimet.2013.08.001. Epub 2013 Aug 13.
4
Rapid detection of intercellular adhesion molecule 1 (G241R and K469E) polymorphisms by a novel PCR-SSP assay.通过新型聚合酶链反应-序列特异性引物分析法快速检测细胞间黏附分子1（G241R和K469E）多态性
Tissue Antigens. 2007 Apr;69(4):338-41. doi: 10.1111/j.1399-0039.2007.00813.x.
5
6
Identification of twelve polymorphisms in the endothelin-1 gene by use of fluorescently labeled oligonucleotides and PCR with restriction fragment polymorphism analysis.
Clin Chem. 2004 Feb;50(2):448-51. doi: 10.1373/clinchem.2003.025593.
7
Residual polymerase activity-induced bias in terminal restriction fragment length polymorphism analysis.末端限制性片段长度多态性分析中残留聚合酶活性诱导的偏差
Environ Microbiol. 2007 Feb;9(2):555-9. doi: 10.1111/j.1462-2920.2006.01169.x.
8
Simplified AFLP protocol: replacement of primer labeling by the incorporation of alpha-labeled nucleotides during PCR.简化的扩增片段长度多态性（AFLP）方案：通过在聚合酶链式反应（PCR）过程中掺入α-标记的核苷酸来替代引物标记。
Biotechniques. 2000 Apr;28(4):622-3. doi: 10.2144/00284bm01.
9
Rapid and direct detection of apolipoprotein E genotypes using whole blood from humans.利用人类全血快速直接检测载脂蛋白 E 基因型。
J Toxicol Environ Health A. 2010;73(21-22):1502-10. doi: 10.1080/15287394.2010.511573.
10
Detection of hotspot mutations and polymorphisms using an enhanced PCR-RFLP approach.使用改进的聚合酶链反应-限制性片段长度多态性方法检测热点突变和多态性。
Hum Mutat. 2003 May;21(5):535-41. doi: 10.1002/humu.10184.
引用本文的文献
1
A transcribed polymorphism and sub-localisation of MDM2.MDM2的转录多态性与亚定位
Hum Genet. 1994 May;93(5):611-2. doi: 10.1007/BF00202837.
本文引用的文献
1
RsaI polymorphism in c-Ki-ras.c-Ki-ras基因中的RsaI多态性
Nucleic Acids Res. 1991 Feb 25;19(4):968. doi: 10.1093/nar/19.4.968-a.
2
PstI polymorphism within the 3' untranslated region of the insulin gene detectable by the polymerase chain reaction (INS).通过聚合酶链反应（INS）可检测到的胰岛素基因3'非翻译区内的PstI多态性。
Nucleic Acids Res. 1991 Aug 25;19(16):4576. doi: 10.1093/nar/19.16.4576-a.
3
PCR primers to convert c-Ki-ras to a four allele RsaI system (KRAS2).用于将c-Ki-ras转化为四等位基因RsaI系统（KRAS2）的PCR引物。
Nucleic Acids Res. 1991 Dec 25;19(24):6966. doi: 10.1093/nar/19.24.6966-a.
4
A MaeIII polymorphism within intron A of the insulin (INS) gene detectable by PCR.通过聚合酶链反应（PCR）可检测到胰岛素（INS）基因内含子A内的MaeIII多态性。
Nucleic Acids Res. 1991 Sep 25;19(18):5091. doi: 10.1093/nar/19.18.5091-a.
5
BsmI polymorphism in N-ras intron I (RASN).N-ras基因内含子I中的BsmI多态性（RASN）
Nucleic Acids Res. 1991 Feb 11;19(3):682. doi: 10.1093/nar/19.3.682.
Zotero 插件