PCR-based detection of two MspI polymorphic sites at D18S8.
作者信息
Parry P J, Markie D, Fearon E R, Nigro J M, Vogelstein B, Bodmer W F
机构信息
Department of Clinical Genetics, Royal Free School of Medicine, Hampstead, London, UK.
出版信息
Nucleic Acids Res. 1991 Dec 25;19(24):6983. doi: 10.1093/nar/19.24.6983-a.
Abstract
摘要
相似文献
1
PCR-based detection of two MspI polymorphic sites at D18S8.基于聚合酶链反应（PCR）检测18号染色体短臂上D18S8位点的两个MspI多态性位点
Nucleic Acids Res. 1991 Dec 25;19(24):6983. doi: 10.1093/nar/19.24.6983-a.
2
PCR detection of the MspI (Aa) RFLP at the human phenylalanine hydroxylase (PAH) locus.在人苯丙氨酸羟化酶（PAH）基因座上对MspI（Aa）限制性片段长度多态性（RFLP）进行聚合酶链反应（PCR）检测。
Nucleic Acids Res. 1991 Apr 25;19(8):1959. doi: 10.1093/nar/19.8.1959.
3
The MspI polymorphism in intron 6 of p53 (TP53) detected by digestion of PCR products.通过PCR产物酶切检测p53（TP53）第6内含子中的MspI多态性。
Nucleic Acids Res. 1991 Sep 11;19(17):4796. doi: 10.1093/nar/19.17.4796-a.
4
PCR detection of the MspI polymorphism in the human IRBP gene (RPB3).人视网膜间维生素A结合蛋白基因（RPB3）中MspI多态性的聚合酶链反应检测
Nucleic Acids Res. 1991 Jul 25;19(14):4016. doi: 10.1093/nar/19.14.4016-a.
5
Polymerase chain reaction (PCR) for detection of MspI polymorphism at the D3S30 locus.
Nucleic Acids Res. 1991 Jul 11;19(13):3757.
6
MspI RFLP of FSHB on chromosome 11p.11号染色体短臂上卵泡刺激素β亚基基因的MspI限制性片段长度多态性
Nucleic Acids Res. 1991 Dec 25;19(24):6981. doi: 10.1093/nar/19.24.6981-a.
7
Polymerase chain reaction (PCR) for detection of MspI polymorphism at the D3S3 locus.
Nucleic Acids Res. 1991 Jul 11;19(13):3759.
8
MspI polymorphism of the human CYP2E gene.人类CYP2E基因的MspI多态性
Nucleic Acids Res. 1991 Oct 25;19(20):5797. doi: 10.1093/nar/19.20.5797.
9
Two MspI polymorphisms within the APC gene.
Hum Mol Genet. 1992 Aug;1(5):352. doi: 10.1093/hmg/1.5.352-a.
10
Polymerase chain reaction (PCR) for detection of MspI polymorphism at the D3S6 locus.
Nucleic Acids Res. 1991 Jul 11;19(13):3759.
引用本文的文献
1
Loss of heterozygosity and mRNA expression at deleted in colorectal cancer gene locus in gastric cancer.胃癌中结直肠癌缺失基因位点的杂合性缺失及mRNA表达
World J Gastroenterol. 1997 Sep 15;3(3):156-9. doi: 10.3748/wjg.v3.i3.156.
2
Fluorescence polarization in homogeneous nucleic acid analysis.均相核酸分析中的荧光偏振
Genome Res. 1999 May;9(5):492-8.
3
Loss of heterozygosity and loss of expression of the DCC gene in gastric cancer.胃癌中DCC基因的杂合性缺失和表达缺失
J Clin Pathol. 1998 Aug;51(8):593-6. doi: 10.1136/jcp.51.8.593.
4
Template-directed dye-terminator incorporation (TDI) assay: a homogeneous DNA diagnostic method based on fluorescence resonance energy transfer.模板导向的染料终止剂掺入（TDI）分析：一种基于荧光共振能量转移的均相DNA诊断方法。
Nucleic Acids Res. 1997 Jan 15;25(2):347-53. doi: 10.1093/nar/25.2.347.
5
Numerical chromosome alterations in colorectal carcinomas detected by fluorescence in situ hybridization. Relationship to 17p and 18q allelic losses.通过荧光原位杂交检测结直肠癌中的染色体数目改变。与17p和18q等位基因缺失的关系。
Virchows Arch. 1996 Jul;428(4-5):243-51. doi: 10.1007/BF00196697.
6
Loss of expression and loss of heterozygosity in the DCC gene in neoplasms of the human female reproductive tract.人类女性生殖道肿瘤中DCC基因的表达缺失和杂合性缺失。
Br J Cancer. 1995 Mar;71(3):462-7. doi: 10.1038/bjc.1995.94.
本文引用的文献
1
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8).通过位于18q21.3的匿名DNA片段OL VII E10鉴定的限制性片段长度多态性（HGM编号：D18S8）。
Nucleic Acids Res. 1987 Feb 11;15(3):1348. doi: 10.1093/nar/15.3.1348.
2
Identification of a chromosome 18q gene that is altered in colorectal cancers.在结直肠癌中发生改变的18号染色体长臂基因的鉴定。
Science. 1990 Jan 5;247(4938):49-56. doi: 10.1126/science.2294591.
Zotero 插件