DOP-PCR amplification of whole genomic DNA and microchip-based capillary electrophoresis.
作者信息
Fortina P, Cheng J, Kricka L J, Waters L C, Jacobson S C, Wilding P, Ramsey J M
机构信息
Department of Pediatrics, University of Pennsylvania School of Medicine, Children's Hospital of Philadelphia, Abramson Pediatric Research Center, Philadelphia, PA, USA.
出版信息
Methods Mol Biol. 2001;163:211-9. doi: 10.1385/1-59259-116-7:211.
PMID:11242946
Abstract
摘要
相似文献
1
DOP-PCR amplification of whole genomic DNA and microchip-based capillary electrophoresis.
Methods Mol Biol. 2001;163:211-9. doi: 10.1385/1-59259-116-7:211.
2
Degenerate oligonucleotide primed-polymerase chain reaction and capillary electrophoretic analysis of human DNA on microchip-based devices.基于微芯片设备的人类DNA简并寡核苷酸引物聚合酶链反应及毛细管电泳分析
Anal Biochem. 1998 Mar 15;257(2):101-6. doi: 10.1006/abio.1997.2531.
3
Toward effective PCR-based amplification of DNA on microfabricated chips.
Methods Mol Biol. 2001;163:191-204. doi: 10.1385/1-59259-116-7:191.
4
Integration of gene amplification and capillary gel electrophoresis on a polydimethylsiloxane-glass hybrid microchip.基因扩增与毛细管凝胶电泳在聚二甲基硅氧烷-玻璃混合微芯片上的集成。
Electrophoresis. 2001 Jan;22(2):328-33. doi: 10.1002/1522-2683(200101)22:2<328::AID-ELPS328>3.0.CO;2-C.
5
Multiplex ligation-dependent probe amplification is superior for detecting deletions/duplications in Duchenne muscular dystrophy.多重连接依赖探针扩增技术在检测杜氏肌营养不良症的缺失/重复方面更具优势。
Clin Genet. 2005 Feb;67(2):189-91. doi: 10.1111/j.1399-0004.2004.00382.x.
6
DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.基于变性梯度凝胶电泳的杜兴氏和贝克氏肌营养不良症患者肌营养不良蛋白基因全基因突变扫描
Hum Mutat. 2004 Jan;23(1):57-66. doi: 10.1002/humu.10283.
7
Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene.
Eur J Hum Genet. 2008 Jan;16(1):53-61. doi: 10.1038/sj.ejhg.5201916. Epub 2007 Aug 29.
8
Microchip capillary electrophoresis/electrochemistry.微芯片毛细管电泳/电化学
Electrophoresis. 2001 Aug;22(12):2526-36. doi: 10.1002/1522-2683(200107)22:12<2526::AID-ELPS2526>3.0.CO;2-K.
9
Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.夸祖鲁-纳塔尔省杜兴氏和贝克氏肌肉营养不良症患者的分子缺失模式
J Neurol Sci. 2007 Jan 15;252(1):1-3. doi: 10.1016/j.jns.2006.06.025. Epub 2006 Dec 1.
10
dcDegenerate oligonucleotide primed-PCR for multilocus, genome-wide analysis from limited quantities of DNA.用于从有限量DNA进行多位点、全基因组分析的简并寡核苷酸引物PCR
Diagn Mol Pathol. 2009 Sep;18(3):165-75. doi: 10.1097/PDM.0b013e31818d34d1.
Zotero 插件