Titlebook: Neurogenetics; Methods and Protocol Nicholas T. Potter Book 2003 Humana Press 2003

冠軍

書目名稱Neurogenetics影響因子(影響力)




書目名稱Neurogenetics影響因子(影響力)學科排名




書目名稱Neurogenetics網(wǎng)絡公開度




書目名稱Neurogenetics網(wǎng)絡公開度學科排名




書目名稱Neurogenetics被引頻次




書目名稱Neurogenetics被引頻次學科排名




書目名稱Neurogenetics年度引用




書目名稱Neurogenetics年度引用學科排名




書目名稱Neurogenetics讀者反饋




書目名稱Neurogenetics讀者反饋學科排名

鴕鳥

Molecular Detection of Galactosemia Mutations by PCR-ELISAalactose is the main treatment. However, this does not prevent secondary complications such as growth retardation, mental retardation, dyspraxia, cataracts, ataxia, and ovarian failure later in life (.).

spinal-stenosis

Multiplexed Fluorescence Analysis for Mutations Causing Tay-Sachs Diseaseuals since the 1970s, which has greatly reduced the number of affected children in this population. The standard method of carrier testing is by biochemical analysis for reduced Hex A activity in serum (.).

安撫

Determination of Gene Dosagethe carrier state, for disorders such as Duchenne muscular dystrophy and spinal muscular atrophy, the accurate determination of heterozygous deletions is essential. This chapter will describe two methods for the determination of gene dosage, using Duchenne muscular dystrophy and spinal muscular atrophy as examples.

去才蔑視

Extreme Expansion Detection in Spinocerebellar Ataxia Type 2 and Type 7plification of the repeat region, separation of PCR products by gel electrophoresis or capillary electrophoresis, and visualization of products by incorporation of radioactivity or dye into PCR products or staining with dye after product separation (.–.).

有抱負者

Arable

Subjugate

PHON

Denaturing Gradient Gel Electrophoresis (DGGE) for Mutation Detection in Duchenne Muscular Dystrophyd the remaining 30% are mutations that are very difficult to identify by current diagnostic screening strategies (.–.). The great majority of deletions can be detected by polymerase chain reaction . multiplex approach (.,.) or Southern blot analysis probed with dystrophin . (.).

不能平靜

Fluorescence PCR and GeneScan? Analysis for the Detection of CAG Repeat Expansions Associated with Honal specific death predominantly within the neostratum (.). Huntington is widely expressed in both the brain and nonneural tissues (.) and interestingly, N-terminal fragments of huntingtin, containing the elongated polyglutamine residues form aggregates, and can be visualized as cytoplasmic and nuclear inclusions (.).