Reagent DNA RNA synthesis

Purine Nucleoside Analogs Universal Solid Support and Trimers (Sponsored Link)
http://www.metkinenchemistry.com/

 

Trinucleotide repeats

Get the Answers You're Looking For. Trinucleotide repeats (Sponsored Link)
http://www.RightHealth.com/Genetic/

 

BioMed Central |Full text |COPASAAR - A database for proteomic analysis of single amino acid repeats

Skip to main content ... LeProust EM, Pearso CE, Sinden RR, Gao XL: Unexpected formation of parallel duplex in GAA and TTC trinucleotide repeats of Friedreich's ataxia. ... Karlin S, Burge C: Trinucleotide...
http://www.biomedcentral.com/1471-2105/6/196

 

Hereditary Disease Foundation Homepage

--WARNING-- / If you are here it is because you have turned off the Javascript functionality of your browser. To fully appreciate all the features of this site, Please enable Javascript and press the refresh button. System Requirements / 800x600...
http://www.hdfoundation.org/

 

Science : Anticipating schizophrenia in twins - 23 November 1996 - New Scientist

New Scientist| / Space| / Technology| / Environment| / New Scientist Jobs|Subscribe to New Scientist / NEWS | / EXPLORE BY SUBJECT | ... As they are passed down the generations, mutated trinucleotide repeats usually increase...
http://www.newscientist.com/article/mg15220572.900-science--anticipating-schizophrenia-in-twins.html

 

Antithrombin Mutation Database

Return to the Imperial homepage / Research / Courses / Faculties & Departments / Campus / Life / News & Events / Admin & Services ... Two of these Alu5 and Alu8 within intron 4 have tails composed of ATT trinucleotide...
http://www1.imperial.ac.uk/medicine/about/divisions/is/haemo/coag/antithrombin/

 

Anita Harding - Wikipedia

Anita Harding / From Wikipedia ... Her major achievements are the classification of the peripheral neuropathies and hereditary ataxias, the first identification of a mitochondrial DNA mutation in human disease and the identification of...
http://en.wikipedia.org/wiki/Anita_Harding

 

Genome Biology |Full text |Mutation patterns of amino acid tandem repeats in the human proteome

Log on / register / BioMed Central home | / Journals A-Z | / Feedback | / Support / home | comment | / reviews | / reports | / deposited research | / refereed research | ... Jodice C, Giovannone B, Calabresi V, Bellocchi M, Terrenato L, Novelletto...
http://genomebiology.com/2006/7/4/R33

 

Glasgow ePrints Service - Mouse tissue culture models of unstable triplet repeats: in vitro selection for larger alleles, mutational expansion bias and tissue s

GLASGOW ePRINTS SERVICE / Published material by members of the University of Glasgow / ePrints Home | / About | / Browse | / Search | / Register | / User Area | / Help ... The expansion of CAG.CTG trinucleotide repeats has...
http://eprints.gla.ac.uk/502/

 

Cambridge Multiple Sclerosis Genetics Group

Multiple Sclerosis / Genetics Group / Abstract ... Expanded CAG trinucleotide repeats are known to be responsible for five of the autosomal dominant spinocerebellar ataxias (SCA1, SCA2, SCA3, SCA6, and SCA7). We have typed...
http://www-gene.cimr.cam.ac.uk/MSgenetics/Abstracts/sca.shtml

 

Fragile X Syndrome: Fmr1 Gene

... The diagnosis of the fragile X syndrome is confirmed by the detection of an increased number of CGG trinucleotide repeats (over 230) in the FMR1 gene, usually with aberrant methylation of the FMR1 gene. The increased...
http://www.lycos.com/info/fragile-x-syndrome--fmr1-gene.html

 

C S CHOONG and E M WILSON: CAG Repeat in the androgen receptor (Journal of Molecular Endocrinology)

REVIEW: Trinucleotide repeats in the human androgen receptor: a molecular basis for disease / C S Choong1 and E M Wilson2 ...
http://journals.endocrinology.org/jme/021/jme0210235.htm

 
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