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Neurobiology of Disease|September 9, 2019
Friedreich ataxia- pathogenesis and implications for therapiesMartin B Delatycki, Sanjay I Bidichandani
The Journal of the Oklahoma State Medical Association|March 5, 2004
What Mendel did not discover: exceptions in Mendelian genetics and their role in inherited human diseaseLaura M Hern, Sanjay I Bidichandani
Nucleic Acids Research|November 30, 2007
Repair of DNA double-strand breaks within the (GAA*TTC)n sequence results in frequent deletion of the triplet-repeat sequenceLaura M Pollard, Rebecka L Bourn, Sanjay I Bidichandani
Methods in Molecular Biology (Clifton, N.J.)|June 18, 2004
Analysis of unstable triplet repeats using small-pool polymerase chain reactionMário Gomes-Pereira, Sanjay I Bidichandani, Darren G Monckton
The Journal of Biological Chemistry|April 17, 2014
Altered nucleosome positioning at the transcription start site and deficient transcriptional initiation in Friedreich ataxiaYogesh K Chutake, Whitney N Costello, Christina Lam, et al.
Mutation Research|December 3, 2008
E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequenceRebecka L Bourn, Paul M Rindler, Laura M Pollard, et al.
Annals of Neurology|August 13, 2014
Epigenetic promoter silencing in Friedreich ataxia is dependent on repeat lengthYogesh K Chutake, Christina Lam, Whitney N Costello, et al.
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