Andrew J Griffith

University of Tennessee Health Science Center Memphis - Memphis / United States

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AD Scientific Index ID: 1639097

Universität Konstanz

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Andrew J Griffith's MOST POPULAR ARTICLES

1-) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23JM Bork, LM Peters, S Riazuddin, SL Bernstein, ZM Ahmed, SL Ness, ...The American Journal of Human Genetics 68 (1), 26-37, 20016002001

2-) Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29ER Wilcox, QL Burton, S Naz, S Riazuddin, TN Smith, B Ploplis, ...Cell 104 (1), 165-172, 20015372001

3-) Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell functionK Kurima, LM Peters, Y Yang, S Riazuddin, ZM Ahmed, S Naz, D Arnaud, ...Nature genetics 30 (3), 277-284, 20024492002

4-) Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZM Ahmed, S Riazuddin, SL Bernstein, Z Ahmed, S Khan, AJ Griffith, ...The American Journal of Human Genetics 69 (1), 25-34, 20014832001

5-) Binding of Ku protein to DNA. Measurement of affinity for ends and demonstration of binding to nicks.PR Blier, AJ Griffith, J Craft, JA Hardinjournal of Biological Chemistry 268 (10), 7594-7601, 19934261993

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