Age-Related Macular Degeneration—a Genome Scan in Extended Families von Majewski, Jacek, Schultz, Dennis W., Weleber, Richard G., Schain, Mitchell B., Edwards, Albert O., Matise, Tara C., Acott, Ted S., Ott, Jurg, Klein, Michael L.

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Analysis of the ARMD1 locus: evidence that a mutation in HEMICENTIN-1 is associated with age-related macular degeneration in a large family von Schultz, Dennis W., Klein, Michael L., Humpert, Andrea J., Luzier, Christina W., Persun, Vesna, Schain, Mitchell, Mahan, Alison, Runckel, Charles, Cassera, Maria, Vittal, Vasavi, Doyle, Trudy M., Martin, Tammy M., Weleber, Richard G., Francis, Peter J., Acott, Ted S.

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Genetic and phenotypic heterogeneity in pattern dystrophy von Francis, P J, Schultz, D W, Gregory, A M, Schain, M B, Barra, R, Majewski, J, Ott, J, Acott, T, Weleber, R G, Klein, M L

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Phase 2 randomized placebo controlled double blind study to assess the efficacy and safety of tecfidera in patients with amyotrophic lateral sclerosis (TEALS Study): Study protocol... von Vucic, Steve, Ryder, Julie, Mekhael, Linda, RD, Henderson, Mathers, Susan, Needham, Merilee, DW, Schultz, MC, Kiernan

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Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human β-Crystallin Gene CRYBB2 von Litt, Michael, Carrero-Valenzuela, Roque, LaMorticella, Dante M., Schultz, Dennis W., Mitchell, Thomas N., Kramer, Patricia, Maumenee, Irene H.

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Transfer RNA Mutation and the Malleability of the Genetic Code von Schultz, Dennis W., Yarus, Michael

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On malleability in the genetic code von Schultz, D W, Yarus, M

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Expanded genome scan in extended families with age-related macular degeneration von Barral, S, Francis, P.J, Schultz, D.W, Schain, M.B, Haynes, C, Majewski, J, Ott, J, Acott, T, Weleber, R.G, Klein, M.L

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Further comments on codon reassignment. Response von Yarus, M, Schultz, D W

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Age-related Macular Degeneration: Clinical Features in a Large Family and Linkage to Chromosome 1q von Klein, Michael L, Schultz, Dennis W, Edwards, Al, Matise, Tara C, Rust, Kristal, Berselli, C. Blair, Trzupek, Karmen, Weleber, Richard G, Ott, Jurg, Wirtz, Mary K, Acott, Ted S

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Lack of an Association of Apolipoprotein E Gene Polymorphisms With Familial Age-Related Macular Degeneration von Schultz, Dennis W, Klein, Michael L, Humpert, Andrea, Majewski, Jacek, Schain, Mitchell, Weleber, Richard G, Ott, Jurg, Acott, Ted S

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RecBC enzyme nicking at chi sites during DNA unwinding: Location and orientation-dependence of the cutting von Taylor, Andrew F., Schultz, Dennis W., Ponticelli, Alfred S., Smith, Gerald R.

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Behavioural disturbance and visual hallucinations in a 78 year old man von Schultz, David W, Lennox, Graham G, Ironside, James W, Warlow, Charles P

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Chi-dependent DNA strand cleavage by RecBC enzyme von Ponticelli, Alfred S., Schultz, Dennis W., Taylor, Andrew F., Smith, Gerald R.

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Structure of chi hotspots of generalized recombination von Smith, Gerald R., Kunes, Sam Martin, Schultz, Dennis W., Taylor, Andrew, Triman, Kathleen L.

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High dose oral methylprednisolone in patients with rheumatoid arthritis: pharmacokinetics and clinical response von Hayball, P J, Cosh, D G, Ahern, M J, Schultz, D W, Roberts-Thomson, P J

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Escherichia coli RecBC pseudorevertants lacking chi recombinational hotspot activity von SCHULTZ, D. W, TAYLOR, A. F, SMITH, G. R

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Conservation of Chi cutting activity in terrestrial and marine enteric bacteria von Schultz, Dennis W., Smith, Gerald R.

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Nucleotide sequence of the lysozyme gene of bacteriophage T4. Analysis of mutations involving repeated sequences von Owen, J E, Schultz, D W, Taylor, A, Smith, G R

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Clustering of mutations inactivating a Chi recombinational hotspot von Schultz, Dennis W., Swindle, John, Smith, Gerald R.

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