The sources of forgetting in working memory are a matter of intense debate: is there a time-related decay of memory traces or is forgetting uniquely due to representation-based interference? In a previous study, we claimed to have provided evidence supporting the temporal decay hypothesis (Portrat, Barrouillet, & Camos, 2008). However, reanalyzing our data, Lewandowsky and Oberauer (2009) demon...

Farming of finfish in sea cages is gaining popularity worldwide. These systems are a suitable environment for the emergence, establishment and transmission of parasites or pathogens, such as sea lice (Copepoda: Caligidae), known to cause serious diseases and economic losses in finfish aquaculture worldwide. In coastal waters of Jaramijó, Ecuador, there are plans to culture spotted rose snapper ...

2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 BORIS FELDMAN, State Bar No . 128838 (boris [email protected]) IGNACIO E. SALCEDA, State Bar No . 164017 ([email protected]) CHERYL W. FOUNG, State Bar No . 108868 (cfoung@wsgr .com) WILSON SONSINI GOODRICH & ROSAT I Professional Corporation 650 Page Mill Road Palo Alto, CA 94304-1050 Telephone: (650) 493-9300 Facsimile: (...

Recently R. M. Wilson used Fleck’s congruence and Weisman’s extension to present a useful lemma on polynomials modulo prime powers, and applied this lemma to reprove the Ax-Katz theorem on solutions of congruences modulo p and deduce various results on codewords in p-ary linear codes with weights. In light of the recent generalizations of Fleck’s congruence given by D. Wan, and D. M. Davis and ...

Flavocytochromes: transceivers and relays in biological electron transfer S. K. Chapman*’, F. Welsh*, R. Moysey*, C. Mowat*, M. K. Dohemy*, K. L. Turner*, A. W. Munro* and G. A. Reidt “Department of Chemistry, University of Edinburgh, West Mains Road, Edinburgh EH9 3JJ, Scotland, U.K., and tlnstitute of Cell and Molecular Biology, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JR, Scotl...

Actin nucleation factors function to organize, shape, and move membrane-bound organelles, yet they remain poorly defined in relation to disease. Galloway-Mowat syndrome (GMS) is an inherited disorder characterized by microcephaly and nephrosis resulting from mutations in the WDR73 gene. This core clinical phenotype appears frequently in the Amish, where virtually all affected individuals harbor...

Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly-mental retardation complex caused by mutations in the Zinc Finger Homeobox 1 B gene (ZFHX1B). MWS has been reported in association with Hirschsprung disease (HSCR). MWS is sometimes difficult to diagnose clinically, especially when HSCR is absent. Thus, it is necessary to detect gene abnormalities at the molecular level. Here we repor...