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Biomedical subjects

G Fisk

Publications and source records attributed to G Fisk.

7 recordsLinked to original sources
PubMed2001

Confidence in word detection predicts word identification: implications for an unconscious perception paradigm.

The present experiments extend the scope of the independent observation model based on signal detection theory (Macmillan & Creelman, 1991) to complex (word) stimulus sets. In the first experiment, the model predicts the relationship between uncertain detection and subsequent correct identification, thereby providing an alternative interpretation to a phenomenon often described as unconscious perception. Our second experiment used an exclusion task (Jacoby, Toth, & Yonelinas, 1993), which, according to theories of unconscious perception, should show qualitative differences in performance based on stimulus detection accuracy and provide a relative measure of conscious versus unconscious influences (Merikle, Joordens, & Stoltz, 1995). Exclusion performance was also explained by the model, suggesting that undetected words did not unconsciously influence identification responses.

Adult↗
PubMed1993

Biochemical characterization of binding of multiple HIV-1 Rev monomeric proteins to the Rev responsive element.

Recombinant HIV-1 Rev protein was overexpressed in Escherichia coli using translational coupling to the beta-glucuronidase gene and demonstrated to interact with high affinity and specificity with the Rev responsive element (RRE). A complex Rev-dependent binding pattern was observed using the gel shift assay which could be simplified to one or two primary bands in the presence of stoichiometric concentrations of RRE. Competition of these bands with a series of homopolymer RNA species demonstrated that Rev is essentially a poly-G binding protein, although poly-I was also shown to compete for specific RRE binding. The stoichiometry of the Rev-dependent gel shift complexes was determined using 125I-labeled Rev. The stable, lowest mobility complex was determined to possess a ratio of between 7 and 8 Rev molecules per RRE containing RNA fragment while the two fastest migrating complexes contained ratios of one and two Rev molecules per RRE, respectively. Using the Hill equation as a model for cooperative interactions, a Hill coefficient of n(app) = 2 was obtained from fitting of direct nitrocellulose filter binding assays, reflecting cooperatively bound Rev molecules on the RRE under equilibrium binding conditions. An increase in ionic strength from 0.0 to 0.3 M NaCl reduced cooperative Rev binding to the RRE, but specificity of Rev for the RRE relative to antisense RNA was increased 100,000-fold. At molar ratios of Rev to RRE above 2, Rev dissociated from the RRE with a T1/2 of approximately 20-25 min.(ABSTRACT TRUNCATED AT 250 WORDS)

Base Sequence↗
PubMed1992

Impaired learning and memory in mature spontaneously hypertensive rats.

In very old, normotensive rats, a disorganization occurs selectively in the retrosplenial cortex, and a similar disorganization occurs in this area in spontaneously hypertensive rats (SHR) at a much earlier age. Since this breakdown compromises a neural circuit involved in learning and memory, this study tests the hypotheses that these functions are disturbed in mature SHR and that they can be prevented or attenuated by long-term, anti-hypertensive therapy. SHR and Sprague Dawley rats (SD) at 3- and 12 months of age, and a group of SHR that had been normotensive from 3 to 12 months of age (CAP-SHR) were trained on an 8 arm radial maze task. Of the 12-month-old groups, SD reached criterion earliest (28 +/- 2 days) and made the least number of total errors. In comparison, 12-month-old SHR took significantly longer to reach criterion (39 +/- 2 days) and made nearly twice as many total errors. CAP-SHR were intermediate between the other two groups (32 +/- 2 days). Three-month-old SD learned the task at the same rate as the 12-month-old SD. In contrast, 3-month-old SHR learned the task significantly faster (21 +/- 1 days) and with fewer errors than any other group. These data indicate that, in SHR, learning and memory are compromised by 12 months of age, and that anti-hypertensive therapy with captopril partially prevents this decline.

Animals↗
PubMed1991

The C. elegans unc-104 gene encodes a putative kinesin heavy chain-like protein.

Mutations in the unc-104 gene of the nematode C. elegans result in uncoordinated and slow movement. Transposon insertions in three unc-104 alleles (e2184, rh1016, and rh1017) were used as physical markers to clone the unc-104 gene. DNA sequence analysis of unc-104 cDNAs revealed an open reading frame capable of encoding a 1584 amino acid protein with similarities to kinesin heavy chain. The similarities are greatest in the amino-terminal ATPase and microtubule-binding domains. Although the primary sequence relatedness to kinesin is weak in the remainder of the molecule, the predicted secondary structure and regional isoelectric points are similar to kinesin heavy chain.

Adenosine Triphosphatases↗