2,608 research outputs found

    AFSCME\u27s Success with Public Sector Clericals

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    [Excerpt] In December 1985 the American Federation of State, County & Municipal Employees (AFSCME) was certified as the bargaining agent for more than 11,000 State of Ohio clerical employees. This victory followed a string of similar successes: 1981, Florida, 23,000, and Connecticut, 7,500; 1983, California university clericals, 19,500; 1984, Iowa, 6,000

    Accelerated Quantum Dynamics

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    In this dissertation we develop a formalism for the computation of observables due to acceleration-induced particle physics processes. By using the spacetime structure produced by acceleration, we examine the properties of accelerated particle detectors as well as accelerated fields. General expressions for the transition rate, multiplicity, power, spectra, and displacement law of particles undergoing time-dependent acceleration and transitioning into a final state of arbitrary particle number are obtained. The transition rate, power, and spectra are characterized by unique polynomials of multiplicity and thermal distributions of both bosonic and fermionic statistics. The acceleration-dependent multiplicities are computed in terms of the branching fractions of the associated inertial processes. The displacement law of the spectra predicts that the energy of the emitted particles is directly proportional to the accelerated temperature

    The Meaning of Imagination In William Wordsworth\u27s Prelude

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    Jim Lynch Oral History Interview

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    https://scholarlycommons.pacific.edu/raymond-college/1157/thumbnail.jp

    Sebaceous Skin Lesions as Clues to Hereditary Non-Polyposis Colorectal Cancer

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    Cutaneous lesions consonant with Muir–Torre syndrome strongly suggest hereditary non-polyposis colorectal cancer (HNPCC). Ponti et al. discuss the importance of combining molecular genetic features of the sebaceous neoplasms, including microsatellite instability and immunohistochemistry, with family history, to determine the likelihood of HNPCC. Proof of diagnosis is identification of one of the mismatch repair germline mutations

    HNPCC (Lynch Syndrome): Differential Diagnosis, Molecular Genetics and Management - a Review

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    HNPCC (Lynch syndrome) is the most common form of hereditary colorectal cancer (CRC), wherein it accounts for between 2-7 percent of the total CRC burden. When considering the large number of extracolonic cancers integral to the syndrome, namely carcinoma of the endometrium, ovary, stomach, hepatobiliary system, pancreas, small bowel, brain tumors, and upper uroepithelial tract, these estimates of its frequency are likely to be conservative. The diagnosis is based upon its natural history in concert with a comprehensive cancer family history inclusive of all anatomic sites. In order for surveillance and management to be effective and, indeed, lifesaving, among these high-risk patients, the linchpin to cancer control would be the physician, who must be knowledgeable about hereditary cancer syndromes, their molecular and medical genetics, genetic counseling, and, most importantly, the natural history of the disorders, so that the entirety of this knowledge can be melded to highly-targeted management

    Current Hypotheses on How Microsatellite Instability Leads to Enhanced Survival of Lynch Syndrome Patients

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    High levels of microsatellite instability (MSI-high) are a cardinal feature of colorectal tumors from patients with Lynch Syndrome. Other key characteristics of Lynch Syndrome are that these patients experience fewer metastases and have enhanced survival when compared to patients diagnosed with microsatellite stable (MSS) colorectal cancer. Many of the characteristics associated with Lynch Syndrome including enhanced survival are also observed in patients with sporadic MSI-high colorectal cancer. In this review we will present the current state of knowledge regarding the mechanisms that are utilized by the host to control colorectal cancer in Lynch Syndrome and why these same mechanisms fail in MSS colorectal cancers

    A Cation-π Interaction in the Binding Site of the Glycine Receptor Is Mediated by a Phenylalanine Residue

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    Cys-loop receptor binding sites characteristically contain many aromatic amino acids. In nicotinic ACh and 5-HT3 receptors, a Trp residue forms a cation-{pi} interaction with the agonist, whereas in GABAA receptors, a Tyr performs this role. The glycine receptor binding site, however, contains predominantly Phe residues. Homology models suggest that two of these Phe side chains, Phe159 and Phe207, and possibly a third, Phe63, are positioned such that they could contribute to a cation-{pi} interaction with the primary amine of glycine. Here, we test this hypothesis by incorporation of a series of fluorinated Phe derivatives using unnatural amino acid mutagenesis. The data reveal a clear correlation between the glycine EC50 value and the cation-{pi} binding ability of the fluorinated Phe derivatives at position 159, but not at positions 207 or 63, indicating a single cation-{pi} interaction between glycine and Phe159. The data thus provide an anchor point for locating glycine in its binding site, and demonstrate for the first time a cation-{pi} interaction between Phe and a neurotransmitter

    Alumnae Bulletin - Number 3

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    Greetings to Alumnae Members and Graduates Alumnae Officers Membership Financial Statement as of 3-1-37 Sick Committee Are You? Alumnae Days Were You at the Bazaar? History of the Nurses\u27 Relief Fund Forget-Me-Not In Memoriam Here and There Marriages Reported During 1936-1937 A Resume Student Nurse Activity Jefferson Nurses Choral Club The Bulletin - Publicity Committee Do You Know? Bazaar Accoun

    Nonparametric versus Parametric Statistical Approaches for Genetic Anticipation: The Pancreatic Cancer Case

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    2000 Mathematics Subject Classi cation: 62N01, 62N05, 62P10, 92D10, 92D30.Genetic anticipation for a particular disease can involve an earlier age of onset, greater severity, and/or a higher number of affected individuals in successive generations within a family. Comparison between nonparametric and semiparametric tests is studied for matched data, and is one of the main focuses of this study. This comparison is investigated for the variable age of diagnosis among different birth cohorts, before and after adjustment for time under observation. The comparison is illustrated on an example of familial pancreatic cancer, which example is the second main focus of this study. The nonparametric test performed on our example better than the two semi-parametric tests, and was less sensitive to right censoring. After adjusting for follow up time, all methods detected genetic anticipation.This work was supported in part by a grant from the National Cancer Institute (1 R33 CA10595-01A2) to S. A. Sherman. G. R. Haynatzki thanks Mr. Oleg Shats and Mrs. Marsha Ketcham for their help with the PCCR
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