588 research outputs found

    Diversification of a University Faculty: Women Faculty in the MIT Schools of Science and Engineering

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    A broadly diverse faculty is critical to MIT’s educational mission, and significant efforts have been made to achieve a faculty whose diversity reflects that of the students we train. To assess the success of some of these efforts, I examined the percentage of women faculty in the Schools of Science and Engineering over time. In Science, the increased number (and percentage) of women faculty today is the consequence of: pressures associated with the civil rights movement in the early 1970s; unusual efforts between 1996 and 2000 by former Dean of Science Bob Birgeneau in response to the 1996 Report on Women Faculty in Science; and efforts that sustained the progress made as a result of these two initiatives. The women faculty hired in the School of Science as a result of these pressures achieved tenure at the same rate as men and have achieved at least the same level of professional success as their male colleagues as measured by election to the prestigious National Academy of Sciences. In the School of Engineering, the number of women faculty rose more steadily with time and with the increasing number of women receiving PhDs. But as in Science, a recent rapid increase in the number of women faculty resulted from the leadership of its Dean, Tom Magnanti, working collaboratively with then Provost Bob Brown, in response to the “Report on Women Faculty in the School of Engineering.” The data suggest that usual departmental hiring processes do not always identify exceptional female candidates. But, women faculty were readily hired by involvement of the central administration, including the use of novel hiring procedures, collaborations among the Provost, Deans, Department Heads, and women faculty committees, all with the visible support of the President

    Re University of Saskatchewan Faculty Association and University of Saskatchewan

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    On behalf of Professor Vandervort, The Association, pursuant to article 31.5.5 of the 1991-2 Collective Agreement, contests the President’s recommendation to the Board of Governors that she be dismissed, on the ground that reasons for dismissal do not exist

    Re University of Saskatchewan Faculty Association and University of Saskatchewan

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    This is the determination of an Arbitration Committee established to hear and determine whether or not the grounds for the President\u27s recommendation for the dismissal of Lucinda Vandervort, a tenured Associate Professor, are established and, if established, whether or not they constitute good and sufficient cause for dismissal. The Committee has already issued an interim decision that, even if established, the grounds for the President\u27s recommendation for dismissal do not constitute good and sufficient cause for dismissal and Professor Vandervort has been fully reinstated pending this determination. We advised the parties of our conclusion to that effect after the University had put in its case, in the hope that time and money would be saved. It suffices to say that it did not have that effect

    Two Factors that Bind to Highly Conserved Sequences in Mammalian Type C Retroviral Enhancers.

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    The transcriptional enhancers of the Moloney and Friend murine leukemia viruses (MLV) are important determinants of viral pathogenicity. We used electrophoretic mobility shift and methylation interference assays to study nuclear factors which bind to a region of these enhancers whose sequence is identical between Moloney and Friend viruses and particularly highly conserved among 35 mammalian type C retroviruses whose enhancer sequences have been aligned (E. Golemis, N. A. Speck, and N. Hopkins, J. Virol. 64:534-542, 1990). Previous studies identified sites for the leukemia virus factor b (LVb) and core proteins in this region (N. A. Speck and D. Baltimore, Mol. Cell. Biol. 7:1101-1110, 1987) as well as a site, overlapping those for LVb and core, for a third factor (N. R. Manley, M. A. O\u27Connell, P. A. Sharp, and N. Hopkins, J. Virol. 63:4210-4223, 1989). Surprisingly, the latter factor appeared to also bind two sites identified in the Friend MLV enhancer, Friend virus factor a and b1 (FVa and FVb1) sites, although the sequence basis for the ability of the protein to bind these diverse sites was not apparent. Here we describe the further characterization of this binding activity, termed MCREF-1 (for mammalian type C retrovirus enhancer factor 1), and the identification of a consensus sequence for its binding, GGN8GG. We also identify a factor, abundant in mouse T-cell lines and designated LVt, which binds to two sites in the Moloney MLV enhancer, overlapping the previously identified LVb and LVc binding sites. These sites contain the consensus binding site for the Ets family of proteins. We speculate on how distinct arrays of these factors may influence the disease-inducing phenotype

    Reflecting on Fifty Years of Progress for Women in Science

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    Like young women today, 50 years ago I too assumed that gender discrimination in science was a thing of the past. Girls who grew up in America in the Sputnik era, as I did, were encouraged to become scientists. By 1964, when I graduated from college with a major in biology, I thought it entirely possible I’d win a Nobel prize. Why not? Dorothy Hodgkin won one that year. At Harvard, my professors had strongly encouraged me to go to graduate school. When I finished my postdoc in 1973, I was actively recruited to the MIT faculty. What were those feminists complaining about

    Expression of ZebrafishragGenes during Early Development Identifies the Thymus

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    AbstractRecent experiments have demonstrated that zebrafish is a vertebrate in which it is possible to carry out large-scale mutagenic screens to identify genes involved in specific developmental pathways. To follow development of the immune system in zebrafish, we have analyzed the expression of the recombination activating genes,rag1andrag2,which we have previously isolated and characterized. These genes catalyze the rearrangement of immunoglobulin genes in immature B lymphocytes and of T cell receptor genes in immature T lymphocytes and are therefore appropriate markers to follow the development of organs containing these cells. By whole-mountin situhybridization, we detected expression of bothraggenes in a paired organ in the head, beginning on the fourth day after fertilization. Histological examination of this organ indicated that it corresponds to the thymus, as described for other fish, an organ that has not previously been identified in zebrafish. By histological analysis, the thymus primordium appears at 54 hr but does not enlarge significantly until 30 hr later. The thymus continues to enlarge and reaches its mature histological organization at 1 month. The pronephros, the major hematopoietic organ in the adult fish, begins to develop hematopoietic tissue about 2 weeks after fertilization. By 1 month, mature lymphocytes are distinguishable in the tissue surrounding renal tubules. Lymphocytes appear in the kidney too late for screening by whole-mountin situhybridization; however, the pattern ofrag1expression in the thymus forms the basis of an assay for mutations affecting development of the thymus or its constituent lymphocytes

    Estudos radiométricos sobre a oxidação de (U-14C) L-aminoácidos por micobactérias sensíveis e resistentes a drogas

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    A radiometric assay system has been used to study oxidation patterns of (U-14C) L-amino acids by drug-susceptible and drug-resistant mycobacteria. Drug-susceptible M. tuberculosis (H37Rv TMC 102 and Erdman) along with the drug-resistant organism M. tuberculosis (H37 Rv TMC 303), M. bovis, M. avium, M. intracellulare, M. kansasii and M. chelonei were used. The organisms were inoculated into a sterile reaction system with liquid 7H9 medium and one of the (U-14C) L-amino acids. Each organism displayed a different pattern of amino acid oxidation, but these patterns were not distinctive enough for identification of the organism. Complex amino acids such as proline, phenylalanine and tyrosine were of no use in identification of mycobacteria, since virtually all organisms failed to oxidize them. There was no combination of substrates able to separate susceptible from resistant organisms.Um sistema radiométrico foi utilizado para estudar os padrões de oxidação dos (U-14C) L-aminoácidos por micobactérias sensíveis e resis tentes a drogas. Foram usadas duas cepas do M. tuberculosis sensíveis a todas as drogas, H37Rv e Erdman. As micobactérias resistentes foram M. tuberculosis H37Rv resistente a 5 ug/ml de hidrazida, M. bovis, M. avium, M. intracellulare, M. kansasii e M. chelonei. As micobac térias foram inoculadas em frascos estéreis contendo o meio líquido 7H9 e um dos (U-14C) L-aminoácidos. Cada micobactéria apresentou um padrão de oxidação de aminoácidos, mas estes padrões não foram suficientemente diferentes para identificá-la. Aminoácidos complexos como a prolina, fenilalanina e tirosina não tiveram utilidade na identificação das micobactérias, pois praticamente todos os microorganismos foram incapazes de oxidá-los. Nenhuma combinação de aminoácidos foi capaz de separar as micobactérias sensíveis das resistentes a drogas

    Identification of Native Defects (Vacancies and Antisites) in CdSiP2 Crystals

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    Electron paramagnetic resonance (EPR) is used to identify four native defects in single crystals of CdSiP2. This nonlinear optical material is used in optical parametric oscillators to generate tunable output in the mid-infrared. The performance of these frequency-conversion devices is limited when infrared absorption bands associated with native defects overlap a pump wavelength. Cadmium, silicon, and phosphorus vacancies and also silicon-on-cadmium antisites are present in the as-grown undoped CdSiP2 crystals. Using near-band-edge 632.8 nm light from a He-Ne laser, a paramagnetic charge state, and thus an EPR spectrum, is formed at liquid-helium temperatures for three of the four defects. The EPR spectrum from the singly ionized silicon vacancy (V-Si) is present without light and has five hyperfine lines due to equal interactions with the four neighboring 31P nuclei. In contrast, the photoinduced EPR spectrum from the singly ionized cadmium vacancy (V-Cd) has a three-line hyperfine pattern due to equal interactions with only two of its four neighboring 31P nuclei. The light-induced spectrum from the singly ionized silicon-on-cadmium antisite (Si+Cd) also has a three-line hyperfine pattern, thus indicating that the unpaired spin interacts primarily with only two 31P neighbors. For the neutral phosphorus vacancy (V0P), the unpaired spin is primarily localized on the nearest-neighbor silicon ions and the photoinduced EPR spectrum has no resolved 31P hyperfine interactions. The silicon and cadmium vacancies are acceptors, and the silicon-on-cadmium antisite and the phosphorus vacancy are donors

    Electron Paramagnetic Resonance and Optical Absorption Study of Acceptors in CdSiP\u3csub\u3e2\u3c/sub\u3e Crystals

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    Cadmium silicon diphosphide (CdSiP2) is a nonlinear material often used in optical parametric oscillators (OPOs) to produce tunable laser output in the mid-infrared. Absorption bands associated with donors and acceptors may overlap the pump wavelength and adversely affect the performance of these OPOs. In the present investigation, electron paramagnetic resonance (EPR) is used to identify two unintentionally present acceptors in large CdSiP2 crystals. These are an intrinsic silicon-on-phosphorus antisite and a copper impurity substituting for cadmium. When exposed to 633 µm laser light at temperatures near or below 80 K, they convert to their neutral paramagnetic charge states (Si0P and Cu0Cd) and can be monitored with EPR. The corresponding donor serving as the electron trap is the silicon-on-cadmium antisite (Si2+Cd before illumination and Si+Cd after illumination). Removing the 633 µm light and warming the crystal above 90 K quickly destroys the EPR signals from both acceptors and the associated donor. Broad optical absorption bands peaking near 0.8 and 1.4 μm are also produced at low temperature by the 633 µm light. These absorption bands are associated with the Si0P and Cu0Cd acceptors
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