292 research outputs found

    Radiographic Features of Anterior Cruciate Ligament Reconstruction

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    Anterior cruciate ligament disruption is a common injury that occurs in contact sports such as football. The treating orthopedic surgeon may elect any of a variety of therapeutic options. Surgical management may consist of primary repair of the torn ligament or replacement of the torn ligament with graft material, known as anterior cruciate ligament reconstruction (ACER). Many physicians, including radiologists, are unfamiliar with the surgical procedure or the expected postoperative radiographic appearance of ACER. Assessment of radiographs following ACER, as with many surgical procedures, requires understanding of the surgical procedure. We present our experience in assessing the postoperative radiographs of 24 patients who underwent ACER. We describe the expected postoperative radiographic appearance, based on the particular type of ACER performed, which allows the recognition of normal postoperative radiographic anatomy as well as sequelae or complications of the procedure

    Human glucocorticoid receptor cDNA contains sequences sufficient for receptor down-regulation.

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    Glucocorticoid receptors are ligand-dependent transcription factors that are subject to down-regulation by their cognate ligand; however, the mechanisms mediating this physiological response are not completely understood. Since analysis of the human glucocorticoid receptor (hGR) cDNA sequence revealed the presence of sequences with homology to both positive and negative glucocorticoid regulatory elements, we have examined the potential of hGR to bind to the hGR cDNA by Southwestern blot analysis. The data revealed that glucocorticoid receptors exhibited specific binding to their own cDNA. To determine whether this binding was of functional significance in the down-regulation of glucocorticoid receptors, we analyzed the effect of glucocorticoids on hGR protein levels from COS 1 cells transfected with an hGR cDNA expression vector. These transfected cells produced intact hGR that were capable of ligand-dependent regulation of a co-transfected glucocorticoid-responsive reporter gene. Glucocorticoid treatment of hGR-transfected cells resulted in down-regulation of hGR (assayed by both glucocorticoid binding capacity and hGR protein levels) within 24 h of steroid administration. To determine if the glucocorticoid-induced down-regulation of transfected hGR was compatible with effects at the levels of receptor gene expression and RNA stability, we examined hGR mRNA steady state levels. Reductions from 2- to 6-fold were observed in hGR mRNA levels following glucocorticoid treatment of transfected COS 1 cells. This down-regulation of transfected hGR mRNA could not be attributed to either the Rous sarcoma virus promoter, which drives hGR expression, or to other sequences present in the vector plasmid since transcription of a related plasmid containing a chloramphenicol acetyltransferase gene in place of the hGR cDNA was not regulated by glucocorticoids. Down-regulation of hGR mRNA by glucocorticoids in transfected cells occurred in a time- and dose-dependent manner that is consistent with a glucocorticoid receptor-mediated process. Glucocorticoid-induced down-regulation of hGR mRNa steady state levels was not observed in COS 1 cells transfected with cDNAs encoding mutant hGR (defective in either steroid or DNA binding), which indicates that functional steroid and DNA binding domains of the expressed hGR were required for down-regulation. Interestingly, treatment of transfected COS 1 cells with the glucocorticoid antagonist RU486 also resulted in down-regulation of transfected hGR mRNA. Deletion analysis revealed that the region of the hGR cDNA that was responsible in part for the observed down-regulation in response to glucocorticoid was contained within a 1-kilobase restriction fragment (from base pair +527 to +1526).(ABSTRACT TRUNCATED AT 400 WORDS

    Linearization of donor DNA during plasmid transformation in Neisseria gonorrhoeae.

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    We examined the fate of plasmid DNA after uptake during transformation in Neisseria gonorrhoeae. An 11.5-kilobase plasmid, pFA10, was processed to linear double-stranded DNA during uptake by competent cells, but cleavage of pFA10 was not site specific. A minority of pFA10 entered as open circles. A 42-kilobase plasmid, pFA14, was degraded into small fragments during uptake; no intracellular circular forms of pFA14 were evident. Since pFA10 DNA linearized by a restriction enzyme was not further cut during uptake, the endonucleolytic activity associated with entry of plasmid DNA appeared to act preferentially on circular DNA. Although linear plasmid DNA was taken up into a DNase-resistant state as efficiently as circular DNA, linear plasmid DNA transformed much less efficiently than circular plasmid DNA. These data suggest that during entry transforming plasmid DNA often is processed to double-stranded linear molecules; transformants may arise when some molecules are repaired to form circles. Occasional molecules which enter as intact circles may also lead to transformants

    Distance to the Active Galaxy NGC 6951 via the Type Ia Supernova 2000E

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    CCD-photometry and low-resolution spectroscopy of the bright supernova SN 2000E in NGC 6951 are presented. Both the light curve extending up to 150 days past maximum and the spectra obtained at 1 month past maximum confirm that SN 2000E is of Type Ia. The reddening of SN 2000E is determined as E(B-V)=0.36+/-0.15, its error is mainly due to uncertainties in the predicted SN (B-V) colour at late epochs. The V(RI)_C light curves are analyzed with the Multi-Colour Light Curve Shape (MLCS) method. The shape of the late light curve suggests that SN 2000E was overluminous by about 0.5 mag at maximum comparing with a fiducial SN Ia. This results in an updated distance of 33+/-8 Mpc of NGC 6951 (corrected for interstellar absorption). The SN-based distance modulus is larger by about +0.7 mag than the previous Tully-Fisher estimates. However, possible systematic errors due to ambiguities in the reddening determination and estimates of the maximum luminosity of SN 2000E may plague the present distance measurement.Comment: 9 p., 5 figs, accepted for publication in A&A. A reference correcte

    Evidence for the Decay Sigma+ -> p mu+ mu-

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    We report the first evidence for the decay Sigma+ -> p mu+ mu- from data taken by the HyperCP experiment(E871) at Fermilab. Based on three observed events, the branching ratio is B(Sigma+ -> p,mu+,mu-) = [8.6 +6.6,-5.4(stat) +/-5.5(syst)] x 10**-8. The narrow range of dimuon masses may indicate that the decay proceeds via a neutral intermediate state, Sigma+ -> p P0, P0 -> mu+ mu-, with a P0 mass of 214.3 +/- 0.5 MeV/c**2 and branching ratio B(Sigma+ -> p P0; P0 -> mu+ mu-) = [3.1 +2.4,-1.(stat) +/-1.5(syst)] x 10**-8.Comment: As published in PR

    Search for the Lepton-Number-Violating Decay Ξ−→pμ−μ−\Xi^- \to p \mu^- \mu^-

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    A sensitive search for the lepton-number-violating decay Ξ−→pμ−μ−\Xi^-\to p \mu^-\mu^- has been performed using a sample of ∼109\sim10^9 Ξ−\Xi^- hyperons produced in 800 GeV/cc pp-Cu collisions. We obtain B(Ξ−→pμ−μ−)<4.0×10−8\mathcal{B}(\Xi^-\to p \mu^-\mu^-)< 4.0\times 10^{-8} at 90% confidence, improving on the best previous limit by four orders of magnitude.Comment: 9 pages, 5 figures, to be published in Phys. Rev. Let

    Measurement of the Alpha Asymmetry Parameter for the Omega- to Lambda K- Decay

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    We have measured the alpha parameter of the Omega- to Lambda K- decay using data collected with the HyperCP spectrometer during the 1997 fixed-target run at Fermilab. Analyzing a sample of 0.96 million Omega- to Lambda K^-, Lambda to p pi- decays, we obtain alpha_Omega*alpha_Lambda = [1.33+/-0.33(stat)+/-0.52(syst)] x 10^{-2}. With the accepted value of alpha_Lambda, alpha_Omega is found to be [2.07+/-0.51(stat)+/-0.81(syst)] x 10^{-2}.Comment: 5 pages, 4 figures, to be appeared as a Rapid Communication in Phys. Rev.

    On the K^+D Interaction at Low Energies

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    The Kd reactions are considered in the impulse approximation with NN final-state interactions (NN FSI) taken into account. The realistic parameters for the KN phase shifts are used. The "quasi-elastic" energy region, in which the elementary KN interaction is predominantly elastic, is considered. The theoretical predictions are compared with the data on the K^+d->K^+pn, K^+d->K^0pp, K^+d->K^+d and K^+d total cross sections. The NN FSI effect in the reaction K^+d->K^+pn has been found to be large. The predictions for the Kd cross sections are also given for slow kaons, produced from phi(1020) decays, as the functions of the isoscalar KN scattering length a_0. These predictions can be used to extract the value of a_0 from the data.Comment: 22 pages, 5 figure

    Search for the Flavor-Changing Neutral-Current Decays D+→π+μ+μ−D^+\to \pi^+ \mu^+ \mu^- and D+→π+e+e−D^+\to \pi^+ e^+ e^-

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    We report the results of a search for the flavor-changing neutral-current decays D+→π+μ+μ−D^+\rightarrow \pi^+ \mu^+ \mu^- and D+→π+e+e−D^+\rightarrow \pi^+ e^+ e^- in data from Fermilab charm hadroproduction experiment E791. No signal above background is found, and we obtain upper limits on branching fractions, B(D+→π+μ+μ−)<1.8×10−5B(D^+\rightarrow \pi^+ \mu^+ \mu^-) < 1.8 \times 10^{-5} and B(D+→π+e+e−)<6.6×10−5B(D^+\rightarrow \pi^+ e^+ e^-) < 6.6 \times 10^{-5}, at the 90\% confidence level.Comment: nine pages with figures; compressed, uuencoded postscrip
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