355 research outputs found
Does spinal manipulation relieve back pain?
Spinal manipulation therapy (SMT) reduces lower back pain and improves the ability to perform everyday activities more than sham therapies (strength of recommendation [SOR]: A, multiple randomized controlled trials [RCTs] and systematic reviews), but it�۪s no more or less effective than pain medication, physical therapy, exercise, back school, or care given by a general practitioner (SOR: A, meta-analysis)
Automated Data for DevSecOps Programs
Symposium PresentationApproved for public release; distribution is unlimited
Automated Data for DevSecOps Programs
Excerpt from the Proceedings of the Nineteenth Annual Acquisition Research SymposiumAutomation in DevSecOps (DSO) transforms the practice of building, deploying, and managing software intensive programs. Although this automation supports continuous delivery and rapid builds, the persistent manual collection of information delays (by weeks) the release of program status metrics and the decisions they are intended to inform. Emerging DSO metrics (e.g., deployment rates, lead times) provide insight into how software development is progressing but fall short of replacing program control metrics for assessing progress (e.g., burn rates against spend targets, integration capability tar-get dates, and schedule for the minimum viable capability release). By instrumenting the (potentially in-teracting) DSO pipelines and supporting environments, the continuous measurement of status, identifica-tion of emerging risks, and probabilistic projections are possible and practical. In this paper, we discuss our research on the information modeling, measurement, metrics, and indicators necessary to establish a continuous program control capability that can keep pace with DSO management needs. We discuss the importance of interactive visualization dashboards for addressing program information needs. We also identify and address the gaps and barriers in the current state of the practice. Finally, we recommend future research needs based on our initial findings.Approved for public release; distribution is unlimited
Automated Data for DevSecOps Programs
Excerpt from the Proceedings of the Nineteenth Annual Acquisition Research SymposiumAutomation in DevSecOps (DSO) transforms the practice of building, deploying, and managing software intensive programs. Although this automation supports continuous delivery and rapid builds, the persistent manual collection of information delays (by weeks) the release of program status metrics and the decisions they are intended to inform. Emerging DSO metrics (e.g., deployment rates, lead times) provide insight into how software development is progressing but fall short of replacing program control metrics for assessing progress (e.g., burn rates against spend targets, integration capability tar-get dates, and schedule for the minimum viable capability release). By instrumenting the (potentially in-teracting) DSO pipelines and supporting environments, the continuous measurement of status, identifica-tion of emerging risks, and probabilistic projections are possible and practical. In this paper, we discuss our research on the information modeling, measurement, metrics, and indicators necessary to establish a continuous program control capability that can keep pace with DSO management needs. We discuss the importance of interactive visualization dashboards for addressing program information needs. We also identify and address the gaps and barriers in the current state of the practice. Finally, we recommend future research needs based on our initial findings.Approved for public release; distribution is unlimited
Earnings Surprises and the Options Market
Numerous articles over the past few decades have documented a consistent relationship between earnings surprises and subsequent stock price performance. [See, for example, Ball and Brown (1968), Rendleman, Jones, and Latane (1982), Foster, Olsen, and Shevlin (1984), and Bernard and Thomas (1989).] Specifically when firms announce quarterly earnings figures that are higher (lower) than market expectations, as proxied by either mechanical time-series models or commercially available analysts’ forecasts, the stock price performance following the announcement tends to be abnormally good (bad). This phenomenon is referred to as post-earnings-announcement drift or the standardized unexpected earnings effect, SUE for short
Earnings Surprises and the Options Market
Numerous articles over the past few decades have documented a consistent relationship between earnings surprises and subsequent stock price performance. [See, for example, Ball and Brown (1968), Rendleman, Jones, and Latane (1982), Foster, Olsen, and Shevlin (1984), and Bernard and Thomas (1989).] Specifically when firms announce quarterly earnings figures that are higher (lower) than market expectations, as proxied by either mechanical time-series models or commercially available analysts’ forecasts, the stock price performance following the announcement tends to be abnormally good (bad). This phenomenon is referred to as post-earnings-announcement drift or the standardized unexpected earnings effect, SUE for short
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia
BACKGROUND: Most patients with familial primary pulmonary hypertension have defects in the gene for bone morphogenetic protein receptor II (BMPR2), a member of the transforming growth factor beta (TGF-beta) superfamily of receptors. Because patients with hereditary hemorrhagic telangiectasia may have lung disease that is indistinguishable from primary pulmonary hypertension, we investigated the genetic basis of lung disease in these patients.
METHODS: We evaluated members of five kindreds plus one individual patient with hereditary hemorrhagic telangiectasia and identified 10 cases of pulmonary hypertension. In the two largest families, we used microsatellite markers to test for linkage to genes encoding TGF-beta-receptor proteins, including endoglin and activin-receptor-like kinase 1 (ALK1), and BMPR2. In subjects with hereditary hemorrhagic telangiectasia and pulmonary hypertension, we also scanned ALK1 and BMPR2 for mutations.
RESULTS: We identified suggestive linkage of pulmonary hypertension with hereditary hemorrhagic telangiectasia on chromosome 12q13, a region that includes ALK1. We identified amino acid changes in activin-receptor-like kinase 1 that were inherited in subjects who had a disorder with clinical and histologic features indistinguishable from those of primary pulmonary hypertension. Immunohistochemical analysis in four subjects and one control showed pulmonary vascular endothelial expression of activin-receptor-like kinase 1 in normal and diseased pulmonary arteries.
CONCLUSIONS: Pulmonary hypertension in association with hereditary hemorrhagic telangiectasia can involve mutations in ALK1. These mutations are associated with diverse effects, including the vascular dilatation characteristic of hereditary hemorrhagic telangiectasia and the occlusion of small pulmonary arteries that is typical of primary pulmonary hypertension
Genetics and genomics of pulmonary arterial hypertension.
Since 2000 there have been major advances in our understanding of the genetic and genomics of pulmonary arterial hypertension (PAH), although there remains much to discover. Based on existing knowledge, around 25-30% of patients diagnosed with idiopathic PAH have an underlying Mendelian genetic cause for their condition and should be classified as heritable PAH (HPAH). Here, we summarise the known genetic and genomic drivers of PAH, the insights these provide into pathobiology, and the opportunities afforded for development of novel therapeutic approaches. In addition, factors determining the incomplete penetrance observed in HPAH are discussed. The currently available approaches to genetic testing and counselling, and the impact of a genetic diagnosis on clinical management of the patient with PAH, are presented. Advances in DNA sequencing technology are rapidly expanding our ability to undertake genomic studies at scale in large cohorts. In the future, such studies will provide a more complete picture of the genetic contribution to PAH and, potentially, a molecular classification of this disease
Prospectus, May 7, 1981
SPEECH TEAM 11TH RANKED; National Forensics Top 20; C of C V-P, Neils predicts downtown area will change; Overcast and Snyder receive award; Co-Editors named for 1981-82; Barnes looks back on his Parkland experiences; Letters to the Editor: Student criticizes review; Classifieds; Our mistake! Stugo candidate got platform in on time; Convocations Wants You!!; Now is the time to get married; More letters to the Editor: New Stugo senator, Jackson appreciates support; Schumacher\u27s final notes...; Trail, Hillary win in close Stugo election last week; Trail expresses gratitude for the voters; Be kind to animals ; Japan King of bicycle road; Motocross bikes good for kids; Rogers, Gayle at Assembly Hall May 13.; Off Broadway: Dynamic, Aggressive; Gayle not living under Lorett\u27s shadow now!; Piloting not as easy as you may think!; Drug problem is going to get worse. ; Art Thesis Exhibit disappointing; Latin may be on its way back; Parkland secretaries enjoy the good life; Model Rockets popular; RWS\u27S help each other; PC offers one-day driving course; Ramblin\u27: Alender\u27s rambles are over; Rundgren just changing with the times; Do you want hard rock...?; Frazier, Turpin part of Senior May Fest; Here\u27s the 1981 Prospectus staff; CIRS has the info on day care; Did You Know That...Some Superstitions; \u27Recent rains still not enough\u27: Burwash; Barkstall appalled by Atlanta slayings: Urban League director says blacks are still discriminated against; Are we running out of natural resources?; Get out your horses for PC\u27s Horse Show; Parkland Happenings: Spring concerts feature Irving Berlin; Awards Banquet a success!; Winning Intellectual Freedom Essay; A child\u27s world is important throughout all stages; Dental classes named for \u2781-82; Final Examinations -- Spring, 1981; Cobras bow to Lake Land; Patrick to Tennessee; Softball team beats Danville; ...beat Lincoln Land three; Letter to the Sports Editor: Student upset; Walder wins final Fast Freddy; scoreboard; Baseballhttps://spark.parkland.edu/prospectus_1981/1017/thumbnail.jp
Copy Number Variation in Familial Parkinson Disease
Copy number variants (CNVs) are known to cause Mendelian forms of Parkinson disease (PD), most notably in SNCA and PARK2. PARK2 has a recessive mode of inheritance; however, recent evidence demonstrates that a single CNV in PARK2 (but not a single missense mutation) may increase risk for PD. We recently performed a genome-wide association study for PD that excluded individuals known to have either a LRRK2 mutation or two PARK2 mutations. Data from the Illumina370Duo arrays were re-clustered using only white individuals with high quality intensity data, and CNV calls were made using two algorithms, PennCNV and QuantiSNP. After quality assessment, the final sample included 816 cases and 856 controls. Results varied between the two CNV calling algorithms for many regions, including the PARK2 locus (genome-wide p = 0.04 for PennCNV and p = 0.13 for QuantiSNP). However, there was consistent evidence with both algorithms for two novel genes, USP32 and DOCK5 (empirical, genome-wide p-values<0.001). PARK2 CNVs tended to be larger, and all instances that were molecularly tested were validated. In contrast, the CNVs in both novel loci were smaller and failed to replicate using real-time PCR, MLPA, and gel electrophoresis. The DOCK5 variation is more akin to a VNTR than a typical CNV and the association is likely caused by artifact due to DNA source. DNA for all the cases was derived from whole blood, while the DNA for all controls was derived from lymphoblast cell lines. The USP32 locus contains many SNPs with low minor allele frequency leading to a loss of heterozygosity that may have been spuriously interpreted by the CNV calling algorithms as support for a deletion. Thus, only the CNVs within the PARK2 locus could be molecularly validated and associated with PD susceptibility
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