671 research outputs found

    The convergent validity of two sensory processing scales used with school - age children : comparing the sensory profile and the sensory processing measure

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    Abstract: Aim: To investigate the convergent validity between the Sensory Profile, the Sensory Profile School Companion, and the Home and Main Classroom Forms of the Sensory Processing Measure. Method: Thirty mothers completed the Sensory Profile and the Sensory Processing Measure - Home Form on one child each. Nineteen teachers of the same children completed the Sensory Profile School Companion and the Sensory Processing Measure - Main Classroom Form. Results: The Sensory Profile and the Sensory Processing Measure - Home Form were significantly correlated (rho=0.86, p less-than .01). The Sensory Profile School Companion and Sensory Processing Measure - Main Classroom Form were also significantly correlated (rho=.74, p less-than .01). Conclusion: The two sets of sensory processing scales had moderate levels of convergent validity.<br /

    Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS)

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    Background: Amyotrophic lateral sclerosis (ALS), a common late-onset neurodegenerative disease, is associated with fronto-temporal dementia (FTD) in 3-10% of patients. A mutation in CHMP2B was recently identified in a Danish pedigree with autosomal dominant FTD. Subsequently, two unrelated patients with familial ALS, one of whom also showed features of FTD, were shown to carry missense mutations in CHMP2B. The initial aim of this study was to determine whether mutations in CHMP2B contribute more broadly to ALS pathogenesis. Methodology/Principal Findings: Sequencing of CHMP2B in 433 ALS cases from the North of England identified 4 cases carrying 3 missense mutations, including one novel mutation, p. Thr104Asn, none of which were present in 500 neurologically normal controls. Analysis of clinical and neuropathological data of these 4 cases showed a phenotype consistent with the lower motor neuron predominant (progressive muscular atrophy (PMA)) variant of ALS. Only one had a recognised family history of ALS and none had clinically apparent dementia. Microarray analysis of motor neurons from CHMP2B cases, compared to controls, showed a distinct gene expression signature with significant differential expression predicting disassembly of cell structure; increased calcium concentration in the ER lumen; decrease in the availability of ATP; down-regulation of the classical and p38 MAPK signalling pathways, reduction in autophagy initiation and a global repression of translation. Transfection of mutant CHMP2B into HEK-293 and COS-7 cells resulted in the formation of large cytoplasmic vacuoles, aberrant lysosomal localisation demonstrated by CD63 staining and impairment of autophagy indicated by increased levels of LC3-II protein. These changes were absent in control cells transfected with wild-type CHMP2B. Conclusions/Significance: We conclude that in a population drawn from North of England pathogenic CHMP2B mutations are found in approximately 1% of cases of ALS and 10% of those with lower motor neuron predominant ALS. We provide a body of evidence indicating the likely pathogenicity of the reported gene alterations. However, absolute confirmation of pathogenicity requires further evidence, including documentation of familial transmission in ALS pedigrees which might be most fruitfully explored in cases with a LMN predominant phenotype

    The Grizzly, April 2, 1982

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    PA Special Olympics This Weekend • Room Selection Continues • Student Publications Staffs Chosen • Parents Day Plans Offer Variety of Talents • USGA Notes • Letters to the Editor • Dean of College Accepting Nominations for Lindback Award • Class Elections Next Week • News Briefs: Hooters Concert Tickets Now Available; Friends of Library Book Sale; Senior Women Invited to Parents Day Reception; Photography in Space Topic of Final Forum; Scholarship Offered for Students of Hellenic Descent • Food Day: A Chance to Share the Wealth • New Library Survey Conducted • Alumna Presents DuPont Grant • Students Direct Comedy Series • Duet Takes First in Talent Show • F&M Tops Track Team • W\u27s Tennis Drops Warm-up • Division 1 West Chester a Little Too Strong • MAC Champs Back • Harvard Slips by Lady Bears • Batsmen Split Twin Bill • Softball Team Takes Two Out of Threehttps://digitalcommons.ursinus.edu/grizzlynews/1077/thumbnail.jp

    The Grizzly, January 30, 1981

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    Gambling Investigation Prompts Student Withdrawals • Thornburgh Discusses Education At Conference • Todd Hall Fined $200 For Alcohol Violation • Tower Restoration Scheduled • McQuillan Presents Financial Aid Workshop • Magazine Addresses Students • J-Board Workings Explained By Barth • Fraternity Theories • Bids Distribution • Top Ten Albums of 1980 • Greaseband Unable To Return This Semester • Spiritwood: A Different Coffeehouse • Theatre: A Midsummer Night\u27s Dream • Shipping Delay Postpones NMD Window Installation • Departmental Focus: Health And Physical Education • Swim Coach Hopes For .500 Season • Men\u27s Basketball Holding 1st Place In MAC • Grapplers Having An Up & Down Year • Haag Leads Lady Hoopsters Past Widenerhttps://digitalcommons.ursinus.edu/grizzlynews/1050/thumbnail.jp

    The modified Glasgow prognostic score in prostate cancer: results from a retrospective clinical series of 744 patients

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    &lt;p&gt;Background: As the incidence of prostate cancer continues to rise steeply, there is an increasing need to identify more accurate prognostic markers for the disease. There is some evidence that a higher modified Glasgow Prognostic Score (mGPS) may be associated with poorer survival in patients with prostate cancer but it is not known whether this is independent of other established prognostic factors. Therefore the aim of this study was to describe the relationship between mGPS and survival in patients with prostate cancer after adjustment for other prognostic factors.&lt;/p&gt; &lt;p&gt;Methods: Retrospective clinical series on patients in Glasgow, Scotland, for whom data from the Scottish Cancer Registry, including Gleason score, Prostate Specific Antigen (PSA), C-reactive protein (CRP) and albumin, six months prior to or following the diagnosis, were included in this study.&lt;/p&gt; &lt;p&gt;The mGPS was constructed by combining CRP and albumin. Five-year and ten-year relative survival and relative excess risk of death were estimated by mGPS categories after adjusting for age, socioeconomic circumstances, Gleason score, PSA and previous in-patient bed days.&lt;/p&gt; &lt;p&gt;Results: Seven hundred and forty four prostate cancer patients were identified; of these, 497 (66.8%) died during a maximum follow up of 11.9 years. Patients with mGPS of 2 had poorest 5-year and 10-year relative survival, of 32.6% and 18.8%, respectively. Raised mGPS also had a significant association with excess risk of death at five years (mGPS 2: Relative Excess Risk = 3.57, 95% CI 2.31-5.52) and ten years (mGPS 2: Relative Excess Risk = 3.42, 95% CI 2.25-5.21) after adjusting for age, socioeconomic circumstances, Gleason score, PSA and previous in-patient bed days.&lt;/p&gt; &lt;p&gt;Conclusions: The mGPS is an independent and objective prognostic indicator for survival of patients with prostate cancer. It may be useful in determining the clinical management of patients with prostate cancer in addition to established prognostic markers.&lt;/p&gt

    The Grizzly, November 6, 1981

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    Changing Role of Women • Spanish Professor Speaks At Literature Conference • Ursinus Grad Anticipates Changes • Whatley Invited to Testing of Nuclear Sub • USGA Notes • Canterbury Tales: Bawdy Production Rates 10 • Fashion Forum • Myrin Hosts Alumna\u27s Art • Study Abroad Series: Continental Culture • Bear Pack Travels to MACs • Bears Fall to Swarthmore 27-10 • Questionable End to Hockey Seasonhttps://digitalcommons.ursinus.edu/grizzlynews/1066/thumbnail.jp

    Cases, Regulations, and Statutes

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    With the exception of ApoE4, genome-wide association studies have failed to identify strong genetic risk factors for late-onset Alzheimer's disease, despite strong evidence of heritability, suggesting that many low penetrance genes may be involved. Additionally, the nature of the identified genetic risk factors and their relation to disease pathology is also largely obscure. Previous studies have found that a cancer-associated variant of the cell cycle inhibitor gene p21cip1 is associated with increased risk of Alzheimer's disease. The aim of this study was to confirm this association and to elucidate the effects of the variant on protein function and Alzheimer-type pathology. We examined the association of the p21cip1 variant with Alzheimer's disease and Parkinson's disease with dementia. The genotyping studies were performed on 719 participants of the Oxford Project to Investigate Memory and Ageing, 225 participants of a Parkinson's disease DNA bank, and 477 participants of the Human Random Control collection available from the European Collection of Cell Cultures. The post mortem studies were carried out on 190 participants. In the in-vitro study, human embryonic kidney cells were transfected with either the common or rare p21cip1 variant; and cytometry was used to assess cell cycle kinetics, p21cip1 protein expression and sub-cellular localisation. The variant was associated with an increased risk of Alzheimer's disease, and Parkinson's disease with dementia, relative to age matched controls. Furthermore, the variant was associated with an earlier age of onset of Alzheimer's disease, and a more severe phenotype, with a primary influence on the accumulation of tangle pathology. In the in-vitro study, we found that the SNPs reduced the cell cycle inhibitory and anti-apoptotic activity of p21cip1. The results suggest that the cancer-associated variant of p21cip1 may contribute to the loss of cell cycle control in neurons that may lead to Alzheimer-type neurodegeneration

    The Grizzly, October 30, 1981

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    Founders Day 100th Year of Coeducation • Board of Directors Approve Tuition Increase • Stevens Talks on Hazing to Packed House • Comment: What Eileen Stevens Didn\u27t Say • Drexel-Ursinus Offer Evening Courses at Limerick and UC • Old Men\u27s Undergoes Heating Renovations • ZX Business Society Grows • Lee Savary: Contrasting Natural and Man-made • Study Abroad Series: Seize the Day • Law of the Sea, Law of the Nations • Gridders to Enter New League in 1983 • Bears Lose Homecoming Heartbreaker • X-Country: 38 Straight W\u27s • Field Hockey Trips West Chester 3-0https://digitalcommons.ursinus.edu/grizzlynews/1065/thumbnail.jp

    The Grizzly, January 29, 1982

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    Two Alumni Join Administration • So Much, POD, in College Bowl Finals • Hermann Eilts on The Middle East • College Receives $500,000 • Teachers Audition For EC/BA Positions • Honor Societies Meet to Discuss Future Plans • Union Undergoes Attractive Renovations • Evening School Expands • Spiritwood Returns for Coffeehouse • German Students Sample American College Life • Mozart Concert to Conclude Winterfest! • Myrin Exhibits Storybook Etchings • Collegeville Claustrophobia? • Schaff Plagued With Repeated Break-ins • Forums, Forums, Forums • Mens Basketball Has Good Vacation • Gymnasts\u27 Work Pays Off • Badminton Opens Season With Temple • Grapplers Impressive in Latest Victories • Hoopsters Lose to Widener • Karas Resigns; New Coach Expected Soon • Widener Drownshttps://digitalcommons.ursinus.edu/grizzlynews/1070/thumbnail.jp
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