35 research outputs found

    Distinctive Inactivation Defects of Differing Mutant Calcium Channels Underlying Timothy Syndrome

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    The Ursinus Weekly, November 17, 1952

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    Faculty show is considered huge success • Dean addresses freshman class • Bus. Ad. Club sponsors debate on current economic issues • Y cabinet hears program plans of commissions • Dorm reps chosen to sell yearbooks • Speaker explains international bank • 11 articles, three books left in lost and found department • Ruby to give show on Friday • Benefit fashion show enjoyed by audience • I.R.C. attends model U.N. • Chest Drive opens today; $1300 set as final goal • Two Messiah soloists chosen • Lord to speak at Forum on November 25 • Freshmen petition to give breakage fees to Union • Rev. James tells What on earth God is doing • Alpha Psi sees play • Kratz, Moser describe Paris to French Club • Marine captain to speak • Editorials: Fashionable trend?; Let\u27s all give • No more expansiveness • Don Juan in Hell judged fine show • Engagements • Scribe reviews Russian movie • F.T.A. holds roast • Not as dead as you think claims fightin\u27st college • Time for change; Ursinus in 1870 • Go west young man ; Dawkins finds rare rattler • Snell\u27s Belles defeat Chestnut Hill in shutout • Court men begin pre-season drills • Drexel defeats Ursinus in final home tilt, 7-1 • Bakermen close season with 7-2 loss to Lehigh • Bears to try for equalizing victory • Juniata topples Bears in rain and mud, 7-0 • Two Ursinus Belles honored • Playoffs to decide champhttps://digitalcommons.ursinus.edu/weekly/1506/thumbnail.jp

    Protein and Overtraining: Potential Applications for Free-Living Athletes

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    Despite a more than adequate protein intake in the general population, athletes have special needs and situations that bring it to the forefront. Overtraining is one example. Hard-training athletes are different from sedentary persons from the sub-cellular to whole-organism level. Moreover, competitive, "free-living" (less-monitored) athletes often encounter negative energy balance, sub-optimal dietary variety, injuries, endocrine exacerbations and immune depression. These factors, coupled with "two-a-day" practices and in-season demands require that protein not be dismissed as automatically adequate or worse, deleterious to health. When applying research to practice settings, one should consider methodological aspects such as population specificity and control variables such as energy balance. This review will address data pertinent to the topic of athletic protein needs, particularly from a standpoint of overtraining and soft tissue recovery. Research-driven strategies for adjusting nutrition and exercise assessments will be offered for consideration. Potentially helpful nutrition interventions for preventing and treating training complications will also be presented

    Atrasentan and renal events in patients with type 2 diabetes and chronic kidney disease (SONAR): a double-blind, randomised, placebo-controlled trial

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    Background: Short-term treatment for people with type 2 diabetes using a low dose of the selective endothelin A receptor antagonist atrasentan reduces albuminuria without causing significant sodium retention. We report the long-term effects of treatment with atrasentan on major renal outcomes. Methods: We did this double-blind, randomised, placebo-controlled trial at 689 sites in 41 countries. We enrolled adults aged 18–85 years with type 2 diabetes, estimated glomerular filtration rate (eGFR)25–75 mL/min per 1·73 m 2 of body surface area, and a urine albumin-to-creatinine ratio (UACR)of 300–5000 mg/g who had received maximum labelled or tolerated renin–angiotensin system inhibition for at least 4 weeks. Participants were given atrasentan 0·75 mg orally daily during an enrichment period before random group assignment. Those with a UACR decrease of at least 30% with no substantial fluid retention during the enrichment period (responders)were included in the double-blind treatment period. Responders were randomly assigned to receive either atrasentan 0·75 mg orally daily or placebo. All patients and investigators were masked to treatment assignment. The primary endpoint was a composite of doubling of serum creatinine (sustained for ≥30 days)or end-stage kidney disease (eGFR <15 mL/min per 1·73 m 2 sustained for ≥90 days, chronic dialysis for ≥90 days, kidney transplantation, or death from kidney failure)in the intention-to-treat population of all responders. Safety was assessed in all patients who received at least one dose of their assigned study treatment. The study is registered with ClinicalTrials.gov, number NCT01858532. Findings: Between May 17, 2013, and July 13, 2017, 11 087 patients were screened; 5117 entered the enrichment period, and 4711 completed the enrichment period. Of these, 2648 patients were responders and were randomly assigned to the atrasentan group (n=1325)or placebo group (n=1323). Median follow-up was 2·2 years (IQR 1·4–2·9). 79 (6·0%)of 1325 patients in the atrasentan group and 105 (7·9%)of 1323 in the placebo group had a primary composite renal endpoint event (hazard ratio [HR]0·65 [95% CI 0·49–0·88]; p=0·0047). Fluid retention and anaemia adverse events, which have been previously attributed to endothelin receptor antagonists, were more frequent in the atrasentan group than in the placebo group. Hospital admission for heart failure occurred in 47 (3·5%)of 1325 patients in the atrasentan group and 34 (2·6%)of 1323 patients in the placebo group (HR 1·33 [95% CI 0·85–2·07]; p=0·208). 58 (4·4%)patients in the atrasentan group and 52 (3·9%)in the placebo group died (HR 1·09 [95% CI 0·75–1·59]; p=0·65). Interpretation: Atrasentan reduced the risk of renal events in patients with diabetes and chronic kidney disease who were selected to optimise efficacy and safety. These data support a potential role for selective endothelin receptor antagonists in protecting renal function in patients with type 2 diabetes at high risk of developing end-stage kidney disease. Funding: AbbVie

    Live Cell Biochemistry Implicates Protein Kinase a Modulation of L-Type CaV1.4 Channels

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