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Your search keyword '"Hesterlee, Sharon E"' showing total 8 results
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8 results on '"Hesterlee, Sharon E"'

2. A call for transparent reporting to optimize the predictive value of preclinical research

Author

Landis, Story C, Amara, Susan G, Asadullah, Khusru, Austin, Chris P, Blumenstein, Robi, Bradley, Eileen W, Crystal, Ronald G, Darnell, Robert B, Ferrante, Robert J, Fillit, Howard, Finkelstein, Robert, Fisher, Marc, Gendelman, Howard E, Golub, Robert M, Goudreau, John L, Gross, Robert A, Gubitz, Amelie K, Hesterlee, Sharon E, Howells, David W, Huguenard, John, Kelner, Katrina, Koroshetz, Walter, Krainc, Dimitri, Lazic, Stanley E, Levine, Michael S, Macleod, Malcolm R, McCall, John M, Moxley III, Richard T, Narasimhan, Kalyani, Noble, Linda J, Perrin, Steve, Porter, John D, Steward, Oswald, Unger, Ellis, Utz, Ursula, and Silberberg, Shai D

Subjects
Accounting, Auditing and Accountability, Biomedical and Clinical Sciences, Commerce, Management, Tourism and Services, Animals, Publishing, Random Allocation, Research Design, Sample Size, Statistics as Topic, General Science & Technology
Abstract

The US National Institute of Neurological Disorders and Stroke convened major stakeholders in June 2012 to discuss how to improve the methodological reporting of animal studies in grant applications and publications. The main workshop recommendation is that at a minimum studies should report on sample-size estimation, whether and how animals were randomized, whether investigators were blind to the treatment, and the handling of data. We recognize that achieving a meaningful improvement in the quality of reporting will require a concerted effort by investigators, reviewers, funding agencies and journal editors. Requiring better reporting of animal studies will raise awareness of the importance of rigorous study design to accelerate scientific progress.

Published
2012

4. Whole-genome analysis of sporadic amyotrophic lateral sclerosis

Author

Dunckley, Travis, Huentelman, Matthew J., Craig, David W., Pearson, John V., Szelinger, Szabolcs, Joshipura, Keta, Halperin, Rebecca F., Stamper, Chelsea, Jensen, Kendall R., Letizia, David, Hesterlee, Sharon E., Pestronk, Alan, Levine, Todd, Bertorini, Tulio, Graves, Michael C., Mozaffar, Tahseen, Jackson, Calayne E., Bosch, Peter, McVey, April, Dick, Arthur, Barohn, Richard, Lomen-Hoerth, Catherine, Rosenfeld, Jeffrey, OEConnor, Daniel T., Kuixing Zhang, Crook, Richard, Ryberg, Henrik, Hutton, Michael, Katz, Jonathan, Simpson, Ericka P., Hiroshi MitsumotoBowser, Robert, Miller, Robert G., Appel, Stanley H., and Stephan, Dietrich A.

Subjects
Amyotrophic lateral sclerosis -- Genetic aspects, Genetic susceptibility -- Research
Abstract

A genomewide case control association study is carried out to identify the specific genetic variants associated with sporadic amyotrophic lateral sclerosis (ALS). Results concluded that variants of the uncharacterized gene, FLJ10986 may confer susceptibility to sporadic ALS.

Published
2007

7. Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents

Author

Landrum Peay, Holly, primary, Fischer, Ryan, additional, Tzeng, Janice P., additional, Hesterlee, Sharon E., additional, Morris, Carl, additional, Strong Martin, Amy, additional, Rensch, Colin, additional, Smith, Edward, additional, Ricotti, Valeria, additional, Beaverson, Katherine, additional, Wand, Hannah, additional, and Mansfield, Carol, additional

Published
2019
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