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Neurology. Genetics|December 20, 2024
Updated Structure of CNBP Repeat Expansions in Patients With Myotonic Dystrophy Type 2 and Its Implication for Standard DiagnosticsMartin Wendlandt, Hannes Erdmann, Simone Rost, et al.
Administration and Policy in Mental Health|November 29, 2019
Mental Healthcare Needs in World Trade Center Responders: Results from a Large, Population-Based Health Monitoring CohortOlivia Diab, Jonathan DePierro, Leo Cancelmo, et al.
Journal of Immunotherapy (Hagerstown, Md. : 1997)|February 27, 2009
Differential responsiveness to IL-2, IL-7, and IL-15 common receptor gamma chain cytokines by antigen-specific peripheral blood naive or memory cytotoxic CD8+ T cells from healthy donors and melanoma patientsRachel Rosenthal, Célia Groeper, Laura Bracci, et al.
The Review of Scientific Instruments|November 2, 2010
The ITER core imaging x-ray spectrometer: x-ray calorimeter performanceP Beiersdorfer, G V Brown, J Clementson, et al.
Journal of Medical Genetics|December 16, 2021
Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancerFlorentine Scharf, Rafaela Magalhaes Leal Silva, Monika Morak, et al.
Molecular Ecology|July 13, 2013
Evidence for a recent horizontal transmission and spatial spread of Wolbachia from endemic Rhagoletis cerasi (Diptera: Tephritidae) to invasive Rhagoletis cingulata in EuropeHannes Schuler, Coralie Bertheau, Scott P Egan, et al.
Depression and Anxiety|July 22, 2021
Moral distress in frontline healthcare workers in the initial epicenter of the COVID-19 pandemic in the United States: Relationship to PTSD symptoms, burnout, and psychosocial functioningSonya B Norman, Jordyn H Feingold, Halley Kaye-Kauderer, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 14, 2026
eQTL Meta-Analysis Reveals Conserved and Population-Specific Regulatory Variation Underlying Nutritional Trait Evolution and Domestication in TomatoJiantao Zhao, Xin Wang, Jing Zhang, et al.
European Journal of Human Genetics : EJHG|February 28, 2008
Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCCMonika Morak, Hans Konrad Schackert, Nils Rahner, et al.
Gastroenterology|November 15, 2006
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated proteinSaara Ollila, Laura Sarantaus, Reetta Kariola, et al.
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