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Psychiatry Research|August 15, 2015
Psychopathic traits in adolescents are associated with higher structural connectivityLouise E Pape, Moran D Cohn, Matthan W A Caan, et al.
Frontiers in Immunology|June 5, 2023
The human Stat1 gain-of-function T385M mutation causes expansion of activated T-follicular helper/T-helper 1-like CD4 T cells and sex-biased autoimmunity in specific pathogen-free miceOri Scott, Shagana Visuvanathan, Emily Reddy, et al.
Lancet (London, England)|June 1, 2000
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathyW M Franz, M Müller, O J Müller, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Pediatrics|May 3, 2006
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T geneStacie B Peddy, Luca A Vricella, Jane E Crosson, et al.
The Journal of Allergy and Clinical Immunology. in Practice|July 12, 2017
Sensitization and Exposure to Pets: The Effect on Asthma Morbidity in the US PopulationPeter J Gergen, Herman E Mitchell, Agustin Calatroni, et al.
Environmental Health Perspectives|March 27, 2007
Dust weight and asthma prevalence in the National Survey of Lead and Allergens in Housing (NSLAH)Leslie Elliott, Samuel J Arbes, Eric S Harvey, et al.
Experimental Neurology|January 22, 2013
Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilizationRan Xu, Eva Andres-Mateos, Rebeca Mejias, et al.
Bone Marrow Transplantation|September 20, 2011
Immunohistochemistry of affected tissue may guide cGVHD treatment decisionsK M Williams, L W Ostrow, D M Loeb, et al.
The Journal of Pediatrics|January 31, 2016
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1LGrace Yoon, Zeenat Malam, Tara Paton, et al.
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