Zobrazeno 1 - 10
of 287
pro vyhledávání: '"Joseph Alroy"'
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 2 (2014)
Lysosomal storage diseases are a group of inherited and acquired disorders. They are characterized by interruption of recycling of cellular and extracellular molecules. Clinically, they are presented as developmental and neurological symptoms similar
Externí odkaz:
https://doaj.org/article/b05d92653c084761901a9c323f0e9b37
Autor:
Xianbao He, Robert Berland, Samrawit Mekasha, Thomas G Christensen, Joseph Alroy, Igor Kramnik, Robin R Ingalls
Publikováno v:
PLoS Pathogens, Vol 9, Iss 8, p e1003569 (2013)
The sst1, "supersusceptibility to tuberculosis," locus has previously been shown to be a genetic determinant of host resistance to infection with the intracellular pathogen, Mycobacterium tuberculosis. Chlamydia pneumoniae is an obligate intracellula
Externí odkaz:
https://doaj.org/article/9e951af5a7304459943b55d04428e27b
Autor:
Xianbao He, Anjali Nair, Samrawit Mekasha, Joseph Alroy, Catherine M O'Connell, Robin R Ingalls
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e20846 (2011)
Chlamydia trachomatis is a common sexually transmitted pathogen and is associated with infant pneumonia. Data from the female mouse model of genital tract chlamydia infection suggests a requirement for TLR2-dependent signaling in the induction of inf
Externí odkaz:
https://doaj.org/article/a3761742b2e74c89920563d881fa3a93
Autor:
Damiana Chiavolini, Javier Rangel-Moreno, Gretchen Berg, Kate Christian, Laura Oliveira-Nascimento, Susan Weir, Joseph Alroy, Troy D Randall, Lee M Wetzler
Publikováno v:
PLoS ONE, Vol 5, Iss 6, p e11156 (2010)
Francisella tularensis causes severe pulmonary disease, and nasal vaccination could be the ideal measure to effectively prevent it. Nevertheless, the efficacy of this type of vaccine is influenced by the lack of an effective mucosal adjuvant.Mice wer
Externí odkaz:
https://doaj.org/article/21a8c7e6b2cd4cc9804af3037d4e0ad5
Autor:
Sara E. Mole, Rodrigo Gutierrez-Quintana, Celia Kun-Rodrigues, Rita Guerreiro, Jose Bras, Kiterie M. E. Faller, Jacques Penderis, Lee Darwent, Samuel Sharpe, Glenn Anderson, Joseph Alroy
Publikováno v:
Journal of Neuroscience Research. 94:339-347
Neuronal ceroid lipofuscinoses (NCLs) are a group of incurable lysosomal storage disorders characterized by neurodegeneration and accumulation of lipopigments mainly within the neurons. We studied two littermate Chihuahua dogs presenting with progres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae41c0038a8db47b71e1de8304fb2130
https://doi.org/10.1002/jnr.23710
https://doi.org/10.1002/jnr.23710
Autor:
Alan Mejia Maza, Danitza G Dávila-Villacorta, Manuela Verastegui, Hector H. Garcia, Cesar M. Gavidia, Javier Mamani, Gino Castillo, Emma S Carter, Armando E. Gonzalez, Robert H. Gilman, Joseph Alroy, Charles R. Sterling, Jemina D Morales, Randy Woltjer, Rogger P Carmen-Orozco
Publikováno v:
Brain Pathol
Neurocysticercosis is a parasitic brain disease caused by the larval form (Cysticercus cellulosae) of the Taenia solium and is the leading cause of preventable epilepsy world-wide. However, the pathophysiology and relation to the wide range of clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dded2568e0f7dd610a243f9a24def00
https://hdl.handle.net/20.500.12866/4012
https://hdl.handle.net/20.500.12866/4012
Publikováno v:
Pediatric and Developmental Pathology. 17:474-477
Galactosialidosis (GS) is a rare autosomal recessive lysosomal storage disease caused by a combined deficiency of lysosomal β-galactosidase and neuraminidase as a result of a genetic defect in the protective protein/cathepsin A gene. We report a cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24bd6cf4ffd4b96d3d539534b74bcb0
https://doi.org/10.2350/14-05-1500-cr.1
https://doi.org/10.2350/14-05-1500-cr.1
Publikováno v:
Virchows Archiv. 463:843-846
Inflammatory pseudotumors have a diverse etiology, mycobacterial pseudotumor (MP) being one of them. MP is a rare entity; it has been reported infrequently in various organs and is extremely rare in the skin. We report a cutaneous MP in an immunosupp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec6d25f05b9d9b2985d26b5efe0b5521
https://doi.org/10.1007/s00428-013-1491-4
https://doi.org/10.1007/s00428-013-1491-4
Publikováno v:
Diagnostic Electron Microscopy-A Practical Guide to Interpretation and Technique
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8c89fd9ae41e99c2ee06e25125ff8a5
https://doi.org/10.1002/9781118452813.ch8
https://doi.org/10.1002/9781118452813.ch8
Publikováno v:
Veterinary Pathology. 49:723-726
A 14-year-old female alpaca ( Vicugna pacos) was presented with a 1-week history of lethargy and anorexia and a 2-day history of recumbency, trembling, and hypothermia. There were no significant gross findings on postmortem examination. Hematoxylin a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c36ee179597dcd8ce3456097ed5abdd2
https://doi.org/10.1177/0300985811406886
https://doi.org/10.1177/0300985811406886