Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rachel E. Kneeland"'
Publikováno v:
Abstracts.
Background Sulfamethoxazole and trimethoprim (TMP-SMX) is frequently used for urinary tract infections and Pneumocystis prophylaxis in patients on high dose systemic steroids or cyclophosphamide. Recommendations on avoiding TMP-SMX in systemic lupus
Autor:
Timothy D. Folsom, S. Hossein Fatemi, Stephanie B. Liesch, Paul Thuras, Rachel E. Kneeland, Mahtab K Yousefi
Publikováno v:
Journal of Neuroscience Research. 95:1110-1122
Prenatal viral infection has been identified as a potential risk factor for the development of neurodevelopmental disorders such as schizophrenia and autism. Additionally, dysfunction in gamma-aminobutyric acid, Reelin, and fragile X mental retardati
Autor:
S. Hossein Fatemi, Rachel E. Kneeland
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 42:35-48
Schizophrenia is a severe neurodevelopmental disorder with genetic and environmental etiologies. Prenatal viral/bacterial infections and inflammation play major roles in the genesis of schizophrenia. In this review, we describe a viral model of schiz
Autor:
Kegang Hua, Timothy D. Folsom, Teri J. Reutiman, Susumu Mori, John Hsu, Stephanie B. Liesch, Rachel E. Kneeland, Divyen H. Patel, Tess E. Kornfield, Robert Rooney, S. Hossein Fatemi
Publikováno v:
Neuropharmacology. 62:1290-1298
Researchers have long noted an excess of patients with schizophrenia were born during the months of January and March. This winter birth effect has been hypothesized to result either from various causes such as vitamin D deficiency (McGrath, 1999; Mc
Autor:
Paul Thuras, Timothy D. Folsom, S. Hossein Fatemi, Mahtab K Yousefi, Stephanie B. Liesch, Rachel E. Kneeland
Publikováno v:
Schizophrenia Research. 146:376-378
Recent work has demonstrated the impact of dysfunction of the GABAergic signaling system in brain and the resultant behavioral pathologies in subjects with autism. In animal models, altered expression of Fragile X mental retardation protein (FMRP) ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fd7e40e884b847fad096523822a66f9
https://europepmc.org/articles/PMC3177171/
https://europepmc.org/articles/PMC3177171/
Publikováno v:
Schizophrenia Research. 124:246-247
In individuals with fragile X syndrome (FXS), there is a silencing of the fragile X mental retardation (FMR1) gene, usually due to an expansion of a CGG repeat in the 5’ untranslated region (Oostra and Willemsen, 2009). The subsequent loss of the F
Autor:
Timothy D. Folsom, Stephanie B. Liesch, Rachel E. Kneeland, Paul Thuras, SHossein Fatemi, Mahtab K Yousefi
Publikováno v:
Molecular Autism
Background Candidate genes associated with idiopathic forms of autism overlap with other disorders including fragile X syndrome. Our laboratory has previously shown reduction in fragile X mental retardation protein (FMRP) and increase in metabotropic