Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Sutha K. John"'
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Akademický článek
The effect of Abi3 locus deletion on the progression of Alzheimer’s disease-related pathologies
Autor: Hande Karahan, Daniel C. Smith, Byungwook Kim, Brianne McCord, Jordan Mantor, Sutha K. John, Md Mamun Al-Amin, Luke C. Dabin, Jungsu Kim
Publikováno v: Frontiers in Immunology, Vol 14 (2023)
Human genetics studies of Alzheimer’s disease (AD) have identified the ABI3 gene as a candidate risk gene for AD. Because ABI3 is highly expressed in microglia, the brain’s immune cells, it was suggested that ABI3 might impact AD pathogenesis by
Externí odkaz: https://doaj.org/article/6efcf4a66fa64855ad808fa16b336f87
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2
Low-Magnitude Mechanical Signals Combined with Zoledronic Acid Reduce Musculoskeletal Weakness and Adiposity in Estrogen-Deprived Mice
Autor: Gabriel M. Pagnotti, Trupti Trivedi, Laura E. Wright, Sutha K. John, Sreemala Murthy, Ryan R. Pattyn, Monte S. Willis, Yun She, Sukanya Suresh, William R. Thompson, Clinton T. Rubin, Khalid S. Mohammad, Theresa A. Guise
Publikováno v: bioRxiv
Combination treatment of Low-Intensity Vibration (LIV) with zoledronic acid (ZA) was hypothesized to preserve bone mass and muscle strength while reducing adipose tissue accrual associated with complete estrogen (E2)-deprivation in young and skeletal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec43956c074715b41cab60f3b02bcf4c
https://doi.org/10.1101/2023.03.12.531571
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3
Tumor necrosis factor inhibits ligand-stimulated EGF receptor activation through a TNF receptor 1-dependent mechanism
Autor: Sutha K. John, Mark R. Frey, D. Brent Polk, Jeremy A. Goettel, Karen L. Edelblum, Steven J. McElroy, Fang Yan
Publikováno v: American Journal of Physiology-Gastrointestinal and Liver Physiology. 295:G285-G293
Tumor necrosis factor (TNF) and epidermal growth factor (EGF) are key regulators in the intricate balance maintaining intestinal homeostasis. Previous work from our laboratory shows that TNF attenuates ligand-driven EGF receptor (EGFR) phosphorylatio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec699eb12837fd567b5b67827018dab
https://doi.org/10.1152/ajpgi.00425.2007
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5
Tumor necrosis factor regulates intestinal epithelial cell migration by receptor-dependent mechanisms
Autor: Julissa Corredor, Guinn Wilson, Sutha K. John, D. Brent Polk, Robert H. Whitehead, Christopher C. Shen, Fang Yan, Wei Tong
Publikováno v: American Journal of Physiology-Cell Physiology. 284:C953-C961
Altered mucosal integrity and increased cytokine production, including tumor necrosis factor (TNF), are the hallmarks of inflammatory bowel disease (IBD). In this study, we addressed the role of TNF receptors (TNFR) on intestinal epithelial cell migr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c6906941d62a54bf4bfc7ec1c51fc86
https://doi.org/10.1152/ajpcell.00309.2002
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6
Single-Limb Irradiation Induces Local and Systemic Bone Loss in a Murine Model
Autor: Laura E, Wright, Jeroen T, Buijs, Hun-Soo, Kim, Laura E, Coats, Anne M, Scheidler, Sutha K, John, Yun, She, Sreemala, Murthy, Ning, Ma, Helen J, Chin-Sinex, Teresita M, Bellido, Ted A, Bateman, Marc S, Mendonca, Khalid S, Mohammad, Theresa A, Guise
Publikováno v: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 30(7)
Increased fracture risk is commonly reported in cancer patients receiving radiotherapy, particularly at sites within the field of treatment. The direct and systemic effects of ionizing radiation on bone at a therapeutic dose are not well-characterize
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a278822321e155b441e6445b85de3e6b
https://pubmed.ncbi.nlm.nih.gov/25588731
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7
The human HNP36 gene is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia, type 1 (MEN I) syndrome
Autor: Thomas B. Shows, John A. Phillips, L.L. Haley, Sarada Sirripurapu, Shiela N.J. Sait, Carissa M. Smith, John B. Williams, Daniela S. Gerhard, Brent N. Rexer, Richard E. Goldstein, Sutha K. John
Publikováno v: Genomics. 42(2)
Multiple endocrine neoplasia, type 1 (MEN I), is an autosomal dominant syndrome of selected endocrine neoplasms whose causative gene, a suspected tumor suppressor, has been localized to chromosome 11q13, but has not been identified. Recently, the HNP
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2537a127dcc9d7a767a57fea51923247
https://pubmed.ncbi.nlm.nih.gov/9192854
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