Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Stephanie M. Carleton"'
Autor:
Salah A Daghlas, Arin K. Oestreich, Xiaomei Yao, Laura C. Schulz, William M. Kamp, Yong Wang, Natalia G. Karasseva, Ferris M. Pfeiffer, Marcus G. McCray, Youngjae Jeong, Stephanie M. Carleton, Kristin L. Lenz, Charlotte L. Phillips, Mark R. Ellersieck
Publikováno v:
Proceedings of the National Academy of Sciences. 113:13522-13527
During fetal development, the uterine environment can have effects on offspring bone architecture and integrity that persist into adulthood; however, the biochemical and molecular mechanisms remain unknown. Myostatin is a negative regulator of muscle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfac1d0c32656fb7632f2b8f8b2ca6ca
https://doi.org/10.1073/pnas.1607644113
https://doi.org/10.1073/pnas.1607644113
Autor:
Yuanji Zhang, Gregory E. Frierdich, Michael S. Koch, Jay S. Petrick, Stephanie M. Carleton, Colton R. Kessenich, Andre Silvanovich
Publikováno v:
Regulatory Toxicology and Pharmacology. 81:57-68
Genetically modified (GM) crops have been developed and commercialized that utilize double stranded RNAs (dsRNA) to suppress a target gene(s), producing virus resistance, nutritional and quality traits. MON 87411 is a GM maize variety that leverages
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117527788f54f944d1ae1df3cf4f992b
Autor:
Xiaomei Yao, Yong Wang, Ashlee M Williams, Marybeth Brown, Arin K. Oestreich, Marcus G. McCray, David R. Eyre, J. Andries Ferreira, Youngjae Jeong, Daniel J. Salamango, Stephanie M. Carleton, MaryAnn Weis, Charlotte L. Phillips, Bettina A. Gentry
Publikováno v:
Journal of Bone and Mineral Research. 30:1874-1886
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder associated with reduced bone mineral density and skeletal fragility. Bone is inherently mechanosensitive, with bone strength being proportional to muscle mass and st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72852ffd6c394ca0af2bb5fd724ca1d8
https://doi.org/10.1002/jbmr.2518
https://doi.org/10.1002/jbmr.2518
Autor:
Stephanie M. Carleton, Yuanji Zhang, Andre Silvanovich, Colton R. Kessenich, Michael S. Koch, Jay S. Petrick, G.E. Frierdich
Publikováno v:
Regulatory toxicology and pharmacology : RTP. 82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cef4b9053d11240f83dc63ac6e5304bb
https://pubmed.ncbi.nlm.nih.gov/27436086
https://pubmed.ncbi.nlm.nih.gov/27436086
Autor:
Steven A. Goldstein, Charlotte L. Phillips, Elizabeth A. Streeten, Daniel J. McBride, Joan C. Marini, Stephanie M. Carleton, Natalia V. Kuznetsova, John D. Sorkin, Alan R. Shuldiner, Sergey Leikin, Sue A. Shapses, Ethan L.H. Daley
Publikováno v:
Journal of Bone and Mineral Research
Osteogenesis imperfecta (OI) is a heritable form of bone fragility typically associated with a dominant COL1A1 or COL1A2 mutation. Variable phenotype for OI patients with identical collagen mutations is well established, but phenotype variability is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::788a1302df5751731198a4f6b7adebd6
https://doi.org/10.1359/jbmr.090720
https://doi.org/10.1359/jbmr.090720
Publikováno v:
Journal of Radioanalytical and Nuclear Chemistry. 276:65-69
Osteogenesis imperfecta (OI) is a heritable osteoporotic bone disease, due to defects in either type I procollagen genes (COL1A1 or COL1A2), resulting in abnormal and/or reduced levels of type I procollagen and alterations in bone mineralization. Our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b483263ba70f13167c0f8d0b18bd86
https://doi.org/10.1007/s10967-007-0411-y
https://doi.org/10.1007/s10967-007-0411-y
Autor:
Xiaomei Yao, Ferris M. Pfeiffer, Yong Wang, Bettina A. Gentry, Charlotte L. Phillips, Marybeth Brown, Stephanie M. Carleton, C. E. Raw, Arin K. Oestreich
Publikováno v:
Osteoporos Int
SUMMARY: Mice with osteogenesis imperfecta (+/oim), a disorder of bone fragility, were bred to mice with muscle over growth to test whether increasing muscle mass genetically would improve bone quality and strength. The results demonstrate that femor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2beb383ef1f69cdad7b494b7e6a28754
https://europepmc.org/articles/PMC8018583/
https://europepmc.org/articles/PMC8018583/
Autor:
Steven L. Levine, Geoffrey M. Mueller, Zihong Song, William Urquhart, Joshua P. Uffman, Tim Perez, Jason M. Ward, Stephanie M. Carleton, Peter D. Jensen
Publikováno v:
Regulatory toxicology and pharmacology : RTP. 73(2)
A biotechnology-derived corn variety, MON 87411, containing a suppression cassette that expresses an inverted repeat sequence that matches the sequence of western corn rootworm (WCR; Diabrotica virgifera virgifera) has been developed. The expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc8a87c250f149c8795f56c7c6d83381
https://pubmed.ncbi.nlm.nih.gov/26361852
https://pubmed.ncbi.nlm.nih.gov/26361852
Animal models have played major roles in understanding the pathogenesis and etiology of disease and this is no less true for osteogenesis imperfecta (OI). Since 1983, at least 15 animal models have been generated or identified representing the broad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8765d8c770cc5a39e2dea8b3c9a32ddd
https://doi.org/10.1016/b978-0-12-397165-4.00021-6
https://doi.org/10.1016/b978-0-12-397165-4.00021-6