Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Megan K Cox"'
Autor:
Benjamin Greene, Ryan J Russo, Shannon Dwyer, Katie Malley, Errin Roberts, Joseph Serrielo, Peter Piepenhagen, Sheila Cummings, Susan Ryan, Christine Zarazinski, Sasidhar Uppuganti, Nikolai Bukanov, Jeffry S Nyman, Megan K Cox, Shiguang Liu, Oxana Ibraghimov‐Beskrovnaya, Yves Sabbagh
Publikováno v:
JBMR Plus, Vol 5, Iss 9, Pp n/a-n/a (2021)
ABSTRACT Osteogenesis imperfecta (OI), is a genetic disorder of bone fragility caused by mutations in collagen I or proteins involved in collagen processing. Previous studies in mice and human OI bones have shown that excessive activation of TGF‐β
Externí odkaz:
https://doaj.org/article/e9260be1938a4cbb897d1633289d0ae3
Autor:
Martin R. Graf, Shruti Apte, Esteban Terzo, Simran Padhye, Shuhao Shi, Megan K. Cox, Roger B. Clark, Vijay Modur, Vasudeo Badarinarayana
Publikováno v:
Journal of Molecular Medicine. 101:375-385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f15234d1587adb9352abe4d77020c45
https://doi.org/10.1007/s00109-023-02291-x
https://doi.org/10.1007/s00109-023-02291-x
Autor:
Katie Malley, Yves Sabbagh, Joseph Serrielo, Christine Zarazinski, Oxana Ibraghimov-Beskrovnaya, Megan K. Cox, Sasidhar Uppuganti, Nikolai Bukanov, Jeffry S. Nyman, Errin Roberts, Benjamin Greene, Ryan J. Russo, Shiguang Liu, Peter A. Piepenhagen, Sheila Cummings, Susan Ryan, Shannon Dwyer
Publikováno v:
JBMR Plus
JBMR Plus, Vol 5, Iss 9, Pp n/a-n/a (2021)
JBMR Plus, Vol 5, Iss 9, Pp n/a-n/a (2021)
Osteogenesis imperfecta (OI), is a genetic disorder of bone fragility caused by mutations in collagen I or proteins involved in collagen processing. Previous studies in mice and human OI bones have shown that excessive activation of TGF‐β signalin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1ac922b70c5f7821fd4561f97246fb2
https://doi.org/10.1002/jbm4.10530
https://doi.org/10.1002/jbm4.10530
Autor:
null Benjamin Greene, null Ryan J Russo, null Shannon Dwyer, null Katie Malley, null Errin Roberts, null Joseph Serrielo, null Peter Piepenhagen, null Sheila Cummings, null Susan Ryan, null Christine Zarazinski, null Sasidhar Uppuganti, null Nikolai Bukanov, null Jeffry S. Nyman, null Megan K. Cox, null Shiguang Liu, null Oxana Ibraghimov‐Beskrovnaya, null Yves Sabbagh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bf23b65b1a3b634cb6529f2f8a76c36
https://doi.org/10.1002/jbm4.10530/v2/response1
https://doi.org/10.1002/jbm4.10530/v2/response1
Autor:
Michelle Matsuura, Heiko L. Schoenfuss, Satomi Kohno, Raingsey Aing, Jessica L. Ward, Megan K. Cox
Publikováno v:
Science of The Total Environment. 692:519-528
Environmental estrogens from anthropogenic activities are ubiquitous in aquatic ecosystems. Ambient temperature in these systems also fluctuates in daily, seasonal, and long-term rhythms. While both factors have been studied extensively, their intera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d074f8f7b48d52c5c561ce34fc36627
https://doi.org/10.1016/j.scitotenv.2019.07.142
https://doi.org/10.1016/j.scitotenv.2019.07.142
Autor:
Robert Fogle, Ying Mu, Kuldeep Singh, William Weber, Yves Sabbagh, Cynthia T. Pryce, Megan K. Cox, Mohammed Salman Shazeeb, Anurag Gupta, Wen Tang, Dinesh S. Bangari, Xiaoyou Ying
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Scientific Reports
Scientific Reports
Achondroplasia, the most common form of dwarfism, affects more than a quarter million people worldwide and remains an unmet medical need. Achondroplasia is caused by mutations in the fibroblast growth factor receptor 3 (FGFR3) gene which results in o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f69022a2c4c6da8f4717141ffab09f57
http://link.springer.com/article/10.1038/s41598-017-18801-0
http://link.springer.com/article/10.1038/s41598-017-18801-0
Publikováno v:
Journal of Cellular Biochemistry. 108:668-674
Phosphate is required for terminal differentiation of hypertrophic chondrocytes during postnatal growth plate maturation. In vitro models of chondrocyte differentiation demonstrate that 7mM phosphate, a concentration analogous to that of the late ges
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2995c1a658f288c039bdf91eb1172dd0
https://doi.org/10.1002/jcb.22302
https://doi.org/10.1002/jcb.22302
Transforming growth factor β (TGF-β) signaling plays an integral role in skeletal development. Conditional deletion of the TGF-β type II receptor (Tgfbr2) from type II Collagen (Col2a) expressing cells results in defects in development of the annu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d36be1c84fb5405f80681bf058b67bf
https://europepmc.org/articles/PMC4252592/
https://europepmc.org/articles/PMC4252592/
Publikováno v:
Developmental biology. 382(1)
It has been difficult to examine the role of TGF-s in post-natal tooth development due to perinatal lethality in many of the signaling deficient mouse models. To address the role of Tgfbr2 in postnatal tooth development, we generated a mouse in which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56b1bef3e08af546e6f9b08104960315
https://pubmed.ncbi.nlm.nih.gov/23933490
https://pubmed.ncbi.nlm.nih.gov/23933490
Autor:
Rosa Serra, Megan K. Cox
Publikováno v:
The Intervertebral Disc ISBN: 9783709115343
Intervertebral discs are derived from embryonic structures called the sclerotome and notochord (Paavola et al. 1980; Theiler 1988; Rufai et al. 1995). The nucleus pulposus, the cushioning core of the mature intervertebral disc, is derived from the no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f9a57d565bd70aacc498fc9caa059d0
https://doi.org/10.1007/978-3-7091-1535-0_3
https://doi.org/10.1007/978-3-7091-1535-0_3