Zobrazeno 1 - 10
of 1 160
pro vyhledávání: '"H Roehl"'
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 9 (2019)
Reduced bone quality or mineral density predict susceptibility to fracture and also attenuate subsequent repair. Bone regrowth is also compromised by bacterial infection, which exacerbates fracture site inflammation. Because of the cellular complexit
Externí odkaz:
https://doaj.org/article/be2871490c584ddcaf613790f841781e
Autor:
Keh-Weei Tzung, Robert L. Lalonde, Karin D. Prummel, Harsha Mahabaleshwar, Hannah R. Moran, Jan Stundl, Amanda N. Cass, Yao Le, Robert Lea, Karel Dorey, Monika J. Tomecka, Changqing Zhang, Eline C. Brombacher, William T. White, Henry H. Roehl, Frank J. Tulenko, Christoph Winkler, Peter D. Currie, Enrique Amaya, Marcus C. Davis, Marianne E. Bronner, Christian Mosimann, Tom J. Carney
Publikováno v:
Nature.
The development of paired appendages was a key innovation during evolution and facilitated the aquatic to terrestrial transition of vertebrates. Largely derived from the lateral plate mesoderm (LPM), one hypothesis for the evolution of paired fins in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::467e218457f50e8ddc9901c2866d6cfb
https://doi.org/10.1038/s41586-023-06100-w
https://doi.org/10.1038/s41586-023-06100-w
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0144982 (2015)
Osteoblast differentiation from mesenchymal cells is regulated by multiple signalling pathways. Here we have analysed the roles of Fibroblast Growth Factor (FGF) and canonical Wingless-type MMTV integration site (Wnt/β-Catenin) signalling pathways o
Externí odkaz:
https://doaj.org/article/1a3ba4d865ee4a169b1d9eaedcf09e24
Autor:
Malgorzata I Wiweger, Zhe Zhao, Richard J P van Merkesteyn, Henry H Roehl, Pancras C W Hogendoorn
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e29734 (2012)
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dominant genetic condition that is characterized by the formation of cartilaginous bone tumours (osteochondromas) at multiple sites in the skeleton, seco
Externí odkaz:
https://doaj.org/article/9dc12d49d2174de89a56e3772aa111f8
Autor:
Aurélie Clément, Malgorzata Wiweger, Sophia von der Hardt, Melissa A Rusch, Scott B Selleck, Chi-Bin Chien, Henry H Roehl
Publikováno v:
PLoS Genetics, Vol 4, Iss 7, p e1000136 (2008)
Mutations in human Exostosin genes (EXTs) confer a disease called Hereditary Multiple Exostoses (HME) that affects 1 in 50,000 among the general population. Patients with HME have a short stature and develop osteochondromas during childhood. Here we
Externí odkaz:
https://doaj.org/article/b06bc09025b8402dade8eb2046f5791d
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Virology. 67:4964-4971
We examined the regulation of the cellular thymidine kinase (TK) gene promoter in simian virus 40 (SV40)-infected simian CV1 cells. Nuclear run-on transcription assays demonstrated a three- to fourfold increase in the rate of transcription of the end
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e760afa806b453d6c21dc945177113f5
https://doi.org/10.1128/jvi.67.8.4964-4971.1993
https://doi.org/10.1128/jvi.67.8.4964-4971.1993
Akademický článek
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Autor:
Holger H. Roehl, Susan E. Conrad
Publikováno v:
Molecular and Cellular Biology. 10:3834-3837
The authors have identified a regulatory region in the human thymidine kinase gene promoter. A set of promoter deletion mutants was constructed, linked to the bacterial neomycin resistance gene, and stably transfected into Rat3 cells. It was shown th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32a348e2700acacd55a516b046ade375
https://doi.org/10.1128/mcb.10.7.3834
https://doi.org/10.1128/mcb.10.7.3834