Zobrazeno 1 - 10
of 23
pro vyhledávání: '"G. Simmer"'
Autor:
Yervant Ichkhanian, Taha Ashraf, Faisal M. Nimri, Omar Shamaa, Brianna Shinn, William Hirsch, Christa Smaltz, Thomas E. Kowalski, David E. Loren, Anand Kumar, Alex Schlachterman, Alina Tantau, Martha Arevalo-Mora, Mouen A. Khashab, Sumit Singla, Stephen G. Simmer, Cyrus Piraka, Tobias Zuchelli
Publikováno v:
Gastrointestinal Endoscopy. 95:AB493-AB494
Autor:
Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, Figen Seymen, Amelia S Richardson, Yuanyuan Hu, Rachel N Milkovich, Ninna M R P Estrella, Mine Yildirim, Merve Bayram, Chiung-Fen Chen, James P Simmer
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52052 (2012)
Amelogenesis imperfecta (AI) is a group of inherited conditions featuring isolated enamel malformations. About 5% of AI cases show an X-linked pattern of inheritance, which are caused by mutations in AMELX. In humans there are two, non-allelic amelog
Externí odkaz:
https://doaj.org/article/972dfad1b5f744f4bb77348a80ac8709
Publikováno v:
Radiation Measurements. 45:1-9
Since many decades, Bonner sphere spectrometers (BSSs) are routinely used for assessment of neutron spectra over a wide energy range from some meV to GeV. Typically, a spectrometer consists of a neutron detector sensitive to thermal neutrons located
Autor:
S. Rollet, F. Wissmann, A. Fiechtner, M. Zielczyński, B. Wiegel, Natalia Golnik, M. Ferrarini, Georg Fehrenbacher, E. Cale, Stefano Agosteo, Carmen Villagrasa, E. Weitzenegger, Marco Caresana, S Sandri, Peter Beck, L. Donadille, Torsten Radon, Carles Domingo, V. Mares, M.J. García, François Trompier, H. Reithmeier, Hartmut Roos, D. Schardt, N. Dubourg, Adolfo Esposito, A. Zechner, Roberto Bedogni, Sabine Mayer, M. Latocha, A. Fuchs, G. Simmer, F. Gutermuth, S. Khurana, W. Rühm, Francisco V. Fernández, Th. Klages, František Spurný, Marco Silari, M. Wielunski
Publikováno v:
Radiation Measurements. 44:673-691
The European Commission has funded within its 6th Framework Programme a three-year project (2005–2007) called CONRAD, COordinated Network for RAdiation Dosimetry. The organizational framework for this project was provided by the European radiation
Publikováno v:
Clinical Genetics. 83:195-197
To the Editor: Amelogenesis imperfecta (AI) is a collection of non-syndromic inherited diseases featuring a variety of abnormal enamel phenotypes, patterns of inheritance, and causative genes. The term is also used to indicate the presence of an enam
Autor:
Figen Seymen, Chiung Fen Chen, Yuanyuan Hu, James P. Simmer, Amelia S. Richardson, Ninna M R P Estrella, Merve Bayram, Jan C.-C. Hu, Hui Chen Chan, Rachel N. Milkovich, Stephen G. Simmer, M. Yildirim
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52052 (2012)
PLoS ONE, Vol 7, Iss 12, p e52052 (2012)
Amelogenesis imperfecta (AI) is a group of inherited conditions featuring isolated enamel malformations. About 5% of AI cases show an X-linked pattern of inheritance, which are caused by mutations in AMELX. In humans there are two, non-allelic amelog
Publikováno v:
Radiation protection dosimetry. 136(4)
Two Bonner sphere spectrometers (BSSs) have recently been installed to measure secondary neutrons from cosmic radiation continuously, one at the environmental research station 'Schneefernerhaus' at an altitude of 2650 m in Germany and the other at th
Autor:
D. Schardt, C. Hranitzky, G. Simmer, S. Rollet, V. Mares, Marco Caresana, Adolfo Esposito, Marco Silari, Stefano Agosteo, Marcel Reginatto, Eike Hohmann, Roberto Bedogni, Werner Rühm, E. Weitzenegger, B. Wiegel, S. Khurana, M. Ferrarini, Georg Fehrenbacher, A. Kasper
The European Commission has funded within its 6th Framework Programme a three-year project (2005–2007) called CONRAD, COordinated Network for RAdiation Dosimetry . A major task of the CONRAD Work Package “ complex mixed radiation fields at workpl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f00f0972fba0906dfc95615b09021a3
http://hdl.handle.net/11311/545131
http://hdl.handle.net/11311/545131
Akademický článek
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Publikováno v:
Biology of reproduction. 62(3)
Estrogen receptor-alpha (ERalpha) knockout (ERalphaKO) female mice are infertile. Initially, they exhibit normal follicular development, but by 4-5 wk of age, they begin to develop hemorrhagic ovarian cysts. Follicles in adult ERalphaKO female mice p