Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lilia J. Tabassian"'
Autor:
Hiroe Ohyama, Nami Akiba, Lilia J Tabassian, Aisha K. Ba, Katsumi Uoshima, Yosuke Akiba, Masako Nagasawa
Publikováno v:
Journal of Dental Education. 86:21-28
Purpose/objectives Self-assessment is an essential skill for dental professionals. Understanding global trends in self-assessment can highlight the learning needs of students across a diversity of cultural backgrounds. The aim of this study is to com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::190f074c92dd780972added6918737fd
https://doi.org/10.1002/jdd.12779
https://doi.org/10.1002/jdd.12779
Publikováno v:
Journal of dental educationREFERENCES. 86(10)
Admission to dental school is based on various factors including academic achievements in undergraduate coursework and the Dental Admission Test (DAT) scores. Students' success in an operative course requires fundamental knowledge, hand skills, spati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41db73d4fde0dff2786eab85f23287b
https://pubmed.ncbi.nlm.nih.gov/35534921
https://pubmed.ncbi.nlm.nih.gov/35534921
Autor:
Timothy M. Miller, Jon B. Toledo, Jennifer Farren, Jeffrey D. Rothstein, John Q. Trojanowski, Luc Pregent, Michael G. Heckman, Alessandro Prelle, Aliesha D. O’Raw, Beth K. Rush, Bryan J. Traynor, Laura Braun, Matthew D. Disney, Yari Carlomagno, Veronique V. Belzil, Antonia Ratti, Lilia J. Tabassian, Monica Castanedes-Casey, Dennis W. Dickson, Michael Tierney, John C. van Swieten, Adam L. Boxer, Jeannie Chew, Lauren Elman, Murray Grossman, Emilie A. Perkerson, Mercedes Prudencio, Ana M. Caputo, Frank Rigo, Lillian M. Daughrity, Casey Cook, Otto Pedraza, James D. Berry, David Lacomis, Christina Fournier, Jennifer Jockel-Balsarotti, Leonard Petrucelli, Giovanna Antognetti, Marka van Blitterswijk, Lindsey R. Hayes, Robert H. Brown, Joanne Wuu, Kevin B. Boylan, Jimei Tong, Edythe Wiggs, Amelia Robertson, Linda Rousseau, Karen Jansen-West, Mary Kay Floeter, Yuping Song, John D. Fryer, Tania D Gendron, Robert Bowser, Barbara Poletti, Jennifer D. McBride, Shafeeq Ladha, Federica Solca, Alexander McCampbell, Leo McCluskey, Bruce L. Miller, Weixing Yang, Rosa Rademakers, Virginia Phillips, Chris W. Lee, Mei Yue, Denitza Raitcheva, Carla Palmucci, Jonathan D. Glass, Nancy N. Diehl, Vincenzo Silani, Jeannette N. Stankowski, Pamela Desaro, Cinzia Tiloca, Claudia Morelli, Abhishek Datta, William T. Hu, Yong Jie Zhang, Michael Benatar, Christine Ambrose
Publikováno v:
Science Translational Medicine, 9(383):eaai7866. American Association for the Advancement of Science
Science translational medicine, vol 9, iss 383
Science translational medicine
Science translational medicine, vol 9, iss 383
Science translational medicine
There is no effective treatment for amyotrophic lateral sclerosis (ALS), a devastating motor neuron disease. However, discovery of a G(4)C(2) repeat expansion in the C9ORF72 gene as the most common genetic cause of ALS has opened up new avenues for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::476c09df1772869d16b8d12d922e0b01
https://doi.org/10.1126/scitranslmed.aai7866
https://doi.org/10.1126/scitranslmed.aai7866
Autor:
Luc Pregent, Karen Jansen-West, Yanan Feng, Aliesha Garrett, Casey Cook, Neill R. Graff-Radford, Nicholas J. Kramer, Joseph W. Paul, Tania F. Gendron, Ronald C. Petersen, Jeannie Chew, Mercedes Prudencio, Marka van Blitterswijk, Nancy M. Bonini, Kevin B. Boylan, David S. Knopman, Fen-Biao Gao, Rosa Rademakers, Stanley N. Cohen, Bradley F. Boeve, Christopher D. Link, Lilia J. Tabassian, Lindsey D. Goodman, Sandra Almeida, Yari Carlomagno, Dennis W. Dickson, Ning Deng, Veronique V. Belzil, Leonard Petrucelli, Yong Jie Zhang, Joseph E. Parisi, Tzu Hao Cheng, Keith A. Josephs, Julien Couthouis, Lillian M. Daughrity, Aaron D. Gitler
Publikováno v:
Science
Targeting three defects with one strategy The neurodegenerative diseases amyotrophic lateral sclerosis and frontotemporal dementia are most commonly caused by a mutation in the C9orf72 gene. The mutation is an expanded hexanucleotide repeat in a nonc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c663f3c6a55485e870e65c09d3f6ff72