Zobrazeno 1 - 7
of 7
pro vyhledávání: '"David A. Liebelt"'
Autor:
Sun Jin Kim, Jonathan Krystal, Benjamin J. Levy, Robert Li, Yossef Blum, David A. Liebelt, David M. Hirsh, Ajay Lall, Praveen K. Kadimcherla
Publikováno v:
Current Orthopaedic Practice. 24:509-512
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c78e473eb8b544839888ab3b8f0e55b
https://doi.org/10.1097/bco.0b013e31829c4476
https://doi.org/10.1097/bco.0b013e31829c4476
Autor:
Paul Hinchey, David A. Liebelt, Natalia Louneva, Joseph Hinchey, Allison M. Terlizzi, Steven J. Siegel, Francois V. Bolduc, Danielle Emerson, Ali Sharma, Brian P. Schoenfeld, Maria Kollaros, R. Suzanne Zukin, Michael Gertner, Catherine H. Choi, Sean Campbell, Aaron J. Bell, Neal J. Ferrick, Cory Rosenfelt, Steven Langer, Richard J. Choi, Eric Koenigsberg, Daniel B. Chambers, Steven E. Arnold, Robert E. Featherstone, Sean M.J. McBride, David Ferreiro, Thomas V. McDonald, Steven Sust, Aatika Malik, Thomas A. Jongens
Publikováno v:
Frontiers in Behavioral Neuroscience
Fragile X is the most common monogenic disorder associated with intellectual disability (ID) and autism spectrum disorders (ASD). Additionally, many patients are afflicted with executive dysfunction, ADHD, seizure disorder and sleep disturbances. Fra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bf00f6be203960a473f293f93172249
https://doi.org/10.3389/fnbeh.2016.00136
https://doi.org/10.3389/fnbeh.2016.00136
Autor:
Catherine H. Choi, Steven E. Arnold, Michael Gertner, Newton H. Woo, Thomas V. McDonald, Aaron J. Bell, Steven J. Siegel, Paul Hinchey, David A. Liebelt, Thomas A. Jongens, Eliana D. Weisz, Francois V. Bolduc, Brian P. Schoenfeld, Joseph Hinchey, Allison M. Terlizzi, Maria Kollaros, Nicole L. Yohn, R. Suzanne Zukin, Eric Koenigsberg, Neal J. Ferrick, Sean M.J. McBride, Natalia Louneva, Richard J. Choi, Michael R. Tranfaglia, Daniel B. Chambers
Fragile X syndrome (FXS) is the leading cause of both intellectual disability and autism resulting from a single gene mutation. Previously, we characterized cognitive impairments and brain structural defects in aDrosophilamodel of FXS and demonstrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f91fc0f7403f93081fe985fac884bec3
https://europepmc.org/articles/PMC4287155/
https://europepmc.org/articles/PMC4287155/
Autor:
David A. Liebelt, Jason B. Dictenberg, T. Eom, Honglai Zhang, Shailesh M. Shenoy, Robert H. Singer, Gary J. Bassell, Yuri Oleynikov
Publikováno v:
Neuron. 31(2):261-275
Neurotrophin regulation of actin-dependent changes in growth cone motility may depend on the signaling of beta-actin mRNA transport. Formation of an RNP complex between the beta-actin mRNA zipcode sequence and Zipcode Binding Protein 1 (ZBP1) was req
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19008737e2d837df8c9b117d6be74766
Autor:
Mark E. Fortini, Eric Koenigsberg, Thomas A. Jongens, Sean M.J. McBride, Paul Hinchey, David A. Liebelt, Neal J. Ferrick, Stephanie Chiorean, Hanh T. Nguyen, Catherine H. Choi, Richard J. Choi, Brian P. Schoenfeld, Allison M. Terlizzi, Maria Kollaros, Ai Sumida, David Ferreiro, Thomas V. McDonald, Rebecca L. Rudominer, Kathleen K. Siwicki, Aaron J. Bell
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 30(28)
Alzheimer9s disease (AD) is the leading cause of cognitive loss and neurodegeneration in the developed world. Although its genetic and environmental causes are not generally known, familial forms of the disease (FAD) are attributable to mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74d98310050b7beb5d5536e953616ef8
https://pubmed.ncbi.nlm.nih.gov/20631179
https://pubmed.ncbi.nlm.nih.gov/20631179
Autor:
Ai Sumida, Paul Hinchey, David A. Liebelt, Catherine H. Choi, Thomas A. Jongens, Eric Koenigsberg, Maria Kollaros, Aaron J. Bell, Neal J. Ferrick, Sean M.J. McBride, Hanh T. Nguyen, David Ferreiro, Thomas V. McDonald, Rebecca L. Rudominer, Yan Wang, Allison M. Terlizzi, Brian P. Schoenfeld
Publikováno v:
Biogerontology. 11(3)
Fragile X syndrome afflicts 1 in 2,500 individuals and is the leading heritable cause of mental retardation worldwide. The overriding clinical manifestation of this disease is mild to severe cognitive impairment. Age-dependent cognitive decline has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c1d38f361f019ec15e5750602ef78e2
https://pubmed.ncbi.nlm.nih.gov/20039205
https://pubmed.ncbi.nlm.nih.gov/20039205
Autor:
David C. Reeves, Paul D. Roepe, David A. Liebelt, David A. Fidock, Viswanathan Lakshmanan, Myles H. Akabas
The emergence of chloroquine-resistant Plasmodium falciparum malaria imperils the lives of millions of people in Africa, Southeast Asia and South America. Chloroquine resistance is associated with mutations in the Plasmodium falciparum chloroquine re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b400c7370a8c43e3bcbb9bd211416f7d
https://europepmc.org/articles/PMC1687154/
https://europepmc.org/articles/PMC1687154/