Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Michael R. Santoro"'
Autor:
Rick S. Bienkowski, Ayan Banerjee, J. Christopher Rounds, Jennifer Rha, Omotola F. Omotade, Christina Gross, Kevin J. Morris, Sara W. Leung, ChangHui Pak, Stephanie K. Jones, Michael R. Santoro, Stephen T. Warren, James Q. Zheng, Gary J. Bassell, Anita H. Corbett, Kenneth H. Moberg
Publikováno v:
Cell Reports, Vol 20, Iss 6, Pp 1372-1384 (2017)
The Drosophila dNab2 protein is an ortholog of human ZC3H14, a poly(A) RNA binding protein required for intellectual function. dNab2 supports memory and axon projection, but its molecular role in neurons is undefined. Here, we present a network of in
Externí odkaz:
https://doaj.org/article/04da1a1516b5427eb44d99b3fc79f925
The discovery of the FMR1 gene and its associated unstable CGG trinucleotide repeat mutation in May of 1991 marked a watershed moment in genetics. Along with the subsequent recognition of expansion of unstable repetitive elements as causative mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5de434a68d80fbd33d2b6cb32a8d2a90
https://doi.org/10.1016/b978-0-12-804461-2.00002-0
https://doi.org/10.1016/b978-0-12-804461-2.00002-0
Autor:
Han Bao, Mark F. Bear, Tamir Ben-Hur, Nissim Benvenisty, Elizabeth Berry-Kravis, Aditi Bhattacharya, Pietro Chiurazzi, Jeffrey Cohen, Lynda El-Hassar, Douglas W. Ethell, Andreas Frick, Christine M. Gall, Fabrizio Gasparini, Inbal Gazy, Melanie Ginger, Christina Gross, Jacalyn Guy, Randi Hagerman, Becky Hardiman, Charles Hoeffer, Jessica E. Hunter, Molly M. Huntsman, Aia E. Jønch, Sébastien Jacquemont, Peng Jin, Richard S. Jope, Leonard K. Kaczmarek, Peter Kind, R. Frank Kooy, Julie C. Lauterborn, Andrew Ligsay, Lothar Lindemann, Olivier J.J. Manzoni, Henry G.S. Martin, Montserrat Milà, David L. Nelson, Giovanni Neri, Daniela Neuhofer, Emily K. Osterweil, Jörg Richstein, Michael R. Santoro, Gaia Scerif, Sebastian S. Scharf, Stephanie L. Sherman, Harpreet Sidhu, Will Spooren, Laura J. Stoppel, Joshua Suhl, Elisabetta Tabolacci, Flora Tassone, Sally Till, Karen Usdin, Dan Vershkov, Stephen T. Warren, Rob Willemsen, Xiao-Nan Zhao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3e6c849b4f83ac11b71cbc2abf0a3bb
https://doi.org/10.1016/b978-0-12-804461-2.00026-3
https://doi.org/10.1016/b978-0-12-804461-2.00026-3
Autor:
Gary J. Bassell, Rick Bienkowski, Ayan Banerjee, Stephen T. Warren, Kenneth H. Moberg, Michael R. Santoro, James Q. Zheng, Omotola F. Omotade, Stephanie K. Jones, Anita H. Corbett, Christina Gross, Kevin J. Morris, ChangHui Pak, Jennifer Rha, Sara W. Leung, J. Christopher Rounds
Publikováno v:
Cell Reports, Vol 20, Iss 6, Pp 1372-1384 (2017)
The Drosophila dNab2 protein is an ortholog of human ZC3H14, a poly(A) RNA binding protein required for intellectual function. dNab2 supports memory and axon projection, but its molecular role in neurons is undefined. Here, we present a network of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9523cbd813de7ac8d6eddeddc1f35c9
https://pubmed.ncbi.nlm.nih.gov/28793261
https://pubmed.ncbi.nlm.nih.gov/28793261
Publikováno v:
Annual review of pathology. 7
Fragile X syndrome (FXS) is a common form of inherited intellectual disability and is one of the leading known causes of autism. The mutation responsible for FXS is a large expansion of the trinucleotide CGG repeat in the 5′ untranslated region of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3776209da10a2b6ce2386b41dc9391b1
https://pubmed.ncbi.nlm.nih.gov/22017584
https://pubmed.ncbi.nlm.nih.gov/22017584