Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Noriko Wakabayashi-Ito"'
Autor:
Naoto Ito, William T. Hendriks, Jyotsna Dhakal, Christine A. Vaine, Christina Liu, David Shin, Kyle Shin, Noriko Wakabayashi-Ito, Marisela Dy, Trisha Multhaupt-Buell, Nutan Sharma, Xandra O. Breakefield, D. Cristopher Bragg
Publikováno v:
Disease Models & Mechanisms, Vol 9, Iss 4, Pp 451-462 (2016)
X-linked dystonia-parkinsonism (XDP) is a hereditary neurodegenerative disorder involving a progressive loss of striatal medium spiny neurons. The mechanisms underlying neurodegeneration are not known, in part because there have been few cellular mod
Externí odkaz:
https://doaj.org/article/b20ed9bd4a20450ea8d555d3d5d51d53
Autor:
Noriko Wakabayashi-Ito, Rami R. Ajjuri, Benjamin W. Henderson, Olugbenga M. Doherty, Xandra O. Breakefield, Janis M. O'Donnell, Naoto Ito
Publikováno v:
Biology Open, Vol 4, Iss 5, Pp 585-595 (2015)
Dystonia represents the third most common movement disorder in humans with over 20 genetic loci identified. TOR1A (DYT1), the gene responsible for the most common primary hereditary dystonia, encodes torsinA, an AAA ATPase family protein. Most cases
Externí odkaz:
https://doaj.org/article/393daecd50f04d25a31ca190b07d6e3f
Autor:
Vahbiz Jokhi, James Ashley, John Nunnari, Akiko Noma, Naoto Ito, Noriko Wakabayashi-Ito, Melissa J. Moore, Vivian Budnik
Publikováno v:
Cell Reports, Vol 3, Iss 4, Pp 988-995 (2013)
A previously unrecognized mechanism through which large ribonucleoprotein (megaRNP) granules exit the nucleus is by budding through the nuclear envelope (NE). This mechanism is akin to the nuclear egress of herpes-type viruses and is essential for pr
Externí odkaz:
https://doaj.org/article/0935ec74da864d77939b924ff64c9c52
Autor:
Majid Kazemian, Charles Blatti, Adam Richards, Michael McCutchan, Noriko Wakabayashi-Ito, Ann S. Hammonds, Susan E. Celniker, Sudhir Kumar, Scot A. Wolfe, Michael H. Brodsky, Saurabh Sinha
Publikováno v:
PLoS Biology, Vol 11, Iss 10 (2013)
Externí odkaz:
https://doaj.org/article/2cba5540bb8842bc81e710f31d0b0a20
Autor:
Noriko Wakabayashi-Ito, Olugbenga M Doherty, Hideaki Moriyama, Xandra O Breakefield, James F Gusella, Janis M O'Donnell, Naoto Ito
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26183 (2011)
Dystonia represents the third most common movement disorder in humans. At least 15 genetic loci (DYT1-15) have been identified and some of these genes have been cloned. TOR1A (formally DYT1), the gene responsible for the most common primary hereditar
Externí odkaz:
https://doaj.org/article/f577069ad7a34a17a0a5af6311ff640a
Autor:
Noriko Wakabayashi-Ito, Olugbenga M. Doherty, Hideaki Moriyama, Xandra O. Breakefield, James F. Gusella, Janis M. O'Donnell, Naoto Ito
Publikováno v:
PLoS ONE, Vol 6, Iss 10 (2011)
Externí odkaz:
https://doaj.org/article/c413924d167d45eba7cfc1742a8676eb
Autor:
Majid Kazemian, Charles Blatti, Adam Richards, Michael McCutchan, Noriko Wakabayashi-Ito, Ann S Hammonds, Susan E Celniker, Sudhir Kumar, Scot A Wolfe, Michael H Brodsky, Saurabh Sinha
Publikováno v:
PLoS Biology, Vol 8, Iss 8, p e1000456 (2010)
Cis-regulatory modules that drive precise spatial-temporal patterns of gene expression are central to the process of metazoan development. We describe a new computational strategy to annotate genomic sequences based on their "pattern generating poten
Externí odkaz:
https://doaj.org/article/8623d3269ad24e4f923079e9b1f726d1
Autor:
Trisha Multhaupt-Buell, Xandra O. Breakefield, Kyle Shin, Jyotsna Dhakal, D. Cristopher Bragg, Marisela E. Dy, Naoto Ito, David Shin, Noriko Wakabayashi-Ito, Christina H. Liu, Christine A. Vaine, Nutan Sharma, William T. Hendriks
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 9, Iss 4, Pp 451-462 (2016)
Disease Models & Mechanisms, Vol 9, Iss 4, Pp 451-462 (2016)
X-linked dystonia-parkinsonism (XDP) is a hereditary neurodegenerative disorder involving a progressive loss of striatal medium spiny neurons. The mechanisms underlying neurodegeneration are not known, in part because there have been few cellular mod
Autor:
Janis M. O'Donnell, Xandra O. Breakefield, Noriko Wakabayashi-Ito, Olugbenga M. Doherty, Benjamin W. Henderson, Rami R. Ajjuri, Naoto Ito
Publikováno v:
Biology Open, Vol 4, Iss 5, Pp 585-595 (2015)
Biology Open
Biology Open
Dystonia represents the third most common movement disorder in humans with over 20 genetic loci identified. TOR1A (DYT1), the gene responsible for the most common primary hereditary dystonia, encodes torsinA, an AAA ATPase family protein. Most cases
Autor:
Melissa J. Moore, Noriko Wakabayashi-Ito, Akiko Noma, Vivian Budnik, James A. Ashley, Naoto Ito, Vahbiz Jokhi, John J. Nunnari
Publikováno v:
Cell Reports, Vol 3, Iss 4, Pp 988-995 (2013)
SUMMARY A previously unrecognized mechanism through which large ribonucleoprotein (megaRNP) granules exit the nucleus is by budding through the nuclear envelope (NE). This mechanism is akin to the nuclear egress of herpes-type viruses and is essentia