Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Aldrin E"'
Autor:
Eduardo E. Arteaga-Bracho, Maria Gulinello, Michael L. Winchester, Nandini Pichamoorthy, Jenna R. Petronglo, Alicia D. Zambrano, Julio Inocencio, Chirstopher D. De Jesus, Joseph O. Louie, Solen Gokhan, Mark F. Mehler, Aldrin E. Molero
Publikováno v:
Neurobiology of Disease, Vol 96, Iss , Pp 144-155 (2016)
The mutation in huntingtin (mHtt) leads to a spectrum of impairments in the developing forebrain of Huntington's disease (HD) mouse models. Whether these developmental alterations are due to loss- or gain-of-function mechanisms and contribute to HD p
Externí odkaz:
https://doaj.org/article/033914eac2624c8087987ee040422140
Autor:
Giang D Nguyen, Solen Gokhan, Aldrin E Molero, Seung-Min Yang, Byung-Ju Kim, Arthur I Skoultchi, Mark F Mehler
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96858 (2014)
H1 linker histone proteins are essential for the structural and functional integrity of chromatin and for the fidelity of additional epigenetic modifications. Deletion of H1c, H1d and H1e in mice leads to embryonic lethality by mid-gestation with a b
Externí odkaz:
https://doaj.org/article/1e0c99051a3441faac370874d1e16f6a
Autor:
Aldrin E. Sweeney
Publikováno v:
ETD: Educação Temática Digital, Vol 2, Iss 2, Pp 59-79 (2001)
The rapid growth of information and communication technology since the early 1990s has greatly influenced the accessibility of information on a global level and also has played a critical role in restructuring the mechanisms by which specialized acad
Externí odkaz:
https://doaj.org/article/756e6f05139b41a8a5f8487919d3e96f
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e64368 (2013)
Huntington's disease (HD) is a neurodegenerative disorder caused by abnormal polyglutamine expansion in the amino-terminal end of the huntingtin protein (Htt) and characterized by progressive striatal and cortical pathology. Previous reports have sho
Externí odkaz:
https://doaj.org/article/d5471c28f13b41ddafe1883b6f55c73b
Publikováno v:
PLoS ONE, Vol 8, Iss 9 (2013)
Externí odkaz:
https://doaj.org/article/9fe56710d14b4e69b1c012f7d4cfa0c9
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e72698 (2013)
Huntington's disease (HD) is a neurodegenerative disease caused by abnormal polyglutamine expansion in the huntingtin protein (Htt). Although both Htt and the HD pathogenic mutation (mHtt) are implicated in early developmental events, their individua
Externí odkaz:
https://doaj.org/article/5dfc3b19ef6b4afe82a27403129b97e4
Autor:
Yung, Shau-Yu, Gokhan, Solen, Jurcsak, Jennifer, Molero, Aldrin E., Abrajano, Joseph J., Mehler, Mark F.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2002 Dec 01. 99(25), 16273-16278.
Externí odkaz:
https://www.jstor.org/stable/3073944
Autor:
Arteaga-Bracho, Eduardo E., Gulinello, Maria, Winchester, Michael L., Pichamoorthy, Nandini, Petronglo, Jenna R., Zambrano, Alicia D., Inocencio, Julio, De Jesus, Chirstopher D., Louie, Joseph O., Gokhan, Solen, Mehler, Mark F., Molero, Aldrin E.
Publikováno v:
In Neurobiology of Disease December 2016 96:144-155
Autor:
Molero, Aldrin E., Arteaga-Bracho, Eduardo E., Chen, Christopher H., Gulinello, Maria, Winchester, Michael L., Pichamoorthy, Nandini, Gokhan, Solen, Khodakhah, Kamran, Mehler, Mark F.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2016 May . 113(20), 5736-5741.
Externí odkaz:
https://www.jstor.org/stable/26469920
Autor:
Bramwell-Lalor, Sharon, Ferguson, Therese, Roofe, Carmel, Cook, Loraine D., Sweeney, Aldrin E., Gentles, Carol Hordatt
Publikováno v:
Caribbean Journal of Education; Apr2023, Vol. 45 Issue 1, p126-155, 30p