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Search Results - Harrington, Emily P.
Search Results - Harrington, Emily P.
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The Central Nervous System-Restricted Transcription Factor Olig2 Opposes p53 Responses to Genotoxic Damage in Neural Progenitors and Malignant Glioma
by
Mehta, Shwetal
,
Huillard, Emmanuelle
,
Kesari, Santosh
,
Maire, Cecile L.
,
Golebiowski, Diane
,
Harrington, Emily P.
,
Alberta, John A.
,
Kane, Michael F.
,
Theisen, Matthew
,
Ligon, Keith L.
,
Rowitch, David H.
,
Stiles, Charles D.
Published in
Cancer cell
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Overcoming remyelination failure in multiple sclerosis and other myelin disorders
by
Fancy, Stephen P.J.
,
Kotter, Mark R.
,
Harrington, Emily P.
,
Huang, Jeffrey K.
,
Zhao, Chao
,
Rowitch, David H.
,
Franklin, Robin J.M.
Published in
Experimental neurology
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COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans
by
Labelle-Dumais, Cassandre
,
Dilworth, David J
,
Harrington, Emily P
,
de Leau, Michelle
,
Lyons, David
,
Kabaeva, Zhyldyz
,
Manzini, M Chiara
,
Dobyns, William B
,
Walsh, Christopher A
,
Michele, Daniel E
,
Gould, Douglas B
Published in
PLoS genetics
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Immune cell modulation of oligodendrocyte lineage cells
by
Harrington, Emily P.
,
Bergles, Dwight E.
,
Calabresi, Peter A.
Published in
Neuroscience letters
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Altered Glutamate Receptor—Transporter Expression and Spontaneous Seizures in Rats Exposed to Methylazoxymethanol in Utero
by
Harrington, Emily P.
,
Möddel, Gabriel
,
Najm, Imad M.
,
Baraban, Scott C.
Published in
Epilepsia (Copenhagen)
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Oligodendrocyte PTEN is required for myelin and axonal integrity, not remyelination
by
Harrington, Emily P.
,
Zhao, Chao
,
Fancy, Stephen P. J.
,
Kaing, Sovann
,
Franklin, Robin J. M.
,
Rowitch, David H.
Published in
Annals of neurology
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COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans: e1002062
by
Labelle-Dumais, Cassandre
,
Dilworth, David J
,
Harrington, Emily P
,
Leau, Michelle de
,
Lyons, David
,
Kabaeva, Zhyldyz
,
Manzini, M Chiara
,
Dobyns, William B
,
Walsh, Christopher A
,
Michele, Daniel E
,
Gould, Douglas B
Published in
PLoS genetics
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Overcoming remyelination failure in multiple sclerosis and other myelin disorders : Axonal/neuronal pathology and neuroprotective treatment strategies in Multiple Sclerosis
by
FANCY, Stephen P. J
,
KOTTER, Mark R
,
HARRINGTON, Emily P
,
HUANG, Jeffrey K
,
CHAO ZHAO
,
ROWITCH, David H
,
FRANKLIN, Robin J. M
Published in
Experimental neurology
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Multivariate prediction of motor diagnosis in Huntington's disease: 12 years of PREDICT-HD
by
Long, Jeffrey D.
,
Paulsen, Jane S.
Published in
Movement disorders
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High and Low Levels of an NTRK2-Driven Genetic Profile Affect Motor- and Cognition-Associated Frontal Gray Matter in Prodromal Huntington's Disease
by
Ciarochi, Jennifer A
,
Liu, Jingyu
,
Calhoun, Vince
,
Johnson, Hans
,
Misiura, Maria
,
Bockholt, H Jeremy
,
Espinoza, Flor A
,
Caprihan, Arvind
,
Plis, Sergey
,
Turner, Jessica A
,
Paulsen, Jane S
Published in
Brain sciences
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