Works by Wertz, Mary H.

Results: 8

Developing therapies for spinal muscular atrophy.

Published in:

Annals of the New York Academy of Sciences, 2016, v. 1366, n. 1, p. 5, doi. 10.1111/nyas.12813

By:

Wertz, Mary H.;
Sahin, Mustafa

Publication type:

Article

The E280A Presenilin Mutation Reduces Voltage-Gated Sodium Channel Levels in Neuronal Cells.

Published in:

Neurodegenerative Diseases, 2014, v. 13, n. 2/3, p. 64, doi. 10.1159/000354669

By:

Kim, Doo Yeon;
Wertz, Mary H.;
Gautam, Vivek;
D'Avanzo, Carla;
Bhattacharyya, Raja;
Kovacs, Dora M.

Publication type:

Article

Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.

Published in:

Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-16

By:

Sek Won Kong;
Sahin, Mustafa;
Collins, Christin D.;
Wertz, Mary H.;
Campbell, Malcolm G.;
Leech, Jarrett D.;
Krueger, Dilja;
Bear, Mark F.;
Kunkel, Louis M.;
Kohane, Isaac S.

Publication type:

Article

BACE1 regulates voltage-gated sodium channels and neuronal activity.

Published in:

Nature Cell Biology, 2007, v. 9, n. 7, p. 755, doi. 10.1038/ncb1602

By:

Doo Yeon Kim;
Carey, Bryce W.;
Wang, Haibin;
Ingano, Laura A. M.;
Binshtok, Alexander M.;
Wertz, Mary H.;
Pettingell, Warren H.;
Ping He;
Lee, Virginia M.-Y.;
Woolf, Clifford J.;
Kovacs, Dora M.

Publication type:

Article

Interleukin-6 deficiency exacerbates Huntington's disease model phenotypes.

Published in:

Molecular Neurodegeneration, 2020, v. 15, n. 1, p. 1, doi. 10.1186/s13024-020-00379-3

By:

Wertz, Mary H.;
Pineda, S. Sebastian;
Lee, Hyeseung;
Kulicke, Ruth;
Kellis, Manolis;
Heiman, Myriam

Publication type:

Article

Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophy.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 11, p. 2168, doi. 10.1093/hmg/ddw084

By:

Wertz, Mary H.;
Winden, Kellen;
Neveu, Pierre;
Shi-Yan Ng;
Ercan, Ebru;
Sahin, Mustafa

Publication type:

Article

SMN regulates axonal local translation via miR-183/mTOR pathway.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 23, p. 6318, doi. 10.1093/hmg/ddu350

By:

Kye, Min Jeong;
Niederst, Emily D.;
Wertz, Mary H.;
Gonçalves, Inês do Carmo G.;
Akten, Bikem;
Dover, Katarzyna Z.;
Peters, Miriam;
Riessland, Markus;
Neveu, Pierre;
Wirth, Brunhilde;
Kosik, Kenneth S.;
Sardi, S. Pablo;
Monani, Umrao R.;
Passini, Marco A.;
Sahin, Mustafa

Publication type:

Article

Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 14, p. 3865, doi. 10.1093/hmg/ddu101

By:

Di Nardo, Alessia;
Wertz, Mary H.;
Kwiatkowski, Erica;
Tsai, Peter T.;
Leech, Jarrett D.;
Greene-Colozzi, Emily;
Goto, June;
Dilsiz, Pelin;
Talos, Delia M.;
Clish, Clary B.;
Kwiatkowski, David J.;
Sahin, Mustafa

Publication type:

Article