Search details
1.
Myospreader improves gene editing in skeletal muscle by myonuclear propagation.
Proc Natl Acad Sci U S A
; 121(19): e2321438121, 2024 May 07.
Article
in English
| MEDLINE | ID: mdl-38687782
2.
Vitamin C regulates Schwann cell myelination by promoting DNA demethylation of pro-myelinating genes.
J Neurochem
; 157(6): 1759-1773, 2021 06.
Article
in English
| MEDLINE | ID: mdl-32219848
3.
In vitro derived female hPGCLCs are unable to complete meiosis in embryoid bodies.
Exp Cell Res
; 397(2): 112358, 2020 12 15.
Article
in English
| MEDLINE | ID: mdl-33160998
4.
Dysregulation of the histone demethylase KDM6B in alcohol dependence is associated with epigenetic regulation of inflammatory signaling pathways.
Addict Biol
; 26(1): e12816, 2021 01.
Article
in English
| MEDLINE | ID: mdl-31373129
5.
Enhancement of BDNF Expression and Memory by HDAC Inhibition Requires BET Bromodomain Reader Proteins.
J Neurosci
; 39(4): 612-626, 2019 01 23.
Article
in English
| MEDLINE | ID: mdl-30504275
6.
EZH1 is an antipsychotic-sensitive epigenetic modulator of social and motivational behavior that is dysregulated in schizophrenia.
Neurobiol Dis
; 119: 149-158, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30099093
7.
The FMR1 promoter is selectively hydroxymethylated in primary neurons of fragile X syndrome patients.
Hum Mol Genet
; 25(22): 4870-4880, 2016 11 15.
Article
in English
| MEDLINE | ID: mdl-28173181
8.
Cocaine alters Homer1 natural antisense transcript in the nucleus accumbens.
Mol Cell Neurosci
; 85: 183-189, 2017 12.
Article
in English
| MEDLINE | ID: mdl-29055697
9.
Investigating the Synergistic Potential of Low-Dose HDAC3 Inhibition and Radiotherapy in Alzheimer's Disease Models.
Mol Neurobiol
; 60(8): 4811-4827, 2023 Aug.
Article
in English
| MEDLINE | ID: mdl-37171575
10.
Myospreader improves gene editing in skeletal muscle by myonuclear propagation.
bioRxiv
; 2023 Nov 06.
Article
in English
| MEDLINE | ID: mdl-37986992
11.
CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro.
Nat Commun
; 13(1): 6286, 2022 10 21.
Article
in English
| MEDLINE | ID: mdl-36271076
12.
Epigenetic Small Molecules Rescue Nucleocytoplasmic Transport and DNA Damage Phenotypes in C9ORF72 ALS/FTD.
Brain Sci
; 11(11)2021 Nov 20.
Article
in English
| MEDLINE | ID: mdl-34827542
13.
Dipeptide repeat proteins inhibit homology-directed DNA double strand break repair in C9ORF72 ALS/FTD.
Mol Neurodegener
; 15(1): 13, 2020 02 24.
Article
in English
| MEDLINE | ID: mdl-32093728
14.
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.
Nat Genet
; 51(4): 649-658, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30926972
15.
Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.
Nat Genet
; 51(5): 920, 2019 05.
Article
in English
| MEDLINE | ID: mdl-31028356
16.
A C9ORF72 BAC mouse model recapitulates key epigenetic perturbations of ALS/FTD.
Mol Neurodegener
; 12(1): 46, 2017 06 12.
Article
in English
| MEDLINE | ID: mdl-28606110
Results
1 -
16
de 16
1
Next >
>>