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Integrated Genome-Wide DNA Methylation and RNAseq Analysis of Hippocampal Specimens Identifies Potential Candidate Genes and Aberrant Signalling Pathways in Patients with Hippocampal Sclerosis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Genome-wide DNA Methylation and RNAseq Analyses Identify Aberrant Signalling Pathways in Focal Cortical Dysplasia (FCD) Type II.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35892-5
- By:
- Publication type:
- Article
Transcriptomic profiling of high- and low-spiking regions reveals novel epileptogenic mechanisms in focal cortical dysplasia type II patients.
- Published in:
- Molecular Brain, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13041-021-00832-4
- By:
- Publication type:
- Article
A novel duplication in the PAX6 gene in a North Indian family with aniridia.
- Published in:
- International Ophthalmology, 2014, v. 34, n. 6, p. 1183, doi. 10.1007/s10792-013-9882-8
- By:
- Publication type:
- Article
Role of Altered Expression, Activity and Sub-cellular Distribution of Various Histone Deacetylases (HDACs) in Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis.
- Published in:
- Cellular & Molecular Neurobiology, 2022, v. 42, n. 4, p. 1049, doi. 10.1007/s10571-020-00994-0
- By:
- Publication type:
- Article