Pages that link to "Q35254765"
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The following pages link to EpilepsyGene: a genetic resource for genes and mutations related to epilepsy. (Q35254765):
Displaying 25 items.
- Molecular mechanisms of epilepsy (Q28087505) (← links)
- Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm (Q30838585) (← links)
- Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies (Q33670246) (← links)
- PCOSKB: A KnowledgeBase on genes, diseases, ontology terms and biochemical pathways associated with PolyCystic Ovary Syndrome (Q36434711) (← links)
- NSDNA: a manually curated database of experimentally supported ncRNAs associated with nervous system diseases (Q37556725) (← links)
- Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing (Q37579472) (← links)
- Disruption of the ATP/adenosine balance in CD39-/- mice is associated with handling-induced seizures. (Q38662497) (← links)
- A genomic view on epilepsy and autism candidate genes (Q38698306) (← links)
- Identification of diverse astrocyte populations and their malignant analogs. (Q45864365) (← links)
- VarCards: an integrated genetic and clinical database for coding variants in the human genome. (Q47097898) (← links)
- Genome-wide profiling reveals functional diversification of ∆FosB gene targets in the hippocampus of an Alzheimer's disease mouse model. (Q48097765) (← links)
- Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing (Q50345064) (← links)
- Global characterization of copy number variants in epilepsy patients from whole genome sequencing. (Q52591846) (← links)
- Clinical utility of a 377 gene custom next-generation sequencing epilepsy panel. (Q53086383) (← links)
- Common terms for rare epilepsies: Synonyms, associated terms, and links to structured vocabularies. (Q53834379) (← links)
- Rare gene deletions in genetic generalized and Rolandic epilepsies (Q57573937) (← links)
- Pediatric Epilepsy Mechanisms: Expanding the Paradigm of Excitation/Inhibition Imbalance (Q64243500) (← links)
- Functional Nutrients for Epilepsy (Q66679720) (← links)
- A comparative study of the genetic components of three subcategories of autism spectrum disorder (Q89014726) (← links)
- Genome-wide, integrative analysis of circular RNA dysregulation and the corresponding circular RNA-microRNA-mRNA regulatory axes in autism (Q95007425) (← links)
- Identifying Common Genes, Cell Types and Brain Regions Between Diseases of the Nervous System (Q92072933) (← links)
- Insights about multi-targeting and synergistic neuromodulators in Ayurvedic herbs against epilepsy: integrated computational studies on drug-target and protein-protein interaction networks (Q92092467) (← links)
- De Novo Germline Mutations in SEMA5A Associated With Infantile Spasms (Q92240275) (← links)
- OncoBase: a platform for decoding regulatory somatic mutations in human cancers (Q93177497) (← links)
- MYT1L haploinsufficiency in human neurons and mice causes autism-associated phenotypes that can be reversed by genetic and pharmacologic intervention (Q117197403) (← links)