354 results on '"Liao, Wei-Ping"'
Search Results
2. ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy
3. Association of LONP1 gene with epilepsy and the sub-regional effect
4. Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy
5. DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders
6. Epilepsy-associated genes: an update
7. BCOR variants are associated with X-linked recessive partial epilepsy
8. Ilepcimide inhibited sodium channel activity in mouse hippocampal neurons
9. Functional Differences Between Two Kv1.1 RNA Editing Isoforms: a Comparative Study on Neuronal Overexpression in Mouse Prefrontal Cortex
10. Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus
11. DLG3 variants caused X-linked epilepsy with/without neurodevelopmental disorders and the genotype-phenotype correlation
12. Epilepsy-associated genes: discovery, clinical significance, and underlying principles of genetic medicine
13. A missense mutation in SLC6A1 associated with Lennox-Gastaut syndrome impairs GABA transporter 1 protein trafficking and function
14. Effect of Nd-incorporation and K-modification on catalytic performance of Co3O4 for N2O decomposition
15. Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies
16. CCDC88C variants are associated with focal epilepsy and genotype–phenotype correlation.
17. Development-related aberrations in Kv1.1 α-subunit exert disruptive effects on bioelectrical activities of neurons in a mouse model of fragile X syndrome
18. Clinical concordance evaluation of the causality of sequence variants
19. Genetic Dependence and Genetic Diseases
20. Variants inSBF1, CELSR2,andTENM1cause childhood epileptic encephalopathies
21. Epilepsy-associated genes
22. Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism
23. Laminar Distribution of Neurochemically-Identified Interneurons and Cellular Co-expression of Molecular Markers in Epileptic Human Cortex
24. Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy
25. HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism
26. Common genetic epilepsies, pathogenicity of genes/variants, and genetic dependence
27. Altered intrinsic properties and bursting activities of neurons in layer IV of somatosensory cortex from Fmr-1 knockout mice
28. ZFHX3variants cause childhood partial epilepsy and infantile spasms with favourable outcomes
29. ABCB1 G2677T/A polymorphism is associated with the risk of drug-resistant epilepsy in Asians
30. Hydrogen production from steam reforming of ethylene glycol over supported nickel catalysts
31. Alteration of Scn3a expression is mediated via CpG methylation and MBD2 in mouse hippocampus during postnatal development and seizure condition
32. ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation
33. Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy
34. A Point Mutation in SCN1A 5′ Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic Drug
35. Involvement of FMRP in Primary MicroRNA Processing via Enhancing Drosha Translation
36. Epigenetic Downregulation of Scn3a Expression by Valproate: a Possible Role in Its Anticonvulsant Activity
37. Variants inBSNgene associated with epilepsy with favourable outcome
38. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients
39. Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome
40. Editorial: Sub-molecular mechanism of genetic epilepsy
41. Cutaneous reactions induced by oxcarbazepine in Southern Han Chinese: Incidence, features, risk factors and relation to HLA-B alleles
42. A MicroRNA Profile in Fmr1 Knockout Mice Reveals MicroRNA Expression Alterations with Possible Roles in Fragile X Syndrome
43. I-line photolithographic metalenses enabled by distributed optical proximity correction with a deep-learning model
44. Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy
45. Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation
46. ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus
47. Supplementary document for I-line photolithographic metalenses enabled by distributed optical proximity correction with a deep-learning model - 5840259.pdf
48. Functional characterization of novel NPRL3mutations identified in three families with focal epilepsy
49. Evaluation of cell damage in organotypic hippocampal slice culture from adult mouse: A potential model system to study neuroprotection
50. Influence of KOH modification on TiO 2 structure and Au/TiO 2 catalyst activity in CO oxidation
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