222 results on '"Erdin, Serkan"'
Search Results
2. Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system
3. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.
4. Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
5. Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
6. Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder
7. Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
8. A deep learning approach to identify gene targets of a therapeutic for human splicing disorders
9. Vortex Chain States in a Ferromagnet/Superconductor Bilayer
10. A Mechanism for Photoinduced Effects In Tetracyanoethylene-Based Organic Magnets
11. Vortex Lattices in Stripe Domains of Ferromagnet/Superconductor Bilayer
12. The London Study of Vortex States in a Superconducting Film Due to a Magnetic Dot
13. Magnetic Superconducting Heterostructures
14. Vortex Penetration in Magneto-Superconducting Heterostructures
15. A large-scale evaluation of computational protein function prediction
16. Symmetry Violation in a Superconducting Film with a Square Array of Ferromagnetic Dots
17. Oscillations of Spherical and Cylindrical Shells
18. Interaction of Mesoscopic Magnetic Textures with Superconductors
19. Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons
20. TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling
21. Proteasomal pathway inhibition as a potential therapy for NF2-associated meningioma and schwannoma.
22. P159: Variants in cohesin release factors WAPL, PDS5A, and PDS5B define a new class of cohesinopathies*
23. CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing
24. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
25. Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
26. CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
27. Pain correlates with germline mutation in schwannomatosis
28. Prediction and experimental validation of enzyme substrate specificity in protein structures
29. Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage
30. TFEB Links Autophagy to Lysosomal Biogenesis
31. Potential molecular consequences of transgene integration: The R6/2 mouse example
32. Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin
33. Htt CAG repeat expansion confers pleiotropic gains of mutant huntingtin function in chromatin regulation
34. Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome
35. Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells
36. GnRH Neurogeneration from Human Stem Cell
37. A lysosome‐to‐nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB
38. MOESM1 of TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling
39. mTOR kinase inhibition disrupts neuregulin 1-ERBB3 autocrine signaling and sensitizes NF2-deficient meningioma cellular models to IGF1R inhibition
40. New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders
41. Accounting for epistatic interactions improves the functional analysis of protein structures
42. ETAscape: analyzing protein networks to predict enzymatic function and substrates in Cytoscape
43. Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice
44. De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features
45. BiallelicGRM7variants cause epilepsy, microcephaly, and cerebral atrophy
46. Evolutionary Trace Annotation Server: automated enzyme function prediction in protein structures using 3D templates
47. Brigatinib causes tumor shrinkage in both NF2-deficient meningioma and schwannoma through inhibition of multiple tyrosine kinases but not ALK.
48. NetWalker: a contextual network analysis tool for functional genomics
49. Hypomorphic mutation of the mouse Huntington’s disease gene orthologue
50. Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions
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