320 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. TSC2 loss in neural progenitor cells suppresses translation of ASD/NDD-associated transcripts in an mTORC1- and MNK1/2-reversible fashion
6. Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
7. Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder
8. Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
9. Age dependent association of inbreeding with risk for schizophrenia in Egypt
10. A deep learning approach to identify gene targets of a therapeutic for human splicing disorders
11. Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system.
12. Vortex Chain States in a Ferromagnet/Superconductor Bilayer
13. A Mechanism for Photoinduced Effects In Tetracyanoethylene-Based Organic Magnets
14. Vortex Lattices in Stripe Domains of Ferromagnet/Superconductor Bilayer
15. The London Study of Vortex States in a Superconducting Film Due to a Magnetic Dot
16. Magnetic Superconducting Heterostructures
17. Vortex Penetration in Magneto-Superconducting Heterostructures
18. A large-scale evaluation of computational protein function prediction
19. Symmetry Violation in a Superconducting Film with a Square Array of Ferromagnetic Dots
20. Oscillations of Spherical and Cylindrical Shells
21. Interaction of Mesoscopic Magnetic Textures with Superconductors
22. Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons
23. TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling
24. Proteasomal pathway inhibition as a potential therapy for NF2-associated meningioma and schwannoma.
25. P159: Variants in cohesin release factors WAPL, PDS5A, and PDS5B define a new class of cohesinopathies*
26. CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing
27. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
28. Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
29. STATISTICAL AND FUNCTIONAL CONVERGENCE OF COMMON AND RARE VARIANT RISK FOR AUTISM SPECTRUM DISORDERS AT CHROMOSOME 16P
30. CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
31. Pain correlates with germline mutation in schwannomatosis
32. Heterogeneous Magnetic Superconducting Systems
33. Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage
34. Prediction and experimental validation of enzyme substrate specificity in protein structures
35. Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage
36. A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings
37. Tissue and cell-type specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
38. TFEB Links Autophagy to Lysosomal Biogenesis
39. Potential molecular consequences of transgene integration: The R6/2 mouse example
40. Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin
41. Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel–Feil syndrome
42. Htt CAG repeat expansion confers pleiotropic gains of mutant huntingtin function in chromatin regulation
43. Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome
44. Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells
45. GnRH Neurogeneration from Human Stem Cell
46. A lysosome‐to‐nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB
47. Ab initio studies of tetracyanoethylene-based organic magnets
48. Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome
49. Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage
50. MOESM1 of TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling
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