797 results on '"Ishiura, Shoichi"'
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2. Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy
3. Dopamine regulates body size in Caenorhabditis elegans
4. Splicing of human chloride channel 1
5. Suppressor Mutations for Presenilin 1 Familial Alzheimer Disease Mutants Modulate γ-Secretase Activities
6. Exon Skipping by Ultrasound-Enhanced Delivery of Morpholino with Bubble Liposomes for Myotonic Dystrophy Model Mice
7. Functional analysis of SERCA1b, a highly expressed SERCA1 variant in myotonic dystrophy type 1 muscle
8. Genetic Variants of the Dopaminergic System in Humans and Model Organisms
9. Usefulness of Monitoring γ-H2AX and Cell Cycle Arrest in HepG2 Cells for Estimating Genotoxicity Using a High-Content Analysis System
10. ADAM9
11. Alzheimer’s disease and proteinases
12. BMP4 induction of trophoblast from mouse embryonic stem cells in defined culture conditions on laminin
13. Molecular Links among the Causative Genes for Ocular Malformation: Otx2 and Sox2 Coregulate Rax Expression
14. Comparison of Presenilin 1 and Presenilin 2 γ-Secretase Activities Using a Yeast Reconstitution System
15. Effect of rice-expressed amyloid β in the Tg2576 Alzheimer's disease transgenic mouse model
16. β-Secretase Inhibitor Potency Is Decreased by Aberrant β-Cleavage Location of the “Swedish Mutant” Amyloid Precursor Protein
17. Identification of Putative Amyloid A4-Splitting Enzymes with Two Endopeptidases Widely Distributed in Mammalian Cells
18. Production of the herb Ruta chalepensis L. expressing amyloid β-GFP fusion protein
19. Nuclear localization of MBNL1: splicing-mediated autoregulation and repression of repeat-derived aberrant proteins
20. ABLIM1 splicing is abnormal in skeletal muscle of patients with DM1 and regulated by MBNL, CELF and PTBP1
21. Nicastrin Is Dispensable for γ-Secretase Protease Activity in the Presence of Specific Presenilin Mutations
22. Proteomic and histochemical analysis of proteins involved in the dying-back-type of axonal degeneration in the gracile axonal dystrophy ( gad) mouse
23. Oxytocin hypersensitivity in pregnant P-LAP deficient mice
24. Dystrophin Diagnosis: Comparison of Dystrophin Abnormalities by Immunofluorescence and Immunoblot Analyses
25. Aβ46 Is Processed to Aβ40 and Aβ43, but Not to Aβ42, in the Low Density Membrane Domains
26. Design and Synthesis of β-Secretase Inhibitors: Optimization at the P4 and P1′ Positions
27. Distant N- and C-terminal Domains Are Required for Intrinsic Kinase Activity of SMG-1, a Critical Component of Nonsense-mediated mRNA Decay
28. Berberine alters the processing of Alzheimer’s amyloid precursor protein to decrease Aβ secretion
29. Expression of MBNL and CELF mRNA transcripts in muscles with myotonic dystrophy
30. Identification of an estrogenic hormone receptor in Caenorhabditis elegans
31. Neuroligins 3 and 4X interact with syntrophin-γ2, and the interactions are affected by autism-related mutations
32. ADAM19 is tightly associated with constitutive Alzheimer’s disease APP α-secretase in A172 cells
33. Genetic Variants of the Dopaminergic System in Humans and Model Organisms
34. Metabolism of amyloid precursor protein in COS cells transfected with a β-secretase candidate
35. Alternative splicing of myomesin 1 gene is aberrantly regulated in myotonic dystrophy type 1
36. Polypyrimidine tract-binding protein 1 regulates the alternative splicing of dopamine receptor D2
37. Immunolocalization of myotonic dystrophy protein kinase in corbular and junctional sarcoplasmic reticulum of human cardiac muscle
38. MBNL and CELF proteins regulate alternative splicing of the skeletal muscle chloride channel CLCN1
39. Polyalanine tracts directly induce the release of cytochrome c, independently of the mitochondrial permeability transition pore, leading to apoptosis
40. Comparative analysis of the cytotoxicity of homopolymeric amino acids
41. Csk-homologous kinase interacts with SHPS-1 and enhances neurite outgrowth of PC12 cells
42. Quantitative Analysis of CUG-BP1 Binding to RNA Repeats
43. Endoplasmic reticulum stress caused by aggregate-prone proteins containing homopolymeric amino acids
44. Interactions between homopolymeric amino acids (HPAAs)
45. Degradation of nicastrin involves both proteasome and lysosome
46. The novel β-secretase inhibitor KMI-429 reduces amyloid β peptide production in amyloid precursor protein transgenic and wild-type mice
47. Characterization of a novel D2-like dopamine receptor with a truncated splice variant and a D1-like dopamine receptor unique to invertebrates from Caenorhabditis elegans
48. Denervation Enhances the Expression of SHPS-1 in Rat Skeletal Muscle
49. Identification and Characterization of the Hesr1/Hey1 as a Candidate trans-Acting Factor on Gene Expression through the 3′ Non-Coding Polymorphic Region of the Human Dopamine Transporter (DAT1) Gene
50. Intracellular Localization of Homopolymeric Amino Acid-containing Proteins Expressed in Mammalian Cells
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