44 results on '"Kinoshita, Koshi"'
Search Results
2. Edoxaban suppresses the progression of atrial fibrosis and atrial fibrillation in a canine congestive heart failure model
3. A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction
4. Anomalous origin of the right coronary artery from the left coronary sinus with an intramural course: comparison between sudden-death and non-sudden-death cases
5. Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series
6. Effect of irbesartan on development of atrial fibrosis and atrial fibrillation in a canine atrial tachycardia model with left ventricular dysfunction, association with p53
7. A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction
8. Epilepsy‐related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next‐generation DNA sequencing
9. Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death
10. Pathological features of preclinical or early clinical stages of corticobasal degeneration: a comparison with advanced cases
11. Neuropathologic Features of Suicide Victims Who Presented With Acute Poststroke Depression: Significance of Association With Neurodegenerative Disorders
12. High takeoff of the left main coronary artery at autopsy after sudden unexpected death in a male
13. A rapid and efficient single-cell manipulation method for screening antigen-specific antibody–secreting cells from human peripheral blood
14. A Novel Missense Mutation Causing a G487R Substitution in the S2–S3 Loop of Human ether-à-go-go-Related Gene Channel
15. 3D-Cell device with aligned and multilayered myocardial tissue derived from iPS-cells for predictive drug safety applications
16. Ternary complex formation of pVHL, elongin B and elongin C visualized in living cells by a fluorescence resonance energy transfer–fluorescence lifetime imaging microscopy technique
17. Altered DNA binding specificity of Arnt by selection of partner bHLH–PAS proteins
18. Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature
19. MicroRNA-145-5p and microRNA-320a encapsulated in endothelial microparticles contribute to the progression of vasculitis in acute Kawasaki Disease
20. Argyrophilic grain disease in a 46-year-old male suicide victim
21. An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing
22. Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature.
23. Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing study
24. Epilepsy‐related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next‐generation DNA sequencing
25. Pseudoaneurysmal defect of mitral-aortic intervalvular fibrosa is likely to be a cerebral embolic source. An autopsy study in remote period from the stroke
26. SCN5A(K817E), a novel Brugada syndrome–associated mutation that alters the activation gating of NaV1.5 channel
27. MicroRNA-93 may control vascular endothelial growth factor A in circulating peripheral blood mononuclear cells in acute Kawasaki disease
28. The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors
29. Sudden unexpected death owing to unilateral medial medullary infarction with early involvement of the respiratory center
30. An Autopsy Case of Acute and Nonalcoholic Thiamine-Deficient Encephalopathy
31. Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K+ Currents
32. Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domain
33. Abstract 049: Functional Characterization of KCNQ1 Channel Subunit With an A590T Mutation
34. Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death
35. Identification and Characterization of a Novel Mutation M579Fs+75X in HERG
36. A CASE OF ESOPHAGEAL PERFORATION DUE TO ESD FOR WHICH TREATMENT SELECTION WAS DIFFICULT
37. Identification of antigen‐specific B cells by concurrent monitoring of intracellular Ca2+ mobilization and antigen binding with microwell array chip system equipped with a CCD imager
38. Identification of amino acid residues in the Ah receptor involved in ligand binding
39. Cell-microarray analysis of antigen-specific B-cells: Single cell analysis of antigen receptor expression and specificity
40. The endoscopic atrophic border is the significant indicator for evaluating the extent of chronic atrophic gastritis
41. The first report of imaging study of primary hepatic malt lymphoma
42. A590T mutation in KCNQ1 C-terminal helix D decreases I Ks channel trafficking and function but not Yotiao interaction.
43. Identification of antigen-specific B cells by concurrent monitoring of intracellular Ca2+ mobilization and antigen binding with microwell array chip system equipped with a CCD imager
44. An autopsy case of infantile-onset vanishing white matter disease related to an EIF2B2 mutation (V85E) in a hemizygous region.
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