478 results on '"Kato, Zenichiro"'
Search Results
2. Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency
3. Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan
4. Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases
5. Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3
6. Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3
7. IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation
8. HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy
9. Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants
10. Effective Valproic Acid Treatment in Motor Function Is Caused by Possible Mechanism of Elevated Survival Motor Neuron Protein Related With Splicing Factor Gene Expression in Spinal Muscular Atrophy
11. Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency
12. An innate interaction between IL-18 and the propeptide that inactivates its precursor form
13. Clinical and neuroimaging findings in children with posterior reversible encephalopathy syndrome
14. Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan
15. Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases
16. Functional assessment of the mutational effects of human IRAK4 and MyD88 genes
17. Genetics of Pediatric Asthma
18. Molecular analysis of the binding mode of Toll/interleukin-1 receptor (TIR) domain proteins during TLR2 signaling
19. Promoting tolerance to proteolipid protein-induced experimental autoimmune encephalomyelitis through targeting dendritic cells
20. Structural Basis for the Multiple Interactions of the MyD88 TIR Domain in TLR4 Signaling
21. Positioning of Autoimmune TCR-Ob.2F3 and TCR-Ob.3D1 on the MBP85-99/HLA-DR2 Complex
22. Amino Acid Copolymer-Specific IL-10-Secreting Regulatory T Cells That Ameliorate Autoimmune Diseases in Mice
23. A Complement Factor B Mutation in a Large Kindred with Atypical Hemolytic Uremic Syndrome
24. Lymphocyte Responses to Chymotrypsin- or Trypsin V-Digested β-Lactoglobulin in Patients with Cow's Milk Allergy
25. Outbreak of immediate-type hydrolyzed wheat protein allergy due to a facial soap in Japan
26. The autoimmune TCR-Ob.2F3 can bind to MBP85–99/HLA-DR2 having an unconventional mode as in TCR-Ob.1A12
27. Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica
28. In Vitro Analysis of the Functional Effects of an NLRP3 G809S Variant with the co-Existence of MEFV Haplotype Variants in Atypical Autoinflammatory Syndrome
29. Sweet’s syndrome in a neonate with non-B54 types of human leukocyte antigen
30. Characterization of NLRP3 Variants in Japanese Cryopyrin-Associated Periodic Syndrome Patients
31. Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II
32. A Novel Homozygous Mutation Destabilizes IKKβ and Leads to Human Combined Immunodeficiency
33. Acute cerebellitis associated with rotavirus infection
34. Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype
35. Development of Fluorescence-linked Immunosorbent Assay for High Throughput Screening of Interferon-γ
36. Apparition of iodinated contrast agents in twin neonatal gastrointestinal tracts after maternal contrast-enhanced computed tomography
37. A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome
38. Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy
39. 1H, 13C, and 15N resonance assignment of the TIR domain of human MyD88
40. Pediatric acute lymphoblastic leukemia mimicking Henoch–Schönlein purpura
41. ADA-SCID with ‘WAZA-ARI’ mutations that synergistically abolished ADA protein stability
42. IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation
43. Theophylline-associated status epilepticus in an infant: pharmacokinetics and the risk of suppository use
44. Brain infarction localized on left inferior temporal gyrus of presumed fetal onset
45. Diffuse large B-cell lymphoma presenting with osteolytic lesions in the bilateral femur
46. New Methods for Clinical Proteomics in Allergy
47. The response of bovine beta-lactoglobulin-specific T-cell clones to single amino acid substitution of T-cell core epitope
48. Interstitial deletion of the short arm of chromosome 10: Report of a case and review of the literature
49. Suppression of IFN-gamma production in atopic group at the acute phase of RSV infection
50. Acute cerebellitis in primary human herpesvirus-6 infection
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