久留米大学研究者紹介

【詳細】	タイトル　種類　／　単著・共著等　／　発行・発表年　発行所、発行・発表雑誌等の名称　／　巻号頁

西小森　隆太の著書・論文・学会発表等
No.	詳細
1	Promoting awareness of terminology related to unmet medical needs in context of rheumatic diseases in Japan: a systematic review for evaluating unmet medical needs 雑誌　／　共著　／　2023年 8月 Rheumatol Int
2	Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases 雑誌　／　共著　／　2023年 2月 J Clin Immunol ／　Vol.43 No.2 466-478
3	Immunoglobulin G deposition on proximal tubules and the tubular basement membrane in acute tubular injury complicated with focal segmental glomerulosclerosis (FSGS): A possible prediction tool for subclinical FSGS. 雑誌　／　共著　／　2023年 Ann Diagn Pathol. ／　Vol.66 152154
4	Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease 雑誌　／　共著　／　2023年 Kidney Int Rep ／　Vol.8 No.5 1127-1129
5	STING signalling is terminated through ESCRT-dependent microautophagy of vesicles originating from recycling endosomes. 雑誌　／　共著　／　2023年 Nat Cell Biol. ／　Vol.25 No.3 453-466
6	Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity. 雑誌　／　共著　／　2023年 J Exp Med. ／　Vol.220 No.9
7	Efficacy and safety of baricitinib in Japanese patients with autoinflammatory type I interferonopathies (NNS/CANDLE, SAVI, And AGS). 雑誌　／　共著　／　2023年 Pediatr Rheumatol Online J. ／　Vol.21 No.1 38
8	Editorial: A new frontier in translational research on autoinflammatory diseases - various aspects of innate immunity on human diseases. 雑誌　／　共著　／　2023年 Front Immunol. ／　Vol.14 1147202
9	Efficient detection of somatic UBA1 variants and clinical scoring system predicting patients with variants in VEXAS syndrome. 雑誌　／　共著　／　2023年 Rheumatology (Oxford).
10	A case of cryopyrin-associated periodic syndrome due to somatic mosaic mutation complicated with recurrent circinate erythematous psoriasis. 雑誌　／　共著　／　2023年 Mod Rheumatol Case Rep.
11	Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL-6/STAT3 signaling. 雑誌　／　共著　／　2023年 Neuropathology. ／　Vol.43 No.3 244-251
12	A Case of STAT1 Mutations in Chronic Mucocutaneous Candidiasis Diagnosed in an Adult. 雑誌　／　共著　／　2023年 Intern Med.
13	Novel AP3B1 mutations in a Hermansky-Pudlak syndrome type2 with neonatal interstitial lung disease. 雑誌　／　共著　／　2022年 Pediatr Allergy Immunol. ／　Vol.33 No.2 e13748
14	Assessment of type I interferon signatures in undifferentiated inflammatory diseases: A Japanese multicenter experience. 雑誌　／　共著　／　2022年 Front Immunol. ／　Vol.13 905960
15	Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation. 雑誌　／　共著　／　2022年 J Exp Med ／　Vol.219 No.6
16	Intracellular virus sensor MDA5 mutation develops autoimmune myocarditis and nephritis. 雑誌　／　共著　／　2022年 J Autoimmun ／　Vol.127 102794
17	Allograft dysfunction after lung transplantation for COPA syndrome: A case report and literature review. 雑誌　／　共著　／　2022年 Mod Rheumatol Case Rep. ／　Vol.6 No.2 314-318
18	Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome. 雑誌　／　共著　／　2022年 Ann Rheum Dis. ／　Vol.81 No.10 1453-1464
19	Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL-6/STAT3 signaling. 雑誌　／　共著　／　2022年 Neuropathology
20	Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis. 雑誌　／　共著　／　2022年 Front Immunol. ／　Vol.13 917398
21	Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease. 雑誌　／　共著　／　2022年 Kidney Int Rep. ／　Vol.7 No.4 857-866
22	Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases. 雑誌　／　共著　／　2022年 J Clin Immunol ／　Vol.43 No.2 466-478
23	Induced Pluripotent Stem Cell-Derived Monocytes/Macrophages in Autoinflammatory Diseases. 雑誌　／　共著　／　2022年 Front Immunol. ／　Vol.13 870535
24	Dysregulation of the Intestinal Microbiome in Patients With Haploinsufficiency of A20. 雑誌　／　共著　／　2022年 Front Cell Infect Microbiol. ／　Vol.11 787667
25	Ultrasound and biopsy findings in arthritis with familial Mediterranean fever. 雑誌　／　共著　／　2022年 J Med Ultrason (2001) ／　Vol.49 No.1 115-116
26	NOD2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination. 雑誌　／　共著　／　2021年 Children (Basel). ／　Vol.8 No.2
27	Dysregulation of the Intestinal Microbiome in Patients With Haploinsufficiency of A20. 雑誌　／　共著　／　2021年 Front Cell Infect Microbiol. ／　Vol.11 787667
28	Case Report: Rituximab Improved Epileptic Spasms and EEG Abnormalities in an Infant With West Syndrome and Anti-NMDAR Encephalitis Associated With APECED. 雑誌　／　共著　／　2021年 Front Neurol ／　Vol.12 679164
29	Aicardi-Goutières syndrome-like encephalitis in mutant mice with constitutively active MDA5. 雑誌　／　共著　／　2021年 Int Immunol ／　Vol.33 No.4 225-240
30	Necrotizing Funisitis as an Intrauterine manifestation of Cryopyrin-Associated Periodic Syndrome: a case report and review of the literature. 雑誌　／　共著　／　2021年 Pediatr Rheumatol Online J ／　Vol.19 No.1 77
31	A novel mutation in early-onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes. 雑誌　／　共著　／　2021年 Pediatr Rheumatol Online J ／　Vol.19 No.1 18
32	Augmentation of Stimulator of Interferon Genes-Induced Type I Interferon Production in COPA Syndrome. 雑誌　／　共著　／　2021年 Arthritis Rheumatol ／　Vol.73 No.11 2105-2015
33	Multiomic technologies for analyses of inborn errors of immunity: from snapshot of the average cell to dynamic temporal picture at single-cell resolution. 雑誌　／　共著　／　2021年 Inflamm Regen. ／　Vol.41 No.1 19
34	MEFV E148Q variant is more associated with familial Mediterranean fever when combined with other non-exon 10 MEFV variants in Japanese patients with recurrent fever. 雑誌　／　共著　／　2021年 Mod Rheumatol. ／　Vol.31 No.6 1208-1214
35	Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation. 雑誌　／　共著　／　2021年 J Allergy Clin Immunol. ／　Vol.148 No.2 550-562
36	Hematopoietic Cell Transplantation Ameliorates Autoinflammation in A20 Haploinsufficiency. 雑誌　／　共著　／　2021年 J Clin Immunol. ／　Vol.41 No.8 1954-1956
37	Haploinsufficiency of A20 with a novel mutation of deletion of exons 2-3 of TNFAIP3. 雑誌　／　共著　／　2021年 Mod Rheumatol. ／　Vol.31 No.2 493-497
38	Clinical phenotypes and genetic analyses for diagnosis of systemic autoinflammatory diseases in adult patients with unexplained fever. 雑誌　／　共著　／　2021年 Mod Rheumatol. ／　Vol.31 No.3 704-709
39	Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency. 雑誌　／　共著　／　2021年 Nat Commun. ／　Vol.12 No.1 6819
40	Enzyme activity in dried blood spot as a diagnostic tool for adenosine deaminase 2 deficiency. 雑誌　／　共著　／　2021年 Anal Biochem ／　Vol.628 114292
41	Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants. 雑誌　／　共著　／　2021年 J Clin Immunol ／　Vol.41 No.6 1187-1197
42	Case of cryopyrin-associated periodic syndrome who recovered from growth delay by treatment with canakinumab. 雑誌　／　共著　／　2021年 J Dermatol ／　Vol.48 No.2 e98-e99
43	Simple and Sensitive Analysis for Dried Blood Spot Proteins by Sodium Carbonate Precipitation for Clinical Proteomics. 雑誌　／　共著　／　2020年 J Proteome Res. ／　Vol.19 No.7 2821-2827
44	ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era. 雑誌　／　共著　／　2020年 Clin Chem. ／　Vol.66 No.4 525-536
45	Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation. 雑誌　／　共著　／　2020年 Ann Rheum Dis. ／　Vol.79 No.11 1492-1499
46	Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry. 雑誌　／　共著　／　2020年 Clin Immunol ／　Vol.216 108441
47	別冊医学のあゆみ自己炎症性疾患ー病態解明から診療体制の確立まで単行本　／　編集　／　2019年11月医歯薬出版社
48	Expanding clinical spectrum of autosomal dominant pyrin-associated autoinflammatory disorder caused by the heterozygous MEFV p.Thr577Asn variant. 雑誌　／　共著　／　2019年 Rheumatology (Oxford). ／　Vol.58 No.1 182-184
49	Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency 雑誌　／　共著　／　2019年 J Clin Invest ／　Vol.129 No.2 583-597
50	National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics 雑誌　／　共著　／　2019年 Mod Rheumatol ／　Vol.29 No.1 181-187
51	Low-frequency mosaicism in cryopyrin-associated periodic fever syndrome: mosaicism in systemic autoinflammatory diseases. その他　／　共著　／　2019年 Int Immunol ／　Vol.31 No.10 649-655
52	Functional analysis of a novel G87V TNFRSF1A mutation in patients with TNF receptor-associated periodic syndrome. 雑誌　／　共著　／　2019年 Clin Exp Immunol. ／　Vol.198 No.3 416-429
53	Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell-derived macrophages. 雑誌　／　共著　／　2019年 J Allergy Clin Immunol. ／　Vol.144 No.5 1438-1441. e12.
54	A Rare Case of Cryopyrin-associated Periodic Syndrome in an Elderly Woman with NLRP3 and MEFV Mutations. 雑誌　／　共著　／　2019年 Intern Med. ／　Vol.58 No.7 1017-1022
55	Plasma infliximab monitoring contributes to optimize Takayasu arteritis treatment: a case report. 雑誌　／　共著　／　2019年 J Pharm Health Care Sci. ／　Vol.5 9
56	Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders. 雑誌　／　共著　／　2018年 J Allergy Clin Immunol. ／　Vol.141 No.4 1485-1488.e11
57	Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation. 雑誌　／　共著　／　2018年 Int J Hematol ／　Vol.108 No.1 66-75
58	A sporadic case of granulomatous disease negative for NOD2 mutations and mimicking Blau syndrome. 雑誌　／　共著　／　2018年 Clin Exp Dermatol. ／　Vol.43 No.1 57-58
59	Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency. 雑誌　／　共著　／　2018年 Scand J Rheumatol. ／　Vol.47 No.2 170-172
60	Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency. 雑誌　／　共著　／　2018年 J Allergy Clin Immunol. ／　Vol.141 No.3 1060-1073. e3
61	Flow cytometry-based diagnosis of primary immunodeficiency diseases. 雑誌　／　共著　／　2018年 Allergol Int. ／　Vol.67 No.1 43-54
62	Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3. 雑誌　／　共著　／　2018年 Clin Immunol. ／　Vol.191 63-66
63	Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis. 雑誌　／　共著　／　2018年 Blood. ／　Vol.131 No.18 2016-2025
64	Autoinflammatory phenotypes in Aicardi-Goutières syndrome with interferon upregulation and serological autoimmune features. 雑誌　／　共著　／　2018年 J Allergy Clin Immunol. ／　Vol.141 No.3 1135-1138
65	Pluripotent stem cell models of Blau syndrome reveal an IFN-γ-dependent inflammatory response in macrophages. 雑誌　／　共著　／　2018年 J Allergy Clin Immunol. ／　Vol.141 No.1 339-349. e11.
66	Long-term safety and efficacy of canakinumab in cryopyrin-associated periodic syndrome: results from an open-label, phase III pivotal study in Japanese patients. 雑誌　／　共著　／　2017年 Clin Exp Rheumatol. ／　Vol.108 No.6 19-26
67	Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations. 雑誌　／　共著　／　2017年 Blood. ／　Vol.130 No.12 1456-1467
68	Live-attenuated vaccines in a cryopyrin-associated periodic syndrome patient receiving canakinumab treatment during infancy. 雑誌　／　共著　／　2017年 Clin Case Rep. ／　Vol.5 No.11 1750-1755
69	A CD57(+) CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients. 雑誌　／　共著　／　2017年 J Clin Immunol ／　Vol.37 No.1 92-99
70	High level of serum human interleukin-18 in a patient with pyogenic arthritis, pyoderma gangrenosum and acne syndrome. 雑誌　／　共著　／　2017年 J Eur Acad Dermatol Venereol ／　Vol.31 No.2 e115-e116
71	Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report. 雑誌　／　共著　／　2017年 Medicine (Baltimore) ／　Vol.96 No.46 e8601
72	Reply to Walsh et al. その他　／　共著　／　2017年 Eur J Hum Genet ／　Vol.25 No.8 907
73	Identification of a High-Frequency Somatic NLRC4 Mutation as a Cause of Autoinflammation by Pluripotent Cell-Based Phenotype Dissection 雑誌　／　共著　／　2017年 Arthritis Rheumatol ／　Vol.69 No.2 447-459
74	A Case with Spondyloenchondrodysplasia Treated with Growth Hormone. 雑誌　／　共著　／　2017年 Front Endocrinol (Lausanne). ／　Vol.8 157
75	Cryopyrin-associated Periodic Syndromes in Italian Patients: Evaluation of the Rate of Somatic NLRP3 Mosaicism and Phenotypic Characterization. 雑誌　／　共著　／　2017年 J Rheumatol ／　Vol.44 No.11 1667-1673
76	Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren. 雑誌　／　共著　／　2017年 Pediatr Allergy Immunol. ／　Vol.28 No.8 793-800
77	Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq. 雑誌　／　共著　／　2017年 Biochem Biophys Rep. ／　Vol.9 146-152
78	Sports activities enhance the prevalence of rhinitis symptoms in schoolchildren. 雑誌　／　共著　／　2016年 Pediatr Allergy Immunol. ／　Vol.27 No.2 209-213
79	Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children. 雑誌　／　共著　／　2016年 Clin Exp Rheumatol. ／　Vol.34 No.6 Suppl 102 S115-S120
80	Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease. 雑誌　／　共著　／　2016年 Dig Endosc. ／　Vol.28 No.5 548-555
81	Secondary bladder amyloidosis with familial Mediterranean fever in a living donor kidney transplant recipient: a case report. 雑誌　／　共著　／　2016年 BMC Res Notes ／　Vol.9 No.1 473
82	The first case of adult-onset PFAPA syndrome in Japan. 雑誌　／　共著　／　2016年 Mod Rheumatol ／　Vol.26 No.2 286-287
83	Brief Report: Late-Onset Cryopyrin-Associated Periodic Syndrome Due to Myeloid-Restricted Somatic NLRP3 Mosaicism. 雑誌　／　共著　／　2016年 Arthritis Rheumatol. ／　Vol.68 No.12 3035-3041
84	Febrile attacks triggered by milk allergy in an infant with mevalonate kinase deficiency. 雑誌　／　共著　／　2016年 Rheumatol Int. ／　Vol.36 No.10 1477-1478
85	Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function. 雑誌　／　共著　／　2016年 Eur J Hum Genet. ／　Vol.24 No.3 408-414
86	Tumor in chest wall caused by Mycobacterium bovis BCG infection: Identification on polymerase chain reaction of formalin-fixed specimen. 雑誌　／　共著　／　2016年 Pediatr Int ／　Vol.58 No.4 317-318
87	Clinical and Genetic Features of Patients With TNFRSF1A Variants in Japan: Findings of a Nationwide Survey. 雑誌　／　共著　／　2016年 Arthritis Rheumatol. ／　Vol.68 No.11 2760-2771
88	A 2-year-old Japanese girl with TNF receptor-associated periodic syndrome: A case report of the youngest diagnosed proband in Japan. 雑誌　／　共著　／　2016年 Mod Rheumatol ／　Vol.26 No.5 798-801
89	自己炎症症候群の臨床単行本　／　分担執筆　／　2015年 4月新興医学出版社
90	Enhanced chondrogenesis of induced pluripotent stem cells from patients with neonatal-onset multisystem inflammatory disease occurs via the caspase 1-independent cAMP/protein kinase A/CREB pathway 雑誌　／　共著　／　2015年 Arthritis Rheumatol ／　Vol.67 No.1 302-314
91	Somatic mosaicism for a NRAS mutation associates with disparate clinical features in RAS-associated leukoproliferative disease: a report of two cases. 雑誌　／　共著　／　2015年 J Clin Immunol. ／　Vol.35 No.5 454-458
92	Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis. 雑誌　／　共著　／　2015年 Br J Haematol ／　Vol.170 No.4 532-538
93	Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with Inflammatory Bowel Disease. 雑誌　／　共著　／　2015年 Inflamm Bowel Dis. ／　Vol.21 No.7 1529-1540
94	Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes 雑誌　／　共著　／　2015年 Ann Rheum Dis ／　Vol.73 No.4 603-610
95	Successful resolution of stromal keratitis and uveitis using canakinumab in a patient with chronic infantile neurologic, cutaneous, and articular syndrome: a case study. 雑誌　／　共著　／　2015年 J Ophthalmic Inflamm Infect ／　Vol.5 No.1 34
96	A nationwide survey of Aicardi-Goutieres syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study 雑誌　／　共著　／　2014年 Rheumatology (Oxford) ／　Vol.53 No.3 448-458
97	BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies. 雑誌　／　共著　／　2014年 J Allergy Clin Immunol ／　Vol.133 No.4 1134-1141
98	Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome. 雑誌　／　共著　／　2014年 Arthritis Res Ther ／　Vol.16 No.2 R89
99	Real-time single-cell imaging of protein secretion. 雑誌　／　共著　／　2014年 Sci Rep. ／　Vol.4 4736
100	Aicardi-Goutieres syndrome is caused by IFIH1 mutations 雑誌　／　共著　／　2014年 Am J Hum Genet ／　Vol.95 No.1 121-25
101	A Japanese pediatric patient with coexisting systemic lupus erythematosus and familial Mediterranean fever. 雑誌　／　共著　／　2013年 Lupus ／　Vol.22 No.10 1056-1059
102	Guidance on the use of canakinumab in patients with cryopyrin-associated periodic syndrome in Japan. その他　／　共著　／　2013年 Mod Rheumatol. ／　Vol.23 No.3 425-429
103	Safety and efficacy of canakinumab in Japanese patients with phenotypes of cryopyrin-associated periodic syndrome as established in the first open-label, phase-3 pivotal study (24-week results). 雑誌　／　共著　／　2013年 Clin Exp Rheumatol ／　Vol.31 No.2 302-309
104	MEFV Variants in Patients with PFAPA Syndrome in Japan. 雑誌　／　共著　／　2013年 Open Rheumatol J. ／　Vol.7 22-25
105	Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus. 雑誌　／　共著　／　2013年 Rheumatology (Oxford). ／　Vol.52 No.2 406-408
106	Effect of eczema on the association between season of birth and food allergy in Japanese children. 雑誌　／　共著　／　2013年 Pediatr Int ／　Vol.55 No.1 7-10
107	Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation. 雑誌　／　共著　／　2013年 J Clin Immunol ／　Vol.33 No.7 1165-1174
108	実地医家のためのクリオピリン関連周期性発熱症候群治療症例集―カナキヌマブ使用の実際単行本　／　分担執筆　／　2012年10月医歯薬ジャーナル社
109	Frequent somatic mosaicism of NEMO in T cells of patients with X-linked anhidrotic ectodermal dysplasia with immunodeficiency 雑誌　／　共著　／　2012年 Blood ／　Vol.119 No.23 5458-66
110	Multiple reversions of an IL2RG mutation restore T cell function in an X-linked severe combined immunodeficiency patient. 雑誌　／　共著　／　2012年 J Clin Immunol ／　Vol.32 No.4 690-697
111	Successful treatment with infliximab for inflammatory colitis in a patient with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. 雑誌　／　共著　／　2012年 J Clin Immunol. ／　Vol.32 No.1 39-49
112	Novel mutations of MVK gene in Japanese family members affected with hyperimmunoglobulinemia D and periodic fever syndrome. 雑誌　／　共著　／　2012年 Rheumatol Int. ／　Vol.32 No.12 3761-3764
113	Birth order effect on childhood food allergy. 雑誌　／　共著　／　2012年 Pediatr Allergy Immunol ／　Vol.23 No.3 250-254
114	Guidelines for the genetic diagnosis of hereditary recurrent fevers 雑誌　／　共著　／　2012年 Ann Rheum Dis ／　Vol.71 No.10 1599-605
115	Dominant-negative STAT1 SH2 domain mutations in unrelated patients with Mendelian susceptibility to mycobacterial disease. 雑誌　／　共著　／　2012年 Hum Mutat. ／　Vol.33 No.9 1377-1387
116	Detection of base substitution-type somatic mosaicism of the NLRP3 gene with >99.9% statistical confidence by massively parallel sequencing 雑誌　／　共著　／　2012年 DNA Res ／　Vol.19 No.2 143-52
117	Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency. その他　／　共著　／　2012年 Allergol Int. ／　Vol.61 No.2 207-217
118	Induced pluripotent stem cells from CINCA syndrome patients as a model for dissecting somatic mosaicism and drug discovery 雑誌　／　共著　／　2012年 Blood ／　Vol.120 No.6 1299-1308
119	Characterization of NLRP3 variants in Japanese cryopyrin-associated periodic syndrome patients. 雑誌　／　共著　／　2012年 J Clin Immunol. ／　Vol.32 No.2 221-229
120	Gastric ulcer and gastroenteritis caused by Epstein-Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis. 雑誌　／　共著　／　2012年 Rheumatology (Oxford). ／　Vol.51 No.11 2107-2109
121	The CD40-CD40L axis and IFN-γ play critical roles in Langhans giant cell formation. 雑誌　／　共著　／　2012年 Int Immunol. ／　Vol.24 No.1 5-15
122	Acute liver failure in young children with systemic-onset juvenile idiopathic arthritis without macrophage activation syndrome: report of two cases. 雑誌　／　共著　／　2012年 J Paediatr Child Health. ／　Vol.48 No.3 E122-125
123	Guidelines for the genetic diagnosis of hereditary recurrent fevers. 雑誌　／　共著　／　2012年 Ann Rheum Dis. ／　Vol.71 No.10 1599-1605
124	Cryopyrin-associated periodic syndrome: a case report and review of the Japanese literature. 雑誌　／　共著　／　2012年 Acta Derm Venereol. ／　Vol.95 No.4 395-398
125	Nationwide survey of patients with primary immunodeficiency diseases in Japan. 雑誌　／　共著　／　2011年 J Clin Immunol. ／　Vol.31 No.6 968-976
126	Decreased expression in nuclear factor-κB essential modulator due to a novel splice-site mutation causes X-linked ectodermal dysplasia with immunodeficiency. 雑誌　／　共著　／　2011年 J Clin Immunol ／　Vol.31 No.5 762-772
127	Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein. 雑誌　／　共著　／　2011年 Blood. ／　Vol.118 No.5 1225-1230
128	High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study 雑誌　／　共著　／　2011年 Arthritis Rheum ／　Vol.63 No.11
129	Total and low-density lipoprotein cholesterol levels are associated with atopy in schoolchildren. 雑誌　／　共著　／　2011年 J Pediatr ／　Vol.158 No.2 334-336
130	Disseminated BCG infection mimicking metastatic nasopharyngeal carcinoma in an immunodeficient child with a novel hypomorphic NEMO mutation. 雑誌　／　共著　／　2011年 J Clin Immunol ／　Vol.31 No.5 802-810
131	Patient with neonatal-onset chronic hepatitis presenting with mevalonate kinase deficiency with a novel MVK gene mutation. 雑誌　／　共著　／　2011年 Mod Rheumatol. ／　Vol.21 No.6 641-645
132	Familial cases of periodic fever with aphthous stomatitis, pharyngitis, and cervical adenitis syndrome. 雑誌　／　共著　／　2011年 J Pediatr. ／　Vol.158 No.1 155-159
133	A case of early-onset sarcoidosis with a six-base deletion in the NOD2 gene. 雑誌　／　共著　／　2010年 Rheumatology (Oxford) ／　Vol.49 No.1 194-196
134	The inflammasome, an innate immunity guardian, participates in skin urticarial reactions and contact hypersensitivity. その他　／　共著　／　2010年 Allergol Int ／　Vol.59 No.2 105-113
135	Breastfeeding and the prevalence of allergic diseases in schoolchildren: Does reverse causation matter? 雑誌　／　共著　／　2010年 Pediatr Allergy Immunol. ／　Vol.21 No.1 Pt 1 60-66
136	The effect of past food avoidance due to allergic symptoms on the growth of children at school age. 雑誌　／　共著　／　2010年 Allergol Int. ／　Vol.59 No.4 369-374
137	Enhanced NF-κB activation with an inflammasome activator correlates with activity of autoinflammatory disease associated with NLRP3 mutations outside of exon 3: comment on the article by Jéru et al. その他　／　共著　／　2010年 Arthritis Rheum ／　Vol.62 No.10 3123-3124
138	Changing prevalence and severity of childhood allergic diseases in kyoto, Japan, from 1996 to 2006. 雑誌　／　共著　／　2009年 Allergol Int. ／　Vol.58 No.4 543-548
139	Allergic status of schoolchildren with food allergy to eggs, milk or wheat in infancy. 雑誌　／　共著　／　2009年 Pediatr Allergy Immunol ／　Vol.20 No.7 642-647
140	Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15. 雑誌　／　共著　／　2009年 Rheumatology (Oxford). ／　Vol.48 No.6 706-707
141	Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis 雑誌　／　共著　／　2009年 Arthritis Rheum ／　Vol.60 No.1 242-50
142	A Japanese case of familial Mediterranean fever with a MEFV gene mutation. 雑誌　／　共著　／　2009年 Hokkaido Igaku Zasshi ／　Vol.84 No.6 419-422
143	Obesity and the prevalence of allergic diseases in schoolchildren. 雑誌　／　共著　／　2008年 Pediatr Allergy Immunol. ／　Vol.19 No.6 527-534
144	A CIAS1 mutation in a Japanese girl with familial cold autoinflammatory syndrome. 雑誌　／　共著　／　2008年 Eur J Pediatr ／　Vol.167 No.2 245-247
145	Early-onset sarcoidosis mimicking refractory cutaneous histiocytosis. 雑誌　／　共著　／　2008年 Pediatr Blood Cancer. ／　Vol.50 No.3 723-726
146	A combination therapy of whole lung lavage and GM-CSF inhalation in pulmonary alveolar proteinosis. 雑誌　／　共著　／　2008年 Pediatr Pulmonol. ／　Vol.43 No.8 828-830
147	Disease-associated CIAS1 mutations induce monocyte death, revealing low-level mosaicism in mutation-negative cryopyrin-associated periodic syndrome patients 雑誌　／　共著　／　2008年 Blood ／　Vol.111 No.4 2132-41
148	Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen. 雑誌　／　共著　／　2007年 Bone Marrow Transplant. ／　Vol.39 No.12 801-804
149	Disease-associated mutations in CIAS1 induce cathepsin B-dependent rapid cell death of human THP-1 monocytic cells. 雑誌　／　共著　／　2007年 Blood. ／　Vol.109 No.7 2903-2911
150	MR imaging findings of eosinophilic cystitis in an 8-year-old girl. 雑誌　／　共著　／　2007年 Pediatr Radiol. ／　Vol.37 No.8 836-839
151	Tumor necrosis factor receptor-associated periodic syndrome mimicking systemic juvenile idiopathic arthritis. 雑誌　／　共著　／　2006年 Allergol Int. ／　Vol.55 No.3 337-341
152	Familial hemophagocytic lymphohistiocytosis with the MUNC13-4 mutation: a case report. 雑誌　／　共著　／　2006年 Eur J Pediatr. ／　Vol.165 No.6 384-388
153	SPINK5 polymorphism is associated with disease severity and food allergy in children with atopic dermatitis. 雑誌　／　共著　／　2005年 J Allergy Clin Immunol ／　Vol.115 No.3 636-638
154	Limited ability of antigen-specific Th1 responses to inhibit Th2 cell development in vivo. 雑誌　／　共著　／　2005年 J Immunol ／　Vol.174 No.3 1325-1331
155	Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome. 雑誌　／　共著　／　2005年 Blood ／　Vol.105 No.3 1195-1197
156	Expanding clinical spectrum of autosomal dominant pyrin-associated autoinflammatory disorder caused by the heterozygous MEFV p.Thr577Asn variant. 雑誌　／　共著　／　2005年 Rheumatology (Oxford). ／　Vol.58 No.1 182-184
157	The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders. その他　／　共著　／　2005年 J Dermatol Sci ／　Vol.39 No.2 71-80
158	Somatic mosaicism of CIAS1 in a patient with chronic infantile neurologic, cutaneous, articular syndrome 雑誌　／　共著　／　2005年 Arthritis Rheum ／　Vol.52 No.11 3579-85
159	Development of both human connective tissue-type and mucosal-type mast cells in mice from hematopoietic stem cells with identical distribution pattern to human body. 雑誌　／　共著　／　2004年 Blood ／　Vol.103 No.3 860-867
160	Differential requirement for the CD40-CD154 costimulatory pathway during Th cell priming by CD8 alpha+ and CD8 alpha- murine dendritic cell subsets. 雑誌　／　共著　／　2004年 J Immunol ／　Vol.172 No.8 4826-4833
161	X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival. 雑誌　／　2004年 Blood. ／　Vol.103 No.12 4565-4572
162	FR901228 induces tumor regression associated with induction of Fas ligand and activation of Fas signaling in human osteosarcoma cells. 雑誌　／　共著　／　2003年 Oncogene ／　Vol.22 No.58 9231-9242
163	Complete reconstitution of human lymphocytes from cord blood CD34+ cells using the NOD/SCID/gammacnull mice model 雑誌　／　共著　／　2003年 Blood ／　Vol.102 No.3 873-80
164	GATA-3 suppresses Th1 development by downregulation of Stat4 and not through effects on IL-12Rbeta2 chain or T-bet. 雑誌　／　共著　／　2003年 Immunity. ／　Vol.18 No.3 415-428
165	Activated STAT4 has an essential role in Th1 differentiation and proliferation that is independent of its role in the maintenance of IL-12R beta 2 chain expression and signaling. 雑誌　／　共著　／　2002年 J Immunol. ／　Vol.169 No.8 4388-4398
166	STAT4 serine phosphorylation is critical for IL-12-induced IFN-gamma production but not for cell proliferation. 雑誌　／　共著　／　2002年 Proc Natl Acad Sci U S A. ／　Vol.99 No.19 12281-12286
167	BALB/c mice bearing a transgenic IL-12 receptor beta 2 gene exhibit a nonhealing phenotype to Leishmania major infection despite intact IL-12 signaling. 雑誌　／　共著　／　2001年 J Immunol. ／　Vol.166 No.11 6776-6783
168	T helper type 2 cell differentiation occurs in the presence of interleukin 12 receptor beta2 chain expression and signaling 雑誌　／　共著　／　2000年 J Exp Med ／　Vol.191 No.5 847-58
169	Administration of mAb against alpha E beta 7 prevents and ameliorates immunization-induced colitis in IL-2-/- mice. 雑誌　／　共著　／　1999年 J Immunol ／　Vol.162 No.8 4975-4982
170	Cis-acting DNA elements of mouse granulocyte-macrophage colony-stimulating factor gene responsive to Fc epsilon receptor cross-linking stimulation in the mouse mast cell line MC/9. 雑誌　／　共著　／　1995年 J Immunol. ／　Vol.154 No.2 694-702
171	Pyrrolidine dithiocarbamate inhibits intercellular adhesion molecule-1 biosynthesis induced by cytokines in human fibroblasts. 雑誌　／　共著　／　1995年 J Immunol ／　Vol.154 No.5 2333-2341
172	Pyrrolidine dithiocarbamate, a potent inhibitor of nuclear factor kappa B (NF-kappa B) activation, prevents apoptosis in human promyelocytic leukemia HL-60 cells and thymocytes. 雑誌　／　共著　／　1994年 Biochem Pharmacol. ／　Vol.48 No.10 1883-1889
173	Molecular basis for developmental changes of GM-CSF gene inducibility in embryonal carcinoma cells. 雑誌　／　共著　／　1994年 Biochem Biophys Res Commun. ／　Vol.198 No.2 473-479
174	Developmental changes of GM-CSF gene inducibility in embryonal carcinoma cells. 雑誌　／　共著　／　1994年 Mol Immunol. ／　Vol.31 No.16 1269-1275
175	A case of Farber disease. 雑誌　／　共著　／　1992年 Acta Paediatr Jpn. ／　Vol.34 No.1 72-79
176	Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndrome. 雑誌　／　共著　／　1990年 J Pediatr. ／　Vol.116 No.1 84-87

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