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1. Pharmacokinetics, safety, and efficacy of 20% subcutaneous immunoglobulin (Ig20Gly) administered weekly or every 2 weeks in Japanese patients with primary immunodeficiency diseases: a phase 3, open-label study.

4. STING signalling is terminated through ESCRT-dependent microautophagy of vesicles originating from recycling endosomes

7. Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease

8. Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency

9. Aberrant RNA sensing in regulatory T cells causes systemic autoimmunity

13. Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry

16. Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency

19. BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies.

20. Efficient detection of somatic UBA1 variants and clinical scoring system predicting patients with variants in VEXAS syndrome

23. Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency

24. Pyoderma gangrenosum, acne, and unclassified inflammatory bowel disease syndrome: A case report on a new subtype of pyogenic arthritis, pyoderma gangrenosum, and acne syndrome

25. Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity

26. Corrigendum to “Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease”Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.

27. Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations

32. Additional file 1 of Efficacy and safety of baricitinib in Japanese patients with autoinflammatory type I interferonopathies (NNS/CANDLE, SAVI, And AGS)

34. Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases

35. Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1 :: CREM fusion presenting associated with IL ‐6/ STAT3 signaling

36. Anti–Integrin αvβ6 Antibody as a Diagnostic Marker for Pediatric Patients With Ulcerative Colitis

38. Assessment of type I interferon signatures in undifferentiated inflammatory diseases: A Japanese multicenter experience

39. Gain-of-function mutations inALPK1cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

44. Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL‐6/STAT3 signaling.

46. Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis

47. Fever of unknown origin caused by an intracranial mesenchymal tumor with a EWSR1-CREM fusion presenting associated with IL-6/STAT3 signaling

49. Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation

50. Author response for 'Novel AP3B1 mutations in a Hermansky-Pudlak syndrome type2 with neonatal interstitial lung disease'

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