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1. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations. (30th June 2020)

2. Discovery of potent α1L-adrenoceptor agonists: Design and synthesis of bicyclic derivatives. Issue 16 (15th August 2015)

3. Discovery of potent α1L-adrenoceptor agonists: Design and synthesis of bicyclic derivatives. Issue 16 (15th August 2015)

5. Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation. (19th April 2018)

6. Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation. Issue 2 (29th September 2017)

7. High‐throughput analysis revealed the unique immunoglobulin gene rearrangements in plasmacytoma‐like post‐transplant lymphoproliferative disorder. (19th March 2020)

8. Novel compound heterozygous mutations in a Japanese girl with Janus kinase 3 deficiency. Issue 10 (4th September 2016)

9. Prominent dermal Langerhans cells in an Omenn syndrome patient with a novel mutation in the IL2RG gene. Issue 11 (27th August 2019)

10. Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations. (16th September 2021)