講演・口頭発表等 - 森尾　友宏

101. Kamae C, Nakagawa N, Sato H, Honma K, Mitsuiki N, Ohara O, Kanegane H, Pasic S, Pan-Hammarström Q, MC van Zelm, Morio T, Imai K, Nonoyama S.. Classification of common variable immunodeficiency by quantification of T cell receptor recombination excision circles (TREC) and Ig kappa-deleting recombination excision circles (KREC). . 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

102. Hirata O, Tsumura M, Mizoguchi Y, Okada S, Minegishi S, Morio T, Kobayashi M. . Gain-of-function mutations of STAT1 in Japanese patients with CMCD.. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

103. Hayase T, Morimoto A, Ikeda T, Katsube N, Kawahara Y, Fukuda T. Kasii Y, Morio T, Momoi M.. HLA-matched unrelated CBT without conditioning in a SCID patient with Artemis abnormality. . 第74回日本血液学会学術集会 2012.10 京都

104. Sato T, Kuramitsu M, Sato-Otsubo A, Yoshida K, Toki T, Terui K, Wang R, Kanno H, Morio T, Ohga S, Ohara A, Kitoh T, Kudo K, Kojima S, Ogawa S, Hamaguchi I,. Frequent mutations in the RPS17 gene in Japanese DBA Patients.. 第74回日本血液学会学術集会 2012.10 京都

105. Kumaki S, Sasahara Y, Kamachi Y, Muramatsu H, Morio T, Goi K, SugitaK, Urabe T, Takada H, Tsuchiya S, Hara T. . Long-term B cell function after unrelated CBT using a RIC regimen in patients with X-SCID.. 第74回日本血液学会学術集会 2012.10 京都

106. H. Takada, M. Ishimura, T. Doi, K. Imai, Y. Sasahara, H Kanegane, R. Nishikomori, T. Morio, T. Heike, M. Kobayashi, T. Ariga, S. Tsuchiya, S. Nonoyama, T. Miyawaki, T. Hara. Nation-wide survey of patients with primary immunodeficiency diseases in japan:2008. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

107. Isoda T, Takagi M, Piao J, Nakagama S, Sato M, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S.. Immune defect and visualization of chromosome 14 breaks and translocations involving TCRa/d loci during early T-cell development lacking ATM. . 17th congress of the European Hematology Association (EHA). 2012.06 Amsterdam, Netherlands.

108. Takasawa K, Kashimada K, Ono M, Matsubara Y, Hijikata A, Katsumata N, Takagi M, Morio T, Ohara O, Mizutani S.. Two Novel Hsd3b2 Miss-Sense Mutations With Different Enzymatic Activity For Δ5 Steroids: Possible Cause For Elevated Levels Of 17-Hydroxyprogesterone (17-OHP) In 3β-Hydroxysteroid Dehydrogenase (3Β-HSD) Deficiency Patients.. ENDO 2012 (The Endocrine Society’s 94th Annual Meeting & Expo). 2012.06 Houston, Texas, USA.

109. Motoyoshi Y, Udagawa T, Chiga M, Yoshida Y, Fujimura Y, Nagasawa M, Morio T, Mizutani S, Nagata M. . A case of atypical hemolytic uremic syndrome successfully treated with anti-C5 antibody. Continuous Professional Development program of International Pediatric Nephrology Association.. Japan-Korea The 10th Pediatric Nephrology Seminar 2012. 2012.05 Tokyo, Japan.

110. Morio T.. An old and new regulator of ROS production in neutrophils. . Seminar of Brain Korea 21 Project for Functional Foods and Nutrigenomics. 2012.03 Seoul, Korea.

111. Isoda T, Takagi M, Piao J, Sato M, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S. Visualization of chromosomal translocation and early T-cell development failure in ATM deficiency.. Ataxia telangiectagia workshop. 2012.02 New Delhi, INDIA.

112. Isoda T, Takagi M, Piao J, Nakagama S, Sato M, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S.. T-Cell Development Failure At β-Selection Checkpoint and TCRα/δ Locus Break Formation Associated with Chromosome 14 Translocation in Ataxia-Telangiectagia Mutated Deficient Mice.. 53rd American society of hematology, annual meeting. 2011.12 San Diego, California, USA.

113. Kuramitsu M, Matsubara A, Morio T, Takagi M, Toki T, Terui K, Wang R, Kanno H, Ohga S, Ohara A, Masumi A, Momose H, Mizukami T, Takizawa K, Yamaguchi K, Ogawa S, Ito E, Hamaguchi I. Extensive gene deletions in Japanese patients with Diamond Blackfan anemia.. Extensive gene deletions in Japanese patients with Diamond Blackfan anemia. . 第73回日本血液学会学術集会 2011.10 名古屋

114. Nagasawa M, Okawa T, Endo A, Mitsuiki N, Aoki Y, Ono T, Isoda T, Tomizawa D, Takagi M, Morio T, Mizutani S, Kajiwara M, Ishiwata Y, Yasuhara M.. Retrospective PK/PD analysis of oral and intravenous busulfan in pediatric patient having SCT.. 第73回日本血液学会学術集会 2011.10 名古屋

115. Nagasawa M, Miyatake H, Hayakawa T, Hayashi Y, Katsumoto Y, Takagi M, Morio T, Ohmori S, Mizutani S. . Analysis of dielectricity and membrane proteins of erythrocytes in patient having allogenic SCT.. 第73回日本血液学会学術集会 2011.10 名古屋

116. Isoda T, Takagi M, Piao J, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S.. DN3 T-cell development failure in Ataxia telangiectagia (AT).. 第73回日本血液学会学術集会 2011.10 名古屋

117. Isoda T, Ford A, Tomizawa D, Frederik van Delft, David Gonzalez De Castro, Score J, Takagi M, Morio T, Greaves M, Mizutani S. . Transmission and Ingenious Clonal Evolution of Maternal Cancer Cells in the Infant. . PAS/ASPR (Pediatric Academic Societies and Asian Society for Pediatric Research) 2011. 2011.05 Denver, Colorado, USA.

118. Morio T. . Dissection of Common Variable immunodeficiency With Distinct Phenotype. . 2011 Pediatric Academic Societies &Asian Society for Pediatric Research Joint Meeting. 2011.04 Denver, Colorado, USA.

119. Imai K, Mitsui K, Kajiwara M, Tomizawa D, Nagasawa M, Kogawa K, Morio T, Nonoyama S.. Retrospective analysis of stem cell transplantations for X-linked hyper-IgM syndrome. . 37th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2011.04 Paris, France.

120. Morio T.. Unrelated umbilical cord blood transplantation for patients with primary immunodeficiency in Japan. . The 52nd ASH Annual Meeting. 2010.12 Orlando, Florida, USA.