S. Yasunaga

发表

Synergistic and persistent effect of T‐cell immunotherapy with anti‐CD19 or anti‐CD38 chimeric receptor in conjunction with rituximab on B‐cell non‐Hodgkin lymphoma

K. Yanagihara, A. Kimura, C. Imai, 2010, British journal of haematology.

Overexpression of BMI‐1 correlates with drug resistance in B‐cell lymphoma cells through the stabilization of survivin expression

K. Yanagihara, M. Ohtsubo, M. Hoshi, 2012, Cancer science.

Bmi-1 is useful as a novel molecular marker for predicting progression of myelodysplastic syndrome and patient prognosis.

A. Kimura, K. Mihara, Y. Takihara, 2006, Blood.

Different contribution of HLA-DR and -DQ genes in susceptibility and resistance to insulin-dependent diabetes mellitus (IDDM).

T. Sasazuki, K. Hamaguchi, K. Rønningen, 1996, Tissue antigens.

Scmh1 Has E3 Ubiquitin Ligase Activity for Geminin and Histone H2A and Regulates Geminin Stability Directly or Indirectly via Transcriptional Repression of Hoxa9 and Hoxb4

J. Miyoshi, M. Ohtsubo, H. Brock, 2012, Molecular and Cellular Biology.

Dominant‐negative STAT1 SH2 domain mutations in unrelated patients with mendelian susceptibility to mycobacterial disease

J. Casanova, A. Abhyankar, M. Ohtsubo, 2012, Human mutation.

Polycomb-group complex 1 acts as an E3 ubiquitin ligase for Geminin to sustain hematopoietic stem cell activity

M. Ohtsubo, M. Tsumura, Masao Kobayashi, 2008, Proceedings of the National Academy of Sciences.

A new predictive model for insulin-dependent diabetes mellitus susceptibility based on combinations of molecular HLA-DRB1 and HLA-DQB1 pockets.

T. Sasazuki, B. Maillère, M. Busson, 1999, Tissue antigens.

The negative-feedback regulation of the IL-13 signal by the IL-13 receptor alpha2 chain in bronchial epithelial cells.

Qing Yang, S. Toda, K. Izuhara, 2003, Cytokine.

Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15.

S. Okada, M. Tsumura, Masao Kobayashi, 2009, Rheumatology.

IL-4 and IL-13: their pathological roles in allergic diseases and their potential in developing new therapies.

K. Izuhara, K. Arima, S. Yasunaga, 2002, Current drug targets. Inflammation and allergy.

Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia

O. Ohara, I. Matsumura, S. Okada, 2015, Journal of Clinical Immunology.

Manipulation of Cell Cycle and Chromatin Configuration by Means of Cell-Penetrating Geminin

S. Hanazawa, K. Naka, M. Ohtsubo, 2016, PloS one.

Analysis of tumor necrosis factor-alpha promoter polymorphism in type 1 diabetes: HLA-B and -DRB1 alleles are primarily associated with the disease in Japanese.

T. Sasazuki, K. Hamaguchi, A. Kimura, 2000, Tissue antigens.

Transcription of the Geminin gene is regulated by a negative-feedback loop

J. Voncken, Kenichi Yoshida, M. Ohtsubo, 2014, Molecular biology of the cell.

Role of Geminin in cell fate determination of hematopoietic stem cells (HSCs)

M. Ohtsubo, N. Shirasu, Y. Takihara, 2016, International Journal of Hematology.

Significance of ACADM mutations identified through newborn screening of MCAD deficiency in Japan.

M. Ohtsubo, S. Okada, M. Tsumura, 2016, Molecular genetics and metabolism.

Simple diagnosis of STAT1 gain‐of‐function alleles in patients with chronic mucocutaneous candidiasis

J. Casanova, T. Morio, A. Puel, 2014, Journal of leukocyte biology.

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

M. Cohen-Salmon, C. Petit, M. Mustapha, 1999, Nature Genetics.

Hoxa9 Transduction Induces Hematopoietic Stem and Progenitor Cell Activity through Direct Down-Regulation of Geminin Protein

M. Ohtsubo, S. Janmohamed, N. Iscove, 2013, PloS one.

Decreased Expression in Nuclear Factor-κB Essential Modulator Due to a Novel Splice-Site Mutation Causes X-linked Ectodermal Dysplasia with Immunodeficiency

M. Ohtsubo, S. Okada, M. Tsumura, 2011, Journal of Clinical Immunology.

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

C. Petit, S. Chardenoux, T. Friedman, 2000, American journal of human genetics.

Poly-ADP ribosylation of Miki by tankyrase-1 promotes centrosome maturation.

T. Inaba, Miho Ohsugi, Tadashi Yamamoto, 2012, Molecular cell.

DNA typing of HLA class II genes (HLA-DR, -DQ and -DP) in Japanese patients with histiocytic necrotizing lymphadenitis (Kikuchi's disease).

M. Kikuchi, S. Yasunaga, K. Ohshima, 1999, Tissue antigens.

DNA typing of HLA class I (HLA-A) and class II genes (HLA-DR, -DQ and -DP) in Japanese patients with gastric cancer.

Y. Maehara, K. Sugimachi, S. Yasunaga, 1997, Tissue antigens.

BMI-1 expression is enhanced through transcriptional and posttranscriptional regulation during the progression of chronic myeloid leukemia

Masaharu Hoshi, M. Hoshi, A. Kimura, 2009, Annals of Hematology.

Induction and activation of the aryl hydrocarbon receptor by IL-4 in B cells.

M. Kubo, A. Shinagawa, K. Izuhara, 2005, International immunology.

A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients

M. Ohtsubo, S. Okada, Masao Kobayashi, 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-gamma receptor 1 and has a dominant-negative effect on interferon-gamma signal transduction.

M. Ohtsubo, S. Okada, M. Tsumura, 2007, Journal of medical genetics.

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency

M. Ohtsubo, S. Okada, M. Tsumura, 2010, Human Genetics.

Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia

O. Ohara, I. Matsumura, S. Okada, 2015, Journal of Clinical Immunology.

Hoxb4 transduction down-regulates Geminin protein, providing hematopoietic stem and progenitor cells with proliferation potential

T. Ohta, M. Ohtsubo, K. Ohtani, 2010, Proceedings of the National Academy of Sciences.

Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals.

C. Cobbs, J. Volanakis, T. Horiuchi, 1996, Journal of immunology.

Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene

M. Ohtsubo, S. Okada, M. Tsumura, 2008, Journal of Medical Genetics.

The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-γ receptor 1 and has a dominant-negative effect on interferon-γ signal transduction

M. Ohtsubo, S. Okada, M. Tsumura, 2007, Journal of Medical Genetics.