Y. Ohashi

发表

Detection of the PGP9.5 and tyrosine hydroxylase mRNAs for minimal residual neuroblastoma cells in bone marrow and peripheral blood.

M. Minegishi, R. Ohi, S. Tsuchiya, 1998, The Tohoku journal of experimental medicine.

Epstein‐Barr virus‐associated Hodgkin's disease in a patient with Wiskott‐Aldrich syndrome

M. Minegishi, S. Tsuchiya, Y. Sasahara, 2001, Acta paediatrica.

Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations.

J. Derry, M. Minegishi, K. Horibe, 2002, Journal of immunological methods.

Tyrosine Phosphorylation of Crk-associated Substrates by Focal Adhesion Kinase

K. Kamiguchi, S. Iwata, H. Fujita, 1997, The Journal of Biological Chemistry.

Identification of anti-herpes simplex virus antibody-producing B cells in a patient with an atypical RAG1 immunodeficiency.

A. Villa, M. Minegishi, A. Villa, 2001, Blood.

Familial genetic defect in a case of leukocyte adhesion deficiency

H. Kikuchi, S. Tsuchiya, T. Konno, 1993, Human mutation.

Aberrant responsiveness to RANTES in synovial fluid T cells from patients with rheumatoid arthritis.

C. Morimoto, N. Hisakawa, Hirotoshi Tanaka, 2002, The Journal of rheumatology.

The first infant case with hepatosplenic gammadelta T-cell lymphoma after acute disseminated encephalomyelitis (ADEM)-like exacerbation.

T. Morio, M. Minegishi, K. Haginoya, 2006, Journal of pediatric hematology/oncology.

Deficient Activity of von Willebrand Factor-Cleaving Protease in Patients With Upshaw-Schulman Syndrome

M. Minegishi, F. Bessho, S. Tsuchiya, 2001, International journal of hematology.

Isolation and characterization of two monoclonal antibodies that recognize different epitopes of the human c-kit receptor.

M. Minegishi, S. Tsuchiya, T. Konno, 1996, The Tohoku journal of experimental medicine.

Immunological reconstitution by allogeneic bone marrow transplantation in a child with the X-linked hyper-IgM syndrome

M. Minegishi, S. Tsuchiya, T. Konno, 1999, European Journal of Pediatrics.

Prolonged secretion of IL-15 in patients with severe forms of acute graft-versus-host disease after allogeneic bone marrow transplantation in children.

M. Minegishi, S. Tsuchiya, T. Konno, 1998, International journal of hematology.

Successful umbilical cord blood transplantation from an unrelated donor for a patient with Epstein–Barr virus-associated hemophagocytic lymphohistiocytosis

M. Minegishi, S. Tsuchiya, T. Sato, 2001, Bone Marrow Transplantation.

Altered tyrosine phosphorylation via the very late antigen (VLA)/beta1 integrin stimulation is associated with impaired T-cell signaling through VLA-4 after allogeneic bone marrow transplantation.

J. Ritz, R. Soiffer, C. Morimoto, 1997, Blood.

Beta 1-integrin-mediated cell signaling in T lymphocytes.

K. Kamiguchi, S. Iwata, C. Morimoto, 2000, Journal of dermatological science.

Cas-L Is Required for β1 Integrin-Mediated Costimulation in Human T Cells

K. Kamiguchi, S. Iwata, C. Morimoto, 1999, The Journal of Immunology.

Cas-L is required for beta 1 integrin-mediated costimulation in human Tcells.

K. Kamiguchi, S. Iwata, C. Morimoto, 1999, Journal of immunology.

T Cell Receptor-mediated Tyrosine Phosphorylation of Cas-L, a 105-kDa Crk-associated Substrate-related Protein, and Its Association of Crk and C3G*

K. Kamiguchi, K. Tachibana, Chika Morimoto, 1998, The Journal of Biological Chemistry.

Tyrosine phosphorylation of Crk-associated substrate lymphocyte-type is a critical element in TCR- and beta 1 integrin-induced T lymphocyte migration.

K. Kamiguchi, S. Iwata, C. Morimoto, 1999, Journal of immunology.

Lymphocyte Migration Integrin-Induced T 1 b Element in TCR- and Substrate Lymphocyte-Type Is a Critical Tyrosine Phosphorylation of Crk-Associated

K. Kamiguchi, S. Iwata, C. Morimoto, 1999 .

Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott-Aldrich syndrome

M. Minegishi, S. Tsuchiya, Y. Sasahara, 2000, European Journal of Pediatrics.

The First Infant Case With Hepatosplenic gd T-cell Lymphoma After Acute Disseminated Encephalomyelitis (ADEM)-like Exacerbation

M. Minegishi, R. Ichinohasama, M. Munakata, 2006 .

Establishment and characterization of a novel human immature megakaryoblastic leukemia cell line, M-MOK, dependent on fibroblasts for its viability.

M. Minegishi, N. Minegishi, S. Tsuchiya, 1995, Experimental hematology.

Mutations of the Epstein‐Barr virus LMP‐1 oncogene in a 10‐year‐old Japanese girl with nasopharyngeal carcinoma

M. Minegishi, S. Tsuchiya, T. Konno, 1996, Acta paediatrica.

Three Monoclonal Antibodies against LFA-1 a and fi Chains with Different Biological Activities

M. Minegishi, T. Konno, Y. Ohashi, 2006 .

Three monoclonal antibodies against human LFA-1 alpha and beta chains with different biological activities.

M. Minegishi, S. Tsuchiya, T. Konno, 1992, The Tohoku journal of experimental medicine.

IL-2 receptor gamma chain expression on CD34 positive hematopoietic progenitor cells from bone marrow and cord blood.

K. Sugamura, M. Minegishi, N. Ishii, 1996, The Tohoku journal of experimental medicine.

Successful treatment of steroid-resistant severe acute GVHD with 24-h continuous infusion of FK506

M. Minegishi, S. Tsuchiya, T. Konno, 1997, Bone Marrow Transplantation.

Allogeneic Malignant Bone Marrow Transplantation for Hematologic Disorders in Children

N. Minegishi, S. Tsuchiya, T. Konno, 2006 .

Allogeneic bone marrow transplantation for malignant hematologic disorders in children.

M. Minegishi, N. Minegishi, S. Tsuchiya, 1992, The Tohoku journal of experimental medicine.

Cell surface c-kit receptors in human leukemia cell lines and pediatric leukemia: selective preservation of c-kit expression on megakaryoblastic cell lines during adaptation to in vitro culture.

M. Endo, M. Minegishi, M. Imaizumi, 1996, Leukemia.

Disseminated nasal T cell lymphoma with a partial deletion of the LMP1 oncogene in a patient with chronic active Epstein-Barr virus infection.

M. Minegishi, R. Ichinohasama, S. Tsuchiya, 1995, Leukemia.

Unusual expression of IgG Fc receptors on peripheral granulocytes from patients with leukocyte adhesion deficiency (CD11/CD18 deficiency).

R. Nagatomi, N. Minegishi, S. Tsuchiya, 1990, Journal of immunology.

Characterization of the γc chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID)

T. Morio, H. Takada, K. Sugamura, 2000, Human Genetics.

A new point mutation involving a highly conserved leucine in the Btk SH2 domain in a family with X linked agammaglobulinaemia.

S. Tsuchiya, T. Konno, Y. Ohashi, 1995, Journal of medical genetics.