TSUCHIYA SHIGERU | Department of Pediatrics, Tohoku University Graduate School of Medicine

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著作論文

The analysis of the functions of human B and T cells in humanized NOD/shi-scid/γc^ (NOG) mice (hu-HSC NOG mice)
Chloride-Dependent Intracellular pH Regulation via Extracellular Calcium-Sensing Receptor in the Medullary Thick Ascending Limb of the Mouse Kidney
Phylogenetic, ontogenetic, and pathological aspects of the urine-concentrating mechanism
Reduced Exposure to Mercury in Patients Receiving Enteral Nutrition
The Nutrient Formula Containing Eicosapentaenoic Acid and Docosahexaenoic Acid Benefits the Fatty Acid Status of Patients Receiving Long-Term Enteral Nutrition
β-Phenylethylamine Inhibits K^+ Currents in Neocortical Neurons of the Rat : A Possible Mechanism of β-phenylethylamine-induced Seizures
Olfactory Stimulation Using Black Pepper Oil Facilitates Oral Feeding in Pediatric Patients Receiving Long-Term Enteral Nutrition
Fludarabine- and Cyclophosphamide-Based Nonmyelobalative Conditioning Regimen for Transplantation of Chronic Granulomatous Disease : Possible Correlation with Prolonged Pure Red Cell Aplasia
A novel JAK3 mutation in a Japanese patient with severe combined immunodeficiency
Genetic Analysis of Shwachman-Diamond Syndrome : Phenotypic Heterogeneity in Patients Carrying Identical SBDS Mutations
Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency
Successful Nonmyeloablative Bone Marrow Transplantation for Leukocyte Adhesion Deficiency Type I from an Unrelated Donor
Refractory chronic immune thrombocytopenic purpura in a child with acute lymphoblastic leukemia
Hypercalcemia due to all-trans retinoic acid therapy for acute promyelocytic leukemia : A case report of effective treatment with bisphosphonate
Improved Survival of Children with Advanced Neuroblastoma Treated by Intensified Therapy Including Myeloablative Chemotherapy with Stem Cell Transplantation : A Retrospective Analysis from the Tohoku Neuroblastoma Study Group
Deficient Activity of von Willebrand Factor-Cleaving Protease in Patients With Upshaw-Schulman Syndrome
PCR-RFLP Analysis of Cytomegalovirus Infections Associated with Bone Marrow Transplantation in Japanese Children
Prolonged secretion of IL-15 in patients with severe forms of acute graft-versus-host disease after allogeneic bone marrow transplantation in children
Detection of the PGP9.5 and Tyrosine Hydroxylase mRNAs for Minimal Residual Neuroblastoma Cells in Bone Marrow and Peripheral Blood
Decrease in Thy-1 Expression on Peripheral CD34 Positive Cells Induced by G-CSF Mobilization
Expression of GATA transcription factors in myelogenous and lymphoblastic leukemia cells
IL-2 Receptor γChain Expression on CD34 Positive Hematopoietic Progenitor Cells from Bone Marrow and Cord Blood
Hypospadias in a Male Patient with 21-hydroxylase Deficiency
Neonatal-Onset Brainstem Reticular Reflex Myoclonus Following a Prenatal Brain Insult : Generalized Myoclonic Jerk and a Brainstem Lesion
Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
A Use of Adaline as an Automatic Method for Interpretation of the Electrocardiogram and the Vectorcardiogram
The Uterus Sustains Stable Biological Clock during Pregnancy
Evaluation of Hematological Reconstitution Potential of Autologous Peripheral Blood Progenitor Cells Cryopreserved by a Simple Controlled-Rate Freezing Method
Abdominal Migraine Associated with Ecchymosis of the Legs and Buttocks : Does the Symptom Imply an Unknown Mechanism of Migraine?
The Cerebrospinal Fluid Level of 5-Methylterahydrofolate in a Japanese Boy with Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
Isolation and Characterization of Two Monoclonal Antibodies that Recognize Different Epitopes of the Human c-kit Receptor
A Case of Ventricular Return Extrasystoles with Two Consecutive Re-entry Sweeps to the Atrium
Molecular analysis of a presymptomatic case of carnitine palmitoyl transferase I (CPT I) deficiency detected by tandem mass spectrometry newborn screening in Japan
Mutation and haplotype analyses of the MUT gene in Japanese patients with methylmalonic acidemia
Quality assessment of umbilical cord blood units at the time of transplantation
Vincristine-resistant Kasabach-Merritt phenomenon successfully treated with low-dose radiotherapy
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

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