Recent advances in the study of the hereditary and environmental basis of childhood leukemia
スポンサーリンク
概要
著者
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MIZUTANI SHUKI
Department of Human Ontogeny and Childhood Development, Tokyo Medical and Dental University
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Mizutani Shuki
Department Of Pediatrics And Developmental Biology Tokyo Medical And Dental University Graduate Scho
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Mizutani Shuki
Tokyo Medical And Dental Univ. Tokyo Jpn
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Mizutani S
Department Of Virology The National Children's Medical Research Center
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Mizutani Shuki
Department Of Developmental Biology Post Graduate School Tokyo Medical And Dental University
関連論文
- Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood
- In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography- Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS)
- Pharmacokinetic monitoring is still required for intravenous busulfan in SCT for small children
- Megalin contributes to the early injury of proximal tubule cells during nonselective proteinuria
- Coordinated Regulation of the Promoter and Enhancer Regions of Human CD23 Gene by Signal Through IL-4R and CD40, and the Role of Ku70/80 in the Enhancer Activity
- Phenotypic variations between affected siblings with ataxia-telangiectasia : ataxia-telangiectasia in Japan
- In Vitro Cleavage of the MLL Gene by Topoisomerase II Inhibitor (Etoposide) in Normal Cord and Peripheral Blood Mononuclear Cells
- New method of chest compression for infants in a single rescuer situation: thumb-index finger technique
- Expression of Cyclin-dependent Kinase Inhibitor p27/Kip1 and AP-1 Coactivator p38/Jab1 Correlates with Differentiation of Embryonal Rhabdomyosarcoma
- A Boy with "transient" Growth Hormone Deficiency in Prepubertal Stage Despite Normal Growth Hormone Secretion in Childhood and after Puberty
- Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes
- Serum Granulysin Is Elevated in Patients with Hemophagocytic Lymphohistiocytosis
- Transient Increase of Serum Granulysin in a Stage IVs Neuroblastoma Patient during Spontaneous Regression : Case Report
- Selective Effect of Imatinib on Serum IgM in a Patient with CML
- Type Two Hyper-IgM Syndrome caused by Mutation in Activation-Induced Cytidine Deaminase
- Recent advances in the study of the hereditary and environmental basis of childhood leukemia
- Liquid chromatography-tandem mass spectrometric method for determination of salivary 17α-hydroxyprogesterone : A noninvasive tool for evaluating efficacy of hormone replacement therapy in congenital adrenal hyperplasia
- Rapid Downregulation of β-actin-based CAG Promoter and Filamentous Actin in Injured Podocytes
- Impaired cell adhesion, apoptosis, and signaling in WASP gene-disrupted Nalm-6 pre-B cells and recovery of cell adhesion using a transducible form of WASp
- Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
- Current evidence for an inherited genetic basis of childhood acute lymphoblastic leukemia
- Initial high dose hydrocortisone (HDC) treatment for 21-hydroxylase deficiency (21-OHD) does not affect linear growth during the first three years of life
- Longitudinal analysis of growth and body composition of Japanese 21-OHD patients in childhood
- Incidence and survival rates of hematological malignancies in Japanesechildren and adolescents (2006-2010): based on registry data from the Japanese Society of Pediatric Hematology