Early lineage switch in an infant acute lymphoblastic leukemia
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-12-15
著者
-
KANEGANE Hirokazu
Department of Pediatrics, Graduate School of Medicine, University of Toyama
-
MIYAWAKI Toshio
Department of Pediatrics, Graduate School of Medicine, University of Toyama
-
MIURA MASAYOSHI
Department of Pediatrics, Toyama City Hospital
-
Nomura Keiko
Department of Pediatrics, Toyama University School of Medicine
-
ISHII Eiichi
Department of Pediatrics, Saga University School of Medicine
-
Nomura Keiko
Department Of Pediatrics Graduate School Of Medicine University Of Toyama
-
Kanegane Hirokazu
富山大学 医学薬学研究部小児科学教室
-
Kanegane Hirokazu
防衛医科大学校 小児科学
-
Kanegane Hirokazu
Department Of Pediatrics Faculty Of Medicine University Of Toyama
-
Kanegane Hirokazu
富山大学 医学薬学研究部小児発達医学
-
Kanegane H
Department Of Pediatrics Graduate School Of Medicine University Of Toyama
-
Miyawaki T
Department Of Dermatology Graduate School Of Medicine University Of Toyama
-
SAKAKI Hisano
Department of Pediatrics, Graduate School of Medicine, University of Toyama
-
GOI Kumiko
Department of Pediatrics, Faculty of Medicine, University of Yamanashi
-
SUGITA Kanji
Department of Pediatrics, Faculty of Medicine, University of Yamanashi
-
Nomura Keiko
Departments Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University
-
Nomura Keiko
Department Of Chemistry And Materials Science Tokyo Institute Of Technology
-
Kanegane Hirokazu
Department Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University
-
Kanegane Hirokazu
Departments Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University
-
Goi Kumiko
Department Of Pediatrics Faculty Of Medicine University Of Yamanashi
-
Sugita Kanji
Department Of Pediatrics Faculty Of Medicine University Of Yamanashi
-
Sakaki Hisano
Department Of Pediatrics Graduate School Of Medicine University Of Toyama
-
Kanegane Hirokazu
Univ. Toyama Toyama Jpn
-
Miyawaki Toshio
Department Of Dermatology Graduate School Of Medicine University Of Toyama
-
Ishii Eiichi
Department Of Pediatrics Graduate School Of Medicine Ehime University
-
Miyawaki Toshio
Department Of Department Of Pediatrics Graduate School Of Medicine University Of Toyama
-
Miura Masayoshi
Department Of Kidney Transplant Surgery Sapporo City General Hospital
-
Ishii Eiichi
Department Of Pediatrics Ehime University Graduate School
-
Kanegane Hirokazu
Faculty Of Medicine University Of Toyama
-
Miyawaki Toshio
Department Of Pediatrics School Of Medicine Toyama Medical And Pharmaceutical University
-
Miura Masayoshi
Department of Industrial Chemistry, Faculty of Engineering, Ibaraki University
関連論文
- ブルトン・チロシン・キナーゼの第1イントロンにおける転写調節異常
- Expansion of activated eosinophils in infants with severe atopic dermatitis
- Novel Fas (CD95/APO-1) mutations in infants with a lymphopro liferative disorder
- lnhibitory action of sulfatide a putative ligand for L-selectiv on B cell proliferation and lg prodrction
- Characterization of Ventricular Myocardial Performance in the Fetus by Tissue Doppler Imaging
- 正常健常児において左室内血流伝搬速度に影響を与える要因の検討
- Open Heart Operation in a Child With Congenital Heart Disease and Hereditary Spherocytosis
- Genetic Analysis in Patients with Left Ventricular Noncompaction and Evidence for Genetic Heterogeneity(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-273 Validation of Myocardial Acceleration during Isovolumic Contraction as a Noninvasive Index of Left Ventricular Contractility(Echo/Doppler 10 (I) : OJ32)(Oral Presentation (Japanese))
- OE-283 Profound S100A12 Expression in Neutrophils in Early Stage of Acute Kawasaki Disease(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
- Clinical features of isolated left ventricular noncompaction : infantile type and juvenile type
- Propagation velocity of transmitral flow is useful for the assessment of left ventricular diastolic function in children with cardiomyopathy
- Novel Gene Mutation in Isolated Left Ventricular Noncompaction
- Dobutamine Stress Radionuclide Ventriculography Reveals Silent Myocardial Dysfunction in Kawasaki Disease
- 0291 ISOLATED NONCOMPACTION OF THE VENTRICULAL MYOCARDIUM (INVM) : CONSIDERATION OF THE DISTINCTIVE CLINICAL ENTITY
- OE-283 Profound S100A12 Expression in Neutrophils in Early Stage of Acute Kawasaki Disease(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
- Successful Outcome of Mismatched Hematopoietic Stem Cell Transplantation from a Related Donor in an Infant with Acute Lymphoblastic Leukemia and 9 ; 11 Translocation : Case Report and Review of the Literature
- Hepatocyte growth factor in transient myeloproliferative disorder of Down syndrome
- Distinct Clones Are Associated with the Development of Transient Myeloproliferative Disorder and Acute Megakaryocytic Leukemia in a Patient with Down Syndrome
- OE-269 Evidence of Genetic Heterogeneity in Left Ventricular Noncompaction(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- M-protein-positive chronic active Epstein-Barr virus infection: features mimicking HIV-1 infection
- Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection
- Outcome of Non-T-Cell-Depleted HLA-Haploidentical Hematopoietic Stem Cell Transplantation from Family Donors in Children and Adolescents
- Chronic Graft-Versus-Host Desease in Children and Adolescents After Bone Marrow Transplantation From HLA-Matched Donors
- Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
- ^Tc-DTPA dynamic SPECT and CT volumetry for measuring split renal function in live kidney donors
- Long-Term Outcome of Coil Occlusion in Patients With Patent Ductus Arteriosus
- Glomerulonephritis induced by methicillin-resistant Staphylococcus aureus infection that progressed during puerperal period
- The Na^+-excreting efficacy of indapamide in combination with furosemide in massive edema
- Three brothers of X-linked agammaglobulinemia : the relation between phenotype and neutropenia
- Peripheral blood lymphocyte subpopulations in three infants with hepatosplenomegaly caused by cytomegalovirus infection
- Mononucleosis-like illness in an infant associated with human herpesvirus 6 infection
- X-Linked Agammaglobulinemia Diagnosed in Adulthood : A Case Report
- X-Linked Lymphoproliferative Disease in an Adult
- Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
- Early lineage switch in an infant acute lymphoblastic leukemia
- Successful Cardiac Resynchronization Therapy in a 3-Year-Old Girl With Isolated Left Ventricular Non-Compaction and Narrow QRS Complex : A Case Report
- Pneumocystis jiroveci pneumonia as an atypical presentation of X-linked agammaglobulinemia
- Spontaneous regression of aleukemic leukemia cutis harboring a NPM/RARA fusion gene in an infant with cutaneous mastosytosis
- Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
- PE-306 SCN5A Variant in Japanese Patients with Left Ventricular Noncompaction and Arrhythmia(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Acute lymphoblastic leukemia after living donor liver transplantation
- Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
- Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients
- The Relationship Between Serum Levels of Interleukin-6 and Thyroid Hormone During the Follow-up Study in Children with Nonthyroidal Illness: Marked Inverse Correlation in Kawasaki and Infectious Disease
- Effective use of corticosteroid in a child with life-threatening plastic bronchitis after Fontan operation
- Quantitative Monitoring of Circulating Epstein-Barr Virus DNA for Predicting the Development of Posttransplantation Lymphoproliferative Disease
- Evaluation of Phenytoin Dosage Regimens Based on Genotyping of CYP2C Subfamily in Routinely Treated Japanese Patients
- Outcome of pediatric patients with Langerhans cell histiocytosis treated with 2 chlorodeoxyadenosine : a nationwide survey in Japan
- A case of severe recurrent hepatitis with common variable immunodeficiency
- Non-Hodgkin's Lymphoma of the Ascending Colon in a Patient with Becker Muscular Dystrophy : Report of a Case
- Nationwide Survey of Hemophagocytic Lymphohistiocytosis in Japan
- Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people
- Immunoblot analysis of cellular expression of Bcl-2 family proteins,Bcl-2,Bax,Bcl-X and Mcl-1,in human perpheral bolld and lymphoid tissues
- Orally Active GPIIb/IIIa Antagonists : Synthesis and Biological Activities of Masked Amidines as Prodrugs of 2-[(3S)-4-[(2S)-2-(4-Amidinobenzoylamino)-3-(4-methoxyphenyl)propanoyl]-3-(2-methoxy-2-oxoethyl)-2-oxopiperazinyl]acetic Acid
- Novel Non-Peptide GPIIb/IIIa Antagonists : Synthesis and Biological Activities of 2-[4-[2-(4-Amidinobenzoylamino)-2-(substituted)acetyl]-3-(2-methoxy-2-oxoethyl)-2-oxopiperazinyl]acetic Acids
- Phenotypic variations between affected siblings with ataxia-telangiectasia : ataxia-telangiectasia in Japan
- Safety and Usefulness of a Novel eMotion^【○!R】 Electric Mesh Nebulizer in Children with Asthma
- Ability of preschool children to use dry powder inhalers as evaluated by In-Check Meter
- Theophylline metabolism in acute asthma with MxA-indicated viral infection
- Trial of intraventricular ribavirin therapy for subacute sclerosing panencephalitis in Japan
- Efficacy of Levocabastine Hydrochloride Ophthalmic Suspension in the Conjunctival Allergen Challenge Test in Japanese Subjects with Seasonal Allergic Conjunctivitis
- A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness
- Mechanism of C-2 Hydroxylation during the Biosynthesis of 20-Hydroxyecdysone in Ajuga Hairy Roots
- Evaluation of left ventricular volume using automatic border detection in children : A comparison with conventional off-line echocardiographic quantification
- Epididymo-orchitis caused by intravesically instillated bacillus Calmette-Guerin : Genetically proven using a multiplex polymerase chain reaction method
- In Vitro Cleavage of the MLL Gene by Topoisomerase II Inhibitor (Etoposide) in Normal Cord and Peripheral Blood Mononuclear Cells
- Atypical X-linked Agammaglobulinemia Diagnosed in Three Adult
- A Novel Perforin Gene Mutation in a Japanese Family with Hemophagocytic Lymphohistiocytosis
- Expression of pericyte, mesangium and muscle markers in malignant rhabdoid tumor cell lines : Differentiation-induction using 5-azacytidine
- The Autocrine Loop of Epidermal Growth Factor Receptor-Epidermal Growth Factor/Transforming Growth Factor-α in Malignant Rhabdoid Tumor Cell Lines:Heterogeneitv of Autocrine Mechanism in TTC549
- Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
- Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
- Non-progressive viral myelitis in X-linked agammaglobulinemia
- identification of an SH2D1A Mutation in a Hypogammaglobulinemic Male Patient with a Diagnosis of Common Variable Immunodeficiency
- Treatment outcome of infant leukemia in Japan
- Outcome of Non-Transplant Surgical Strategy for End-Stage Dilated Cardiomyopathy in Young Children
- Clonal hematopoiesis in acquired aplastic anemia revealed by rearrangement of the immunoglobulin heavy chain gene-JH region
- Autoimmune Neutropenia of Infancy with Multiple Brain Abscesses during the Course of Human Herpesvirus-6 Infection
- Long-Term Outcome of Coil Occlusion in Patients With Patent Ductus Arteriosus
- Analysis of Serum Lactate Dehydrogenase and Its Isozymes During Administration of Granulocyte Colony-Stimulating Factor in Children
- A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
- High-dose chemotherapy and autologous blood stem cell transplantation in children with metastatic neuroblastoma
- Changes in T-Cell Receptor Subsets After Cardiac Surgery in Children
- Saccade eye movements as a quantitative measure of frontostriatal network in children with ADHD
- Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
- エクソン・スキッピング誘導による治療の臨床応用に向けて、適正アンチセンスと適応患者のスクリーニング法
- Serial changes of prefrontal lobe growth in the patients with benign childhood epilepsy with centrotemporal spikes presenting with cognitive impairments/behavioral problems
- Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection
- Atypical case of X-linked agammaglobulinemia diagnosed at 45 years of age
- Mislocalization or low expression of mutated Shwachman-Bodian-Diamond syndrome protein
- A novel method for indexing echocardiographic left ventricular mass in infants, children and adolescents : Evaluation of obesity-induced left ventricular hypertrophy
- Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
- Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
- Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis
- Repeated seizures induce prefrontal growth disturbance in frontal lobe epilepsy
- EEG characteristics predict subsequent epilepsy in children with febrile seizure
- Relapsing Campylobacter Coli Bacteremia with Reactive Arthritis in a Patient with X-linked Agammaglobulinemia
- Therapeutic outcome of multifocal Langerhans cell histiocytosis in adults treated with the Special C regimen formulated by the Japan LCH Study Group
- A Case Report of Dysosteosclerosis Observed from the Prenatal Period