No association between atopic asthma and a coding variant of Fcε R1β in a Japanese population
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 1999-09-01
著者
-
Hamada Hiromi
Department Of Obstetrics And Gynecology Institute Of Clinical Medicine Graduate School Of Comprehens
-
MATSUI AKIRA
Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba
-
Hamaguchi H
Univ. Tsukuba Tsukuba Jpn
-
ARINAMI Tadao
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba
-
NOGUCHI Emiko
Department of Medical Genetics, Graduate School of Comprehensive Human Sciences, University of Tsuku
-
Arinami T
Department Of Medical Genetics Graduate School Of Comprehensive Human Sciences University Of Tsukuba
-
Noguchi Emiko
Department Of Medical Genetics Graduate School Of Comprehensive Human Sciences University Of Tsukuba
-
YAMAKAWA-KOBAYASHI Kimiko
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba
-
ISHIZAWA Mika
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba
-
SHIBASAKI Masanao
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba
-
YOKOUCHI Yukako
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba
-
HAMAGUCHI Hiedo
Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba
-
Ishizawa Mika
Department Of Medical Genetics Institute Of Basic Medical Sciences University Of Tsukuba
-
Arinami Tadao
Department Of Medical Genetics Graduate School Of Comprehensive Human Sciences University Of Tsukuba
-
Yokouchi Yukako
Department Of Medical Genetics Institute Of Basic Medical Sciences University Of Tsukuba
-
Shibasaki Masanao
Department Of Pediatrics Tsukuba College Of Technology
-
Matsui A
Department Of Physics Graduate School Of Science Tohoku University Aramaki
-
Matsui Akira
Department Of Child Health University Of Tsukuba School Of Medicine
-
Arinami Tadao
Medical Genetics Graduate School Of Comprehensive Human Sciences University Of Tsukuba
-
NOGUCHI Emiko
Medical Genetics, Graduate School of Comprehensive Human Sciences, University of Tsukuba
-
Noguchi Emiko
Medical Genetics Graduate School Of Comprehensive Human Sciences University Of Tsukuba
-
Noguchi Emiko
Department of Medical Genetics, Graduate School of Comprehensive Human Sciences, University of Tsukuba
-
Yamakawa-Kobayashi Kimiko
Department of Medical Genetics, Institute of Basic Medical Sciences, Institute of Clinical Medicine, University of Tsukuba
関連論文
- Coagulofibrynolytic Factors Activation is well Correlated with Moya-Moya Echo Severity of Limb Vein in Preganant Women(Thrombosis/Thrombolysis 3 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Intravenous prostacyclin combined with inhaled nitric oxide therapy for an infant with alveolar capillary dysplasia
- A novel susceptibility locus for moyamoya disease on chromosome 8q23
- Clinical and genetic analysis of Fabry disease : report of six cases including three heterozygous females
- Rapid Detection of Chromosome Aneuploidies by Prenatal Interphase FISH (Fluorescence in situ Hybridization) and Its Clinical Utility in Japan
- Guidelines for care of pregnant women carrying hepatitis C virus and their infants
- The 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene is associated with severe preeclampsia
- Filaggrin null mutations are associated with atopic dermatitis and elevated levels of IgE in the Japanese population: a family and case–control study
- Pulmonary veno-occlusive disease associated with partial anomalous pulmonary venous connection
- Brain MRI findings of older patients with Pallister-Killian syndrome
- Laryngeal dystonia in xeroderma pigmentosum
- Human papillomavirus infections among Japanese women : age-related prevalence and type-specific risk for cervical cancer
- JK1-1 Genetic Approach to Identify Susceptibility Genes for Allergic Diseases(Part1 Genetics of Asthma and Allergy Diseases)
- Midtrimester termination of pregnancy using gemeprost in combination with laminaria in women who have previously undergone cesarean section
- Association analysis of nine missense polymorphisms in the coagulation factor V gene with severe preeclampsia in pregnant Japanese women
- Brain Natriuretic Peptide (BNP) and Cyclic Guanosine Monophosphate (cGMP) Levels in Normal Pregnancy and Preeclampsia
- No association between atopic asthma and a coding variant of Fcε R1β in a Japanese population
- A pediatric case of critical illness polyneuropathy : clinical and pathological findings
- A case of listerial meningitis treated with a regimen containing panipenem-betamipron
- Membrane Fusion between Liposomes Composed of Acidic Phospholipids and Neutral Phospholipids Induced by Melittin : A Differential Scanning Calorimetric Study
- Comparison of IgG, IgG1 and IgG2 immune responses to pneumococcal polysaccharide in atopic and nonatopic children
- An association between asthma and TNF-308G/A polymorphism : meta-analysis
- Advanced Research on Dopamine Signaling to Develop Drugs for the Treatment of Mental Disorders: Ser311Cys Polymorphisms of the Dopamine D2–Receptor Gene and Schizophrenia
- IV D2 A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures
- Molecular Genetics of Febrile Seizures
- Mutation and association analysis of the interferon regulatory factor 2 gene (IRF2) with atopic dermatitis
- Failure to Find an Association between CD14-159C/T Polymorphism and Asthma : A Family-based Association Test and Meta-analysis
- Evidence for an association between plasma platelet-activating factor acetylhydrolase deficiency and increased risk of childhood atopic asthma
- ENDOSCOPIC SUBMUCOSAL DISSECTION FOR SUBMUCOSAL INVASIVE GASTRIC CANCER AND CURABILITY CRITERIA
- A rare case of congenital hepatic fibrosis with severe pulmonary hypertension in an adolescent
- An association study between a transcriptional polymorphism in the serotonin transporter gene and panic disorder in a Japanese population
- Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia
- SMAD3 as an atopic dermatitis susceptibility gene in the Japanese population
- Fatal pulmonary veno-occlusive disease after chemotherapy for Burkitt's lymphoma
- Advanced Research on Dopamine Signaling to Develop Drugs for the Treatment of Mental Disorders : Ser311Cys Polymorphisms of the Dopamine D_2-Receptor Gene and Schizophrenia
- Reevaluation of serum p53 antibody as a tumor marker in colorectal cancer patients
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growth
- An association study between the dymeclin gene and schizophrenia in the Japanese population
- A two-stage case-control association study of PADI2 with schizophrenia
- Two-stage case-control association study of polymorphisms in rheumatoid arthritis susceptibility genes with schizophrenia
- Substituent effects in the Diels-Alder reaction of substituted benzynes with hexamethylcyclohexa-2,4-dienone.
- The synthesis of 1,2,3,4-tetramethyl-5-nitronaphthalene and 1,2,3,4-tetramethyl-6-nitronaphthalene.
- Membrane Fusion between Liposomes Composed of Acidic Phospholipids and Neutral Phospholipids Induced by Melittin: A Differential Scanning Calorimetric Study.