Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the 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
• 2002-06-01

著者

• Matsubara Yoichi

  東北大学 医学系研究科遺伝病学分野

• Matsubara Yoichi

  Department Of Medical Genetics Tohoku University School Of Medicine

• Yamada Atsushi

  Department of Cardiology, Juntendo University School of Medicine

• AOKI Yoko

  Department of Medical Genetics, Tohoku University School of Medicine

• KURE Shigeo

  Department of Medical Genetics, Tohoku University School of Medicine

• SUZUKI Yoichi

  Department of Medical Genetics, Tohoku University School of Medicine

• KOJIMA Kanako

  Department of Medical Genetics, Tohoku University School of Medicine

• KANNO Kiyoshi

  Department of Medical Genetics, Tohoku University School of Medicine

• KANNO Kiyosi

  Department of Medical Genetics, Tohoku University School of Medicine

• YANG Xuemei

  Department of Plastic Surgery, Tohoku University School of Medicine

• Yang Xue

  Department Of Plastic Surgery Tohoku University School Of Medicine

• Kure Shigeo

  Tohoku Univ. School Of Medicine Sendai Jpn

• Kure S

  Department Of Medical Genetics Tohoku University School Of Medicine

• Kure Shigeo

  Department Of Medical Genetics Tohoku University Graduate School Of Medicine

• Kure Shigeo

  Department Of Pediatrics And Biochemical Genetics Tohoku University School Of Medicine

• Kojima Kanako

  Department Of Medical Genetics Tohoku University School Of Medicine

• Suzuki Yoichi

  Department Of Public Health Chiba University Graduate School Of Medicine

• Suzuki Yoichi

  Department Of Medical Genetics Tohoku University School Of Medicine

• Sakata Yoshiyuki

  Department Of Medical Genetics Tohoku University School Of Medicine

• Suzuki Yoichi

  Department Of Applied Chemistry Faculty Of Science And Technology Keio University

• Suzuki Y

  Department Of Medical Genetics Tohoku University School Of Medicine

• Konno Kazuaki

  Department Of Bioengineering And Robotics Tohoku University

• SUZUKI Yasuyo

  Department of Clinical Genetics, Medical Institute of Bioregulation, Kyushu University

• Matsubara Y

  Department Of Medical Genetics Tohoku University School Of Medicine

• Matsubara Yoichi

  Department Of Medical Genetics Tohoku University Of Graduate School Of Medicine

• Yamada Atsushi

  Department Of Plastic And Reconstructive Surgery Tohoku University School Of Medicine

• Yamada Atsushi

  Department Of Cardiology Juntendo University School Of Medicine

• Yamaguchi Koichi

  Division Of Allergy National Center For Children Health And Development

• YAMADA Atsushi

  Department of Biochemistry, Showa University School of Dentistry

• AOKI Yoko

  Department of Food and Nutrition, Japan Women's University

• YAMADA ATSUSHI

  DEPARTMENT OF ADMINISTRATION ENGINEERING CHUO UNIVERSITY

関連論文

• DPE-063 Prognostic Value of Urinary Liver-type Fatty Acid-Binding Protein (L-FABP) in Patients with Acute Coronary Syndrome(DPE11,Kidney/Renal Circulation/CKD (H),Digital Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulat
• Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome
• A novel KCNQ4 one-base deletion in a large pedigree with hearing loss : implication for the genotype-phenotype correlation
• A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem
• Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
• Genotyping of Single Nucleotide Polymorphisms (SNPs) Influencing Drug Response by Competitive Allele-specific Short Oligonucleotide Hybridization (CASSOH) with Immunochromatographic Strip
• Novel IRF6 mutations in Japanese patients with Van der Woude Syndrome : two missense mutations (R45Q and P396S) and a 17-kb deletion
• Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population
• Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia
• Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
• A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia
• Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsy
• DINUCLEOTIDE REPEAT POLYMORPHISM IN 65k-GLUTAMATE DECARBOXYLASE GENE
• Potentiating and blocking actions of neonicotinoids on the response to acetylcholine of the neuronal α4β2 nicotinic acetylcholine receptor
• Association study of the C3 gene with adult and childhood asthma
• No Association of Polymorphisms in the 5' Region of the CD14 Gene and Food Allergy in a Japanese Population
• Effects of Probiotics on the Immune System and Allergic Diseases
• 6 Single nucleotide polymorphisms of CD14 and TLR2 is associated with the development of respiratory syncytial virus-induced bronchiolitis in Japanese children(II. Asthma Genetics)
• CIPRO 2.5 : Ciona intestinalis protein database, a unique integrated repository of large-scale omics data, bioinformatic analyses and curated annotation, with user rating and reviewing functionality
• Unique Histopathological Features of a Familial Dilated Cardiomyopathy with Conduction Defect Caused by a Lamin A/C Gene Mutation
• FRS-040 Unique Arrhythmogenesis of a Familial Dilated Cardiomyopathy with Conduction Defect Caused by a Lamin A/C Gene Mutation(Arrhythmia-Clinical : Advances in Diagnosis and Management (A) : FRS5)(Featured Research Session (English))
• Stable Expression of the Motor Protein Prestin in Chinese Hamster Ovary Cells(Bioengineering)
• Sequence analysis, gene expression, and chromosomal assignment of mouse Borg4 gene and its human orthologue
• Anaplastic ganglioglioma with sarcomatous component : An immunohistochemical study and molecular analysis of p53 tumor suppressor gene
• Guidelines for Diagnosis and Management of Pediatric Food Allergy in Japan
• Immunosuppressive Effects of Gallic Acid and Chebulagic Acid on CTL-Mediated Cytotoxicity
• Identification of Low Molecular Weight Probes on Perforin- and Fas-based Killing Mediated by Cytotoxic T Lymphocytes
• Association of the RIP2 Gene with Childhood Atopic Asthma
• Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma
• Impact of unilateral interposition sural nerve graft on the recovery of sexual function after radical prostatectomy in Japanese men : A preliminary study
• Neonatal-Onset Brainstem Reticular Reflex Myoclonus Following a Prenatal Brain Insult : Generalized Myoclonic Jerk and a Brainstem Lesion
• An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway
• Serum Nutritional Status of Tocopherol and Retinol Normalized to Lipids of Persons Living in the Southern Rural Terai Region in Nepal
• Clinical characterization of familial dilated cardiomyopathy with conduction defect caused by a novel lamin A/C gene mutation
• Ultrasonographic Findings in Neonates Screened for Congenital Hypothyroidism
• Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency
• Cloning, expression analysis, and chromosomal localization of a novel butyrophilin-like receptor
• Isolation and chromosomal mapping of a novel human gene showing homology to Na^+/PO4 cotransporter
• A novel human gene whose product shares significant homology with the bovine brain-specific protein p25 on chromosome 5p15.3
• Isolation, tissue expression, and chromosomal assignment of a novel human gene which encodes a protein with RING finger motif
• Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)
• Isolation, tissue expression, and chromosomal assignment of human RGS5, a novel G-protein signaling regulator gene
• B-56. Clinical Significance of Early Epilepsy
• Estimated glomerular filtration rate is an independent predictor for mortality of patients with acute heart failure
• Ehlers-Danlos Syndrome and Congenital Heart Anomalies
• Primary Hypoparathyroidism in Turner's Syndrome
• Acute motor axonal neuropathy during intensive immunosuppressive therapy for macrophage activation syndrome
• A novel therapeutic trial of homogentisic aciduria in a murine model of alkaptonuria
• Filaggrin null mutations are associated with atopic dermatitis and elevated levels of IgE in the Japanese population: a family and case–control study
• Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population
• Resolution of anti-neutrophil cytoplasmic antibody-associated vasculitis after resection of gastric cancer
• 114. Clinical Observations of the Ventriculo-atrial Shunt
• Molecular analysis of methylmalonyl-CoA mutase deficiency : identification of three missense mutations in mut^0 patients
• Nonketotic hyperglycinemia: Pathophysiological studies
• Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
• NONKETOTIC HYPERGLYCINEMIA : BIOCHEMICAL, MOLECULAR, AND NEUROLOGICAL ASPECTS
• Polymerization of Polar Vinyl Monomers by Cobalt Complex-Alkylaluminum Compound
• Polymerization of Polar Vinyl Monomers with Novel Cobalt-based Catalyst
• Influence of Mechanical Loading on Resonance Frequency Analysis and Trabecular Structure of Peri-implant Bone
• A Slow Spread of Adenovirus Type 7 Infection after Its Re-Emergence in Yamagata, Japan, in 1995
• Enzyme-catalyzed Ring-opening Polymerization of β-Butyrolactone Using PHB Depolymerase
• Detection of Chlorophyll Breakdown Products in the Senescent Leaves of Higher Plants
• CHEMICAL SHIFT OF OH PROTONS OF ALKYLPHENOLS IN CARBON TETRACHLORIDE ETHYL ACETATE MIXED SOLVENT IN PRESENCE OF CADMIUM NITRATE
• Tuberculous Hypertrophic Pachymeningitis Involving the Posterior Fossa and High Cervical Region : Case Report
• Multiple Cerebral Arteriovenous Malformations : Case Report
• Efficacy and safety of orally administered pilocarpine hydrochloride for patients with juvenile-onset Sjogren's syndrome
• Japanese pediatric guidelines for the treatment and management of bronchial asthma 2008
• Electronic Band Structures of Cu_2Sb-Type Intermetallic Compounds
• Mutation and haplotype analyses of the MUT gene in Japanese patients with methylmalonic acidemia
• Bright Red Color Formation of Cooked Pork Loin Cured with Lactic Acid Bacteria Starter Culture without Adding Nitrite During Low-Temperature Storage
• 我が国における学童・生徒における肥満と喘息症状との関連
• Endemicity of human metapneumovirus subgenogroups A2 and B2 in Yamagata, Japan, between 2004 and 2009
• Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination
• Sublingual Immunotherapy with House Dust-Extract for House Dust-Mite Allergic Rhinitis in Children
• Evola : Ortholog database of all human genes in H-InvDB with manual curation of phylogenetic trees
• Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones
• Improved genome assembly and evidence-based global gene model set for the chordate Ciona intestinalis : new insight into intron and operon populations
• The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts
• Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
• HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome
• A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
• Two Novel Mutations in the Lactase Gene in a Japanese Infant with Congenital Lactase Deficiency
• Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
• An Outbreak of Exanthematous Disease due to Coxsackievirus A9 in a Nursery in Yamagata, Japan, from February to March 2012
• Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis
• Replication of genetic association studies in asthma and related phenotypes
• Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies
• Linkage and association of childhood asthma with the chromosome 12 genes
• Panax Ginseng : A Newly Identified Cause of Gynecomastia
• Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia
• A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder
• Seasonal Patterns of Respiratory Syncytial Virus, Influenza A Virus, Human Metapneumovirus, and Parainfluenza Virus Type 3 Infections on the Basis of Virus Isolation Data between 2004 and 2011 in Yamagata, Japan
• An Outbreak of Parainfluenza Virus Type 4 Infections among Children with Acute Respiratory Infections during the 2011–2012 Winter Season in Yamagata, Japan
• Production of Hydroxlated Flavonoids with Cytochrome P450 BM3 Variant F87V and Their Antioxidative Activities
• Human Herpes Virus Type 6 Can Cause Skin Lesions at the BCG Inoculation Site Similar to Kawasaki Disease
• Utility of Thallium-201 Scintigraphy in Tolosa-Hunt Syndrome
• Valproic Acid Exacerbated Infantile Spasms and Induced Novel Complex Partial Seizures in an Infant with Non-ketotic Hyperglycinemia
• Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure
• Screening for Five Prevalent Mutations of SLC25A13 Gene in Guangdong, China: A Molecular Epidemiologic Survey of Citrin Deficiency
• Successful treatment with rituximab of an infant with refractory autoimmune hemolytic anemia

もっと見る 閉じる

スポンサーリンク