COMPARISON OF INSERTION RATE OF L1 RETROPOSON INTO INTRON 30 OF THE NEUROFIBROMATOSIS TYPE 1 GENE IN SEVEN ASIAN AND PACIFIC POPULATIONS

スポンサーリンク

概要

• 論文の詳細を見る
• Japan Society of Human Geneticsの論文
• 1996-03-31

著者

• MATSUO Masafumi

  Division of Molecular Medicine, Department of International and Environmental Medical Science

• Ishida Takafumi

  Department of Cardiovascular Medicine, Hiroshima University Graduate School of Biochemical Sciences

• Shirakawa Taku

  Department Of Medical Technology Faculty Of Health Sciences Kobe University School Of Medicine

• Shirakawa Taku

  Faculty Of Health Science Kobe University School Of Medicine

• Ishida Takafumi

  Department Of Biological Sciences Graduate School Of Science The University Of Tokyo

• Poh-san Lai

  Department Of Pediatrics National University Of Singapore

• NISHIYAMA Kaoru

  Faculty of Health Science, Kobe University School of Medicine

• Nishiyama Kaoru

  Department Of Medical Technology Faculty Of Health Sciences Kobe University School Of Medicine

• Matsuo Masafumi

  Division Of Genetics Icmr Kobe University

• Matsuo M

  Kobe University Graduate School Of Medicine

• Ishida Takafumi

  Department Of Anthropology Faculty Of Science The University Of Tokyo

関連論文

• Clinical Types, Molecular Genetic Diagnosis & Genetic : clinical Correlation in Patients with Spinal Muscular Atrophy
• Deletion of the SMN1 and NAIP Genes in Vietnamese Patients with Spinal Muscular Atrophy
• Molecular Genetic Analyses of Five Vietnamese Patients with Spinal Musucular Atrophy
• Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
• Molecular Diagnosis, Correlation of Clinical and Deletion Data in Duchenne Muscular Dystrophy
• OE-175 Low-intensity Pulsed Ultrasound (LIPUS) Enhanced Angiogenesis in a Rat Hind Limb Ischemia Model, VEGF-A Expression and Mobilization in HUVEC(OE30,Preventive Medicine/Epidemiology/Education (H),Oral Presentation (English),The 73rd Annual Scientific
• Nifedipine Interferes with Migration of Vascular Smooth Muscle Cells via Inhibition of Pyk2-Src Axis
• PE-127 Role of Src and Cas in Dorsal Ruffling, Lamellipodia and Migration in Vascular Smooth Muscle Cells(PE022,Atherosclerosis, Basic (IHD),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
• Angiotensin II-Induced Osteopontin Expression in Vascular Smooth Muscle Cells Involves G_, Ras, ERK, Src and Ets-1
• PJ-617 Role of HIF-1-dependent Expression of the VLDL Receptor in the Progression of Atherosclerosis(Atherosclerosis, basic(08)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-621 Feasibility and Optimization of Aortic Valve Planimetry Using Retrospective ECG-gated 64-slice Multidetector-Row Computed Tomography(PJ104,CT/MRI (Myocardium) 3 (I),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circul
• PJ-258 Nonobstructive Aortic Valve Calcification and Cardiovascular Risk Factors as Predictors of Coronary Artery Atherosclerosis Assessed by 64-slice Multidetector-row Computed Tomography(PJ044,Atherosclerosis (Clinical/Diagnosis) 2 (IHD),Poster Session
• PE-184 Lower High Molecular Weight Adiponectin Level is Associated with Unstable Coronary Plaques as Detected by Multi-detecter Computed Tomography(PE031,Metabolic Syndrome 2 (H),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese
• PE-073 Evaluation of Coronary Calcium and Noncalcified Plaque Characteristics in Patients with Acute Coronary Syndrome by Multislice Computed Tomography(PE013,CT/MRI (Coronary/Vascular) (I),Poster Session (English),The 73rd Annual Scientific Meeting of Th
• OJ-208 Usefulness of 64-slice Multidetector-Row Computed Tomography in the Simultaneous Evaluation of Aortic Valve Area and Coronary Artery Disease(OJ35,Valvular Heart Disease/Pericarditis/Cardiac Tumor 1 (M),Oral Presentation (Japanese),The 73rd Annual S
• OE-157 Coronary Plaque Stabilization by Intensive Statin Therapy Decreasing Serum LDL/HDL Cholesterol Ratio on Multislice Computed Tomographic Angiography(OE27,CT/MRI (Coronary/Vascular) 1 (I),Oral Presentation (English),The 73rd Annual Scientific Meeting
• Ablation of the Bach1 Gene Leads to the Suppression of Atherosclerosis in Bach1 and Apolipoprotein E Double Knockout Mice
• PE-125 DNA Double-Strand Breaks and DNA Repair Enzyme Activity are Increased in Human Atherosclerotic Plaque(Atherosclerosis, basic-6, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• OE-277 DEC1, a Member of the Fifth Clock-Gene Family, is Induced by Angiotensin II, Growth Factors, and Hypoxia in Vascular Cells(Hypertension, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• OE-391 Increased Leukocyte Rho Kinase (ROCK) Activity and Endothelial Dysfunction in Cigarette Smokers(OE66,Atherosclerosis (Clinical/Pathophysiology) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society
• PJ-221 Prediction of Heart Failure Death in Hemodialysis Patients by Myocardial Washout Rate of Technetium 99m Sestamibi(PJ037,Nuclear Cardiology (Coronary, Myocardium) 1 (I),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Cir
• The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
• Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase Deficiency in Vietnam
• DELETION OF TWENTY SEVEN NUCLEOTIDES WITHIN EXON 11 OF THE BAND 3GENE IDENTIFIED IN OVALOCYTOSIS IN LOMBOK ISLAND, INDONESIA
• Beneficial Effect of T-Type Calcium Channel Blockers on Endothelial Function in Patients with Essential Hypertension
• Effect of Amlodipine and Cilazapril Treatment on Platelet Ca^ Handling in Spontaneously Hypertensive Rats
• FTO polymorphisms in oceanic populations
• Polymorphisms in the ABO blood group gene in three populations in the New Georgia group of the Solomon Islands
• Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations
• インドネシア東ジャワ地方の前頭骨篩骨脳瘤患者にMTHFR遺伝子のC677T変異は認められなかった
• Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia
• A COMPREHENSIVE METHOD TO SCAN FOR POINT MUTATIONS OF THE GLUCOSE 6 PHOSPHATE DEHYDROGENASE GENE
• COMPARISON OF INSERTION RATE OF L1 RETROPOSON INTO INTRON 30 OF THE NEUROFIBROMATOSIS TYPE 1 GENE IN SEVEN ASIAN AND PACIFIC POPULATIONS
• Comparative study on deletions of the dystrophin gene in three Asian populations
• C TO T TRANSITION AT THE FIRST NUCLEOTIDE OF CODON 63 OF THE β-GLOBIN GENE CORRESPONDING TO HEMOGLOBIN M-SASKATOON IN AN INDONESIAN BOY
• Molecular identification and characterization of a novel gene that is upregulated in obese mouse heart
• Hepatitis B virus-positive blood donors in the early stages of Hepatitis B virus infection : Significance of nucleic acid amplification testing
• Molecular Genetic Analysis of a B^3 Allele in a Rare Subtype A_1B_3 Blood-type Individual
• Screening for glucose-6-phosphate dehydrogenase deficiency using a modified formazan method : A pilot study on Filipino male newborns
• Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase Deficiency in Malays in Malaysia
• A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5
• Molecular genetics of spinal muscular atrophy : contribution of the NAIP gene to clinical severity
• Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient
• Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene : a novel source of genomic instability
• A simple explanation for a case of incompatibility with the reading frame theory in Duchenne muscular dystrophy: failure to detect an aberrant restriction fragment in Southern blot analysis
• Human Papillomavirus Genotypes and the p53 Codon 72 Polymorphism in Cervical Cancer of Northeastern Thailand
• Poor correlation between hemolysis and jaundice in glucose 6-phosphate dehydrogenase-deficient babies
• Hepatic cytotoxic T-cell infiltrates in patients with peripheral T-cell proliferative diseases/lymphomas : Clinicopathological and molecular analysis
• PDGF-alpha Receptor Expression Following Hypoxic-Ischemic Injury in the Neonatal Rat Brain
• Population Genetic Studies on Nine Aboriginal Ethnic Groups of Taiwan, II. Serum Protein Systems
• Coexistence of five G6PD variants indicates ethnic complexity of Phuket islanders, Southern Thailand
• Bacterial Contamination of Bathing Facilities in Day Care Center and the Disinfection Efficiency of Oxidizing Water
• Rescue Mission for Patients with Chronic Diseases such as Diabetes : The Design of the Mobile Laboratory
• Heart Disease Risk Factors and Onset of Heart Problems among the Elderly
• Multicolor Karyotyping of Six Old World Monkey Species
• OE-309 Role of the Ras-ERK Pathway And c-Src in Angiotensin II-Induced Osteopontin Expression in Vascular Smooth Muscle Cells(Hypertension, Basic 3 (H) : OE39)(Oral Presentation (English))
• MAP Kinase Signal-Integrating Kinase-1 (Mnk1), a Novel Substratefor MARK, Is Involved in Angiotensin II-Mediated Protein Synthesis
• The Pacific lineage (2E) of JC polyomavirus is prevalent in Sumba Island, Eastern Indonesia
• Ligand orientation governs conjugation capacity of UDP-glucuronosyltransferase 1A1
• Distinctive distribution of AIM1 polymorphism among major human populations with different skin color
• Duchenne/Becker muscular dystrophy:from molecular diagnosis to gene therapy
• Comparison of the Efficiencies of the Fused Heterocyclic Compounds, 9H-Xanthene-2,7-diols, and Related Chain-Breaking Phenolic Antioxidants
• Molecular basis of glucose-6-phosphate dehydrogenase deficiency among Filipinos
• MET 235 THR POLYMORPHISM OF ANGIOTENSINOGEN IN INDONESIANS
• High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia
• FGFR2 is associated with hair thickness in Asian populations
• DRD4 VNTR polymorphism in Oceanic populations
• Role of DNA Damage in Cardiovascular Disease
• High prevalence of Southeast Asian ovalocytosis in Malays with distal renal tubular acidosis
• Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages
• Hypertension-susceptibility gene prevalence in the Pacific Islands and associations with hypertension in Melanesia

もっと見る 閉じる

スポンサーリンク