A COMPREHENSIVE METHOD TO SCAN FOR POINT MUTATIONS OF THE GLUCOSE 6 PHOSPHATE DEHYDROGENASE GENE

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
• 1997-09-30

著者

• MATSUO Masafumi

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

• 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

• 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

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
• 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
• 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
• 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
• 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
• Ligand orientation governs conjugation capacity of UDP-glucuronosyltransferase 1A1
• Duchenne/Becker muscular dystrophy:from molecular diagnosis to gene therapy
• Molecular basis of glucose-6-phosphate dehydrogenase deficiency among Filipinos
• MET 235 THR POLYMORPHISM OF ANGIOTENSINOGEN IN INDONESIANS
• 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

もっと見る 閉じる

スポンサーリンク