Search Results1-20 of  24

  • 1 / 2
  • Yagi Mariko ID: 9000010045592

    Articles in CiNii:1

    • A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene (2005)
  • Yagi Mariko ID: 9000290355491

    Articles in CiNii:1

    • Identical deletion at 14q13.3 including PAX9 and NKX2-1 in siblings from mosaicism of unaffected parent (2015)
  • Yagi Mariko ID: 9000322731301

    Articles in CiNii:1

    • Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother (2016)
  • YAGI Mariko ID: 1000060362787

    Department of Pediatrics, Kobe University Graduate School of Medicine (2011 from CiNii)

    Articles in CiNii:23

    • Dystrophin Gene Analysis on 76 Families with Dystrophinopathy (2002)
    • Treatment of Duchenne Muscular Dystrophy with Gentamicin (2004)
    • ジストロフィン遺伝子mRNAのトランススプライシングによって発症した Duchenne 型筋ジストロフィー (2001)
  • YAGI Mariko ID: 9000000369598

    Department of Pediatrics, Kakogawa Municipal Hospital (1999 from CiNii)

    Articles in CiNii:4

    • Serial Echocardiographic Assessment of Cardiac Function in Very Low Birth Weight Infant V: Serial Assessment of Left Ventricular Systolic Time Interval using M-Mode Echocardiography (1999)
    • Serial Echocardiographic Assessment of Cardiac Function in Very Low Birth Weight Infant VI: Serial Assessment of Right Ventricular Systolic Time Interval using M-Mode Echocardiography (1999)
    • Perinatal Risk Factors of Decreased Early Cardiac Function in Very Low Birth Weight Infants (1998)
  • YAGI Mariko ID: 9000006169239

    Department of Clinical Pharmacy, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University (2012 from CiNii)

    Articles in CiNii:22

    • A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5 (2002)
    • Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle (2005)
    • Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphoma (2007)
  • YAGI Mariko ID: 9000017512170

    Graduate school of Eng., Univ. of CHIBA (2009 from CiNii)

    Articles in CiNii:2

    • 7542 Relation between urban transformation and building constructor's trend : Research on building constructor's code of good practices for urban revival(VOl. 2) (2009)
    • 7543 About building constructor's activity and conscious of local residents : Research on building constructor's code of good practices for urban revival (VOl.3) (2009)
  • YAGI Mariko ID: 9000248221618

    Department of Pediatrics, Kobe University Graduate School of Medicine (2013 from CiNii)

    Articles in CiNii:1

    • Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28 (2013)
  • YAGI Mariko ID: 9000258071470

    Faculty of Engineering, Shizuoka University (2008 from CiNii)

    Articles in CiNii:1

    • Input of G1 Continuous Aesthetic Curve Segments with Pen Tablet (2008)
  • YAGI Mariko ID: 9000391837843

    Faculty of Engineering, Shizuoka University (2007 from CiNii)

    Articles in CiNii:1

    • Input of Aesthetic Curve Segments with Inflection End Points and Generation of Aesthetic Curves with G² continuity (2007)
  • Yagi Mariko ID: 9000023879879

    Articles in CiNii:1

    • Chemical treatment enhances skipping of a mutated exon in the dystrophin gene. (2011)
  • Yagi Mariko ID: 9000239584994

    Articles in CiNii:1

    • Novel cryptic exons identified in introns 2 and 3 of the human dystrophin gene with duplication of exons 8-11 (2006)
  • Yagi Mariko ID: 9000239600611

    Articles in CiNii:1

    • Mutation Analysis of the Ornithine Transcarbamylase (OTC) Gene in Five Japanese OTC Deficiency Patients Revealed Two Known and Three Novel Mutations Including a Deep Intronic Mutation (2007)
  • Yagi Mariko ID: 9000239600668

    Articles in CiNii:1

    • Mosaic Tetrasomy 9p Case with the Phenotype Mimicking Klinefelter Syndrome and Hyporesponse of Gonadotropin-Stimulated Testosterone Production (2007)
  • Yagi Mariko ID: 9000242079330

    Department of Pediatrics, Kobe University Graduate School of Medicine, Japan (2013 from CiNii)

    Articles in CiNii:1

    • Rapid Progression of Neuromuscular Disorder Related Cardiomyopathy in a Young Patient (2013)
  • Yagi Mariko ID: 9000256119548

    Divisions of Molecular Medicine Kobe University Graduate School of Medicine|Pediatrics Kobe University Graduate School of Medicine (2002 from CiNii)

    Articles in CiNii:1

    • Dystrophin Gene Analysis on 76 Families with Dystrophinopathy. (2002)
  • Yagi Mariko ID: 9000256119973

    Department of Pediatrics, Kobe University Graduate School of Medicine (2004 from CiNii)

    Articles in CiNii:1

    • Treatment of Duchenne Muscular Dystrophy with Gentamicin (2004)
  • Yagi Mariko ID: 9000279202624

    Department of Pediatrics, Graduate School of Medicine, Kobe University (2014 from CiNii)

    Articles in CiNii:1

    • Phosphorothioate Modification of Chimeric 2'-O-Methyl RNA/Ethylene-Bridged Nucleic Acid Oligonucleotides Increases Dystrophin Exon 45 Skipping Capability and Reduces Cytotoxicity (2014)
  • Yagi Mariko ID: 9000283719475

    Department of Pediatrics, Kobe University Graduate School of Medicine (2014 from CiNii)

    Articles in CiNii:1

    • Clinical manifestations of three neonates with family histories of Menkes disease (2014)
  • Yagi Mariko ID: 9000283719555

    神戸大学大学院医学研究科小児科学|にこにこハウス医療福祉センター小児科 (2014 from CiNii)

    Articles in CiNii:1

    • Clinical manifestations of Menkes disease vary according to patient's genotype and the initiation time of treatment with copper-histidine injections (2014)
  • 1 / 2
Page Top