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Disease-causing allele-specific silencing against the ALK2 mutants, R206H and G356D, in fibrodysplasia ossificans progressiva

Gene therapy, 2012-07, Vol.19 (7), p.781-785

2012

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Epigenetic aberration of the human REELIN gene in psychiatric disorders

Molecular psychiatry, 2007-06, Vol.12 (6), p.593-600

2007

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Cytoplasmic ribonucleoprotein complexes containing human LINE‐1 protein and RNA

The EMBO journal, 1996-02, Vol.15 (3), p.630-639

1996

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Allele-specific binding of the ubiquitous transcription factor OCT-1 to the functional single nucleotide polymorphism (SNP) sites in the tumor necrosis factor-alpha gene (TNFA) promoter

Genes and immunity, 2001-04, Vol.2 (2), p.105-109

2001

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T.O.2 Allele-specific silencing against the ALK2 mutants, R206H and G356D, in fibrodysplasia ossificans progressiva (FOP)

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.906-906

2012

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The possible association between epigenetic aberration in DNA methylation in RELN and psychiatric disorders

Molecular psychiatry, 2007-06, Vol.12 (6), p.519-519

2007

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RNA interference (RNAi) induction with various types of synthetic oligonucleotide duplexes in cultured human cells

FEBS letters, 2002-06, Vol.521 (1), p.195-199

Hohjoh, Hirohiko

2002

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Allele-specific silencing by RNA interference

Methods in molecular biology (Clifton, N.J.), 2010, Vol.623, p.67

Hohjoh, Hirohiko

2010

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Expression profile analysis of microRNA (miRNA) in mouse central nervous system using a new miRNA detection system that examines hybridization signals at every step of washing

Gene, 2007-04, Vol.391 (1), p.39-44

2007

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Marked change in microRNA expression during neuronal differentiation of human teratocarcinoma NTera2D1 and mouse embryonal carcinoma P19 cells

Biochemical and biophysical research communications, 2007-10, Vol.362 (2), p.360-367

2007

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Enhancement of RNAi activity by improved siRNA duplexes

FEBS letters, 2004-01, Vol.557 (1), p.193-198

Hohjoh, Hirohiko

2004

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Suppression of regulatory T cells by exosomes via LET-7I-IGF1R/TGFBR1 axis in multiple sclerosis

Journal of the neurological sciences, 2017-10, Vol.381, p.447-447

2017

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Complex HLA-DR and -DQ Interactions Confer Risk of Narcolepsy-Cataplexy in Three Ethnic Groups

American journal of human genetics, 2001-03, Vol.68 (3), p.686-699

2001

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Systematic gene regulation involving miRNAs during neuronal differentiation of mouse P19 embryonic carcinoma cell

Biochemical and biophysical research communications, 2009-10, Vol.388 (4), p.648-653

2009

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Long-lasting RNAi activity in mammalian neurons

FEBS letters, 2004-01, Vol.558 (1), p.89-95

2004

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Genomewide Association Analysis of Human Narcolepsy and a New Resistance Gene

American journal of human genetics, 2006-08, Vol.79 (2), p.252-263

2006

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Novel allele containing a 190C>T nonsynonymous substitution in the N-acetyltransferase (NAT2) gene

Human mutation, 2000-06, Vol.15 (6), p.581-581

2000

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Novel single nucleotide polymorphisms (SNPs) at positions 497 (T/G) and 829 (T/C) in the human c-FOS gene and haplotype association

Human mutation, 2000-09, Vol.16 (3), p.279-279

2000

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Sequence-specific single-strand RNA binding protein encoded by the human LINE-1 retrotransposon

The EMBO journal, 1997-10, Vol.16 (19), p.6034-6043

1997

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Molecular cloning and characterization of the common marmoset huntingtin gene

Gene, 2009-03, Vol.432 (1), p.60-66

2009

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Significant association of the arylalkylamine N-acetyltransferase (AA-NAT) gene with delayed sleep phase syndrome

Neurogenetics, 2003-04, Vol.4 (3), p.151-153

2003

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Influence of assembly of siRNA elements into RNA-induced silencing complex by fork-siRNA duplex carrying nucleotide mismatches at the 3′- or 5′-end of the sense-stranded siRNA element

Biochemical and biophysical research communications, 2005-04, Vol.329 (2), p.516-521

2005

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Gene silencing analyses against amyloid precursor protein ( APP) gene family by RNA interference

Cell biology international, 2006-11, Vol.30 (11), p.952-956

2006

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Epigenetic aberration of the human REELIN gene in psychiatric disorders

Molecular psychiatry, 2007-06, Vol.12 (6), p.519-600

2007

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Immunoselected hepatitis B virus mutant

The Lancet (British edition), 1991-01, Vol.337 (8733), p.125-125

1991

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Disease-causing allele-specific silencing against the ALK2 mutants, R206H and G356D, in fibrodysplasia ossificans progressiva

Epigenetic aberration of the human REELIN gene in psychiatric disorders

Cytoplasmic ribonucleoprotein complexes containing human LINE‐1 protein and RNA

Allele-specific binding of the ubiquitous transcription factor OCT-1 to the functional single nucleotide polymorphism (SNP) sites in the tumor necrosis factor-alpha gene (TNFA) promoter

T.O.2 Allele-specific silencing against the ALK2 mutants, R206H and G356D, in fibrodysplasia ossificans progressiva (FOP)

The possible association between epigenetic aberration in DNA methylation in RELN and psychiatric disorders

RNA interference (RNAi) induction with various types of synthetic oligonucleotide duplexes in cultured human cells

Allele-specific silencing by RNA interference

Expression profile analysis of microRNA (miRNA) in mouse central nervous system using a new miRNA detection system that examines hybridization signals at every step of washing

Marked change in microRNA expression during neuronal differentiation of human teratocarcinoma NTera2D1 and mouse embryonal carcinoma P19 cells

Enhancement of RNAi activity by improved siRNA duplexes

Suppression of regulatory T cells by exosomes via LET-7I-IGF1R/TGFBR1 axis in multiple sclerosis

Complex HLA-DR and -DQ Interactions Confer Risk of Narcolepsy-Cataplexy in Three Ethnic Groups

Systematic gene regulation involving miRNAs during neuronal differentiation of mouse P19 embryonic carcinoma cell

Long-lasting RNAi activity in mammalian neurons

Genomewide Association Analysis of Human Narcolepsy and a New Resistance Gene

Novel allele containing a 190C>T nonsynonymous substitution in the N-acetyltransferase (NAT2) gene

Novel single nucleotide polymorphisms (SNPs) at positions 497 (T/G) and 829 (T/C) in the human c-FOS gene and haplotype association

Sequence-specific single-strand RNA binding protein encoded by the human LINE-1 retrotransposon

Molecular cloning and characterization of the common marmoset huntingtin gene

Significant association of the arylalkylamine N-acetyltransferase (AA-NAT) gene with delayed sleep phase syndrome

Influence of assembly of siRNA elements into RNA-induced silencing complex by fork-siRNA duplex carrying nucleotide mismatches at the 3′- or 5′-end of the sense-stranded siRNA element

Gene silencing analyses against amyloid precursor protein ( APP) gene family by RNA interference

Epigenetic aberration of the human REELIN gene in psychiatric disorders

Immunoselected hepatitis B virus mutant

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