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Molecular cloning and chromosomal localization of the human thrombopoietin gene

FEBS letters, 1994-10, Vol.353 (1), p.57-61

1994

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Genetic variations in Lycoris radiata var. radiata in Japan

Genes & Genetic Systems, 2005, Vol.80(3), pp.199-212

2005

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Genetic variations in the chloroplast genome and phylogenetic clustering of Lycoris species

Genes & Genetic Systems, 2006, Vol.81(4), pp.243-253

2006

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R-banding and nonisotopic in situ hybridization : precise localization of the human type II collagen gene (COL2A1)

Human genetics, 1990-11, Vol.86 (1), p.14-16

1990

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Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

Nature genetics, 1994-11, Vol.8 (3), p.236-242

1994

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Expression of NPAT, a novel substrate of cyclin E-CDK2, promotes S-phase entry

Genes & development, 1998-02, Vol.12 (4), p.456-461

1998

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Structure, Chromosomal Location, and Expression Profile of EXTR1 and EXTR2, New Members of the Multiple Exostoses Gene Family

Biochemical and biophysical research communications, 1998-02, Vol.243 (1), p.61-66

1998

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Characterization of Functional Domains of an Embryonic Stem Cell Coactivator UTF1 Which Are Conserved and Essential for Potentiation of ATF-2 Activity

The Journal of biological chemistry, 1998-10, Vol.273 (40), p.25840-25849

1998

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Isolation, tissue expression, and chromosomal assignment of human RGS5, a novel G-protein signaling regulator gene

Journal of human genetics, 1998-01, Vol.43 (3), p.202-205

1998

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ATM mutations in patients with ataxia telangiectasia screened by a hierarchical strategy

Human mutation, 1998, Vol.12 (3), p.186-195

1998

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Structure and regulation of the human interferon regulatory factor 1 (IRF-1) and IRF-2 genes: implications for a gene network in the interferon system

Molecular and Cellular Biology, 1994-02, Vol.14 (2), p.1500-1509

1994

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Chromosome mapping of the human cytidine-5'-triphosphate synthetase (CTPS) gene to band 1p34.1-p34.3 by fluorescence in situ hybridization

Human genetics, 1991-11, Vol.88 (1), p.119-121

1991

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Genomic Organization and Chromosomal Localization of the Human Sepiapterin Reductase Gene

Biochemical and biophysical research communications, 1998-10, Vol.251 (2), p.597-602

1998

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Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)

Journal of human genetics, 1998-01, Vol.43 (4), p.268-271

1998

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Proviral inactivation of the Npat gene of Mpv 20 mice results in early embryonic arrest

Molecular and Cellular Biology, 1997-07, Vol.17 (7), p.4080-4086

1997

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A novel human gene whose product shares significant homology with the bovine brain-specific protein p25 on chromosome 5p15.3

Journal of human genetics, 1999-01, Vol.44 (2), p.121-122

1999

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Structural Analyses of the UTF1 Gene Encoding a Transcriptional Coactivator Expressed in Pluripotent Embryonic Stem Cells

Biochemical and biophysical research communications, 2001-07, Vol.285 (4), p.945-953

2001

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Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family

Genomics (San Diego, Calif.), 1995-01, Vol.25 (2), p.581-583

1995

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Chromosomal assignment of a human apoptosis-associated tyrosine kinase gene on chromosome 17q25.3 by somatic hybrid analysis and fluorescence in situ hybridization

Journal of human genetics, 1999-01, Vol.44 (2), p.141-142

1999

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A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3

Genomics (San Diego, Calif.), 1991-11, Vol.11 (3), p.565-572

1991

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Assignment of the ZIP kinase gene to human chromosome 19p13.3 by somatic hybrid analysis and fluorescence in-situ hybridization

Journal of human genetics, 1998-01, Vol.43 (3), p.209-211

1998

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Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families

Clinical genetics, 1993-01, Vol.43 (1), p.34-38

1993

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Chromosomal Insertion and Amplification of Human Papillomavirus 16 DNA Sequences in a Cell Line of Argyrophil Small Cell Carcinoma of the Uterine Cervix

Cancer science, 1991-04, Vol.82 (4), p.371-375

1991

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Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence

Clinical genetics, 1993-10, Vol.44 (4), p.169-172

1993

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Population cytogenetics of rare fragile sites in Japan

Human genetics, 1988-02, Vol.78 (2), p.121-126

1988

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Molecular cloning and chromosomal localization of the human thrombopoietin gene

Genetic variations in Lycoris radiata var. radiata in Japan

Genetic variations in the chloroplast genome and phylogenetic clustering of Lycoris species

R-banding and nonisotopic in situ hybridization : precise localization of the human type II collagen gene (COL2A1)

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

Expression of NPAT, a novel substrate of cyclin E-CDK2, promotes S-phase entry

Structure, Chromosomal Location, and Expression Profile of EXTR1 and EXTR2, New Members of the Multiple Exostoses Gene Family

Characterization of Functional Domains of an Embryonic Stem Cell Coactivator UTF1 Which Are Conserved and Essential for Potentiation of ATF-2 Activity

Isolation, tissue expression, and chromosomal assignment of human RGS5, a novel G-protein signaling regulator gene

ATM mutations in patients with ataxia telangiectasia screened by a hierarchical strategy

Structure and regulation of the human interferon regulatory factor 1 (IRF-1) and IRF-2 genes: implications for a gene network in the interferon system

Chromosome mapping of the human cytidine-5'-triphosphate synthetase (CTPS) gene to band 1p34.1-p34.3 by fluorescence in situ hybridization

Genomic Organization and Chromosomal Localization of the Human Sepiapterin Reductase Gene

Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)

Proviral inactivation of the Npat gene of Mpv 20 mice results in early embryonic arrest

A novel human gene whose product shares significant homology with the bovine brain-specific protein p25 on chromosome 5p15.3

Structural Analyses of the UTF1 Gene Encoding a Transcriptional Coactivator Expressed in Pluripotent Embryonic Stem Cells

Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family

Chromosomal assignment of a human apoptosis-associated tyrosine kinase gene on chromosome 17q25.3 by somatic hybrid analysis and fluorescence in situ hybridization

A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3

Assignment of the ZIP kinase gene to human chromosome 19p13.3 by somatic hybrid analysis and fluorescence in-situ hybridization

Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families

Chromosomal Insertion and Amplification of Human Papillomavirus 16 DNA Sequences in a Cell Line of Argyrophil Small Cell Carcinoma of the Uterine Cervix

Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence

Population cytogenetics of rare fragile sites in Japan

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