Yusuke Nakamura


Ontology type: schema:Person     


Person Info

NAME

Yusuke

SURNAME

Nakamura

Publications in SciGraph latest 50 shown

  • 2000-05-01 Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 1999-12 Localization of membrane-associated guanylate kinase (MAGI)-1/BAI-associated protein (BAP) 1 at tight junctions of epithelial cells in ONCOGENE
  • 1999-10-06 Retrovirus vectors designed for efficient transduction of cytotoxic or cytostatic genes in GENE THERAPY
  • 1999-10-01 Mapping of a gene responsible for dermatitis in NOA (Naruto Research Institute Otsuka Atrichia) mice, an animal model of allergic dermatitis in JOURNAL OF HUMAN GENETICS
  • 1999-10 Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines in JOURNAL OF HUMAN GENETICS
  • 1999-08-18 Bcl-2/E1B 19 kDa-interacting protein 3-like protein (Bnip3L) interacts with Bcl-2/Bcl-xL and induces apoptosis by altering mitochondrial membrane permeability in ONCOGENE
  • 1999-08-01 Complete cDNA sequence and genomic organization of a human pancreas-specific gene homologous to Caenorhabditis elegans sel-1 in JOURNAL OF HUMAN GENETICS
  • 1999-08-01 Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes in JOURNAL OF HUMAN GENETICS
  • 1999-08-01 Molecular cloning, expression, and mapping of a novel human cDNA, GRP17, highly homologous to human gadd45 and murine MyD118 in JOURNAL OF HUMAN GENETICS
  • 1999-07-30 Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization in BRITISH JOURNAL OF CANCER
  • 1999-07 Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome in JOURNAL OF HUMAN GENETICS
  • 1999-07 Association of the human NPPS gene with ossification of the posterior longitudinal ligament of the spine (OPLL) in HUMAN GENETICS
  • 1999-05-28 Frequent loss of expression or aberrant alternative splicing of P2XM, a p53-inducible gene, in soft-tissue tumours in BRITISH JOURNAL OF CANCER
  • 1999-05-01 Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP) in JOURNAL OF HUMAN GENETICS
  • 1999-05-01 Significantly elevated expression of PF4 (platelet factor 4) and eotaxin in the NOA mouse, a model for atopic dermatitis in JOURNAL OF HUMAN GENETICS
  • 1999-05-01 Isolation and characterization of a human cDNA homologous to the Xenopus laevis XCAP-C gene belonging to the structural maintenance of chromosomes (SMC) family in JOURNAL OF HUMAN GENETICS
  • 1999-04 Identification of the gene responsible for gelatinous drop-like corneal dystrophy in NATURE GENETICS
  • 1999-03-01 Isolation and characterization of a novel serine threonine kinase gene on chromosome 3p22-21.3 in JOURNAL OF HUMAN GENETICS
  • 1999-03-01 A Gln/Arg polymorphism at codon 349 of the hBUBR1 gene in JOURNAL OF HUMAN GENETICS
  • 1999-01-01 Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1 in JOURNAL OF HUMAN GENETICS
  • 1998-12 Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia in HUMAN GENETICS
  • 1998-12-01 Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferases in JOURNAL OF HUMAN GENETICS
  • 1998-11 Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence or Miller-Dieker syndrome in HUMAN GENETICS
  • 1998-10 Genetic diagnosis of cancer in INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY
  • 1998-09 Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD) in HUMAN GENETICS
  • 1998-09-01 Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin in JOURNAL OF HUMAN GENETICS
  • 1998-09-01 Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 1998-09 Molecular cloning of the chromosomal breakpoint in the LIS1 gene of a patient with isolated lissencephaly and balanced t(8;17) in HUMAN GENETICS
  • 1998-09-01 VNTR (variable number of tandem repeat) sequences as transcriptional, translational, or functional regulators in JOURNAL OF HUMAN GENETICS
  • 1998-09 Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome in HUMAN GENETICS
  • 1998-09-01 Dinucleotide repeat polymorphism in the first intron of the CSR gene in JOURNAL OF HUMAN GENETICS
  • 1998-09 Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome in HUMAN GENETICS
  • 1998-07 An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy in NATURE
  • 1998-07 Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine in NATURE GENETICS
  • 1998-06 Positional cloning of the gene for Nijmegen breakage syndrome in NATURE GENETICS
  • 1998-06 Genetic dissection of ``OLETF'', a rat model for non-insulin-dependent diabetes mellitus in MAMMALIAN GENOME
  • 1998-06-01 Identification of brain-specific splicing variants of the hDLG1 gene and altered splicing in neuroblastoma cell lines in JOURNAL OF HUMAN GENETICS
  • 1998-06-01 Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma in JOURNAL OF HUMAN GENETICS
  • 1998-06-01 Genomic organization and mapping of the human activin receptor type IIB (hActR-IIB) gene in JOURNAL OF HUMAN GENETICS
  • 1998-04 Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome in HUMAN GENETICS
  • 1998-04 Frequent Allelic Loss at 6q26-27 in Breast Carcinomas of the Solid-tubular Histologic Type in BREAST CANCER
  • 1998-02 Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3 in HUMAN GENETICS
  • 1998-02-01 Identification by differential display of eight known genes induced during in vivo intimal hyperplasia in JOURNAL OF HUMAN GENETICS
  • 1998-02-01 The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32 in JOURNAL OF HUMAN GENETICS
  • 1998-02 Mapping of a gene responsible for twy (tip-toe walking Yoshimura), a mouse model of ossification of the posterior longitudinal ligament of the spine (OPLL) in MAMMALIAN GENOME
  • 1998-02 Detection of known missense mutation ofhMLH1 in a hereditary non-polyposis colorectal cancer family using DNA extracts from mouthwash samples in INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY
  • 1997-12 Correlation of allelic losses and clinicopathological factors in primary breast cancers in BREAST CANCER
  • 1997-12 Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia in JOURNAL OF HUMAN GENETICS
  • 1997-12 Dual-color fish analysis of breakpoints on robertsonian translocations in JOURNAL OF HUMAN GENETICS
  • 1997-12 Allelic frequencies of twelve dinucleotide repeat marker loci on chromosome 13 in the normal Japanese population in JOURNAL OF HUMAN GENETICS
  • JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

    [
      {
        "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
        "affiliation": [
          {
            "affiliation": {
              "id": "http://www.grid.ac/institutes/grid.26999.3d", 
              "type": "Organization"
            }, 
            "isCurrent": true, 
            "type": "OrganizationRole"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.419280.6", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.272458.e", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.136593.b", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.419953.3", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.486756.e", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.256642.1", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.265073.5", 
            "type": "Organization"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.260975.f", 
            "type": "Organization"
          }
        ], 
        "familyName": "Nakamura", 
        "givenName": "Yusuke", 
        "id": "sg:person.011310672653.44", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011310672653.44"
        ], 
        "sdDataset": "persons", 
        "sdDatePublished": "2022-01-01T19:58", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        }, 
        "sdSource": "s3://com-springernature-scigraph/baseset/20220101/entities/gbq_results/person/person_881.jsonl", 
        "type": "Person"
      }
    ]
     

    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/person.011310672653.44'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/person.011310672653.44'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/person.011310672653.44'

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/person.011310672653.44'


     

    This table displays all metadata directly associated to this object as RDF triples.

    32 TRIPLES      10 PREDICATES      19 URIs      7 LITERALS      2 BLANK NODES

    Subject Predicate Object
    1 sg:person.011310672653.44 schema:affiliation Ne5e5689c46dc4cabaeb2e07f402743dc
    2 grid-institutes:grid.136593.b
    3 grid-institutes:grid.256642.1
    4 grid-institutes:grid.260975.f
    5 grid-institutes:grid.265073.5
    6 grid-institutes:grid.272458.e
    7 grid-institutes:grid.419280.6
    8 grid-institutes:grid.419953.3
    9 grid-institutes:grid.486756.e
    10 schema:familyName Nakamura
    11 schema:givenName Yusuke
    12 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011310672653.44
    13 schema:sdDatePublished 2022-01-01T19:58
    14 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    15 schema:sdPublisher Nf2748ec9bcd845cdb2ff57cd9c587163
    16 sgo:license sg:explorer/license/
    17 sgo:sdDataset persons
    18 rdf:type schema:Person
    19 Ne5e5689c46dc4cabaeb2e07f402743dc schema:affiliation grid-institutes:grid.26999.3d
    20 sgo:isCurrent true
    21 rdf:type schema:OrganizationRole
    22 Nf2748ec9bcd845cdb2ff57cd9c587163 schema:name Springer Nature - SN SciGraph project
    23 rdf:type schema:Organization
    24 grid-institutes:grid.136593.b schema:Organization
    25 grid-institutes:grid.256642.1 schema:Organization
    26 grid-institutes:grid.260975.f schema:Organization
    27 grid-institutes:grid.265073.5 schema:Organization
    28 grid-institutes:grid.26999.3d schema:Organization
    29 grid-institutes:grid.272458.e schema:Organization
    30 grid-institutes:grid.419280.6 schema:Organization
    31 grid-institutes:grid.419953.3 schema:Organization
    32 grid-institutes:grid.486756.e schema:Organization
     




    Preview window. Press ESC to close (or click here)


    ...