E Leroy

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. ncbi request reprint Intron-exon structure of ubiquitin c-terminal hydrolase-L1
    E Leroy
    Genetic Disease Research Branch, NHGRI, NIH, Bethesda, MD 20892, USA
    DNA Res 5:397-400. 1998
  2. ncbi request reprint Genomic organization and expression of the human beta-synuclein gene (SNCB)
    C Lavedan
    National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, 20892, USA
    Genomics 54:173-5. 1998
  3. ncbi request reprint Identification, localization and characterization of the human gamma-synuclein gene
    C Lavedan
    Laboratory of Genetic Disease Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
    Hum Genet 103:106-12. 1998
  4. ncbi request reprint Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease
    C Lavedan
    Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
    DNA Res 5:401-2. 1998
  5. ncbi request reprint Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
    M H Polymeropoulos
    Laboratory of Genetic Disease Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 1430, USA
    Science 276:2045-7. 1997
  6. ncbi request reprint Mapping of the gene (NRAP) encoding N-RAP in the mouse and human genomes
    G Luo
    National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA
    Genomics 45:229-32. 1997
  7. ncbi request reprint The ubiquitin pathway in Parkinson's disease
    E Leroy
    Nature 395:451-2. 1998
  8. ncbi request reprint Mutation screening of the Wolfram syndrome gene in psychiatric patients
    R Torres
    Novartis Pharmaceuticals Corporation, Pharmacogenetics, Gaithersburg, MD 20878, USA
    Mol Psychiatry 6:39-43. 2001
  9. pmc Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein
    A Athanassiadou
    Am J Hum Genet 65:555-8. 1999
  10. ncbi request reprint Novel gene transcripts preferentially expressed in human muscles revealed by quantitative hybridization of a high density cDNA array
    G Pietu
    Centre National de la Recherche Scientifique UPR 420, Villejuif, France
    Genome Res 6:492-503. 1996

Collaborators

Detail Information

Publications11

  1. ncbi request reprint Intron-exon structure of ubiquitin c-terminal hydrolase-L1
    E Leroy
    Genetic Disease Research Branch, NHGRI, NIH, Bethesda, MD 20892, USA
    DNA Res 5:397-400. 1998
  2. ncbi request reprint Genomic organization and expression of the human beta-synuclein gene (SNCB)
    C Lavedan
    National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, 20892, USA
    Genomics 54:173-5. 1998
    ....
  3. ncbi request reprint Identification, localization and characterization of the human gamma-synuclein gene
    C Lavedan
    Laboratory of Genetic Disease Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
    Hum Genet 103:106-12. 1998
    ..The gamma-synuclein gene, also known as BCSG1, was recently found to be overexpressed in advanced infiltrating carcinoma of the breast. Our survey of the EST database indicated that it might also be overexpressed in an ovarian tumor...
  4. ncbi request reprint Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease
    C Lavedan
    Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
    DNA Res 5:401-2. 1998
  5. ncbi request reprint Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
    M H Polymeropoulos
    Laboratory of Genetic Disease Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892 1430, USA
    Science 276:2045-7. 1997
    ..This finding of a specific molecular alteration associated with PD will facilitate the detailed understanding of the pathophysiology of the disorder...
  6. ncbi request reprint Mapping of the gene (NRAP) encoding N-RAP in the mouse and human genomes
    G Luo
    National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA
    Genomics 45:229-32. 1997
    ..Comparative analysis of the mouse and human genomes indicates that the NRAP gene is located in regions of conserved synteny between the two species...
  7. ncbi request reprint The ubiquitin pathway in Parkinson's disease
    E Leroy
    Nature 395:451-2. 1998
  8. ncbi request reprint Mutation screening of the Wolfram syndrome gene in psychiatric patients
    R Torres
    Novartis Pharmaceuticals Corporation, Pharmacogenetics, Gaithersburg, MD 20878, USA
    Mol Psychiatry 6:39-43. 2001
    ..None of the psychiatric patients screened in this study carried these types of mutations. We identified, however, 24 new variations whose significance remains to be determined...
  9. pmc Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein
    A Athanassiadou
    Am J Hum Genet 65:555-8. 1999
  10. ncbi request reprint Novel gene transcripts preferentially expressed in human muscles revealed by quantitative hybridization of a high density cDNA array
    G Pietu
    Centre National de la Recherche Scientifique UPR 420, Villejuif, France
    Genome Res 6:492-503. 1996
    ..All these genes have been registered in the Genexpress Index, such that sequence, map, and expression data can be used to decipher their role in the physiology and pathology of human muscles...
  11. ncbi request reprint Occurrence of hepatitis viruses in wild-born non-human primates: a 3 year (1998-2001) epidemiological survey in Gabon
    M Makuwa
    Centre International de Recherches Medicales, Franceville, Gabon
    J Med Primatol 32:307-14. 2003
    ..9% wild-born and 8.3% at CIRMF harboured HBV-DNA despite the presence of neutralizing HbsAb. Together with previous findings, we confirm the high HBV prevalence not only in humans but also in chimpanzees and gorillas in Gabon and Congo...