Human Molecular Genetics

Published by: Oxford University Press  

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  1. Journal Article (39)
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  1. GSK Faculty (16)
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Results (40)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Intra-nuclear trafficking of the BLM helicase to DNA damage-induced foci is regulated by SUMO modification
    Journal Article

    Eladad, S.; Ye, T. Z.; Hu, P.; Leversha, M.; Beresten, S.; Matunis, M. J.; Ellis, N. A.
    Human Molecular Genetics (2005)

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  • The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants
    Journal Article

    Mattiazzi, M.; Vijayvergiya, C.; Gajewski, C. D.; DeVivo, D. C.; Lenaz, G.; Wiedmann, M.; Manfredi, G.
    Human Molecular Genetics (2004)

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  • Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site
    Journal Article

    Ulaner, G. A.; Vu, T. H.; Li, T.; Hu, J. F.; Yao, X. M.; Yang, Y.; Gorlick, R.; Meyers, P.; Healey, J.; Ladanyi, M.; more...
    Human Molecular Genetics (2003)

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  • Oncogenes and tumor suppressors in the molecular pathogenesis of acute promyelocytic leukemia
    Journal Article

    Pandolfi, P. P.
    Human Molecular Genetics (2001)

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  • Evidence for BLM and Topoisomerase IIIα interaction in genomic stability
    Journal Article

    Hu, P.; Beresten, S. F.; Van Brabant, A.; Ye, T. Z.; Pandolfi, P. P.; Johnson, F. B.; Guarente, L.; Ellis, N. A.
    Human Molecular Genetics (2001)

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  • A common molecular basis for rearrangement disorders on chromosome 22q11
    Journal Article

    Edelmann, L.; Pandita, R. K.; Spiteri, E.; Funke, B.; Goldberg, R.; Palanisamy, N.; Chaganti, R. S. K.; Magenis, E.; Shprintzen, R. J.; Morrow, B. E.
    Human Molecular Genetics (1999)

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  • A model for testing recombinogenic sequences in the mouse germline
    Journal Article

    Moynahan, M. E.; Akgün, E.; Jasin, M.
    Human Molecular Genetics (1996)

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  • Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases
    Journal Article

    Phaneuf, D.; Wakamatsu, N.; Huang, J. Q.; Borowski, A.; Peterson, A. C.; Fortunato, S. R.; Ritter, G.; Igdoura, S. A.; Morales, C. R.; Benoit, G.; more...
    Human Molecular Genetics (1996)

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  • A human homolog of the S.cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region
    Journal Article

    Lamour, V.; Lécluse, Y.; Desmaze, C.; Spector, M.; Bodescot, M.; Aurias, A.; Osley, M. A.; Lipinski, M.
    Human Molecular Genetics (1995)

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  • A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues
    Journal Article

    Tsang, P.; Gilles, F.; Yuan, L.; Kuo, Y. H.; Lupu, F.; Samara, G.; Moosikasuwan, J.; Goye, A.; Zelenetz, A. D.; Selleri, L.; more...
    Human Molecular Genetics (1995)

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    • Human Molecular Genetics – authorized name for:

    Name ISSN / ISBN Publisher
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 09646906 Unknown
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 0964-6906 Unknown
    Human Molecular Genetics 1460-2083 Oxford University Press
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 09646906 The Author 2012
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 09646906 The Author 2008
    Human molecular genetics 1460-2083 Oxford University Press
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 09646906 The Author 2005
    Human molecular genetics 1460-2083 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press