Resultats de la cerca - Ghebranious, Nader

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  1. 1
    Detection of ApoE E2, E3 and E4 alleles using MALDI-TOF mass spectrometry and the homogeneous mass-extend technology

    Detection of ApoE E2, E3 and E4 alleles using MALDI-TOF mass spectrometry and the homogeneous mass-extend technology per Ghebranious, Nader, Ivacic, Lynn, Mallum, Jamie, Dokken, Charles

    Publicat 2005
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  2. 2
    Aging-Associated Truncated Form of p53 Interacts with Wild-Type p53 and Alters p53 Stability, Localization, and Activity

    Aging-Associated Truncated Form of p53 Interacts with Wild-Type p53 and Alters p53 Stability, Localization, and Activity per Moore, Lynette, Lu, Xiongbin, Ghebranious, Nader, Tyner, Stuart, Donehower, Lawrence A.

    Publicat 2007
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  3. 3
    STRP Screening Sets for the human genome at 5 cM density

    STRP Screening Sets for the human genome at 5 cM density per Ghebranious, Nader, Vaske, David, Yu, Adong, Zhao, Chengfeng, Marth, Gabor, Weber, James L

    Publicat 2003
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  4. 4
    A Pilot Study of Gene/Gene and Gene/Environment Interactions in Alzheimer Disease

    A Pilot Study of Gene/Gene and Gene/Environment Interactions in Alzheimer Disease per Ghebranious, Nader, Mukesh, Bickol, Giampietro, Philip F., Glurich, Ingrid, Mickel, Susan F., Waring, Stephen C., McCarty, Catherine A.

    Publicat 2011
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  5. 5
    A Novel Locus for Adolescent Idiopathic Scoliosis on Chromosome 12p

    A Novel Locus for Adolescent Idiopathic Scoliosis on Chromosome 12p per Raggio, Cathleen L., Giampietro, Philip F., Dobrin, Seth, Zhao, Chengfeng, Dorshorst, Donna, Ghebranious, Nader, Weber, James L., Blank, Robert D.

    Publicat 2009
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  6. 6
    Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension

    Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension per Wilke, Russell A, Simpson, Robert U, Mukesh, Bickol N, Bhupathi, Satya V, Dart, Richard A, Ghebranious, Nader R, McCarty, Catherine A

    Publicat 2009
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  7. 7
    Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations

    Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations per Ghebranious, Nader, Raggio, Cathleen L, Blank, Robert D, McPherson, Elizabeth, Burmester, James K, Ivacic, Lynn, Rasmussen, Kristen, Kislow, Jennifer, Glurich, Ingrid, Jacobsen, F Stig, Faciszewski, Thomas, Pauli, Richard M, Boachie-Adjei, Oheneba, Giampietro, Philip F

    Publicat 2007
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