Search Results - MIRZAYANS, F

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  1. 1
    Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis

    Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis by Fetterman, CD, Mirzayans, F, Walter, MA

    Published in Clinical genetics
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  2. 2
    Mutation of the PAX6 gene in patients with autosomal dominant keratitis

    Mutation of the PAX6 gene in patients with autosomal dominant keratitis by MIRZAYANS, F, PEARCE, W. G, MACDONALD, I. M, WALTER, M. A

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  3. 3
    Quantitative Oropharyngeal Epstein-Barr Virus Shedding in Renal and Cardiac Transplant Recipients: Relationship to Immunosuppressive Therapy, Serologic Responses, and the Risk of Posttransplant Lymphoproliferative Disorder

    Quantitative Oropharyngeal Epstein-Barr Virus Shedding in Renal and Cardiac Transplant Recipients: Relationship to Immunosuppressive Therapy, Serologic Responses, and the Risk of P... by Preiksaitis, J. K., Diaz-Mitoma, F., Mirzayans, F., Roberts, S., Tyrrell, D. L. J.

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  4. 4
    Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25

    Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25 by MEARS, A. J, MIRZAYANS, F, GOULD, D. B, PEARCE, W. G, WALTER, M. A

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  5. 5
    Regulation of FOXC1 Stability and Transcriptional Activity by an Epidermal Growth Factor-activated Mitogen-activated Protein Kinase Signaling Cascade

    Regulation of FOXC1 Stability and Transcriptional Activity by an Epidermal Growth Factor-activated Mitogen-activated Protein Kinase Signaling Cascade by Berry, Fred B., Mirzayans, Farideh, Walter, Michael A.

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  6. 6
    Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly

    Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly by Mears, Alan J., Jordan, Tim, Mirzayans, Farideh, Dubois, Stéphane, Kume, Tsutomu, Parlee, Michael, Ritch, Robert, Koop, Benjamin, Kuo, Wen-Lin, Collins, Colin, Marshall, Jody, Gould, Douglas B., Pearce, William, Carlsson, Peter, Enerbäck, Sven, Morissette, Jean, Bhattacharya, Shomi, Hogan, Brigid, Raymond, Vincent, Walter, Michael A.

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  7. 7
    Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting protein

    Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting protein by Acharya, Moulinath, Sharp, Michael W, Mirzayans, Farideh, Footz, Tim, Huang, Lijia, Birdi, Chanchal, Walter, Michael A

    Published in Molecular vision
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  8. 8
    Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray

    Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray by Ekong, Rosemary, Jeremiah, Steve, Judah, David, Lehmann, Ordan, Mirzayans, Farideh, Hung, Ying-Chun, Walter, Michael A., Bhattacharya, Shomi, Gant, Timothy W., Povey, Sue, Wolfe, Jonathan

    Published in Human mutation
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  9. 9
    Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning

    Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning by Mirzayans, Farideh, Mears, Alan J., Guo, Sun-Wei, Pearce, William G., Walter, Michael A.

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  10. 10
    Purification and Characterization of Amine Oxidase from Pea Seedlings

    Purification and Characterization of Amine Oxidase from Pea Seedlings by Vianello, Fabio, Malek-Mirzayans, Armond, Di Paolo, Maria Luisa, Stevanato, Roberto, Rigo, Adelio

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