Search Results - "Berry, F B"

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  1. 1

    Aircraft and road traffic noise and children's cognition and health: a cross-national study by Stansfeld, SA, Berglund, B, Clark, C, Lopez-Barrio, I, Fischer, P, Öhrström, E, Haines, MM, Head, J, Hygge, S, van Kamp, I, Berry, BF

    Published in The Lancet (British edition) (2005)
    “…Exposure to environmental stressors can impair children's health and their cognitive development. The effects of air pollution, lead, and chemicals have been…”
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    Journal Article
  2. 2

    Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1 by Saleem, Ramsey A., Banerjee-Basu, Sharmila, Berry, Fred B., Baxevanis, Andreas D., Walter, Michael A.

    Published in American journal of human genetics (01-03-2001)
    “…Five missense mutations of the winged-helix FOXC1 transcription factor, found in patients with Axenfeld-Rieger (AR) malformations, were investigated for their…”
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    Journal Article
  3. 3

    BRCA1 and GATA3 corepress FOXC1 to inhibit the pathogenesis of basal-like breast cancers by Tkocz, D, Crawford, N T, Buckley, N E, Berry, F B, Kennedy, R D, Gorski, J J, Harkin, D P, Mullan, P B

    Published in Oncogene (09-08-2012)
    “…In this study we describe a novel interaction between the breast/ovarian tumor suppressor gene BRCA1 and the transcription factor GATA3, an interaction, which…”
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    Journal Article
  4. 4

    CaM I mRNA is localized to apical dendrites during postnatal development of neurons in the rat brain by Berry, F.B., Brown, I.R.

    Published in Journal of neuroscience research (01-03-1996)
    “…In the rat, a single calmodulin (CaM) protein is encoded by three separate genes which produce five different transcripts. The significance of the multiple CaM…”
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    Journal Article
  5. 5

    Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1 by Saleem, Ramsey A., Banerjee-Basu, Sharmila, Berry, Fred B., Baxevanis, Andreas D., Walter, Michael A.

    Published in Human molecular genetics (15-11-2003)
    “…Five missense mutations (P79L, P79T, I91S, I91T and R127H) within the forkhead DNA-binding domain of the FOXC1 transcription factor, identified in patients…”
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  6. 6

    FOXC1 Transcriptional Regulation Is Mediated by N- and C-terminal Activation Domains and Contains a Phosphorylated Transcriptional Inhibitory Domain by Berry, Fred B., Saleem, Ramsey A., Walter, Michael A.

    Published in The Journal of biological chemistry (22-03-2002)
    “…Mutations in the FOXC1 gene result in Axenfeld-Rieger malformations of the anterior segment of the eye and lead to an increased susceptibility of glaucoma. To…”
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    Journal Article
  7. 7

    Positive and Negative Regulation of Myogenic Differentiation of C2C12 Cells by Isoforms of the Multiple Homeodomain Zinc Finger Transcription Factor ATBF1 by Berry, F B, Miura, Y, Mihara, K, Kaspar, P, Sakata, N, Hashimoto-Tamaoki, T, Tamaoki, T

    Published in The Journal of biological chemistry (06-07-2001)
    “…The ATBF1 gene encodes two protein isoforms, the 404-kDa ATBF1-A, possessing four homeodomains and 23 zinc fingers, and the 306-kDa ATBF1-B, lacking a…”
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    Journal Article
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