Search Results - "Nummy, K A"

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  1. 1

    Depressive symptoms in mid‐pregnancy, lifetime stressors and the 5‐HTTLPR genotype by Scheid, J. M., Holzman, C. B., Jones, N., Friderici, K. H., Nummy, K. A., Symonds, L. L., Sikorskii, A., Regier, M. K., Fisher, R.

    Published in Genes, brain and behavior (01-07-2007)
    “…Few studies of gene–environment interactions for the serotonin transporter promoter polymorphism (5‐HTTLPR), life stressors and depression have considered…”
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    Journal Article
  2. 2

    Characterization of a chromosomally encoded 2,4-dichlorophenoxyacetic acid/alpha-ketoglutarate dioxygenase from Burkholderia sp. strain RASC by SUWA, Y, WRIGHT, A. D, FUKIMORI, F, NUMMY, K. A, HAUSINGER, R. P, HOLBEN, W. E, FORNEY, L. J

    Published in Applied and Environmental Microbiology (01-07-1996)
    “…The findings of previous studies indicate that the genes required for metabolism of the pesticide 2,4-dichlorophenoxyacetic acid (2,4-D) are typically encoded…”
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  3. 3

    Association and linkage of α-2A adrenergic receptor gene polymorphisms with childhood ADHD by PARK, L, NIGG, J. T, WALDMAN, I. D, MUMMY, K. A, HUANG-POLLOCK, C, RAPPLEY, M, FRIDERICI, K. H

    Published in Molecular psychiatry (01-06-2005)
    “…Attention-deficit hyperactivity disorder (ADHD) is a heritable disorder, prevalent from childhood through adulthood. Although the noradrenergic (NA) system is…”
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    Journal Article
  4. 4

    The ontogeny and cellular distribution of estrogen receptors in normal mouse mammary gland by Haslam, S Z, Nummy, K A

    “…The appearance, epithelial and stromal cell distribution of estrogen receptors (ER) in normal mouse mammary gland were determined between 1 and 10 weeks of age…”
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  5. 5

    Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD by Park, L, Nigg, J T, Waldman, I D, Nummy, K A, Huang-Pollock, C, Rappley, M, Friderici, K H

    Published in Molecular psychiatry (01-06-2005)
    “…Attention-deficit hyperactivity disorder (ADHD) is a heritable disorder, prevalent from childhood through adulthood. Although the noradrenergic (NA) system is…”
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    Journal Article
  6. 6

    EGF receptor regulation in normal mouse mammary gland by Haslam, S Z, Counterman, L J, Nummy, K A

    Published in Journal of cellular physiology (01-09-1992)
    “…Estrogen (E), progesterone (P), and epidermal growth factor (EGF) are known to regulate growth and development of the normal mammary gland, and it is possible…”
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  7. 7

    Effects of epidermal growth factor, estrogen, and progestin on DNA synthesis in mammary cells in vivo are determined by the developmental state of the gland by Haslam, S Z, Counterman, L J, Nummy, K A

    Published in Journal of cellular physiology (01-04-1993)
    “…Estrogen (E), progesterone (P), and epidermal growth factor (EGF) are involved in the growth and development of the normal mammary gland. While studies have…”
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  8. 8

    Association and linkage of -2A adrenergic receptor gene polymorphisms with childhood ADHD by Park, L, Nigg, J T, Waldman, I D, Nummy, K A, Huang-Pollock, C, Rappley, M, Friderici, K H

    Published in Molecular psychiatry (01-06-2005)
    “…Attention-deficit hyperactivity disorder (ADHD) is a heritable disorder, prevalent from childhood through adulthood. Although the noradrenergic (NA) system is…”
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    Journal Article
  9. 9

    Asexual transmission, non-suppressiveness and meiotic extinction of small plasmid-like derivatives of the mitochondrial DNA in Neurospora crassa by Hausner, Georg, Nummy, Katherine A., Bertrand, Helmut

    Published in Fungal genetics and biology (01-02-2006)
    “…For reasons that are not obvious, sets of related plasmid-like elements that consist of short segments of DNA that overlap the 5′ terminal region of the…”
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  10. 10

    Biogenesis and replication of small plasmid-like derivatives of the mitochondrial DNA in Neurospora crassa by Hausner, Georg, Nummy, Katherine A., Stoltzner, Sarah, Hubert, Susannah K., Bertrand, Helmut

    Published in Fungal genetics and biology (01-02-2006)
    “…For reasons that are not obvious, sets of related, small, plasmid-like elements appear spontaneously and become amplified in the mitochondria of some…”
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    Journal Article
  11. 11

    Variable clinical presentation of lysosomal β-mannosidosis in patients with null mutations by Bedilu, Rebecca, Nummy, Katherine A, Cooper, Alan, Wevers, Ron, Smeitink, Jan, Kleijer, Wim J, Friderici, Karen H

    Published in Molecular genetics and metabolism (01-12-2002)
    “…β-Mannosidosis is an autosomal recessive lysosomal storage disease resulting from a deficiency of the lysosomal enzyme β-mannosidase. The clinical…”
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    Journal Article