Search Results - "Ogilvie, Judith M"

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  1. 1

    Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B by Heldermon, Coy D, Hennig, Anne K, Ohlemiller, Kevin K, Ogilvie, Judith M, Herzog, Erik D, Breidenbach, Annalisa, Vogler, Carole, Wozniak, David F, Sands, Mark S

    Published in PloS one (22-08-2007)
    “…Mucopolysaccharidosis (MPS) IIIB (Sanfilippo Syndrome type B) is caused by a deficiency in the lysosomal enzyme N-acetyl-glucosaminidase (Naglu). Children with…”
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    Journal Article
  2. 2

    Inhibition of Caspases Prevents Ototoxic and Ongoing Hair Cell Death by Matsui, Jonathan I, Ogilvie, Judith M, Warchol, Mark E

    Published in The Journal of neuroscience (15-02-2002)
    “…Sensory hair cells die after acoustic trauma or ototoxic insults, but the signal transduction pathways that mediate hair cell death are not known. Here we…”
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  3. 3

    Retinal Degeneration: Short-Term Options and Long-Term Vision for Future Therapy by Majidi, Shabnam, Ogilvie, Judith M, Flaveny, Colin A

    Published in Missouri medicine (01-09-2021)
    “…The leading cause blindness is the loss of retinal ganglion cells which connect the retina to the brain. Degenerative retinal diseases include retinal…”
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  4. 4
  5. 5

    PROJECT DiViNe: DIVERSE VOICES IN NEUROSCIENCE: Profiles of Rita Levi-Montalcini, Ricardo Miledi, Simon LeVay, Erich Jarvis, and Steve Ramirez by Frenzel, Kristen E, Grisham, William, Ogilvie, Judith M, Harrington, Ian A

    “…In this paper we share the first five of what we hope will be many profiles of neuroscientists from historically underrepresented or marginalized groups. This…”
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  6. 6

    Inhibition of dopamine signaling suppresses cGMP accumulation in rd1 retinal organ cultures by Zhang, Ju, Richmond, Angela M, Ogilvie, Judith M

    Published in Neuroreport (28-05-2014)
    “…The rd1 mouse is a model of retinitis pigmentosa, an inherited photoreceptor neurodegenerative disease. In rd1 retina, early onset rod degeneration is caused…”
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  7. 7

    AAV2-mediated Ocular Gene Therapy for Infantile Neuronal Ceroid Lipofuscinosis by Griffey, Megan, Macauley, Shannon L, Ogilvie, Judith M, Sands, Mark S

    Published in Molecular therapy (01-09-2005)
    “…Infantile neuronal ceroid lipofuscinosis (INCL) is a neurodegenerative disorder caused by mutations in the gene encoding the lysosomal enzyme palmitoyl protein…”
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  8. 8

    Cover Image, Volume 528, Issue 9 by Patterson, Sara S., Bordt, Andrea S., Girresch, Rebecca J., Linehan, Conor M., Bauss, Jacob, Yeo, Eunice, Perez, Diego, Tseng, Luke, Navuluri, Sriram, Harris, Nicole B., Matthews, Chaiss, Anderson, James R., Kuchenbecker, James A., Manookin, Michael B., Ogilvie, Judith M., Neitz, Jay, Marshak, David W.

    Published in Journal of comparative neurology (1911) (15-06-2020)
    “…The cover image is based on the Original Article Wide‐field amacrine cell inputs to ON parasol ganglion cells in macaque retina by DAVID W. MARSHAK, Sara…”
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