Search Results - "Ogilvie, Judith M"
-
1
Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B
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…”
Get full text
Journal Article -
2
Inhibition of Caspases Prevents Ototoxic and Ongoing Hair Cell Death
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…”
Get full text
Journal Article -
3
Retinal Degeneration: Short-Term Options and Long-Term Vision for Future Therapy
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…”
Get full text
Journal Article -
4
Wide‐field amacrine cell inputs to ON parasol ganglion cells in macaque retina
Published in Journal of comparative neurology (1911) (15-06-2020)“…Parasol cells are one of the major types of primate retinal ganglion cells. The goal of this study was to describe the synaptic inputs that shape the light…”
Get full text
Journal Article -
5
PROJECT DiViNe: DIVERSE VOICES IN NEUROSCIENCE: Profiles of Rita Levi-Montalcini, Ricardo Miledi, Simon LeVay, Erich Jarvis, and Steve Ramirez
Published in Journal of undergraduate neuroscience education (2022)“…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…”
Get full text
Journal Article -
6
Inhibition of dopamine signaling suppresses cGMP accumulation in rd1 retinal organ cultures
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…”
Get full text
Journal Article -
7
AAV2-mediated Ocular Gene Therapy for Infantile Neuronal Ceroid Lipofuscinosis
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…”
Get full text
Journal Article -
8
Cover Image, Volume 528, Issue 9
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…”
Get full text
Journal Article