Jessica Gardner, Ph.D

Affiliations: 
Pharmacology & Experimental Neuroscience University of Nebraska Medical Center, Omaha, NE, United States 
Area:
neuroinflammation, astrocytes, glia
Website:
http://www.unmc.edu/research_editorial.htm
Google:
"Jessica Gardner"
Mean distance: 21.75 (cluster 52)
 
SNBCP
Cross-listing: Chemistry Tree

Parents

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Anuja Ghorpade grad student 2002-2007 University of Nebraska Medical Center
 (TIMP-1 regulation in astrocytes: Implications for HIV-1-associated dementia.)
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Publications

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Gardner JC, Michaelides M, Hardcastle AJ. (2016) Cone opsins, colour blindness and cone dystrophy: Genotype-phenotype correlations South African Medical Journal. 106: S75-S78
Gardner JC, Liew G, Quan YH, et al. (2014) Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants. Human Mutation. 35: 1354-62
Davidson AE, Cheong SS, Hysi PG, et al. (2014) Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness. Plos One. 9: e104163
Cideciyan AV, Hufnagel RB, Carroll J, et al. (2013) Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy. Human Gene Therapy. 24: 993-1006
Karampelas M, Gardner J, Holder G, et al. (2013) Retinal dysfunction and high myopia in association with 48,XXYY syndrome. Documenta Ophthalmologica. Advances in Ophthalmology. 127: 245-7
Carroll J, Dubra A, Gardner JC, et al. (2012) The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic. Investigative Ophthalmology & Visual Science. 53: 8006-15
Webb TR, Parfitt DA, Gardner JC, et al. (2012) Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23). Human Molecular Genetics. 21: 3647-54
Webb TR, Matarin M, Gardner JC, et al. (2012) X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development. American Journal of Human Genetics. 90: 247-59
Gardner JC, Webb TR, Kanuga N, et al. (2012) A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5). Advances in Experimental Medicine and Biology. 723: 595-601
Slee M, Finkemeyer J, Krupa M, et al. (2011) A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 18: 1318-24
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