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Catherine Spellicy

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Catherine J Spellicy; Sara C Hamon; Mark J Harding; Thomas R Kosten; David A Nielsen
The MTHFR C677T Variant is Associated with Responsiveness to Disulfiram Treatment for Cocaine Dependency.
Catherine J Spellicy; Paul T Cirino; Maureen Dennis; Jack M Fletcher; Carla A Martinez; Alanna C Morrison; Hope Northrup; Kit-Sing Au
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.
Catherine J Spellicy; Dong Xu; Garrett Cobb; Lizbeth Hedstrom; Sara J Bowne; Lori S Sullivan; Stephen P Daiger
Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

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2012: Catherine J Spellicy; Sara C Hamon; Mark J Harding; Thomas R Kosten; David A Nielsen
The MTHFR C677T Variant is Associated with Responsiveness to Disulfiram Treatment for Cocaine Dependency.
Frontiers in psychiatry / Frontiers Research Foundation 2012;3():109.
2012: Catherine J Spellicy; Paul T Cirino; Maureen Dennis; Jack M Fletcher; Carla A Martinez; Alanna C Morrison; Hope Northrup; Kit-Sing Au
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.
PloS one 2012;7(12):e51330.
2010: Catherine J Spellicy; Dong Xu; Garrett Cobb; Lizbeth Hedstrom; Sara J Bowne; Lori S Sullivan; Stephen P Daiger
Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.
Advances in experimental medicine and biology 2010;664():541-8.
2008: Dong Xu; Garrett Cobb; Catherine J Spellicy; Sara J Bowne; Stephen P Daiger; Lizbeth Hedstrom
Retinal isoforms of inosine 5'-monophosphate dehydrogenase type 1 are poor nucleic acid binding proteins.
Archives of biochemistry and biophysics 2008;472(2):100-4.
2007: Catherine J Spellicy; Stephen P Daiger; Lori S Sullivan; Jingya Zhu; Qin Liu; Eric A Pierce; Sara J Bowne
Characterization of retinal inosine monophosphate dehydrogenase 1 in several mammalian species.
Molecular vision 2007;13():1866-72.
2006: Sara J Bowne; Qin Liu; Lori S Sullivan; Jingya Zhu; Catherine J Spellicy; Catherine Bowes Rickman; Eric A Pierce; Stephen P Daiger
Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration?
Investigative ophthalmology & visual science 2006;47(9):3754-65.
2006: Lori S Sullivan; Sara J Bowne; David G Birch; Dianna Hughbanks-Wheaton; John R Heckenlively; Richard Alan Lewis; Charles A Garcia; Richard S Ruiz; S Blanton; Hope Northrup; Anisa I Gire; Robyn Seaman; Hatice Duzkale; Catherine J Spellicy; Jingya Zhu; Suma Shankar; Stephen P Daiger
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.
Investigative ophthalmology & visual science 2006;47(7):3052-64.
2006: Sara J Bowne; Lori S Sullivan; Sarah E Mortimer; Lizbeth Hedstrom; Jingya Zhu; Catherine J Spellicy; Anisa I Gire; Dianna Hughbanks-Wheaton; David G Birch; Richard A Lewis; John R Heckenlively; Stephen P Daiger
Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.
Investigative ophthalmology & visual science 2006;47(1):34-42.
2005: Petra Kozma; Dianna Hughbanks-Wheaton; Kirsten G Locke; Gary E Fish; Anisa I Gire; Catherine J Spellicy; Lori S Sullivan; Sara J Bowne; Stephen P Daiger; David G Birch
Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene.
American journal of ophthalmology 2005;140(5):858-867.