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	1.	Autosomal dominant retinitis pigmentosa mutations in inosine 5'-monophosphate dehydrogenase type I disrupt nucleic acid binding. [electronic resource] by Mortimer, Sarah E Hedstrom, Lizbeth Producer: 20051107 In: The Biochemical journal vol. 390 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Inosine 5'-monophosphate dehydrogenase binds nucleic acids in vitro and in vivo. [electronic resource] by McLean, Jeremy E Hamaguchi, Nobuko Belenky, Peter Mortimer, Sarah E Stanton, Martin Hedstrom, Lizbeth Producer: 20040722 In: The Biochemical journal vol. 379 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mapping the HLA-DO/HLA-DM complex by FRET and mutagenesis. [electronic resource] by Yoon, Taejin Macmillan, Henriette Mortimer, Sarah E Jiang, Wei Rinderknecht, Cornelia H Stern, Lawrence J Mellins, Elizabeth D Producer: 20121005 In: Proceedings of the National Academy of Sciences of the United States of America vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	HLA-DO acts as a substrate mimic to inhibit HLA-DM by a competitive mechanism. [electronic resource] by Guce, Abigail I Mortimer, Sarah E Yoon, Taejin Painter, Corrie A Jiang, Wei Mellins, Elizabeth D Stern, Lawrence J Producer: 20130225 In: Nature structural & molecular biology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	IMP dehydrogenase type 1 associates with polyribosomes translating rhodopsin mRNA. [electronic resource] by Mortimer, Sarah E Xu, Dong McGrew, Dharia Hamaguchi, Nobuko Lim, Hoong Chuin Bowne, Sara J Daiger, Stephen P Hedstrom, Lizbeth Producer: 20090313 In: The Journal of biological chemistry vol. 283 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis. [electronic resource] by Bowne, Sara J Sullivan, Lori S Mortimer, Sarah E Hedstrom, Lizbeth Zhu, Jingya Spellicy, Catherine J Gire, Anisa I Hughbanks-Wheaton, Dianna Birch, David G Lewis, Richard A Heckenlively, John R Daiger, Stephen P Producer: 20060209 In: Investigative ophthalmology & visual science vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)