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A crystallin gene network in the mouse retina.
Templeton JP, Wang X, Freeman NE, Ma Z, Lu A, Hejtmancik F, Geisert EE. Templeton JP, et al. Among authors: hejtmancik f. Exp Eye Res. 2013 Nov;116:129-40. doi: 10.1016/j.exer.2013.08.001. Epub 2013 Aug 24. Exp Eye Res. 2013. PMID: 23978599 Free PMC article.
Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry.
Liu Y, Hauser MA, Akafo SK, Qin X, Miura S, Gibson JR, Wheeler J, Gaasterland DE, Challa P, Herndon LW; International Consortium of African Ancestry REsearch in Glaucoma; Ritch R, Moroi SE, Pasquale LR, Girkin CA, Budenz DL, Wiggs JL, Richards JE, Ashley-Koch AE, Allingham RR. Liu Y, et al. Invest Ophthalmol Vis Sci. 2013 Sep 17;54(9):6248-54. doi: 10.1167/iovs.13-12779. Invest Ophthalmol Vis Sci. 2013. PMID: 23963167 Free PMC article.
A Spontaneous Missense Mutation in Branched Chain Keto Acid Dehydrogenase Kinase in the Rat Affects Both the Central and Peripheral Nervous Systems.
Zigler JS Jr, Hodgkinson CA, Wright M, Klise A, Sundin O, Broman KW, Hejtmancik F, Huang H, Patek B, Sergeev Y, Hose S, Brayton C, Xaiodong J, Vasquez D, Maragakis N, Mori S, Goldman D, Hoke A, Sinha D. Zigler JS Jr, et al. Among authors: hejtmancik f. PLoS One. 2016 Jul 29;11(7):e0160447. doi: 10.1371/journal.pone.0160447. eCollection 2016. PLoS One. 2016. PMID: 27472223 Free PMC article.
Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24.
Lin BR, Le DJ, Chen Y, Wang Q, Chung DD, Frausto RF, Croasdale C, Yee RW, Hejtmancik FJ, Aldave AJ. Lin BR, et al. Among authors: hejtmancik fj. PLoS One. 2016 Jun 16;11(6):e0157418. doi: 10.1371/journal.pone.0157418. eCollection 2016. PLoS One. 2016. PMID: 27309958 Free PMC article.
12 results