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Laura A. Krueger - Publications

Affiliations: 
University of Kentucky, Lexington, KY 
Area:
Experimental Eye Research
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Krueger LA, Bills JD, Lim ZY, Skidmore JM, Martin DM, Morris AC. Chromatin remodeler Chd7 regulates photoreceptor development and outer segment length. Experimental Eye Research. 109299. PMID 36343670 DOI: 10.1016/j.exer.2022.109299  0.598
2022 Krueger LA, Morris AC. Eyes on CHARGE syndrome: Roles of CHD7 in ocular development. Frontiers in Cell and Developmental Biology. 10: 994412. PMID 36172288 DOI: 10.3389/fcell.2022.994412  0.547
2022 Krueger LA, Morris AC. Generation of a zebrafish knock-in line expressing MYC-tagged Sox11a using CRISPR/Cas9 genome editing. Biochemical and Biophysical Research Communications. 608: 8-13. PMID 35378361 DOI: 10.1016/j.bbrc.2022.03.103  0.455
2020 Coomer CE, Wilson SG, Titialii-Torres KF, Bills JD, Krueger LA, Petersen RA, Turnbaugh EM, Janesch EL, Morris AC. Author Correction: Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survival. Scientific Reports. 10: 14843. PMID 32884063 DOI: 10.1038/S41598-020-72314-X  0.555
2020 Coomer CE, Wilson SG, Titialii-Torres KF, Bills JD, Krueger LA, Petersen RA, Turnbaugh EM, Janesch EL, Morris AC. Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survival. Scientific Reports. 10: 11316. PMID 32647335 DOI: 10.1038/S41598-020-68172-2  0.595
2015 Hufnagel RB, Arno G, Hein ND, Hersheson J, Prasad M, Anderson Y, Krueger LA, Gregory LC, Stoetzel C, Jaworek TJ, Hull S, Li A, Plagnol V, Willen CM, Morgan TM, et al. Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. Journal of Medical Genetics. 52: 85-94. PMID 25480986 DOI: 10.1136/Jmedgenet-2014-102856  0.326
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