John Parant, Ph.D.
Affiliations: | University of Alabama, Birmingham, Birmingham, AL, United States |
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"John Parant"
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Publications
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| Wang J, Thomas HR, Thompson RG, et al. (2022) Variable phenotypes and penetrance between and within different zebrafish ciliary transition zone mutants. Disease Models & Mechanisms. 15 |
| Bentley-Ford MR, LaBonty M, Thomas HR, et al. (2021) Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes. Genetics |
| Chumley P, Zhou J, Mrug S, et al. (2018) Truncating PKHD1 and PKD2 mutations alter energy metabolism. American Journal of Physiology. Renal Physiology |
| Lewis WR, Malarkey EB, Tritschler D, et al. (2016) Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease. Plos Genetics. 12: e1006220 |
| Parant JM, Yeh JR. (2016) Approaches to Inactivate Genes in Zebrafish. Advances in Experimental Medicine and Biology. 916: 61-86 |
| Percival SM, Thomas HR, Amsterdam A, et al. (2015) Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome. Disease Models & Mechanisms. 8: 941-55 |
| Crittenden F, Thomas HR, Parant JM, et al. (2015) Activity Suppression Behavior Phenotype in SULT4A1 Frameshift Mutant Zebrafish. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 43: 1037-44 |
| Thomas HR, Percival SM, Yoder BK, et al. (2014) High-throughput genome editing and phenotyping facilitated by high resolution melting curve analysis. Plos One. 9: e114632 |
| Parant JM, George SA, Holden JA, et al. (2010) Genetic modeling of Li-Fraumeni syndrome in zebrafish. Disease Models & Mechanisms. 3: 45-56 |
| Parant JM, George SA, Pryor R, et al. (2009) A rapid and efficient method of genotyping zebrafish mutants. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 3168-74 |