| Year |
Citation |
Score |
| 2021 |
Men H, Hankins MA, Bock AS, Beaton BP, Davis DJ, Chesney KL, Bryda EC. Mutational analyses of novel rat models with targeted modifications in inflammatory bowel disease susceptibility genes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 33843019 DOI: 10.1007/s00335-021-09868-2 |
0.308 |
|
| 2021 |
Chesney K, Men H, Hankins MA, Bryda EC. The Atg16l1 gene: characterization of wild type, knock-in, and knock-out phenotypes in rats. Physiological Genomics. PMID 33818130 DOI: 10.1152/physiolgenomics.00114.2020 |
0.313 |
|
| 2020 |
Men H, Stone BJ, Bryda EC. Media optimization to promote rat embryonic development to the blastocyst stage in vitro. Theriogenology. 151: 81-85. PMID 32311604 DOI: 10.1016/J.Theriogenology.2020.03.007 |
0.332 |
|
| 2019 |
Shababi M, Smith CE, Kacher M, Alrawi Z, Villalón E, Davis D, Bryda EC, Lorson CL. Development of a novel severe mouse model of spinal muscular atrophy with respiratory distress type 1: FVB-nmd. Biochemical and Biophysical Research Communications. PMID 31604525 DOI: 10.1016/J.Bbrc.2019.10.032 |
0.367 |
|
| 2019 |
Bryda EC, Men H, Davis DJ, Bock AS, Shaw ML, Chesney KL, Hankins MA. A novel conditional ZsGreen-expressing transgenic reporter rat strain for validating Cre recombinase expression. Scientific Reports. 9: 13330. PMID 31527612 DOI: 10.1038/S41598-019-49783-W |
0.348 |
|
| 2019 |
Bryda EC, LaVail MM. Letter to the editor announcing the availability of RCS and transgenic rats with P23H and S334ter rhodopsin mutations with inherited retinal degenerations. Experimental Eye Research. 178: 176. PMID 30296413 DOI: 10.1016/J.Exer.2018.10.003 |
0.311 |
|
| 2017 |
Shimoyama M, Smith JR, Bryda E, Kuramoto T, Saba L, Dwinell M. Rat Genome and Model Resources. Ilar Journal. 58: 42-58. PMID 28838068 DOI: 10.1093/Ilar/Ilw041 |
0.365 |
|
| 2017 |
Li S, Lan H, Men H, Wu Y, Li N, Capecchi MR, Bryda EC, Wu S. Derivation of Transgene-Free Rat Induced Pluripotent Stem Cells Approximating the Quality of Embryonic Stem Cells. Stem Cells Translational Medicine. 6: 340-351. PMID 28191784 DOI: 10.5966/Sctm.2015-0390 |
0.347 |
|
| 2016 |
Lan H, Li S, Guo Z, Men H, Wu Y, Li N, Bryda EC, Capecchi MR, Wu S. Efficient Generation of Selection-Gene-Free Rat Knockout Models by Homologous Recombination in ES Cells. Febs Letters. PMID 27597178 DOI: 10.1002/1873-3468.12388 |
0.371 |
|
| 2016 |
Hansen SA, Hart ML, Busi S, Parker T, Goerndt A, Jones KB, Amos-Landgraf JM, Bryda EC. Fischer 344-Tp53 knockout rats exhibit a high rate of bone and brain neoplasia with frequent metastasis. Disease Models & Mechanisms. PMID 27528400 DOI: 10.1242/Dmm.025767 |
0.393 |
|
| 2016 |
Hanson MM, Liu F, Dai S, Kearns A, Qin X, Bryda E. A rapid conditional targeted ablation model for hemolytic anemia in the rat. Physiological Genomics. physiolgenomics.0002. PMID 27368711 DOI: 10.1152/Physiolgenomics.00026.2016 |
0.389 |
|
| 2016 |
Feng D, Dai S, Liu F, Ohtake Y, Zhou Z, Wang H, Zhang Y, Kearns A, Peng X, Zhu F, Hayat U, Li M, He Y, Xu M, Zhao C, ... ... Bryda EC, et al. Cre-inducible human CD59 mediates rapid cell ablation after intermedilysin administration. The Journal of Clinical Investigation. PMID 27159394 DOI: 10.1172/Jci84921 |
0.32 |
|
| 2016 |
Amos-Landgraf J, Hansen S, Hart M, Busi S, Jones K, Bryda E. Abstract LB-032: A rat knockout of p53 that exhibits high rates of osteosarcoma and menigial sarcoma with frequent metastasis Cancer Research. 76. DOI: 10.1158/1538-7445.Am2016-Lb-032 |
0.407 |
|
| 2015 |
Ericsson AC, Akter S, Hanson MM, Busi SB, Parker TW, Schehr RJ, Hankins MA, Ahner CE, Davis JW, Franklin CL, Amos-Landgraf JM, Bryda EC. Differential susceptibility to colorectal cancer due to naturally occurring gut microbiota. Oncotarget. 6: 33689-704. PMID 26378041 DOI: 10.18632/Oncotarget.5604 |
0.355 |
|
| 2015 |
Amos-Landgraf J, Busi S, Ericsson A, McCoy M, Parker T, Schehr R, Hankins M, Franklin C, Bryda E. Abstract 2880: Modulating disease susceptibility in a model of human colon cancer by microbiome rederivation Cancer Research. 75: 2880-2880. DOI: 10.1158/1538-7445.Am2015-2880 |
0.319 |
|
| 2014 |
Seiler MJ, Aramant RB, Jones MK, Ferguson DL, Bryda EC, Keirstead HS. A new immunodeficient pigmented retinal degenerate rat strain to study transplantation of human cells without immunosuppression. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv FüR Klinische Und Experimentelle Ophthalmologie. 252: 1079-92. PMID 24817311 DOI: 10.1007/S00417-014-2638-Y |
0.329 |
|
| 2014 |
Mesner LD, Ray B, Hsu YH, Manichaikul A, Lum E, Bryda EC, Rich SS, Rosen CJ, Criqui MH, Allison M, Budoff MJ, Clemens TL, Farber CR. Bicc1 is a genetic determinant of osteoblastogenesis and bone mineral density. The Journal of Clinical Investigation. 124: 2736-49. PMID 24789909 DOI: 10.1172/Jci73072 |
0.312 |
|
| 2014 |
Taskiran EZ, Korkmaz E, Gucer S, Kosukcu C, Kaymaz F, Koyunlar C, Bryda EC, Chaki M, Lu D, Vadnagara K, Candan C, Topaloglu R, Schaefer F, Attanasio M, Bergmann C, et al. Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD. Journal of the American Society of Nephrology : Jasn. 25: 1653-61. PMID 24610927 DOI: 10.1681/Asn.2013060646 |
0.37 |
|
| 2014 |
Bock AS, Leigh ND, Bryda EC. Effect of Gsk3 inhibitor CHIR99021 on aneuploidy levels in rat embryonic stem cells. In Vitro Cellular & Developmental Biology. Animal. 50: 572-9. PMID 24519175 DOI: 10.1007/S11626-014-9734-5 |
0.372 |
|
| 2013 |
McCoy MR, Montonye D, Bryda EC. Electroejaculation of chimeric rats. Lab Animal. 42: 203-5. PMID 23689457 DOI: 10.1038/Laban.301 |
0.355 |
|
| 2013 |
Men H, Bryda EC. Derivation of a germline competent transgenic Fischer 344 embryonic stem cell line. Plos One. 8: e56518. PMID 23437152 DOI: 10.1371/Journal.Pone.0056518 |
0.384 |
|
| 2012 |
Men H, Bauer BA, Bryda EC. Germline transmission of a novel rat embryonic stem cell line derived from transgenic rats. Stem Cells and Development. 21: 2606-12. PMID 22455749 DOI: 10.1089/Scd.2012.0040 |
0.391 |
|
| 2012 |
Bryda EC, Johnson NT, Ohlemiller KK, Besch-Williford CL, Moore E, Bram RJ. Conditional deletion of calcium-modulating cyclophilin ligand causes deafness in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 270-6. PMID 22170629 DOI: 10.1007/S00335-011-9381-Z |
0.307 |
|
| 2011 |
Hillhouse AE, Myles MH, Taylor JF, Bryda EC, Franklin CL. Quantitative trait loci in a bacterially induced model of inflammatory bowel disease. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 544-55. PMID 21717222 DOI: 10.1007/S00335-011-9343-5 |
0.336 |
|
| 2010 |
Bryda EC, Bauer BA. A Restriction Enzyme-PCR-Based Technique to Determine Transgene Insertion Sites Methods of Molecular Biology. 597: 287-299. PMID 20013241 DOI: 10.1007/978-1-60327-389-3_20 |
0.34 |
|
| 2006 |
Bryda EC, Pearson M, Agca Y, Bauer BA. Method for detection and identification of multiple chromosomal integration sites in transgenic animals created with lentivirus Biotechniques. 41: 715-719. PMID 17191616 DOI: 10.2144/000112289 |
0.321 |
|
| 2003 |
Cogswell C, Price SJ, Hou X, Guay-Woodford LM, Flaherty L, Bryda EC. Positional cloning of jcpk/bpk locus of the mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 242-9. PMID 12682776 DOI: 10.1007/S00335-002-2241-0 |
0.343 |
|
| 2002 |
Price SJ, Chittenden LR, Flaherty L, O'Dell B, Guay-Woodford LM, Stubbs L, Bryda EC. Characterization of the region containing the jcpk PKD gene on mouse Chromosome 10. Cytogenetic and Genome Research. 98: 61-6. PMID 12584442 DOI: 10.1159/000068534 |
0.342 |
|
| 2002 |
Chittenden L, Lu X, Cacheiro NLA, Cain KT, Generoso W, Bryda EC, Stubbs LJ. A new mouse model for autosomal recessive polycystic kidney disease. Genomics. 79: 499-504. PMID 11944981 DOI: 10.1006/Geno.2002.6731 |
0.365 |
|
| 2001 |
Bryda EC, Kim HJ, Legare ME, Frankel WN, Noben-Trauth K. High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (Cdh23v) Genomics. 73: 338-342. PMID 11350126 DOI: 10.1006/Geno.2001.6538 |
0.335 |
|
| 2001 |
Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, Steel KP, Noben-Trauth K. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nature Genetics. 27: 103-7. PMID 11138008 DOI: 10.1038/83660 |
0.338 |
|
| 1996 |
Guay-Woodford LM, Bryda EC, Christine B, Lindsey JR, Collier WR, Avner ED, D'Eustachio P, Flaherty L. Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Kidney International. 50: 1158-65. PMID 8887273 DOI: 10.1038/Ki.1996.423 |
0.366 |
|
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