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James Resnick - Publications

Affiliations: 
University of Florida, Gainesville, Gainesville, FL, United States 
Area:
Genetics, Molecular Biology
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22 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
2018 Lewis MW, Vargas-Franco D, Morse DA, Resnick JL. A mouse model of angelman syndrome imprinting defects. Human Molecular Genetics. PMID 30260400 DOI: 10.1093/hmg/ddy345  0.617
2018 Coulson RL, Powell WT, Yasui DH, Dileep G, Resnick J, LaSalle JM. Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN. Human Molecular Genetics. PMID 30124848 DOI: 10.1093/Hmg/Ddy296  0.367
2016 Golding DM, Rees DJ, Davies JR, Relkovic D, Furby HV, Guschina IA, Hopkins AL, Davies JS, Resnick JL, Isles AR, Wells T. Paradoxical leanness in the imprinting centre deletion mouse model for Prader-Willi syndrome. The Journal of Endocrinology. PMID 27799465 DOI: 10.1530/Joe-16-0367  0.496
2015 Lewis MW, Brant JO, Kramer JM, Moss JI, Yang TP, Hansen PJ, Williams RS, Resnick JL. Angelman syndrome imprinting center encodes a transcriptional promoter. Proceedings of the National Academy of Sciences of the United States of America. 112: 6871-5. PMID 25378697 DOI: 10.1073/pnas.1411261111  0.466
2015 Lim CH, Brower JV, Resnick JL, Oh SP, Terada N. Adenine nucleotide translocase 4 is expressed within embryonic ovaries and dispensable during oogenesis. Reproductive Sciences (Thousand Oaks, Calif.). 22: 250-7. PMID 25031318 DOI: 10.1177/1933719114542026  0.319
2014 Brant JO, Riva A, Resnick JL, Yang TP. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain. Epigenetics : Official Journal of the Dna Methylation Society. 9: 1540-56. PMID 25482058 DOI: 10.4161/15592294.2014.969667  0.562
2013 Yazdi PG, Su H, Ghimbovschi S, Fan W, Coskun PE, Nalbandian A, Knoblach S, Resnick JL, Hoffman E, Wallace DC, Kimonis VE. Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome. Clinical and Translational Science. 6: 347-55. PMID 24127921 DOI: 10.1111/Cts.12083  0.335
2013 Resnick JL, Nicholls RD, Wevrick R. Recommendations for the investigation of animal models of Prader-Willi syndrome. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 165-78. PMID 23609791 DOI: 10.1007/s00335-013-9454-2  0.31
2013 Rodriguez-Jato S, Shan J, Khadake J, Heggestad AD, Ma X, Johnstone KA, Resnick JL, Yang TP. Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain. Plos One. 8: e52390. PMID 23390487 DOI: 10.1371/journal.pone.0052390  0.608
2012 DuBose AJ, Smith EY, Johnstone KA, Resnick JL. Temporal and developmental requirements for the Prader-Willi imprinting center. Proceedings of the National Academy of Sciences of the United States of America. 109: 3446-50. PMID 22331910 DOI: 10.1073/Pnas.1115057109  0.831
2011 Smith EY, Futtner CR, Chamberlain SJ, Johnstone KA, Resnick JL. Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus. Plos Genetics. 7: e1002422. PMID 22242001 DOI: 10.1371/Journal.Pgen.1002422  0.823
2011 Dubose AJ, Smith EY, Yang TP, Johnstone KA, Resnick JL. A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center. Human Molecular Genetics. 20: 3461-6. PMID 21659337 DOI: 10.1093/Hmg/Ddr262  0.844
2010 Relkovic D, Doe CM, Humby T, Johnstone KA, Resnick JL, Holland AJ, Hagan JJ, Wilkinson LS, Isles AR. Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome. The European Journal of Neuroscience. 31: 156-64. PMID 20092561 DOI: 10.1111/j.1460-9568.2009.07048.x  0.471
2010 DuBose AJ, Johnstone KA, Smith EY, Hallett RA, Resnick JL. Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC. Neurogenetics. 11: 145-51. PMID 19894069 DOI: 10.1007/S10048-009-0226-9  0.802
2009 Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM. Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. Human Molecular Genetics. 18: 4227-38. PMID 19656775 DOI: 10.1093/Hmg/Ddp373  0.783
2008 Smith EY, Resnick J. The Roles of E2F6 and DNA Methylation in the Regulation of Gene Expression During Germ Cell Development. Biology of Reproduction. 78: 135-135. DOI: 10.1093/Biolreprod/78.S1.135C  0.447
2007 Peery EG, Elmore MD, Resnick JL, Brannan CI, Johnstone KA. A targeted deletion upstream of Snrpn does not result in an imprinting defect. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 255-62. PMID 17514346 DOI: 10.1007/S00335-007-9019-3  0.754
2006 Maatouk DM, Kellam LD, Mann MR, Lei H, Li E, Bartolomei MS, Resnick JL. DNA methylation is a primary mechanism for silencing postmigratory primordial germ cell genes in both germ cell and somatic cell lineages. Development (Cambridge, England). 133: 3411-8. PMID 16887828 DOI: 10.1242/Dev.02500  0.745
2006 Johnstone KA, DuBose AJ, Futtner CR, Elmore MD, Brannan CI, Resnick JL. A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. Human Molecular Genetics. 15: 393-404. PMID 16368707 DOI: 10.1093/Hmg/Ddi456  0.786
2005 Rodić N, Oka M, Hamazaki T, Murawski MR, Jorgensen M, Maatouk DM, Resnick JL, Li E, Terada N. DNA methylation is required for silencing of ant4, an adenine nucleotide translocase selectively expressed in mouse embryonic stem cells and germ cells. Stem Cells (Dayton, Ohio). 23: 1314-23. PMID 16051982 DOI: 10.1634/Stemcells.2005-0119  0.726
2004 Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI. Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. Human Molecular Genetics. 13: 2971-7. PMID 15459179 DOI: 10.1093/Hmg/Ddh314  0.776
2003 Maatouk DM, Resnick JL. Continuing primordial germ cell differentiation in the mouse embryo is a cell-intrinsic program sensitive to DNA methylation. Developmental Biology. 258: 201-8. PMID 12781693  0.69
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