| Year |
Citation |
Score |
| 2020 |
Plummer NW, Chandler DJ, Powell JM, Scappini EL, Waterhouse BD, Jensen P. An intersectional viral-genetic method for fluorescent tracing of axon collaterals reveals details of noradrenergic locus coeruleus structure. Eneuro. PMID 32354756 DOI: 10.1523/ENEURO.0010-20.2020 |
0.551 |
|
| 2020 |
Tillage RP, Sciolino NR, Plummer NW, Lustberg D, Liles LC, Hsiang M, Powell JM, Smith KG, Jensen P, Weinshenker D. Elimination of galanin synthesis in noradrenergic neurons reduces galanin in select brain areas and promotes active coping behaviors. Brain Structure & Function. PMID 32065256 DOI: 10.1007/S00429-020-02035-4 |
0.589 |
|
| 2019 |
Chen YW, Das M, Oyarzabal EA, Cheng Q, Plummer NW, Smith KG, Jones GK, Malawsky D, Yakel JL, Shih YI, Jensen P. A subset of noradrenergic (NE) neurons defined by developmental expression of Hoxb1 have a distinct role in attenuating the behavioral response to acute stress. Molecular Psychiatry. 24: 625. PMID 31019268 DOI: 10.1038/S41380-019-0418-0 |
0.55 |
|
| 2019 |
Whissell PD, Bang JY, Khan I, Xie YF, Parfitt GM, Grenon M, Plummer NW, Jensen P, Bonin RP, Kim JC. Selective Activation of Cholecystokinin-Expressing GABA (CCK-GABA) Neurons Enhances Memory and Cognition. Eneuro. 6. PMID 30834305 DOI: 10.1523/ENEURO.0360-18.2019 |
0.538 |
|
| 2018 |
Powell JM, Plummer NW, Scappini EL, Tucker CJ, Jensen P. DEFiNE: A Method for Enhancement and Quantification of Fluorescently Labeled Axons. Frontiers in Neuroanatomy. 12: 117. PMID 30687025 DOI: 10.3389/Fnana.2018.00117 |
0.497 |
|
| 2018 |
Alexander GM, Brown LY, Farris S, Lustberg D, Pantazis C, Gloss B, Plummer NW, Jensen P, Dudek SM. CA2 neuronal activity controls hippocampal low gamma and ripple oscillations. Elife. 7. PMID 30387713 DOI: 10.7554/Elife.38052 |
0.532 |
|
| 2018 |
Chen YW, Das M, Oyarzabal EA, Cheng Q, Plummer NW, Smith KG, Jones GK, Malawsky D, Yakel JL, Shih YI, Jensen P. Genetic identification of a population of noradrenergic neurons implicated in attenuation of stress-related responses. Molecular Psychiatry. PMID 30214043 DOI: 10.1038/S41380-018-0245-8 |
0.574 |
|
| 2018 |
Alexander GM, Brown LY, Farris S, Lustberg D, Pantazis C, Gloss B, Plummer NW, Jensen P, Dudek SM. Author response: CA2 neuronal activity controls hippocampal low gamma and ripple oscillations Elife. DOI: 10.7554/Elife.38052.033 |
0.535 |
|
| 2017 |
Plummer NW, Ungewitter EK, Smith KG, Yao HH, Jensen P. A new mouse line for cell ablation by diphtheria toxin subunit A controlled by a Cre-dependent FLEx switch. Genesis (New York, N.Y. : 2000). PMID 28875587 DOI: 10.1002/Dvg.23067 |
0.569 |
|
| 2017 |
Plummer NW, Scappini EL, Smith KG, Tucker CJ, Jensen P. Two Subpopulations of Noradrenergic Neurons in the Locus Coeruleus Complex Distinguished by Expression of the Dorsal Neural Tube Marker Pax7. Frontiers in Neuroanatomy. 11: 60. PMID 28775681 DOI: 10.3389/Fnana.2017.00060 |
0.589 |
|
| 2016 |
Plummer NW, de Marchena J, Jensen P. A knock-in allele of En1 expressing Dre recombinase. Genesis (New York, N.Y. : 2000). PMID 27313055 DOI: 10.1002/Dvg.22954 |
0.587 |
|
| 2016 |
Sciolino NR, Plummer NW, Chen YW, Alexander GM, Robertson SD, Dudek SM, McElligott ZA, Jensen P. Recombinase-Dependent Mouse Lines for Chemogenetic Activation of Genetically Defined Cell Types. Cell Reports. PMID 27264177 DOI: 10.1016/J.Celrep.2016.05.034 |
0.612 |
|
| 2015 |
Robertson SD, Plummer NW, Jensen P. Uncovering diversity in the development of central noradrenergic neurons and their efferents. Brain Research. PMID 26612521 DOI: 10.1016/J.Brainres.2015.11.023 |
0.618 |
|
| 2015 |
Plummer NW, Evsyukova IY, Robertson SD, de Marchena J, Tucker CJ, Jensen P. Expanding the power of recombinase-based labeling to uncover cellular diversity. Development (Cambridge, England). PMID 26586220 DOI: 10.1242/Dev.129981 |
0.595 |
|
| 2013 |
Robertson SD, Plummer NW, de Marchena J, Jensen P. Developmental origins of central norepinephrine neuron diversity. Nature Neuroscience. 16: 1016-23. PMID 23852112 DOI: 10.1038/Nn.3458 |
0.588 |
|
| 2006 |
Plummer NW, Squire TL, Srinivasan S, Huang E, Zawistowski JS, Matsunami H, Hale LP, Marchuk DA. Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 119-28. PMID 16465592 DOI: 10.1007/S00335-005-0098-8 |
0.748 |
|
| 2005 |
Plummer NW, Zawistowski JS, Marchuk DA. Genetics of cerebral cavernous malformations. Current Neurology and Neuroscience Reports. 5: 391-6. PMID 16131422 DOI: 10.1007/S11910-005-0063-7 |
0.738 |
|
| 2004 |
Meisler MH, Plummer NW, Burgess DL, Buchner DA, Sprunger LK. Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions. Genetica. 122: 37-45. PMID 15619959 DOI: 10.1007/S10709-004-1441-9 |
0.782 |
|
| 2004 |
Plummer NW, Gallione CJ, Srinivasan S, Zawistowski JS, Louis DN, Marchuk DA. Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations. The American Journal of Pathology. 165: 1509-18. PMID 15509522 DOI: 10.1016/S0002-9440(10)63409-8 |
0.746 |
|
| 2004 |
Whitehead KJ, Plummer NW, Adams JA, Marchuk DA, Li DY. Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations. Development (Cambridge, England). 131: 1437-48. PMID 14993192 DOI: 10.1242/dev.01036 |
0.549 |
|
| 2003 |
Liquori CL, Berg MJ, Siegel AM, Huang E, Zawistowski JS, Stoffer T, Verlaan D, Balogun F, Hughes L, Leedom TP, Plummer NW, Cannella M, Maglione V, Squitieri F, Johnson EW, et al. Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations. American Journal of Human Genetics. 73: 1459-64. PMID 14624391 DOI: 10.1086/380314 |
0.738 |
|
| 2001 |
Kearney JA, Plummer NW, Smith MR, Kapur J, Cummins TR, Waxman SG, Goldin AL, Meisler MH. A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities. Neuroscience. 102: 307-17. PMID 11166117 DOI: 10.1016/S0306-4522(00)00479-6 |
0.573 |
|
| 1999 |
Plummer NW, Meisler MH. Evolution and diversity of mammalian sodium channel genes Genomics. 57: 323-331. PMID 10198179 DOI: 10.1006/Geno.1998.5735 |
0.519 |
|
| 1998 |
Plummer NW, Galt J, Jones JM, Burgess DL, Sprunger LK, Kohrman DC, Meisler MH. Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A. Genomics. 54: 287-96. PMID 9828131 DOI: 10.1006/Geno.1998.5550 |
0.746 |
|
| 1998 |
Smith MR, Smith RD, Plummer NW, Meisler MH, Goldin AL. Functional analysis of the mouse Scn8a sodium channel. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 6093-102. PMID 9698304 DOI: 10.1523/Jneurosci.18-16-06093.1998 |
0.501 |
|
| 1997 |
Meisler MH, Sprunger LK, Plummer NW, Escayg A, Jones JM. Ion channel mutations in mouse models of inherited neurological disease. Annals of Medicine. 29: 569-74. PMID 9562526 DOI: 10.3109/07853899709007484 |
0.77 |
|
| 1997 |
Plummer NW, McBurney MW, Meisler MH. Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells Journal of Biological Chemistry. 272: 24008-24015. PMID 9295353 DOI: 10.1074/jbc.272.38.24008 |
0.549 |
|
| 1995 |
Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH. Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'. Nature Genetics. 10: 461-5. PMID 7670495 DOI: 10.1038/Ng0895-461 |
0.755 |
|
| 1995 |
Kohrman DC, Plummer NW, Schuster T, Jones JM, Jang W, Burgess DL, Galt J, Spear BT, Meisler MH. Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15. Genomics. 26: 171-7. PMID 7601440 DOI: 10.1016/0888-7543(95)80198-U |
0.741 |
|
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