Karen Muller Smith, Ph.D. - Publications

Affiliations: 
Biology University of Louisiana at Lafayette, Lafayette, LA, United States 
Area:
brain development, Fibroblast Growth Factors, interneurons, astrocytes, attention deficit hyperactivity disorder

21 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
2019 Dias JD, Deoli NT, Rogers D, Vera Ad, Smith KM, Schneider-Broussard R, Whitlow HJ. Development of a biosafety level-2 facility for irradiation of biological cells using MeV ions Nuclear Instruments & Methods in Physics Research Section B-Beam Interactions With Materials and Atoms. 447: 50-54. DOI: 10.1016/J.Nimb.2019.03.002  0.53
2018 Smith KM. Hyperactivity in mice lacking one allele of the glutamic acid decarboxylase 67 gene. Attention Deficit and Hyperactivity Disorders. PMID 29556956 DOI: 10.1007/S12402-018-0254-0  0.351
2017 Collette JC, Choubey L, Smith KM. -Glial and stem cell expression of murine Fibroblast Growth Factor Receptor 1 in the embryonic and perinatal nervous system. Peerj. 5: e3519. PMID 28674667 DOI: 10.7717/Peerj.3519  0.738
2017 Choubey L, Collette JC, Smith KM. Quantitative assessment of fibroblast growth factor receptor 1 expression in neurons and glia. Peerj. 5: e3173. PMID 28439461 DOI: 10.7717/Peerj.3173  0.757
2014 Smith KM, Maragnoli ME, Phull PM, Tran KM, Choubey L, Vaccarino FM. Fgfr1 inactivation in the mouse telencephalon results in impaired maturation of interneurons expressing parvalbumin. Plos One. 9: e103696. PMID 25116473 DOI: 10.1371/Journal.Pone.0103696  0.711
2013 Zhang Y, Cook A, Kim J, Baranov SV, Jiang J, Smith K, Cormier K, Bennett E, Browser RP, Day AL, Carlisle DL, Ferrante RJ, Wang X, Friedlander RM. Melatonin inhibits the caspase-1/cytochrome c/caspase-3 cell death pathway, inhibits MT1 receptor loss and delays disease progression in a mouse model of amyotrophic lateral sclerosis. Neurobiology of Disease. 55: 26-35. PMID 23537713 DOI: 10.1016/J.Nbd.2013.03.008  0.316
2011 Wang X, Sirianni A, Pei Z, Cormier K, Smith K, Jiang J, Zhou S, Wang H, Zhao R, Yano H, Kim JE, Li W, Kristal BS, Ferrante RJ, Friedlander RM. The melatonin MT1 receptor axis modulates mutant Huntingtin-mediated toxicity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 14496-507. PMID 21994366 DOI: 10.1523/Jneurosci.3059-11.2011  0.373
2010 Stevens HE, Smith KM, Rash BG, Vaccarino FM. Neural stem cell regulation, fibroblast growth factors, and the developmental origins of neuropsychiatric disorders. Frontiers in Neuroscience. 4. PMID 20877431 DOI: 10.3389/Fnins.2010.00059  0.595
2010 Stevens HE, Smith KM, Maragnoli ME, Fagel D, Borok E, Shanabrough M, Horvath TL, Vaccarino FM. Fgfr2 is required for the development of the medial prefrontal cortex and its connections with limbic circuits. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 5590-602. PMID 20410112 DOI: 10.1523/Jneurosci.5837-09.2010  0.761
2010 Smith K, Maragnoli M, Phull P, Tran K, Vaccarino F. [P2.33]: Fibroblast growth factor receptor 1 (Fgfr1) participates in postnatal interneuron development International Journal of Developmental Neuroscience. 28: 698-698. DOI: 10.1016/J.Ijdevneu.2010.07.163  0.61
2009 Vaccarino FM, Smith KM. Increased brain size in autism--what it will take to solve a mystery. Biological Psychiatry. 66: 313-5. PMID 19643218 DOI: 10.1016/J.Biopsych.2009.06.013  0.539
2009 Vaccarino FM, Grigorenko EL, Smith KM, Stevens HE. Regulation of cerebral cortical size and neuron number by fibroblast growth factors: implications for autism. Journal of Autism and Developmental Disorders. 39: 511-20. PMID 18850329 DOI: 10.1007/S10803-008-0653-8  0.629
2008 Stevens H, Maragnoli M, Smith K, Fagel D, Okhubo Y, Vaccarino F. [P2.41]: Direct and indirect consequences of Fgf receptor 2 loss of function for cortical development International Journal of Developmental Neuroscience. 26: 880-880. DOI: 10.1016/J.Ijdevneu.2008.09.166  0.74
2008 Smith K, Maragnoli M, Fagel D, Phull P, Tran K, Vaccarino F. [P2.10]: Postnatal maturation of cortical parvalbumin inhibitory neurons is impaired in FGF receptor mutant mice International Journal of Developmental Neuroscience. 26: 870-870. DOI: 10.1016/J.Ijdevneu.2008.09.135  0.763
2007 Stack EC, Dedeoglu A, Smith KM, Cormier K, Kubilus JK, Bogdanov M, Matson WR, Yang L, Jenkins BG, Luthi-Carter R, Kowall NW, Hersch SM, Beal MF, Ferrante RJ. Neuroprotective effects of synaptic modulation in Huntington's disease R6/2 mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 12908-15. PMID 18032664 DOI: 10.1523/Jneurosci.4318-07.2007  0.327
2007 Vaccarino FM, Fagel DM, Ganat Y, Maragnoli ME, Ment LR, Ohkubo Y, Schwartz ML, Silbereis J, Smith KM. Astroglial cells in development, regeneration, and repair. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 13: 173-85. PMID 17404377 DOI: 10.1177/1073858406298336  0.756
2006 Barkley RA, Smith KM, Fischer M, Navia B. An examination of the behavioral and neuropsychological correlates of three ADHD candidate gene polymorphisms (DRD4 7+, DBH TaqI A2, and DAT1 40 bp VNTR) in hyperactive and normal children followed to adulthood. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 487-98. PMID 16741944 DOI: 10.1002/Ajmg.B.30326  0.566
2006 Smith KM, Ohkubo Y, Maragnoli ME, Rasin MR, Schwartz ML, Sestan N, Vaccarino FM. Midline radial glia translocation and corpus callosum formation require FGF signaling. Nature Neuroscience. 9: 787-97. PMID 16715082 DOI: 10.1038/Nn1705  0.64
2005 Smith KM, Bauer L, Fischer M, Barkley R, Navia BA. Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 133: 57-63. PMID 15635701 DOI: 10.1002/Ajmg.B.30127  0.605
2003 Smith KM, Daly M, Fischer M, Yiannoutsos CT, Bauer L, Barkley R, Navia BA. Association of the dopamine beta hydroxylase gene with attention deficit hyperactivity disorder: genetic analysis of the Milwaukee longitudinal study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 119: 77-85. PMID 12707943 DOI: 10.1002/Ajmg.B.20005  0.58
2000 Smith KM, Crandall KA, Kneissl ML, Navia BA. PCR detection of host and HIV-1 sequences from archival brain tissue. Journal of Neurovirology. 6: 164-71. PMID 10822330 DOI: 10.3109/13550280009013160  0.561
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