Vicki L. McGovern, Ph.D.

2003 Ohio State University, Columbus, Columbus, OH 
Drosophila midline axon guidance
"Vicki McGovern"
Mean distance: 16.49 (cluster 11)


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Mark Seeger grad student 2003 Ohio State
 (Analysis of axon guidance in the embryonic central nervous system of Drosophila melanogaster.)
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Blatnik AJ, McGovern VL, Burghes AHM. (2021) What Genetics Has Told Us and How It Can Inform Future Experiments for Spinal Muscular Atrophy, a Perspective. International Journal of Molecular Sciences. 22
Kray KM, McGovern VL, Chugh D, et al. (2021) Dual SMN inducing therapies can rescue survival and motor unit function in symptomatic ∆7SMA mice. Neurobiology of Disease. 159: 105488
McGovern VL, Kray KM, Arnold WD, et al. (2020) Intragenic complementation of amino and carboxy terminal SMN missense mutations can rescue Smn null mice. Human Molecular Genetics
Blatnik AJ, McGovern VL, Le TT, et al. (2020) Conditional deletion of SMN in cell culture identifies functional SMN alleles. Human Molecular Genetics
Ruhno C, McGovern VL, Avenarius MR, et al. (2019) Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype. Human Genetics
Kaspar B, Thomsen G, Hsieh C, et al. (2019) O.24Biodistribution of onasemnogene abeparvovec (AVXS-101) DNA, mRNA, and SMN protein in human tissue Neuromuscular Disorders. 29
Iyer CC, Corlett KM, Massoni-Laporte A, et al. (2018) Mild SMN missense alleles are only functional in the presence of SMN2 in mammals. Human Molecular Genetics
Kolb SJ, Coffey CS, Yankey JW, et al. (2017) Natural History of Infantile-Onset Spinal Muscular Atrophy. Annals of Neurology
Wang X, Renusch SR, Duque SI, et al. (2017) SMN Blood Levels in a Porcine Model of Spinal Muscular Atrophy. Journal of Neuromuscular Diseases. 4: 59-66
Burghes A, McGovern V, Ruhno C, et al. (2017) P.133 - Identification of variants that affect severity of the spinal muscular atrophy phenotype within and outside of the SMN2 gene Neuromuscular Disorders. 27
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