Lyle W. Ostrow

Affiliations: 
2005 State University of New York, Buffalo, Buffalo, NY, United States 
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"Lyle Ostrow"
Mean distance: 17.26 (cluster 11)
 
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Frederick Sachs grad student 2005 SUNY Buffalo (Chemistry Tree)
 (Mechanosensation and endothelin in astrocytes.)
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Publications

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Tam OH, Rozhkov NV, Shaw R, et al. (2019) Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia. Cell Reports. 29: 1164-1177.e5
Pereira GC, Sanchez L, Schaughency PM, et al. (2018) Properties of LINE-1 proteins and repeat element expression in the context of amyotrophic lateral sclerosis. Mobile Dna. 9: 35
Mayer J, Harz C, Sanchez L, et al. (2018) Transcriptional profiling of HERV-K(HML-2) in amyotrophic lateral sclerosis and potential implications for expression of HML-2 proteins. Molecular Neurodegeneration. 13: 39
Nicolas A, Kenna KP, Renton AE, et al. (2018) Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. Neuron. 97: 1268-1283.e6
Ayers JI, Diamond J, Sari A, et al. (2016) Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS. Acta Neuropathologica
Jablonski AM, Lamitina T, Liachko NF, et al. (2015) Loss of RAD-23 Protects Against Models of Motor Neuron Disease by Enhancing Mutant Protein Clearance. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 14286-306
Li W, Lee MH, Henderson L, et al. (2015) Human endogenous retrovirus-K contributes to motor neuron disease. Science Translational Medicine. 7: 307ra153
Zhang K, Donnelly CJ, Haeusler AR, et al. (2015) The C9orf72 repeat expansion disrupts nucleocytoplasmic transport. Nature. 525: 56-61
Zu T, Liu Y, Bañez-Coronel M, et al. (2013) RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia. Proceedings of the National Academy of Sciences of the United States of America. 110: E4968-77
Kang SH, Li Y, Fukaya M, et al. (2013) Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis. Nature Neuroscience. 16: 571-9
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