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Items: 9


Temporal evolution of the microbiome, immune system, and epigenome with disease progression in ALS mice.

Figueroa-Romero C, Guo K, Murdock BJ, Paez-Colasante X, Bassis CM, Mikhail KA, Raue KD, Evans MC, Taubman GF, McDermott AJ, O'Brien PD, Savelieff MG, Hur J, Feldman EL.

Dis Model Mech. 2019 Oct 9. pii: dmm.041947. doi: 10.1242/dmm.041947. [Epub ahead of print]


Abnormal RNA stability in amyotrophic lateral sclerosis.

Tank EM, Figueroa-Romero C, Hinder LM, Bedi K, Archbold HC, Li X, Weskamp K, Safren N, Paez-Colasante X, Pacut C, Thumma S, Paulsen MT, Guo K, Hur J, Ljungman M, Feldman EL, Barmada SJ.

Nat Commun. 2018 Jul 20;9(1):2845. doi: 10.1038/s41467-018-05049-z.


Emerging understanding of the genotype-phenotype relationship in amyotrophic lateral sclerosis.

Goutman SA, Chen KS, Paez-Colasante X, Feldman EL.

Handb Clin Neurol. 2018;148:603-623. doi: 10.1016/B978-0-444-64076-5.00039-9. Review.


Corrigendum: Defective Acetylcholine Receptor Subunit Switch Precedes Atrophy of Slow-Twitch Skeletal Muscle Fibers Lacking ERK1/2 Kinases in Soleus Muscle.

Wang S, Seaberg B, Paez-Colasante X, Rimer M.

Sci Rep. 2017 Mar 30;7:45420. doi: 10.1038/srep45420. No abstract available.


Expression of microRNAs in human post-mortem amyotrophic lateral sclerosis spinal cords provides insight into disease mechanisms.

Figueroa-Romero C, Hur J, Lunn JS, Paez-Colasante X, Bender DE, Yung R, Sakowski SA, Feldman EL.

Mol Cell Neurosci. 2016 Mar;71:34-45. doi: 10.1016/j.mcn.2015.12.008. Epub 2015 Dec 17.


Amyotrophic lateral sclerosis: mechanisms and therapeutics in the epigenomic era.

Paez-Colasante X, Figueroa-Romero C, Sakowski SA, Goutman SA, Feldman EL.

Nat Rev Neurol. 2015 May;11(5):266-79. doi: 10.1038/nrneurol.2015.57. Epub 2015 Apr 21. Review.


Muscle-derived extracellular signal-regulated kinases 1 and 2 are required for the maintenance of adult myofibers and their neuromuscular junctions.

Seaberg B, Henslee G, Wang S, Paez-Colasante X, Landreth GE, Rimer M.

Mol Cell Biol. 2015 Apr;35(7):1238-53. doi: 10.1128/MCB.01071-14. Epub 2015 Jan 20.


Improvement of neuromuscular synaptic phenotypes without enhanced survival and motor function in severe spinal muscular atrophy mice selectively rescued in motor neurons.

Paez-Colasante X, Seaberg B, Martinez TL, Kong L, Sumner CJ, Rimer M.

PLoS One. 2013 Sep 23;8(9):e75866. doi: 10.1371/journal.pone.0075866. eCollection 2013.

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