Scherer SS - Search Results

1

Central nervous system dysfunction in a mouse model of FA2H deficiency.

Potter KA, Kern MJ, Fullbright G, Bielawski J, Scherer SS, Yum SW, Li JJ, Cheng H, Han X, Venkata JK, Khan PA, Rohrer B, Hama H. Potter KA, et al. Among authors: scherer ss. Glia. 2011 Jul;59(7):1009-21. doi: 10.1002/glia.21172. Epub 2011 Apr 13. Glia. 2011. PMID: 21491498 Free PMC article.

2

Cellular mechanisms of connexin32 mutations associated with CNS manifestations.

Kleopa KA, Yum SW, Scherer SS. Kleopa KA, et al. Among authors: scherer ss. J Neurosci Res. 2002 Jun 1;68(5):522-34. doi: 10.1002/jnr.10255. J Neurosci Res. 2002. PMID: 12111842

3

A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.

Yum SW, Zhang J, Mo K, Li J, Scherer SS. Yum SW, et al. Among authors: scherer ss. Ann Neurol. 2009 Dec;66(6):759-70. doi: 10.1002/ana.21728. Ann Neurol. 2009. PMID: 20039262 Free PMC article.

4

Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30.

Yum SW, Zhang J, Scherer SS. Yum SW, et al. Among authors: scherer ss. Neurobiol Dis. 2010 May;38(2):226-36. doi: 10.1016/j.nbd.2010.01.010. Epub 2010 Jan 21. Neurobiol Dis. 2010. PMID: 20096356 Free PMC article.

5

Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26.

Zhang J, Scherer SS, Yum SW. Zhang J, et al. Among authors: scherer ss. Mol Cell Neurosci. 2011 Jun;47(2):71-8. doi: 10.1016/j.mcn.2010.10.002. Epub 2010 Oct 30. Mol Cell Neurosci. 2011. PMID: 21040787 Free PMC article.

6

De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.

Motley WW, Palaima P, Yum SW, Gonzalez MA, Tao F, Wanschitz JV, Strickland AV, Löscher WN, De Vriendt E, Koppi S, Medne L, Janecke AR, Jordanova A, Zuchner S, Scherer SS. Motley WW, et al. Among authors: scherer ss. Brain. 2016 Jun;139(Pt 6):1649-56. doi: 10.1093/brain/aww055. Epub 2016 Mar 23. Brain. 2016. PMID: 27009151 Free PMC article.

7

Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E.

Lancaster E, Li J, Hanania T, Liem R, Scheideler MA, Scherer SS. Lancaster E, et al. Among authors: scherer ss. Exp Neurol. 2018 Oct;308:13-25. doi: 10.1016/j.expneurol.2018.06.010. Epub 2018 Jun 22. Exp Neurol. 2018. PMID: 29940160

8

TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model.

Sase S, Almad AA, Boecker CA, Guedes-Dias P, Li JJ, Takanohashi A, Patel A, McCaffrey T, Patel H, Sirdeshpande D, Curiel J, Shih-Hwa Liu J, Padiath Q, Holzbaur EL, Scherer SS, Vanderver A. Sase S, et al. Among authors: scherer ss. Elife. 2020 May 28;9:e52986. doi: 10.7554/eLife.52986. Elife. 2020. PMID: 32463361 Free PMC article.

9

Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system.

Abrams CK, Lancaster E, Li JJ, Dungan G, Gong D, Scherer SS, Freidin MM. Abrams CK, et al. Among authors: scherer ss. Exp Neurol. 2023 Feb;360:114277. doi: 10.1016/j.expneurol.2022.114277. Epub 2022 Nov 18. Exp Neurol. 2023. PMID: 36403785

10

Modality-based organization of ascending somatosensory axons in the direct dorsal column pathway.

Niu J, Ding L, Li JJ, Kim H, Liu J, Li H, Moberly A, Badea TC, Duncan ID, Son YJ, Scherer SS, Luo W. Niu J, et al. Among authors: scherer ss. J Neurosci. 2013 Nov 6;33(45):17691-709. doi: 10.1523/JNEUROSCI.3429-13.2013. J Neurosci. 2013. PMID: 24198362 Free PMC article.

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