Scherer SS - Search Results

1

Inducible knockout of Clec16a in mice results in sensory neurodegeneration.

Hain HS, Pandey R, Bakay M, Strenkowski BP, Harrington D, Romer M, Motley WW, Li J, Lancaster E, Roth L, Grinspan JB, Scherer SS, Hakonarson H. Hain HS, et al. Among authors: scherer ss. Sci Rep. 2021 Apr 29;11(1):9319. doi: 10.1038/s41598-021-88895-0. Sci Rep. 2021. PMID: 33927318 Free PMC article.

2

Genetic dysmyelination alters the molecular architecture of the nodal region.

Arroyo EJ, Xu T, Grinspan J, Lambert S, Levinson SR, Brophy PJ, Peles E, Scherer SS. Arroyo EJ, et al. Among authors: scherer ss. J Neurosci. 2002 Mar 1;22(5):1726-37. doi: 10.1523/JNEUROSCI.22-05-01726.2002. J Neurosci. 2002. PMID: 11880502 Free PMC article.

3

Kv3.1b is a novel component of CNS nodes.

Devaux J, Alcaraz G, Grinspan J, Bennett V, Joho R, Crest M, Scherer SS. Devaux J, et al. Among authors: scherer ss. J Neurosci. 2003 Jun 1;23(11):4509-18. doi: 10.1523/JNEUROSCI.23-11-04509.2003. J Neurosci. 2003. PMID: 12805291 Free PMC article.

4

Pannexin1 is expressed by neurons and glia but does not form functional gap junctions.

Huang Y, Grinspan JB, Abrams CK, Scherer SS. Huang Y, et al. Among authors: scherer ss. Glia. 2007 Jan 1;55(1):46-56. doi: 10.1002/glia.20435. Glia. 2007. PMID: 17009242

5

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.

6

The in vivo contribution of motor neuron TrkB receptors to mutant SOD1 motor neuron disease.

Zhai J, Zhou W, Li J, Hayworth CR, Zhang L, Misawa H, Klein R, Scherer SS, Balice-Gordon RJ, Kalb RG. Zhai J, et al. Among authors: scherer ss. Hum Mol Genet. 2011 Nov 1;20(21):4116-31. doi: 10.1093/hmg/ddr335. Epub 2011 Aug 4. Hum Mol Genet. 2011. PMID: 21816949 Free PMC article.

7

A novel AARS mutation in a family with dominant myeloneuropathy.

Motley WW, Griffin LB, Mademan I, Baets J, De Vriendt E, De Jonghe P, Antonellis A, Jordanova A, Scherer SS. Motley WW, et al. Among authors: scherer ss. Neurology. 2015 May 19;84(20):2040-7. doi: 10.1212/WNL.0000000000001583. Epub 2015 Apr 22. Neurology. 2015. PMID: 25904691 Free PMC article.

8

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.

9

Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.

Abrams CK, Goman M, Wong S, Scherer SS, Kleopa KA, Peinado A, Freidin MM. Abrams CK, et al. Among authors: scherer ss. Sci Rep. 2017 Jan 10;7:40166. doi: 10.1038/srep40166. Sci Rep. 2017. PMID: 28071741 Free PMC article.

10

A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family.

Dankwa L, Richardson J, Motley WW, Züchner S, Scherer SS. Dankwa L, et al. Among authors: scherer ss. J Peripher Nerv Syst. 2018 Mar;23(1):36-39. doi: 10.1111/jns.12248. Epub 2018 Feb 6. J Peripher Nerv Syst. 2018. PMID: 29341354 Free PMC article.

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