Delpire E - Search Results

1

Temporal manipulation of KCC3 expression in juvenile or adult mice suggests irreversible developmental deficit in hereditary motor sensory neuropathy with agenesis of the corpus callosum.

Flores B, Delpire E. Flores B, et al. Among authors: delpire e. Am J Physiol Cell Physiol. 2021 May 1;320(5):C722-C730. doi: 10.1152/ajpcell.00594.2020. Epub 2021 Feb 17. Am J Physiol Cell Physiol. 2021. PMID: 33596149 Free PMC article.

2

Axonal and periaxonal swelling precede peripheral neurodegeneration in KCC3 knockout mice.

Byun N, Delpire E. Byun N, et al. Among authors: delpire e. Neurobiol Dis. 2007 Oct;28(1):39-51. doi: 10.1016/j.nbd.2007.06.014. Epub 2007 Jun 23. Neurobiol Dis. 2007. PMID: 17659877 Free PMC article.

., George, A.L., Jr., McDonald, M.P., Bouchard, J.P., Mathieu, J., Delpire, E., Rouleau, G.A., 2002. The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. ...

., George, A.L., Jr., McDonald, M.P., Bouchard, J.P., Mathieu, J., Delpire, E., Rouleau, G.A., 2002. The K-Cl cotransporter KC …

3

Deletion of KCC3 in parvalbumin neurons leads to locomotor deficit in a conditional mouse model of peripheral neuropathy associated with agenesis of the corpus callosum.

Ding J, Delpire E. Ding J, et al. Among authors: delpire e. Behav Brain Res. 2014 Nov 1;274:128-36. doi: 10.1016/j.bbr.2014.08.005. Epub 2014 Aug 10. Behav Brain Res. 2014. PMID: 25116249 Free PMC article.

4

Peripheral motor neuropathy is associated with defective kinase regulation of the KCC3 cotransporter.

Kahle KT, Flores B, Bharucha-Goebel D, Zhang J, Donkervoort S, Hegde M, Hussain G, Duran D, Liang B, Sun D, Bönnemann CG, Delpire E. Kahle KT, et al. Among authors: delpire e. Sci Signal. 2016 Aug 2;9(439):ra77. doi: 10.1126/scisignal.aae0546. Sci Signal. 2016. PMID: 27485015 Free PMC article.

5

KCC3 deficiency-induced disruption of paranodal loops and impairment of axonal excitability in the peripheral nervous system.

Sun YT, Tzeng SF, Lin TS, Hsu KS, Delpire E, Shen MR. Sun YT, et al. Among authors: delpire e. Neuroscience. 2016 Oct 29;335:91-102. doi: 10.1016/j.neuroscience.2016.08.031. Epub 2016 Aug 24. Neuroscience. 2016. PMID: 27568057

6

A patient with multisystem dysfunction carries a truncation mutation in human SLC12A2, the gene encoding the Na-K-2Cl cotransporter, NKCC1.

Delpire E, Wolfe L, Flores B, Koumangoye R, Schornak CC, Omer S, Pusey B, Lau C, Markello T, Adams DR. Delpire E, et al. Cold Spring Harb Mol Case Stud. 2016 Nov;2(6):a001289. doi: 10.1101/mcs.a001289. Cold Spring Harb Mol Case Stud. 2016. PMID: 27900370 Free PMC article.

7

The KCC3 cotransporter as a therapeutic target for peripheral neuropathy.

Delpire E, Kahle KT. Delpire E, et al. Expert Opin Ther Targets. 2017 Feb;21(2):113-116. doi: 10.1080/14728222.2017.1275569. Epub 2017 Jan 5. Expert Opin Ther Targets. 2017. PMID: 28019725 No abstract available.

8

A role for KCC3 in maintaining cell volume of peripheral nerve fibers.

Flores B, Schornak CC, Delpire E. Flores B, et al. Among authors: delpire e. Neurochem Int. 2019 Feb;123:114-124. doi: 10.1016/j.neuint.2018.01.009. Epub 2018 Jan 31. Neurochem Int. 2019. PMID: 29366908 Free PMC article. Review.

9

De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy.

Park J, Flores BR, Scherer K, Kuepper H, Rossi M, Rupprich K, Rautenberg M, Deininger N, Weichselbaum A, Grimm A, Sturm M, Grasshoff U, Delpire E, Haack TB. Park J, et al. Among authors: delpire e. J Med Genet. 2020 Apr;57(4):283-288. doi: 10.1136/jmedgenet-2019-106273. Epub 2019 Aug 22. J Med Genet. 2020. PMID: 31439721

10

Osmotic Response of Dorsal Root Ganglion Neurons Expressing Wild-Type and Mutant KCC3 Transporters.

Flores B, Delpire E. Flores B, et al. Among authors: delpire e. Cell Physiol Biochem. 2020 Jun 8;54(4):577-590. doi: 10.33594/000000241. Cell Physiol Biochem. 2020. PMID: 32506846 Free PMC article.

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