Simkin D - Search Results

1

Andersen's syndrome mutants produce a knockdown of inwardly rectifying K⁺ channel in mouse skeletal muscle in vivo.

Simkin D, Robin G, Giuliano S, Vukolic A, Moceri P, Guy N, Wagner KD, Lacampagne A, Allard B, Bendahhou S. Simkin D, et al. Cell Tissue Res. 2018 Feb;371(2):309-323. doi: 10.1007/s00441-017-2696-7. Epub 2017 Oct 10. Cell Tissue Res. 2018. PMID: 29018970 Free article.

2

Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.

Sacconi S, Simkin D, Arrighi N, Chapon F, Larroque MM, Vicart S, Sternberg D, Fontaine B, Barhanin J, Desnuelle C, Bendahhou S. Sacconi S, et al. Among authors: simkin d. Am J Physiol Cell Physiol. 2009 Oct;297(4):C876-85. doi: 10.1152/ajpcell.00519.2008. Epub 2009 Jul 1. Am J Physiol Cell Physiol. 2009. PMID: 19570891 Free article.

3

Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorder.

Simkin D, Léna I, Landrieu P, Lion-François L, Sternberg D, Fontaine B, Bendahhou S. Simkin D, et al. J Physiol. 2011 Jul 1;589(Pt 13):3115-24. doi: 10.1113/jphysiol.2011.207977. Epub 2011 Apr 26. J Physiol. 2011. PMID: 21521764 Free PMC article.

4

Skeletal muscle na channel disorders.

Simkin D, Bendahhou S. Simkin D, et al. Front Pharmacol. 2011 Oct 14;2:63. doi: 10.3389/fphar.2011.00063. eCollection 2011. Front Pharmacol. 2011. PMID: 22016737 Free PMC article.

5

Osteogenic and Chondrogenic Master Genes Expression Is Dependent on the Kir2.1 Potassium Channel Through the Bone Morphogenetic Protein Pathway.

Pini J, Giuliano S, Matonti J, Gannoun L, Simkin D, Rouleau M, Bendahhou S. Pini J, et al. Among authors: simkin d. J Bone Miner Res. 2018 Oct;33(10):1826-1841. doi: 10.1002/jbmr.3474. Epub 2018 Jun 29. J Bone Miner Res. 2018. PMID: 29813186 Free article.

6

Evaluation of HCN2 abnormalities as a cause of juvenile audiogenic seizures in Black Swiss mice.

Shin M, Simkin D, Suyeoka GM, Chetkovich DM. Shin M, et al. Among authors: simkin d. Brain Res. 2006 Apr 14;1083(1):14-20. doi: 10.1016/j.brainres.2006.01.102. Epub 2006 Mar 20. Brain Res. 2006. PMID: 16542642

7

Dyshomeostatic modulation of Ca²⁺-activated K⁺ channels in a human neuronal model of KCNQ2 encephalopathy.

Simkin D, Marshall KA, Vanoye CG, Desai RR, Bustos BI, Piyevsky BN, Ortega JA, Forrest M, Robertson GL, Penzes P, Laux LC, Lubbe SJ, Millichap JJ, George AL Jr, Kiskinis E. Simkin D, et al. Elife. 2021 Feb 5;10:e64434. doi: 10.7554/eLife.64434. Elife. 2021. PMID: 33544076 Free PMC article.

8

Control of the single channel conductance of K2P10.1 (TREK-2) by the amino-terminus: role of alternative translation initiation.

Simkin D, Cavanaugh EJ, Kim D. Simkin D, et al. J Physiol. 2008 Dec 1;586(23):5651-63. doi: 10.1113/jphysiol.2008.161927. Epub 2008 Oct 9. J Physiol. 2008. PMID: 18845607 Free PMC article.

9

Homozygous might be hemizygous: CRISPR/Cas9 editing in iPSCs results in detrimental on-target defects that escape standard quality controls.

Simkin D, Papakis V, Bustos BI, Ambrosi CM, Ryan SJ, Baru V, Williams LA, Dempsey GT, McManus OB, Landers JE, Lubbe SJ, George AL Jr, Kiskinis E. Simkin D, et al. Stem Cell Reports. 2022 Apr 12;17(4):993-1008. doi: 10.1016/j.stemcr.2022.02.008. Epub 2022 Mar 10. Stem Cell Reports. 2022. PMID: 35276091 Free PMC article.

10

'Channeling' therapeutic discovery for epileptic encephalopathy through iPSC technologies.

Simkin D, Ambrosi C, Marshall KA, Williams LA, Eisenberg J, Gharib M, Dempsey GT, George AL Jr, McManus OB, Kiskinis E. Simkin D, et al. Trends Pharmacol Sci. 2022 May;43(5):392-405. doi: 10.1016/j.tips.2022.03.001. Trends Pharmacol Sci. 2022. PMID: 35427475 Free PMC article. Review.

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