R01 NS062869/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2009	3
2010	1
2011	3
2012	3
2013	4
2014	1
2015	3
2020	3
2024	0

1

The nonselective cation channel TRPV4 inhibits angiotensin II receptors.

Zaccor NW, Sumner CJ, Snyder SH. Zaccor NW, et al. J Biol Chem. 2020 Jul 17;295(29):9986-9997. doi: 10.1074/jbc.RA120.014325. Epub 2020 Jun 3. J Biol Chem. 2020. PMID: 32493776 Free PMC article.

2

TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca².

Woolums BM, McCray BA, Sung H, Tabuchi M, Sullivan JM, Ruppell KT, Yang Y, Mamah C, Aisenberg WH, Saavedra-Rivera PC, Larin BS, Lau AR, Robinson DN, Xiang Y, Wu MN, Sumner CJ, Lloyd TE. Woolums BM, et al. Nat Commun. 2020 May 29;11(1):2679. doi: 10.1038/s41467-020-16411-5. Nat Commun. 2020. PMID: 32471994 Free PMC article.

3

Dominant mutations of the Notch ligand Jagged1 cause peripheral neuropathy.

Sullivan JM, Motley WW, Johnson JO, Aisenberg WH, Marshall KL, Barwick KE, Kong L, Huh JS, Saavedra-Rivera PC, McEntagart MM, Marion MH, Hicklin LA, Modarres H, Baple EL, Farah MH, Zuberi AR, Lutz CM, Gaudet R, Traynor BJ, Crosby AH, Sumner CJ. Sullivan JM, et al. J Clin Invest. 2020 Mar 2;130(3):1506-1512. doi: 10.1172/JCI128152. J Clin Invest. 2020. PMID: 32065591 Free PMC article.

4

Astrocytes influence the severity of spinal muscular atrophy.

Rindt H, Feng Z, Mazzasette C, Glascock JJ, Valdivia D, Pyles N, Crawford TO, Swoboda KJ, Patitucci TN, Ebert AD, Sumner CJ, Ko CP, Lorson CL. Rindt H, et al. Hum Mol Genet. 2015 Jul 15;24(14):4094-102. doi: 10.1093/hmg/ddv148. Epub 2015 Apr 24. Hum Mol Genet. 2015. PMID: 25911676 Free PMC article.

5

Non-aggregating tau phosphorylation by cyclin-dependent kinase 5 contributes to motor neuron degeneration in spinal muscular atrophy.

Miller N, Feng Z, Edens BM, Yang B, Shi H, Sze CC, Hong BT, Su SC, Cantu JA, Topczewski J, Crawford TO, Ko CP, Sumner CJ, Ma L, Ma YC. Miller N, et al. J Neurosci. 2015 Apr 15;35(15):6038-50. doi: 10.1523/JNEUROSCI.3716-14.2015. J Neurosci. 2015. PMID: 25878277 Free PMC article.

6

Spinal Muscular Atrophy Therapeutics: Where do we Stand?

d'Ydewalle C, Sumner CJ. d'Ydewalle C, et al. Neurotherapeutics. 2015 Apr;12(2):303-16. doi: 10.1007/s13311-015-0337-y. Neurotherapeutics. 2015. PMID: 25631888 Free PMC article. Review.

7

Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics.

Bricceno KV, Martinez T, Leikina E, Duguez S, Partridge TA, Chernomordik LV, Fischbeck KH, Sumner CJ, Burnett BG. Bricceno KV, et al. Hum Mol Genet. 2014 Sep 15;23(18):4745-57. doi: 10.1093/hmg/ddu189. Epub 2014 Apr 23. Hum Mol Genet. 2014. PMID: 24760765 Free PMC article.

8

SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3'-end formation of histone mRNAs.

Tisdale S, Lotti F, Saieva L, Van Meerbeke JP, Crawford TO, Sumner CJ, Mentis GZ, Pellizzoni L. Tisdale S, et al. Cell Rep. 2013 Dec 12;5(5):1187-95. doi: 10.1016/j.celrep.2013.11.012. Cell Rep. 2013. PMID: 24332368 Free PMC article.

9

A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance.

Sumner CJ, d'Ydewalle C, Wooley J, Fawcett KA, Hernandez D, Gardiner AR, Kalmar B, Baloh RH, Gonzalez M, Züchner S, Stanescu HC, Kleta R, Mankodi A, Cornblath DR, Boylan KB, Reilly MM, Greensmith L, Singleton AB, Harms MB, Rossor AM, Houlden H. Sumner CJ, et al. Am J Hum Genet. 2013 Nov 7;93(5):976-83. doi: 10.1016/j.ajhg.2013.10.006. Epub 2013 Oct 24. Am J Hum Genet. 2013. PMID: 24207122 Free PMC article.

10

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. Paez-Colasante X, et al. PLoS One. 2013 Sep 23;8(9):e75866. doi: 10.1371/journal.pone.0075866. eCollection 2013. PLoS One. 2013. PMID: 24086650 Free PMC article.

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