R01 NS057482/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2008	2
2009	1
2010	2
2011	2
2012	3
2014	4
2015	1
2017	3
2018	2
2020	1
2024	0

1

Spinal muscular atrophy: new and emerging insights from model mice.

Park GH, Kariya S, Monani UR. Park GH, et al. Curr Neurol Neurosci Rep. 2010 Mar;10(2):108-17. doi: 10.1007/s11910-010-0095-5. Curr Neurol Neurosci Rep. 2010. PMID: 20425235 Free PMC article. Review.

2

Spinal muscular atrophy: journeying from bench to bedside.

Awano T, Kim JK, Monani UR. Awano T, et al. Neurotherapeutics. 2014 Oct;11(4):786-95. doi: 10.1007/s13311-014-0293-y. Neurotherapeutics. 2014. PMID: 24990202 Free PMC article. Review.

3

Spectrum of neuropathophysiology in spinal muscular atrophy type I.

Harding BN, Kariya S, Monani UR, Chung WK, Benton M, Yum SW, Tennekoon G, Finkel RS. Harding BN, et al. J Neuropathol Exp Neurol. 2015 Jan;74(1):15-24. doi: 10.1097/NEN.0000000000000144. J Neuropathol Exp Neurol. 2015. PMID: 25470343 Free PMC article.

4

SMN regulates axonal local translation via miR-183/mTOR pathway.

Kye MJ, Niederst ED, Wertz MH, Gonçalves Ido C, Akten B, Dover KZ, Peters M, Riessland M, Neveu P, Wirth B, Kosik KS, Sardi SP, Monani UR, Passini MA, Sahin M. Kye MJ, et al. Hum Mol Genet. 2014 Dec 1;23(23):6318-31. doi: 10.1093/hmg/ddu350. Epub 2014 Jul 4. Hum Mol Genet. 2014. PMID: 25055867 Free PMC article.

5

A pathogenic S250F missense mutation results in a mouse model of mild aromatic l-amino acid decarboxylase (AADC) deficiency.

Caine C, Shohat M, Kim JK, Nakanishi K, Homma S, Mosharov EV, Monani UR. Caine C, et al. Hum Mol Genet. 2017 Nov 15;26(22):4406-4415. doi: 10.1093/hmg/ddx326. Hum Mol Genet. 2017. PMID: 28973165 Free PMC article.

6

A cell autonomous torsinA requirement for cholinergic neuron survival and motor control.

Pappas SS, Li J, LeWitt TM, Kim JK, Monani UR, Dauer WT. Pappas SS, et al. Elife. 2018 Aug 17;7:e36691. doi: 10.7554/eLife.36691. Elife. 2018. PMID: 30117805 Free PMC article.

7

Muscle-specific SMN reduction reveals motor neuron-independent disease in spinal muscular atrophy models.

Kim JK, Jha NN, Feng Z, Faleiro MR, Chiriboga CA, Wei-Lapierre L, Dirksen RT, Ko CP, Monani UR. Kim JK, et al. J Clin Invest. 2020 Mar 2;130(3):1271-1287. doi: 10.1172/JCI131989. J Clin Invest. 2020. PMID: 32039917 Free PMC article.

8

Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein.

Tang M, Gao G, Rueda CB, Yu H, Thibodeaux DN, Awano T, Engelstad KM, Sanchez-Quintero MJ, Yang H, Li F, Li H, Su Q, Shetler KE, Jones L, Seo R, McConathy J, Hillman EM, Noebels JL, De Vivo DC, Monani UR. Tang M, et al. Nat Commun. 2017 Jan 20;8:14152. doi: 10.1038/ncomms14152. Nat Commun. 2017. PMID: 28106060 Free PMC article.

9

Motor neuron biology and disease: A current perspective on infantile-onset spinal muscular atrophy.

Jha NN, Kim JK, Monani UR. Jha NN, et al. Future Neurol. 2018 Aug;13(3):161-172. doi: 10.2217/fnl-2018-0008. Epub 2018 Jul 6. Future Neurol. 2018. PMID: 31396020 Free PMC article.

10

Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy.

Lee AJ, Awano T, Park GH, Monani UR. Lee AJ, et al. PLoS One. 2012;7(9):e46353. doi: 10.1371/journal.pone.0046353. Epub 2012 Sep 27. PLoS One. 2012. PMID: 23029491 Free PMC article.

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