Kothary R - Search Results

1

Optimization of base editors for the functional correction of SMN2 as a treatment for spinal muscular atrophy.

Alves CRR, Ha LL, Yaworski R, Sutton ER, Lazzarotto CR, Christie KA, Reilly A, Beauvais A, Doll RM, de la Cruz D, Maguire CA, Swoboda KJ, Tsai SQ, Kothary R, Kleinstiver BP. Alves CRR, et al. Among authors: kothary r. Nat Biomed Eng. 2024 Feb;8(2):118-131. doi: 10.1038/s41551-023-01132-z. Epub 2023 Dec 6. Nat Biomed Eng. 2024. PMID: 38057426 Free PMC article.

2

SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis.

Bowerman M, Anderson CL, Beauvais A, Boyl PP, Witke W, Kothary R. Bowerman M, et al. Among authors: kothary r. Mol Cell Neurosci. 2009 Sep;42(1):66-74. doi: 10.1016/j.mcn.2009.05.009. Epub 2009 Jun 1. Mol Cell Neurosci. 2009. PMID: 19497369

3

Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model.

Bowerman M, Beauvais A, Anderson CL, Kothary R. Bowerman M, et al. Among authors: kothary r. Hum Mol Genet. 2010 Apr 15;19(8):1468-78. doi: 10.1093/hmg/ddq021. Epub 2010 Jan 22. Hum Mol Genet. 2010. PMID: 20097679

4

Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy.

Liu H, Beauvais A, Baker AN, Tsilfidis C, Kothary R. Liu H, et al. Among authors: kothary r. Dev Neurobiol. 2011 Feb;71(2):153-69. doi: 10.1002/dneu.20840. Dev Neurobiol. 2011. PMID: 20862739

5

Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late.

Hammond SM, Gogliotti RG, Rao V, Beauvais A, Kothary R, DiDonato CJ. Hammond SM, et al. Among authors: kothary r. PLoS One. 2010 Dec 29;5(12):e15887. doi: 10.1371/journal.pone.0015887. PLoS One. 2010. PMID: 21249120 Free PMC article.

6

The proteolipid protein promoter drives expression outside of the oligodendrocyte lineage during embryonic and early postnatal development.

Michalski JP, Anderson C, Beauvais A, De Repentigny Y, Kothary R. Michalski JP, et al. Among authors: kothary r. PLoS One. 2011 May 10;6(5):e19772. doi: 10.1371/journal.pone.0019772. PLoS One. 2011. PMID: 21572962 Free PMC article.

7

A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology.

Bowerman M, Murray LM, Beauvais A, Pinheiro B, Kothary R. Bowerman M, et al. Among authors: kothary r. Neuromuscul Disord. 2012 Mar;22(3):263-76. doi: 10.1016/j.nmd.2011.09.007. Epub 2011 Nov 8. Neuromuscul Disord. 2012. PMID: 22071333

8

Glucose metabolism and pancreatic defects in spinal muscular atrophy.

Bowerman M, Swoboda KJ, Michalski JP, Wang GS, Reeks C, Beauvais A, Murphy K, Woulfe J, Screaton RA, Scott FW, Kothary R. Bowerman M, et al. Among authors: kothary r. Ann Neurol. 2012 Aug;72(2):256-68. doi: 10.1002/ana.23582. Ann Neurol. 2012. PMID: 22926856 Free PMC article.

9

Defects in neuromuscular junction remodelling in the Smn(2B/-) mouse model of spinal muscular atrophy.

Murray LM, Beauvais A, Bhanot K, Kothary R. Murray LM, et al. Among authors: kothary r. Neurobiol Dis. 2013 Jan;49:57-67. doi: 10.1016/j.nbd.2012.08.019. Epub 2012 Aug 30. Neurobiol Dis. 2013. PMID: 22960106

10

Defects in pancreatic development and glucose metabolism in SMN-depleted mice independent of canonical spinal muscular atrophy neuromuscular pathology.

Bowerman M, Michalski JP, Beauvais A, Murray LM, DeRepentigny Y, Kothary R. Bowerman M, et al. Among authors: kothary r. Hum Mol Genet. 2014 Jul 1;23(13):3432-44. doi: 10.1093/hmg/ddu052. Epub 2014 Feb 4. Hum Mol Genet. 2014. PMID: 24497575 Free PMC article.

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