Lutz C - Search Results

1

A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA mice.

Workman E, Saieva L, Carrel TL, Crawford TO, Liu D, Lutz C, Beattie CE, Pellizzoni L, Burghes AH. Workman E, et al. Among authors: lutz c. Hum Mol Genet. 2009 Jun 15;18(12):2215-29. doi: 10.1093/hmg/ddp157. Epub 2009 Mar 27. Hum Mol Genet. 2009. PMID: 19329542 Free PMC article.

2

Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy.

Kariya S, Park GH, Maeno-Hikichi Y, Leykekhman O, Lutz C, Arkovitz MS, Landmesser LT, Monani UR. Kariya S, et al. Among authors: lutz c. Hum Mol Genet. 2008 Aug 15;17(16):2552-69. doi: 10.1093/hmg/ddn156. Epub 2008 May 20. Hum Mol Genet. 2008. PMID: 18492800 Free PMC article.

3

Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy mice.

Sumner CJ, Wee CD, Warsing LC, Choe DW, Ng AS, Lutz C, Wagner KR. Sumner CJ, et al. Among authors: lutz c. Hum Mol Genet. 2009 Sep 1;18(17):3145-52. doi: 10.1093/hmg/ddp253. Epub 2009 May 28. Hum Mol Genet. 2009. PMID: 19477958 Free PMC article.

4

Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice.

Heier CR, Satta R, Lutz C, DiDonato CJ. Heier CR, et al. Among authors: lutz c. Hum Mol Genet. 2010 Oct 15;19(20):3906-18. doi: 10.1093/hmg/ddq330. Epub 2010 Aug 6. Hum Mol Genet. 2010. PMID: 20693262 Free PMC article.

5

Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy.

Lutz CM, Kariya S, Patruni S, Osborne MA, Liu D, Henderson CE, Li DK, Pellizzoni L, Rojas J, Valenzuela DM, Murphy AJ, Winberg ML, Monani UR. Lutz CM, et al. J Clin Invest. 2011 Aug;121(8):3029-41. doi: 10.1172/JCI57291. Epub 2011 Jul 25. J Clin Invest. 2011. PMID: 21785219 Free PMC article.

6

Characterization of behavioral and neuromuscular junction phenotypes in a novel allelic series of SMA mouse models.

Osborne M, Gomez D, Feng Z, McEwen C, Beltran J, Cirillo K, El-Khodor B, Lin MY, Li Y, Knowlton WM, McKemy DD, Bogdanik L, Butts-Dehm K, Martens K, Davis C, Doty R, Wardwell K, Ghavami A, Kobayashi D, Ko CP, Ramboz S, Lutz C. Osborne M, et al. Among authors: lutz c. Hum Mol Genet. 2012 Oct 15;21(20):4431-47. doi: 10.1093/hmg/dds285. Epub 2012 Jul 16. Hum Mol Genet. 2012. PMID: 22802075 Free PMC article.

7

Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMA.

Kong L, Valdivia DO, Simon CM, Hassinan CW, Delestrée N, Ramos DM, Park JH, Pilato CM, Xu X, Crowder M, Grzyb CC, King ZA, Petrillo M, Swoboda KJ, Davis C, Lutz CM, Stephan AH, Zhao X, Weetall M, Naryshkin NA, Crawford TO, Mentis GZ, Sumner CJ. Kong L, et al. Among authors: lutz cm. Sci Transl Med. 2021 Jan 27;13(578):eabb6871. doi: 10.1126/scitranslmed.abb6871. Sci Transl Med. 2021. PMID: 33504650 Free PMC article.

8

SMN protein is required throughout life to prevent spinal muscular atrophy disease progression.

Zhao X, Feng Z, Risher N, Mollin A, Sheedy J, Ling KKY, Narasimhan J, Dakka A, Baird JD, Ratni H, Lutz C, Chen KS, Naryshkin NA, Ko CP, Welch E, Metzger F, Weetall M. Zhao X, et al. Among authors: lutz c. Hum Mol Genet. 2021 Dec 17;31(1):82-96. doi: 10.1093/hmg/ddab220. Hum Mol Genet. 2021. PMID: 34368854

9

Characterization of a commonly used mouse model of SMA reveals increased seizure susceptibility and heightened fear response in FVB/N mice.

Gogliotti RG, Lutz C, Jorgensen M, Huebsch K, Koh S, Didonato CJ. Gogliotti RG, et al. Among authors: lutz c. Neurobiol Dis. 2011 Jul;43(1):142-51. doi: 10.1016/j.nbd.2011.03.002. Epub 2011 Mar 21. Neurobiol Dis. 2011. PMID: 21396450 Free PMC article.

10

Molecular and phenotypic reassessment of an infrequently used mouse model for spinal muscular atrophy.

Gogliotti RG, Hammond SM, Lutz C, Didonato CJ. Gogliotti RG, et al. Among authors: lutz c. Biochem Biophys Res Commun. 2010 Jan 1;391(1):517-22. doi: 10.1016/j.bbrc.2009.11.090. Epub 2009 Dec 4. Biochem Biophys Res Commun. 2010. PMID: 19961830 Free PMC article.

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