McKenna-Yasek D - Search Results

1

Suppression of mutant C9orf72 expression by a potent mixed backbone antisense oligonucleotide.

Tran H, Moazami MP, Yang H, McKenna-Yasek D, Douthwright CL, Pinto C, Metterville J, Shin M, Sanil N, Dooley C, Puri A, Weiss A, Wightman N, Gray-Edwards H, Marosfoi M, King RM, Kenderdine T, Fabris D, Bowser R, Watts JK, Brown RH Jr. Tran H, et al. Among authors: mckenna yasek d. Nat Med. 2022 Jan;28(1):117-124. doi: 10.1038/s41591-021-01557-6. Epub 2021 Dec 23. Nat Med. 2022. PMID: 34949835 Free PMC article.

2

Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel.

McClatchey AI, McKenna-Yasek D, Cros D, Worthen HG, Kuncl RW, DeSilva SM, Cornblath DR, Gusella JF, Brown RH Jr. McClatchey AI, et al. Nat Genet. 1992 Oct;2(2):148-52. doi: 10.1038/ng1092-148. Nat Genet. 1992. PMID: 1338909

3

Apolipoprotein E epsilon 4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis.

Mui S, Rebeck GW, McKenna-Yasek D, Hyman BT, Brown RH Jr. Mui S, et al. Ann Neurol. 1995 Sep;38(3):460-3. doi: 10.1002/ana.410380318. Ann Neurol. 1995. PMID: 7668834

4

Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis.

Bowling AC, Barkowski EE, McKenna-Yasek D, Sapp P, Horvitz HR, Beal MF, Brown RH Jr. Bowling AC, et al. J Neurochem. 1995 May;64(5):2366-9. doi: 10.1046/j.1471-4159.1995.64052366.x. J Neurochem. 1995. PMID: 7722523

5

Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effect.

Grosson CL, Esteban J, McKenna-Yasek D, Gusella JF, Brown RH Jr. Grosson CL, et al. Neuromuscul Disord. 1996 Jan;6(1):27-31. doi: 10.1016/0960-8966(95)00018-6. Neuromuscul Disord. 1996. PMID: 8845715

6

Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.

Cudkowicz ME, McKenna-Yasek D, Chen C, Hedley-Whyte ET, Brown RH Jr. Cudkowicz ME, et al. Ann Neurol. 1998 Jun;43(6):703-10. doi: 10.1002/ana.410430604. Ann Neurol. 1998. PMID: 9629839

7

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort.

Ticozzi N, Silani V, LeClerc AL, Keagle P, Gellera C, Ratti A, Taroni F, Kwiatkowski TJ Jr, McKenna-Yasek DM, Sapp PC, Brown RH Jr, Landers JE. Ticozzi N, et al. Neurology. 2009 Oct 13;73(15):1180-5. doi: 10.1212/WNL.0b013e3181bbff05. Epub 2009 Sep 9. Neurology. 2009. PMID: 19741215 Free PMC article.

8

Mutational analysis of TARDBP in neurodegenerative diseases.

Ticozzi N, LeClerc AL, van Blitterswijk M, Keagle P, McKenna-Yasek DM, Sapp PC, Silani V, Wills AM, Brown RH Jr, Landers JE. Ticozzi N, et al. Neurobiol Aging. 2011 Nov;32(11):2096-9. doi: 10.1016/j.neurobiolaging.2009.11.018. Epub 2009 Dec 23. Neurobiol Aging. 2011. PMID: 20031275 Free PMC article.

9

Paraoxonase gene mutations in amyotrophic lateral sclerosis.

Ticozzi N, LeClerc AL, Keagle PJ, Glass JD, Wills AM, van Blitterswijk M, Bosco DA, Rodriguez-Leyva I, Gellera C, Ratti A, Taroni F, McKenna-Yasek D, Sapp PC, Silani V, Furlong CE, Brown RH Jr, Landers JE. Ticozzi N, et al. Ann Neurol. 2010 Jul;68(1):102-7. doi: 10.1002/ana.21993. Ann Neurol. 2010. PMID: 20582942 Free PMC article.

10

Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules.

Bosco DA, Lemay N, Ko HK, Zhou H, Burke C, Kwiatkowski TJ Jr, Sapp P, McKenna-Yasek D, Brown RH Jr, Hayward LJ. Bosco DA, et al. Hum Mol Genet. 2010 Nov 1;19(21):4160-75. doi: 10.1093/hmg/ddq335. Epub 2010 Aug 10. Hum Mol Genet. 2010. PMID: 20699327 Free PMC article.

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