Pittman SK - Search Results

1

Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis.

Weihl CC, Baloh RH, Lee Y, Chou TF, Pittman SK, Lopate G, Allred P, Jockel-Balsarotti J, Pestronk A, Harms MB. Weihl CC, et al. Among authors: pittman sk. Neuromuscul Disord. 2015 Apr;25(4):289-96. doi: 10.1016/j.nmd.2014.12.009. Epub 2015 Jan 6. Neuromuscul Disord. 2015. PMID: 25617006 Free PMC article.

2

mTOR dysfunction contributes to vacuolar pathology and weakness in valosin-containing protein associated inclusion body myopathy.

Ching JK, Elizabeth SV, Ju JS, Lusk C, Pittman SK, Weihl CC. Ching JK, et al. Among authors: pittman sk. Hum Mol Genet. 2013 Mar 15;22(6):1167-79. doi: 10.1093/hmg/dds524. Epub 2012 Dec 18. Hum Mol Genet. 2013. PMID: 23250913 Free PMC article.

3

Increased autophagy accelerates colchicine-induced muscle toxicity.

Ching JK, Ju JS, Pittman SK, Margeta M, Weihl CC. Ching JK, et al. Among authors: pittman sk. Autophagy. 2013 Dec;9(12):2115-25. doi: 10.4161/auto.26150. Autophagy. 2013. PMID: 24184927

4

Autophagic vacuolar pathology in desminopathies.

Weihl CC, Iyadurai S, Baloh RH, Pittman SK, Schmidt RE, Lopate G, Pestronk A, Harms MB. Weihl CC, et al. Among authors: pittman sk. Neuromuscul Disord. 2015 Mar;25(3):199-206. doi: 10.1016/j.nmd.2014.12.002. Epub 2014 Dec 12. Neuromuscul Disord. 2015. PMID: 25557463 Free PMC article.

5

SQSTM1 splice site mutation in distal myopathy with rimmed vacuoles.

Bucelli RC, Arhzaouy K, Pestronk A, Pittman SK, Rojas L, Sue CM, Evilä A, Hackman P, Udd B, Harms MB, Weihl CC. Bucelli RC, et al. Among authors: pittman sk. Neurology. 2015 Aug 25;85(8):665-74. doi: 10.1212/WNL.0000000000001864. Epub 2015 Jul 24. Neurology. 2015. PMID: 26208961 Free PMC article.

6

Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1D.

Bengoechea R, Pittman SK, Tuck EP, True HL, Weihl CC. Bengoechea R, et al. Among authors: pittman sk. Hum Mol Genet. 2015 Dec 1;24(23):6588-602. doi: 10.1093/hmg/ddv363. Epub 2015 Sep 11. Hum Mol Genet. 2015. PMID: 26362252 Free PMC article.

7

TMEM184b Promotes Axon Degeneration and Neuromuscular Junction Maintenance.

Bhattacharya MR, Geisler S, Pittman SK, Doan RA, Weihl CC, Milbrandt J, DiAntonio A. Bhattacharya MR, et al. Among authors: pittman sk. J Neurosci. 2016 Apr 27;36(17):4681-9. doi: 10.1523/JNEUROSCI.2893-15.2016. J Neurosci. 2016. PMID: 27122027 Free PMC article.

8

Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination.

Lee Y, Chou TF, Pittman SK, Keith AL, Razani B, Weihl CC. Lee Y, et al. Among authors: pittman sk. Cell Rep. 2017 Apr 4;19(1):188-202. doi: 10.1016/j.celrep.2017.03.030. Cell Rep. 2017. PMID: 28380357 Free PMC article.

9

Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination.

Lee Y, Chou TF, Pittman SK, Keith AL, Razani B, Weihl CC. Lee Y, et al. Among authors: pittman sk. Cell Rep. 2017 Aug 22;20(8):1994. doi: 10.1016/j.celrep.2017.08.019. Cell Rep. 2017. PMID: 28834760 Free article. No abstract available.

10

Loss of lipin 1-mediated phosphatidic acid phosphohydrolase activity in muscle leads to skeletal myopathy in mice.

Schweitzer GG, Collier SL, Chen Z, McCommis KS, Pittman SK, Yoshino J, Matkovich SJ, Hsu FF, Chrast R, Eaton JM, Harris TE, Weihl CC, Finck BN. Schweitzer GG, et al. Among authors: pittman sk. FASEB J. 2019 Jan;33(1):652-667. doi: 10.1096/fj.201800361R. Epub 2018 Jul 20. FASEB J. 2019. PMID: 30028636 Free PMC article.

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