Moghadaszadeh B - Search Results

1

Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.

Lawlor MW, Dechene ET, Roumm E, Geggel AS, Moghadaszadeh B, Beggs AH. Lawlor MW, et al. Among authors: moghadaszadeh b. Hum Mutat. 2010 Feb;31(2):176-83. doi: 10.1002/humu.21157. Hum Mutat. 2010. PMID: 19953533 Free PMC article.

2

X-linked myotubular and centronuclear myopathies.

Pierson CR, Tomczak K, Agrawal P, Moghadaszadeh B, Beggs AH. Pierson CR, et al. Among authors: moghadaszadeh b. J Neuropathol Exp Neurol. 2005 Jul;64(7):555-64. doi: 10.1097/01.jnen.0000171653.17213.2e. J Neuropathol Exp Neurol. 2005. PMID: 16042307 Review.

3

Adult-onset nemaline myopathy and monoclonal gammopathy.

Keller CE, Hays AP, Rowland LP, Moghadaszadeh B, Beggs AH, Bhagat G. Keller CE, et al. Among authors: moghadaszadeh b. Arch Neurol. 2006 Jan;63(1):132-4. doi: 10.1001/archneur.63.1.132. Arch Neurol. 2006. PMID: 16401746

4

Selenoproteins and their impact on human health through diverse physiological pathways.

Moghadaszadeh B, Beggs AH. Moghadaszadeh B, et al. Physiology (Bethesda). 2006 Oct;21:307-15. doi: 10.1152/physiol.00021.2006. Physiology (Bethesda). 2006. PMID: 16990451 Free PMC article. Review.

5

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

Parker KC, Kong SW, Walsh RJ; Bch; Salajegheh M, Moghadaszadeh B, Amato AA, Nazareno R, Lin YY, Krastins B, Sarracino DA, Beggs AH, Pinkus JL, Greenberg SA. Parker KC, et al. Among authors: moghadaszadeh b. Muscle Nerve. 2009 Jun;39(6):739-53. doi: 10.1002/mus.21230. Muscle Nerve. 2009. PMID: 19291799 Free PMC article.

6

Cell membrane expression of cardiac sodium channel Na(v)1.5 is modulated by alpha-actinin-2 interaction.

Ziane R, Huang H, Moghadaszadeh B, Beggs AH, Levesque G, Chahine M. Ziane R, et al. Among authors: moghadaszadeh b. Biochemistry. 2010 Jan 12;49(1):166-78. doi: 10.1021/bi901086v. Biochemistry. 2010. PMID: 19943616 Free PMC article.

7

Selenoprotein N deficiency in mice is associated with abnormal lung development.

Moghadaszadeh B, Rider BE, Lawlor MW, Childers MK, Grange RW, Gupta K, Boukedes SS, Owen CA, Beggs AH. Moghadaszadeh B, et al. FASEB J. 2013 Apr;27(4):1585-99. doi: 10.1096/fj.12-212688. Epub 2013 Jan 16. FASEB J. 2013. PMID: 23325319 Free PMC article.

8

SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy.

Agrawal PB, Pierson CR, Joshi M, Liu X, Ravenscroft G, Moghadaszadeh B, Talabere T, Viola M, Swanson LC, Haliloğlu G, Talim B, Yau KS, Allcock RJ, Laing NG, Perrella MA, Beggs AH. Agrawal PB, et al. Among authors: moghadaszadeh b. Am J Hum Genet. 2014 Aug 7;95(2):218-26. doi: 10.1016/j.ajhg.2014.07.004. Epub 2014 Jul 31. Am J Hum Genet. 2014. PMID: 25087613 Free PMC article.

9

X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene.

Shelton GD, Rider BE, Child G, Tzannes S, Guo LT, Moghadaszadeh B, Troiano EC, Haase B, Wade CM, Beggs AH. Shelton GD, et al. Among authors: moghadaszadeh b. Skelet Muscle. 2015 Jan 27;5(1):1. doi: 10.1186/s13395-014-0025-3. eCollection 2015. Skelet Muscle. 2015. PMID: 25664165 Free PMC article.

10

Sarcomeric and nonmuscle α-actinin isoforms exhibit differential dynamics at skeletal muscle Z-lines.

Hsu CP, Moghadaszadeh B, Hartwig JH, Beggs AH. Hsu CP, et al. Among authors: moghadaszadeh b. Cytoskeleton (Hoboken). 2018 May;75(5):213-228. doi: 10.1002/cm.21442. Epub 2018 Apr 1. Cytoskeleton (Hoboken). 2018. PMID: 29518289 Free PMC article.

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