| Year |
Citation |
Score |
| 2024 |
Barraza-Flores P, Moghadaszadeh B, Lee W, Isaac B, Sun L, Troiano EC, Rockowitz S, Sliz P, Beggs AH. Zebrafish and cellular models of -Related Myopathy exhibit novel embryonic and metabolic phenotypes. Biorxiv : the Preprint Server For Biology. PMID 38464009 DOI: 10.1101/2024.02.26.581979 |
0.611 |
|
| 2023 |
Rybalka E, Kourakis S, Bonsett CA, Moghadaszadeh B, Beggs AH, Timpani CA. Adenylosuccinic Acid: An Orphan Drug with Untapped Potential. Pharmaceuticals (Basel, Switzerland). 16. PMID 37375769 DOI: 10.3390/ph16060822 |
0.399 |
|
| 2023 |
Li Q, Lin J, Luo S, Schmitz-Abe K, Agrawal R, Meng M, Moghadaszadeh B, Beggs AH, Liu X, Perrella MA, Agrawal PB. Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complex. Biorxiv : the Preprint Server For Biology. PMID 37162921 DOI: 10.1101/2023.04.24.538136 |
0.645 |
|
| 2021 |
Tabebordbar M, Lagerborg KA, Stanton A, King EM, Ye S, Tellez L, Krunnfusz A, Tavakoli S, Widrick JJ, Messemer KA, Troiano EC, Moghadaszadeh B, Peacker BL, Leacock KA, Horwitz N, et al. Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species. Cell. PMID 34506722 DOI: 10.1016/j.cell.2021.08.028 |
0.562 |
|
| 2021 |
Guo Y, Cao Y, Jardin BD, Sethi I, Ma Q, Moghadaszadeh B, Troiano EC, Mazumdar N, Trembley MA, Small EM, Yuan GC, Beggs AH, Pu WT. Sarcomeres regulate murine cardiomyocyte maturation through MRTF-SRF signaling. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33361330 DOI: 10.1073/pnas.2008861118 |
0.503 |
|
| 2018 |
Hsu CP, Moghadaszadeh B, Hartwig JH, Beggs AH. Sarcomeric and non-muscle α-actinin isoforms exhibit differential dynamics at skeletal muscle Z-lines. Cytoskeleton (Hoboken, N.J.). PMID 29518289 DOI: 10.1002/Cm.21442 |
0.476 |
|
| 2015 |
Shelton GD, Rider BE, Child G, Tzannes S, Guo LT, Moghadaszadeh B, Troiano EC, Haase B, Wade CM, Beggs AH. X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene. Skeletal Muscle. 5: 1. PMID 25664165 DOI: 10.1186/S13395-014-0025-3 |
0.597 |
|
| 2014 |
Agrawal PB, Pierson CR, Joshi M, Liu X, Ravenscroft G, Moghadaszadeh B, Talabere T, Viola M, Swanson LC, HaliloÄŸlu G, Talim B, Yau KS, Allcock RJ, Laing NG, Perrella MA, et al. SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. American Journal of Human Genetics. 95: 218-26. PMID 25087613 DOI: 10.1016/J.Ajhg.2014.07.004 |
0.681 |
|
| 2013 |
Moghadaszadeh B, Rider BE, Lawlor MW, Childers MK, Grange RW, Gupta K, Boukedes SS, Owen CA, Beggs AH. Selenoprotein N deficiency in mice is associated with abnormal lung development. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 27: 1585-99. PMID 23325319 DOI: 10.1096/Fj.12-212688 |
0.645 |
|
| 2010 |
Lawlor MW, Dechene ET, Roumm E, Geggel AS, Moghadaszadeh B, Beggs AH. Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion. Human Mutation. 31: 176-83. PMID 19953533 DOI: 10.1002/Humu.21157 |
0.616 |
|
| 2010 |
Ziane R, Huang H, Moghadaszadeh B, Beggs AH, Levesque G, Chahine M. Cell membrane expression of cardiac sodium channel Na(v)1.5 is modulated by alpha-actinin-2 interaction. Biochemistry. 49: 166-78. PMID 19943616 DOI: 10.1021/Bi901086V |
0.382 |
|
| 2009 |
Parker KC, Kong SW, Walsh RJ, Salajegheh M, Moghadaszadeh B, Amato AA, Nazareno R, Lin YY, Krastins B, Sarracino DA, Beggs AH, Pinkus JL, Greenberg SA. Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis. Muscle & Nerve. 39: 739-53. PMID 19291799 DOI: 10.1002/Mus.21230 |
0.564 |
|
| 2006 |
Moghadaszadeh B, Beggs AH. Selenoproteins and their impact on human health through diverse physiological pathways. Physiology (Bethesda, Md.). 21: 307-15. PMID 16990451 DOI: 10.1152/Physiol.00021.2006 |
0.414 |
|
| 2006 |
Keller CE, Hays AP, Rowland LP, Moghadaszadeh B, Beggs AH, Bhagat G. Adult-onset nemaline myopathy and monoclonal gammopathy. Archives of Neurology. 63: 132-4. PMID 16401746 DOI: 10.1001/Archneur.63.1.132 |
0.512 |
|
| 2005 |
Pierson CR, Tomczak K, Agrawal P, Moghadaszadeh B, Beggs AH. X-linked myotubular and centronuclear myopathies. Journal of Neuropathology and Experimental Neurology. 64: 555-64. PMID 16042307 DOI: 10.1097/01.Jnen.0000171653.17213.2E |
0.632 |
|
| 2004 |
Di Blasi C, Moghadaszadeh B, Ciano C, Negri T, Giavazzi A, Cornelio F, Morandi L, Mora M. Abnormal lysosomal and ubiquitin-proteasome pathways in 19p13.3 distal myopathy. Annals of Neurology. 56: 133-8. PMID 15236412 DOI: 10.1002/ana.20158 |
0.337 |
|
| 2003 |
Moghadaszadeh B, Albrechtsen R, Guo LT, Zaik M, Kawaguchi N, Borup RH, Kronqvist P, Schroder HD, Davies KE, Voit T, Nielsen FC, Engvall E, Wewer UM. Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alpha 7 integrin, utrophin and associated glycoproteins. Human Molecular Genetics. 12: 2467-79. PMID 12915458 DOI: 10.1093/hmg/ddg264 |
0.356 |
|
| 2003 |
Petit N, Lescure A, Rederstorff M, Krol A, Moghadaszadeh B, Wewer UM, Guicheney P. Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression pattern. Human Molecular Genetics. 12: 1045-53. PMID 12700173 DOI: 10.1093/Hmg/Ddg115 |
0.366 |
|
| 2002 |
Kronqvist P, Kawaguchi N, Albrechtsen R, Xu X, Schrøder HD, Moghadaszadeh B, Nielsen FC, Fröhlich C, Engvall E, Wewer UM. ADAM12 alleviates the skeletal muscle pathology in mdx dystrophic mice. The American Journal of Pathology. 161: 1535-40. PMID 12414501 DOI: 10.1016/S0002-9440(10)64431-8 |
0.433 |
|
| 2002 |
Mercuri E, Talim B, Moghadaszadeh B, Petit N, Brockington M, Counsell S, Guicheney P, Muntoni F, Merlini L. Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1). Neuromuscular Disorders : Nmd. 12: 631-8. PMID 12207930 DOI: 10.1016/s0960-8966(02)00023-8 |
0.323 |
|
| 2002 |
Ferreiro A, Quijano-Roy S, Pichereau C, Moghadaszadeh B, Goemans N, Bönnemann C, Jungbluth H, Straub V, Villanova M, Leroy JP, Romero NB, Martin JJ, Muntoni F, Voit T, Estournet B, et al. Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies. American Journal of Human Genetics. 71: 739-49. PMID 12192640 DOI: 10.1086/342719 |
0.323 |
|
| 2002 |
Demir E, Sabatelli P, Allamand V, Ferreiro A, Moghadaszadeh B, Makrelouf M, Topaloglu H, Echenne B, Merlini L, Guicheney P. Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy. American Journal of Human Genetics. 70: 1446-58. PMID 11992252 DOI: 10.1086/340608 |
0.303 |
|
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