Year |
Citation |
Score |
2023 |
Russell AJ, DuVall M, Barthel B, Qian Y, Peter AK, Newell-Stamper BL, Hunt K, Lehman SJ, Madden MR, Schlachter ST, Robertson BD, Van Deusen A, Rodriguez HM, Vera CD, Su Y, et al. Modulating fast skeletal muscle contraction protects skeletal muscle in animal models of Duchenne muscular dystrophy. The Journal of Clinical Investigation. PMID 36995778 DOI: 10.1172/JCI153837 |
0.452 |
|
2020 |
Bjorkman KK, Guess MG, Harrison BC, Polmear MM, Peter AK, Leinwand LA. miR-206 Enforces a Slow Muscle Phenotype. Journal of Cell Science. PMID 32620696 DOI: 10.1242/Jcs.243162 |
0.434 |
|
2020 |
Zhang J, Vincent KP, Peter AK, Klos M, Cheng H, Huang SM, Towne JK, Ferng D, Gu Y, Dalton ND, Chan Y, Li R, Peterson KL, Chen J, McCulloch AD, et al. Cardiomyocyte Expression of ZO-1 Is Essential for Normal Atrioventricular Conduction but Does not Alter Ventricular Function. Circulation Research. PMID 32345129 DOI: 10.1161/Circresaha.119.315539 |
0.419 |
|
2019 |
Chang EI, Rozance PJ, Wesolowski SR, Nguyen LM, Shaw SC, Sclafani RA, Bjorkman KK, Peter AK, Hay W, Brown LD. Rates of myogenesis and myofiber numbers are reduced in late gestation IUGR fetal sheep. The Journal of Endocrinology. PMID 31751294 DOI: 10.1530/Joe-19-0273 |
0.437 |
|
2019 |
Peter AK, Rossi AC, Buvoli M, Ozeroff CD, Crocini C, Perry AR, Buvoli AE, Lee LA, Leinwand LA. Expression of Normally Repressed Myosin Heavy Chain 7b in the Mammalian Heart Induces Dilated Cardiomyopathy. Journal of the American Heart Association. 8: e013318. PMID 31364453 DOI: 10.1161/Jaha.119.013318 |
0.492 |
|
2017 |
Peter AK, Crocini C, Leinwand LA. Expanding our scientific horizons: utilization of unique model organisms in biological research. The Embo Journal. PMID 28694243 DOI: 10.15252/Embj.201797640 |
0.329 |
|
2017 |
Peter AK, Miller G, Capote J, DiFranco M, Solares-Pérez A, Wang EL, Heighway J, Coral-Vázquez RM, Vergara J, Crosbie-Watson RH. Nanospan, an alternatively spliced isoform of sarcospan, localizes to the sarcoplasmic reticulum in skeletal muscle and is absent in limb girdle muscular dystrophy 2F. Skeletal Muscle. 7: 11. PMID 28593034 DOI: 10.1186/s13395-017-0127-9 |
0.431 |
|
2017 |
Peter AK, Miller G, Capote J, DiFranco M, Solares-Pérez A, Wang EL, Heighway J, Coral-Vázquez RM, Vergara J, Crosbie-Watson RH. Nanospan, an alternatively spliced isoform of sarcospan, localizes to the sarcoplasmic reticulum in skeletal muscle and is absent in limb girdle muscular dystrophy 2F. Skeletal Muscle. 7: 11. PMID 28587652 DOI: 10.1186/S13395-017-0127-9 |
0.513 |
|
2016 |
Zhang Z, Mu Y, Veevers J, Peter AK, Manso AM, Bradford WH, Dalton ND, Peterson KL, Knowlton KU, Ross RS, Zhou X, Chen J. Postnatal Loss of Kindlin-2 Leads to Progressive Heart Failure. Circulation. Heart Failure. 9. PMID 27502369 DOI: 10.1161/Circheartfailure.116.003129 |
0.54 |
|
2015 |
Mu Y, Jing R, Peter AK, Lange S, Lin L, Zhang J, Ouyang K, Fang X, Veevers J, Zhou X, Evans SM, Cheng H, Chen J. Cypher and Enigma homolog protein are essential for cardiac development and embryonic survival. Journal of the American Heart Association. 4. PMID 25944877 DOI: 10.1161/Jaha.115.001950 |
0.476 |
|
2014 |
Domenighetti AA, Chu PH, Wu T, Sheikh F, Gokhin DS, Guo LT, Cui Z, Peter AK, Christodoulou DC, Parfenov MG, Gorham JM, Li DY, Banerjee I, Lai X, Witzmann FA, et al. Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice. Human Molecular Genetics. 23: 209-25. PMID 23975679 DOI: 10.1093/Hmg/Ddt412 |
0.579 |
|
2013 |
Lim BK, Peter AK, Xiong D, Narezkina A, Yung A, Dalton ND, Hwang KK, Yajima T, Chen J, Knowlton KU. Inhibition of Coxsackievirus-associated dystrophin cleavage prevents cardiomyopathy. The Journal of Clinical Investigation. 123: 5146-51. PMID 24200690 DOI: 10.1172/Jci66271 |
0.405 |
|
2013 |
Randazzo D, Giacomello E, Lorenzini S, Rossi D, Pierantozzi E, Blaauw B, Reggiani C, Lange S, Peter AK, Chen J, Sorrentino V. Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity. The Journal of Cell Biology. 200: 523-36. PMID 23420875 DOI: 10.1085/Jgp1414Oia9 |
0.521 |
|
2013 |
Randazzo D, Giacomello E, Rossi D, Blaauw B, Reggiani C, Lange S, Peter AK, Chen J, Sorrentino V. Obscurin-Dependent Localization of Ankyrin B is required for the Organization of Sub-Sarcolemma Microtubules, Localization of Dystrophin, and Sarcolemmal Integrity in Skeletal Muscle Biophysical Journal. 104: 146a. DOI: 10.1016/J.Bpj.2012.11.831 |
0.525 |
|
2012 |
Marshall JL, Holmberg J, Chou E, Ocampo AC, Oh J, Lee J, Peter AK, Martin PT, Crosbie-Watson RH. Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration. The Journal of Cell Biology. 197: 1009-27. PMID 22734004 DOI: 10.1083/Jcb.201110032 |
0.701 |
|
2011 |
Peter AK, Cheng H, Ross RS, Knowlton KU, Chen J. The costamere bridges sarcomeres to the sarcolemma in striated muscle. Progress in Pediatric Cardiology. 31: 83-88. PMID 24039381 DOI: 10.1016/J.Ppedcard.2011.02.003 |
0.516 |
|
2011 |
Cheng H, Zheng M, Peter AK, Kimura K, Li X, Ouyang K, Shen T, Cui L, Frank D, Dalton ND, Gu Y, Frey N, Peterson KL, Evans SM, Knowlton KU, et al. Selective deletion of long but not short Cypher isoforms leads to late-onset dilated cardiomyopathy. Human Molecular Genetics. 20: 1751-62. PMID 21303826 DOI: 10.1093/Hmg/Ddr050 |
0.54 |
|
2010 |
Cheng H, Kimura K, Peter AK, Cui L, Ouyang K, Shen T, Liu Y, Gu Y, Dalton ND, Evans SM, Knowlton KU, Peterson KL, Chen J. Loss of enigma homolog protein results in dilated cardiomyopathy. Circulation Research. 107: 348-56. PMID 20538684 DOI: 10.1161/Circresaha.110.218735 |
0.422 |
|
2009 |
Peter AK, Ko CY, Kim MH, Hsu N, Ouchi N, Rhie S, Izumiya Y, Zeng L, Walsh K, Crosbie RH. Myogenic Akt signaling upregulates the utrophin-glycoprotein complex and promotes sarcolemma stability in muscular dystrophy. Human Molecular Genetics. 18: 318-27. PMID 18986978 DOI: 10.1093/Hmg/Ddn358 |
0.714 |
|
2008 |
Peter AK, Marshall JL, Crosbie RH. Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex. The Journal of Cell Biology. 183: 419-27. PMID 18981229 DOI: 10.1083/Jcb.200808027 |
0.69 |
|
2007 |
Peter AK, Miller G, Crosbie RH. Disrupted mechanical stability of the dystrophin-glycoprotein complex causes severe muscular dystrophy in sarcospan transgenic mice. Journal of Cell Science. 120: 996-1008. PMID 17311848 DOI: 10.1242/Jcs.03360 |
0.733 |
|
2007 |
Miller G, Wang EL, Nassar KL, Peter AK, Crosbie RH. Structural and functional analysis of the sarcoglycan-sarcospan subcomplex. Experimental Cell Research. 313: 639-51. PMID 17223103 DOI: 10.1016/J.Yexcr.2006.11.021 |
0.654 |
|
2006 |
Miller G, Peter AK, Espinoza E, Heighway J, Crosbie RH. Over-expression of Microspan, a novel component of the sarcoplasmic reticulum, causes severe muscle pathology with triad abnormalities. Journal of Muscle Research and Cell Motility. 27: 545-58. PMID 16823602 DOI: 10.1007/S10974-006-9069-2 |
0.703 |
|
2006 |
Peter AK, Crosbie RH. Hypertrophic response of Duchenne and limb-girdle muscular dystrophies is associated with activation of Akt pathway. Experimental Cell Research. 312: 2580-91. PMID 16797529 DOI: 10.1016/J.Yexcr.2006.04.024 |
0.685 |
|
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