Year |
Citation |
Score |
2014 |
Liu Y, Satz JS, Vo MN, Nangle LA, Schimmel P, Ackerman SL. Deficiencies in tRNA synthetase editing activity cause cardioproteinopathy. Proceedings of the National Academy of Sciences of the United States of America. 111: 17570-5. PMID 25422440 DOI: 10.1073/Pnas.1420196111 |
0.347 |
|
2013 |
Nguyen H, Ostendorf AP, Satz JS, Westra S, Ross-Barta SE, Campbell KP, Moore SA. Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteins. Acta Neuropathologica Communications. 1: 58. PMID 24252195 DOI: 10.1186/2051-5960-1-58 |
0.589 |
|
2012 |
Myshrall TD, Moore SA, Ostendorf AP, Satz JS, Kowalczyk T, Nguyen H, Daza RA, Lau C, Campbell KP, Hevner RF. Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortex. Journal of Neuropathology and Experimental Neurology. 71: 1047-63. PMID 23147502 DOI: 10.1097/Nen.0B013E318274A128 |
0.499 |
|
2011 |
Hara Y, Kanagawa M, Kunz S, Yoshida-Moriguchi T, Satz JS, Kobayashi YM, Zhu Z, Burden SJ, Oldstone MB, Campbell KP. Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection. Proceedings of the National Academy of Sciences of the United States of America. 108: 17426-31. PMID 21987822 DOI: 10.1073/Pnas.1114836108 |
0.546 |
|
2011 |
Noell S, Wolburg-Buchholz K, Mack AF, Beedle AM, Satz JS, Campbell KP, Wolburg H, Fallier-Becker P. Evidence for a role of dystroglycan regulating the membrane architecture of astroglial endfeet. The European Journal of Neuroscience. 33: 2179-86. PMID 21501259 DOI: 10.1111/J.1460-9568.2011.07688.X |
0.556 |
|
2011 |
Stalnaker SH, Aoki K, Lim JM, Porterfield M, Liu M, Satz JS, Buskirk S, Xiong Y, Zhang P, Campbell KP, Hu H, Live D, Tiemeyer M, Wells L. Glycomic analyses of mouse models of congenital muscular dystrophy. The Journal of Biological Chemistry. 286: 21180-90. PMID 21460210 DOI: 10.1074/Jbc.M110.203281 |
0.492 |
|
2011 |
Hara Y, Balci-Hayta B, Yoshida-Moriguchi T, Kanagawa M, Beltrán-Valero de Bernabé D, Günde?li H, Willer T, Satz JS, Crawford RW, Burden SJ, Kunz S, Oldstone MB, Accardi A, Talim B, Muntoni F, et al. A dystroglycan mutation associated with limb-girdle muscular dystrophy. The New England Journal of Medicine. 364: 939-46. PMID 21388311 DOI: 10.1056/Nejmoa1006939 |
0.541 |
|
2010 |
Satz JS, Ostendorf AP, Hou S, Turner A, Kusano H, Lee JC, Turk R, Nguyen H, Ross-Barta SE, Westra S, Hoshi T, Moore SA, Campbell KP. Distinct functions of glial and neuronal dystroglycan in the developing and adult mouse brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 14560-72. PMID 20980614 DOI: 10.1523/Jneurosci.3247-10.2010 |
0.554 |
|
2010 |
Satz JS, Philip AR, Nguyen H, Kusano H, Lee J, Turk R, Riker MJ, Hernández J, Weiss RM, Anderson MG, Mullins RF, Moore SA, Stone EM, Campbell KP. Visual impairment in the absence of dystroglycan (Journal of Neuroscience (2010) 30, (13136-13146)) Journal of Neuroscience. 30: 797. |
0.367 |
|
2010 |
Satz JS, Philp AR, Nguyen H, Kusano H, Lee J, Turk R, Riker MJ, Hernández J, Weiss RM, Anderson MG, Mullins RF, Moore SA, Stone EM, Campbell KP. Visual impairment in the absence of dystroglycan (The Journal of Neuroscience (2009) (13136-13146)) Journal of Neuroscience. 30: 1983. |
0.367 |
|
2009 |
Satz JS, Philp AR, Nguyen H, Kusano H, Lee J, Turk R, Riker MJ, Hernández J, Weiss RM, Anderson MG, Mullins RF, Moore SA, Stone EM, Campbell KP. Visual impairment in the absence of dystroglycan. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 13136-46. PMID 19846701 DOI: 10.1523/Jneurosci.0474-09.2009 |
0.52 |
|
2008 |
Satz JS, Barresi R, Durbeej M, Willer T, Turner A, Moore SA, Campbell KP. Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblast. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 10567-75. PMID 18923033 DOI: 10.1523/Jneurosci.2457-08.2008 |
0.534 |
|
2008 |
Satz JS, Campbell KP. Unraveling the ribbon synapse. Nature Neuroscience. 11: 857-9. PMID 18660835 DOI: 10.1038/Nn0808-857 |
0.499 |
|
2005 |
Kanagawa M, Michele DE, Satz JS, Barresi R, Kusano H, Sasaki T, Timpl R, Henry MD, Campbell KP. Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function. Febs Letters. 579: 4792-6. PMID 16098969 DOI: 10.1016/J.Febslet.2005.07.059 |
0.654 |
|
2005 |
Méhes E, Czirók A, Hegedüs B, Szabó B, Vicsek T, Satz J, Campbell K, Jancsik V. Dystroglycan is involved in laminin-1-stimulated motility of Müller glial cells: Combined velocity and directionality analysis Glia. 49: 492-500. PMID 15578661 DOI: 10.1002/Glia.20135 |
0.54 |
|
2004 |
Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nature Medicine. 10: 696-703. PMID 15184894 DOI: 10.1038/Nm1059 |
0.649 |
|
2002 |
Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature. 418: 417-22. PMID 12140558 DOI: 10.1038/Nature00837 |
0.681 |
|
2001 |
Sugita S, Saito F, Tang J, Satz J, Campbell K, Südhof TC. A stoichiometric complex of neurexins and dystroglycan in brain. The Journal of Cell Biology. 154: 435-45. PMID 11470830 DOI: 10.1083/Jcb.200105003 |
0.605 |
|
2001 |
Henry MD, Satz JS, Brakebusch C, Costell M, Gustafsson E, Fässler R, Campbell KP. Distinct roles for dystroglycan, beta1 integrin and perlecan in cell surface laminin organization. Journal of Cell Science. 114: 1137-44. PMID 11228157 |
0.484 |
|
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