| Year |
Citation |
Score |
| 2020 |
Klofas LK, Short BP, Snow JP, Sinnaeve J, Rushing GV, Westlake G, Weinstein W, Ihrie RA, Ess KC, Carson RP. DEPDC5 haploinsufficiency drives increased mTORC1 signaling and abnormal morphology in human iPSC-derived cortical neurons. Neurobiology of Disease. 104975. PMID 32574724 DOI: 10.1016/J.Nbd.2020.104975 |
0.353 |
|
| 2020 |
Klofas LK, Short BP, Zhou C, Carson RP. Prevention of premature death and seizures in a Depdc5 mouse epilepsy model through inhibition of mTORC1. Human Molecular Genetics. PMID 32280987 DOI: 10.1093/Hmg/Ddaa068 |
0.335 |
|
| 2019 |
Short B, Kozek L, Harmsen H, Zhang B, Wong M, Ess KC, Fu C, Naftel R, Pearson MM, Carson RP. Cerebral aquaporin-4 expression is independent of seizures in tuberous sclerosis complex. Neurobiology of Disease. PMID 31078684 DOI: 10.1016/J.Nbd.2019.05.003 |
0.314 |
|
| 2015 |
Carson RP, Kelm ND, West KL, Does MD, Fu C, Weaver G, McBrier E, Parker B, Grier MD, Ess KC. Hypomyelination following deletion of Tsc2 in oligodendrocyte precursors. Annals of Clinical and Translational Neurology. 2: 1041-54. PMID 26734657 DOI: 10.1002/Acn3.254 |
0.307 |
|
| 2013 |
Kim SH, Scott SA, Bennett MJ, Carson RP, Fessel J, Brown HA, Ess KC. Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiency. Plos Genetics. 9: e1003563. PMID 23785301 DOI: 10.1371/Journal.Pgen.1003563 |
0.358 |
|
| 2013 |
Carson RP, Fu C, Winzenburger P, Ess KC. Deletion of Rictor in neural progenitor cells reveals contributions of mTORC2 signaling to tuberous sclerosis complex. Human Molecular Genetics. 22: 140-52. PMID 23049074 DOI: 10.1093/Hmg/Dds414 |
0.346 |
|
| 2012 |
Armour EA, Carson RP, Ess KC. Cystogenesis and elongated primary cilia in Tsc1-deficient distal convoluted tubules. American Journal of Physiology. Renal Physiology. 303: F584-92. PMID 22674026 DOI: 10.1152/Ajprenal.00141.2012 |
0.311 |
|
| 2012 |
Carson RP, Van Nielen DL, Winzenburger PA, Ess KC. Neuronal and glia abnormalities in Tsc1-deficient forebrain and partial rescue by rapamycin. Neurobiology of Disease. 45: 369-80. PMID 21907282 DOI: 10.1016/J.Nbd.2011.08.024 |
0.365 |
|
| 2004 |
Oeltmann T, Carson R, Shannon JR, Ketch T, Robertson D. Assessment of O-methylated catecholamine levels in plasma and urine for diagnosis of autonomic disorders. Autonomic Neuroscience : Basic & Clinical. 116: 1-10. PMID 15556832 DOI: 10.1016/J.Autneu.2004.08.013 |
0.395 |
|
| 2002 |
Carson RP, Diedrich A, Robertson D. Autonomic control after blockade of the norepinephrine transporter: a model of orthostatic intolerance. Journal of Applied Physiology (Bethesda, Md. : 1985). 93: 2192-8. PMID 12391111 DOI: 10.1152/Japplphysiol.00033.2002 |
0.462 |
|
| 2002 |
Carson RP, Robertson D. Genetic manipulation of noradrenergic neurons. The Journal of Pharmacology and Experimental Therapeutics. 301: 410-7. PMID 11961038 DOI: 10.1124/Jpet.301.2.410 |
0.443 |
|
| 2001 |
Robertson D, Flattem N, Tellioglu T, Carson R, Garland E, Shannon JR, Jordan J, Jacob G, Blakely RD, Biaggioni I. Familial orthostatic tachycardia due to norepinephrine transporter deficiency. Annals of the New York Academy of Sciences. 940: 527-43. PMID 11458707 DOI: 10.1111/J.1749-6632.2001.Tb03703.X |
0.456 |
|
| 2001 |
Carson RP, Appalsamy M, Diedrich A, Davis TL, Robertson D. Animal model of neuropathic tachycardia syndrome. Hypertension. 37: 1357-61. PMID 11408377 DOI: 10.1161/01.Hyp.37.6.1357 |
0.427 |
|
| 2001 |
Robertson D, Shannon JR, Biaggioni I, Ertl AC, Diedrich A, Carson R, Furlan R, Jacob G, Jordan J. Orthostatic intolerance and the postural tachycardia syndrome: Genetic and environment pathophysiologies Pflugers Archiv European Journal of Physiology. 441: R48-R51. PMID 11200979 DOI: 10.1007/S004240000353 |
0.368 |
|
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