Year |
Citation |
Score |
2020 |
Kapfhamer D, McKenna J, Yoon CJ, Murray-Stewart T, Casero RA, Gambello MJ. Ornithine Decarboxylase, the rate-limiting enzyme of polyamine synthesis, modifies brain pathology in a mouse model of tuberous sclerosis complex. Human Molecular Genetics. PMID 32588887 DOI: 10.1093/Hmg/Ddaa121 |
0.485 |
|
2015 |
Rozas NS, Redell JB, McKenna J, Moore AN, Gambello MJ, Dash PK. Prolonging the survival of Tsc2 conditional knockout mice by glutamine supplementation. Biochemical and Biophysical Research Communications. 457: 635-9. PMID 25613864 DOI: 10.1016/J.Bbrc.2015.01.039 |
0.467 |
|
2013 |
Mietzsch U, McKenna J, Reith RM, Way SW, Gambello MJ. Comparative analysis of Tsc1 and Tsc2 single and double radial glial cell mutants. The Journal of Comparative Neurology. 521: 3817-31. PMID 23749404 DOI: 10.1002/Cne.23380 |
0.698 |
|
2013 |
Reith RM, McKenna J, Wu H, Hashmi SS, Cho SH, Dash PK, Gambello MJ. Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex. Neurobiology of Disease. 51: 93-103. PMID 23123587 DOI: 10.1016/J.Nbd.2012.10.014 |
0.356 |
|
2012 |
Way SW, Rozas NS, Wu HC, McKenna J, Reith RM, Hashmi SS, Dash PK, Gambello MJ. The differential effects of prenatal and/or postnatal rapamycin on neurodevelopmental defects and cognition in a neuroglial mouse model of tuberous sclerosis complex. Human Molecular Genetics. 21: 3226-36. PMID 22532572 DOI: 10.1093/Hmg/Dds156 |
0.688 |
|
2012 |
Chévere-Torres I, Kaphzan H, Bhattacharya A, Kang A, Maki JM, Gambello MJ, Arbiser JL, Santini E, Klann E. Metabotropic glutamate receptor-dependent long-term depression is impaired due to elevated ERK signaling in the ΔRG mouse model of tuberous sclerosis complex. Neurobiology of Disease. 45: 1101-10. PMID 22198573 DOI: 10.1016/J.Nbd.2011.12.028 |
0.323 |
|
2011 |
Reith RM, Way S, McKenna J, Haines K, Gambello MJ. Loss of the tuberous sclerosis complex protein tuberin causes Purkinje cell degeneration. Neurobiology of Disease. 43: 113-22. PMID 21419848 DOI: 10.1016/j.nbd.2011.02.014 |
0.686 |
|
2010 |
Zeng LH, Rensing NR, Zhang B, Gutmann DH, Gambello MJ, Wong M. Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex. Human Molecular Genetics. 20: 445-54. PMID 21062901 DOI: 10.1093/Hmg/Ddq491 |
0.477 |
|
2010 |
Kim S, Lehtinen MK, Sessa A, Zappaterra MW, Cho SH, Gonzalez D, Boggan B, Austin CA, Wijnholds J, Gambello MJ, Malicki J, LaMantia AS, Broccoli V, Walsh CA. The apical complex couples cell fate and cell survival to cerebral cortical development. Neuron. 66: 69-84. PMID 20399730 DOI: 10.1016/J.Neuron.2010.03.019 |
0.368 |
|
2010 |
Cao J, Gong L, Guo DC, Mietzsch U, Kuang SQ, Kwartler CS, Safi H, Estrera A, Gambello MJ, Milewicz DM. Thoracic aortic disease in tuberous sclerosis complex: molecular pathogenesis and potential therapies in Tsc2+/- mice. Human Molecular Genetics. 19: 1908-20. PMID 20159776 DOI: 10.1093/Hmg/Ddq066 |
0.348 |
|
2009 |
Adhikari D, Flohr G, Gorre N, Shen Y, Yang H, Lundin E, Lan Z, Gambello MJ, Liu K. Disruption of Tsc2 in oocytes leads to overactivation of the entire pool of primordial follicles. Molecular Human Reproduction. 15: 765-70. PMID 19843635 DOI: 10.1093/molehr/gap092 |
0.307 |
|
2009 |
Way SW, McKenna J, Mietzsch U, Reith RM, Wu HC, Gambello MJ. Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse. Human Molecular Genetics. 18: 1252-65. PMID 19150975 DOI: 10.1093/hmg/ddp025 |
0.693 |
|
2007 |
Hernandez O, Way S, McKenna J, Gambello MJ. Generation of a conditional disruption of the Tsc2 gene. Genesis (New York, N.Y. : 2000). 45: 101-6. PMID 17245776 DOI: 10.1002/dvg.20271 |
0.68 |
|
2004 |
Au KS, Williams AT, Gambello MJ, Northrup H. Molecular genetic basis of tuberous sclerosis complex: from bench to bedside. Journal of Child Neurology. 19: 699-709. PMID 15563017 DOI: 10.1177/08830738040190091101 |
0.421 |
|
2004 |
Toyo-oka K, Hirotsune S, Gambello MJ, Zhou ZQ, Olson L, Rosenfeld MG, Eisenman R, Hurlin P, Wynshaw-Boris A. Loss of the Max-interacting protein Mnt in mice results in decreased viability, defective embryonic growth and craniofacial defects: relevance to Miller-Dieker syndrome. Human Molecular Genetics. 13: 1057-67. PMID 15028671 DOI: 10.1093/Hmg/Ddh116 |
0.386 |
|
2003 |
Toyo-oka K, Shionoya A, Gambello MJ, Cardoso C, Leventer R, Ward HL, Ayala R, Tsai LH, Dobyns W, Ledbetter D, Hirotsune S, Wynshaw-Boris A. 14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome. Nature Genetics. 34: 274-85. PMID 12796778 DOI: 10.1038/Ng1169 |
0.319 |
|
2003 |
Gambello MJ, Darling DL, Yingling J, Tanaka T, Gleeson JG, Wynshaw-Boris A. Multiple dose-dependent effects of Lis1 on cerebral cortical development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 1719-29. PMID 12629176 DOI: 10.1523/Jneurosci.23-05-01719.2003 |
0.363 |
|
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