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Michael J. Gambello - Publications

Affiliations: 
Pediatrics University of Texas Health Science Center at Houston, Houston, TX, United States 
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17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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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