Michael J. Gambello
Affiliations: | Pediatrics | University of Texas Health Science Center at Houston, Houston, TX, United States |
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Sign in to add trainee| Sharon W. Way | grad student | 2005-2010 | University of Texas Health Science Center at Houston |
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| Kapfhamer D, McKenna J, Yoon CJ, et al. (2020) Ornithine Decarboxylase, the rate-limiting enzyme of polyamine synthesis, modifies brain pathology in a mouse model of tuberous sclerosis complex. Human Molecular Genetics |
| Rozas NS, Redell JB, McKenna J, et al. (2015) Prolonging the survival of Tsc2 conditional knockout mice by glutamine supplementation. Biochemical and Biophysical Research Communications. 457: 635-9 |
| Mietzsch U, McKenna J, Reith RM, et al. (2013) Comparative analysis of Tsc1 and Tsc2 single and double radial glial cell mutants. The Journal of Comparative Neurology. 521: 3817-31 |
| Reith RM, McKenna J, Wu H, et al. (2013) 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 |
| Way SW, Rozas NS, Wu HC, et al. (2012) 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 |
| Chévere-Torres I, Kaphzan H, Bhattacharya A, et al. (2012) 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 |
| Reith RM, Way S, McKenna J, et al. (2011) Loss of the tuberous sclerosis complex protein tuberin causes Purkinje cell degeneration. Neurobiology of Disease. 43: 113-22 |
| Zeng LH, Rensing NR, Zhang B, et al. (2010) 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 |
| Kim S, Lehtinen MK, Sessa A, et al. (2010) The apical complex couples cell fate and cell survival to cerebral cortical development. Neuron. 66: 69-84 |
| Cao J, Gong L, Guo DC, et al. (2010) Thoracic aortic disease in tuberous sclerosis complex: molecular pathogenesis and potential therapies in Tsc2+/- mice. Human Molecular Genetics. 19: 1908-20 |