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Journal Abstract Search

323 related items for PubMed ID: 17376623

  • 21. The tuberous sclerosis gene products hamartin and tuberin are multifunctional proteins with a wide spectrum of interacting partners.
    Rosner M, Hanneder M, Siegel N, Valli A, Hengstschläger M.
    Mutat Res; 2008; 658(3):234-46. PubMed ID: 18291711
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  • 23. Enhanced episodic-like memory and kindling epilepsy in a rat model of tuberous sclerosis.
    Waltereit R, Welzl H, Dichgans J, Lipp HP, Schmidt WJ, Weller M.
    J Neurochem; 2006 Jan; 96(2):407-13. PubMed ID: 16300636
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  • 24. Analysis of TSC2 stop codon variants found in tuberous sclerosis patients.
    Goedbloed MA, Nellist M, Verhaaf B, Reuser AJ, Lindhout D, Sunde L, Verhoef S, Halley DJ, van den Ouweland AM.
    Eur J Hum Genet; 2001 Nov; 9(11):823-8. PubMed ID: 11781698
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  • 25. Hamartin, the tuberous sclerosis complex 1 gene product, interacts with polo-like kinase 1 in a phosphorylation-dependent manner.
    Astrinidis A, Senapedis W, Henske EP.
    Hum Mol Genet; 2006 Jan 15; 15(2):287-97. PubMed ID: 16339216
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  • 26. Evidence for separable functions of tuberous sclerosis gene products in mammalian cell cycle regulation.
    Miloloza A, Kubista M, Rosner M, Hengstschläger M.
    J Neuropathol Exp Neurol; 2002 Feb 15; 61(2):154-63. PubMed ID: 11853018
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  • 27. A role of the tuberous sclerosis gene-2 product during neuronal differentiation.
    Soucek T, Hölzl G, Bernaschek G, Hengstschläger M.
    Oncogene; 1998 Apr 30; 16(17):2197-204. PubMed ID: 9619828
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  • 28. Analysis of 65 tuberous sclerosis complex (TSC) patients by TSC2 DGGE, TSC1/TSC2 MLPA, and TSC1 long-range PCR sequencing, and report of 28 novel mutations.
    Rendtorff ND, Bjerregaard B, Frödin M, Kjaergaard S, Hove H, Skovby F, Brøndum-Nielsen K, Schwartz M, Danish Tuberous Sclerosis Group.
    Hum Mutat; 2005 Oct 30; 26(4):374-83. PubMed ID: 16114042
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  • 30. Heat shock enhances NGF-induced neurite elongation which is not mediated by Hsp25 in PC12 cells.
    Read DE, Reed Herbert K, Gorman AM.
    Brain Res; 2008 Jul 24; 1221():14-23. PubMed ID: 18561899
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  • 31. Distinct effects of single amino-acid changes to tuberin on the function of the tuberin-hamartin complex.
    Nellist M, Sancak O, Goedbloed MA, Rohe C, van Netten D, Mayer K, Tucker-Williams A, van den Ouweland AM, Halley DJ.
    Eur J Hum Genet; 2005 Jan 24; 13(1):59-68. PubMed ID: 15483652
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  • 35. Tuberous sclerosis complex 2 loss-of-function mutation regulates reactive oxygen species production through Rac1 activation.
    Suzuki T, Das SK, Inoue H, Kazami M, Hino O, Kobayashi T, Yeung RS, Kobayashi K, Tadokoro T, Yamamoto Y.
    Biochem Biophys Res Commun; 2008 Mar 28; 368(1):132-7. PubMed ID: 18230340
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  • 36. The TSC1 gene product hamartin interacts with NADE.
    Yasui S, Tsuzaki K, Ninomiya H, Floricel F, Asano Y, Maki H, Takamura A, Nanba E, Higaki K, Ohno K.
    Mol Cell Neurosci; 2007 May 28; 35(1):100-8. PubMed ID: 17355907
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  • 37. NOX1/NADPH oxidase negatively regulates nerve growth factor-induced neurite outgrowth.
    Ibi M, Katsuyama M, Fan C, Iwata K, Nishinaka T, Yokoyama T, Yabe-Nishimura C.
    Free Radic Biol Med; 2006 May 15; 40(10):1785-95. PubMed ID: 16678016
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  • 39. Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex.
    Zeng LH, Rensing NR, Zhang B, Gutmann DH, Gambello MJ, Wong M.
    Hum Mol Genet; 2011 Feb 01; 20(3):445-54. PubMed ID: 21062901
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  • 40. Metastasis of benign tumor cells in tuberous sclerosis complex.
    Henske EP.
    Genes Chromosomes Cancer; 2003 Dec 01; 38(4):376-81. PubMed ID: 14566858
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