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Items: 1 to 20 of 93

1.

Endogenous neuroprotection: hamartin modulates an austere approach to staying alive in a recession.

Hadley G, De Luca GC, Papadakis M, Buchan AM.

Int J Stroke. 2013 Aug;8(6):449-50. doi: 10.1111/ijs.12130. Review.

PMID:
23879750
2.

Tsc1 (hamartin) confers neuroprotection against ischemia by inducing autophagy.

Papadakis M, Hadley G, Xilouri M, Hoyte LC, Nagel S, McMenamin MM, Tsaknakis G, Watt SM, Drakesmith CW, Chen R, Wood MJ, Zhao Z, Kessler B, Vekrellis K, Buchan AM.

Nat Med. 2013 Mar;19(3):351-7. doi: 10.1038/nm.3097. Epub 2013 Feb 24.

3.

Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuber.

Jansen FE, Notenboom RG, Nellist M, Goedbloed MA, Halley DJ, de Graan PN, van Nieuwenhuizen O.

Neurology. 2004 Oct 12;63(7):1293-5.

PMID:
15477556
4.
5.

Dissociate expression of tuberous sclerosis complex 1 product hamartin in a skin and pulmonary lesion of a tuberous sclerosis complex.

Wataya-Kaneda M, Katayama I.

Hum Pathol. 2009 Mar;40(3):430-4. doi: 10.1016/j.humpath.2008.06.026. Epub 2008 Oct 5.

PMID:
18835623
6.

Tuberous-sclerosis complex-related cell signaling in the pathogenesis of lung cancer.

Fuchs A, König K, Heukamp LC, Fassunke J, Kirfel J, Huss S, Becker AJ, Büttner R, Majores M.

Diagn Pathol. 2014 Mar 4;9:48. doi: 10.1186/1746-1596-9-48.

7.

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 Mar-Apr;658(3):234-46. doi: 10.1016/j.mrrev.2008.01.001. Epub 2008 Jan 12. Review.

PMID:
18291711
8.

Developmental expression of the tuberous sclerosis proteins tuberin and hamartin.

Murthy V, Stemmer-Rachamimov AO, Haddad LA, Roy JE, Cutone AN, Beauchamp RL, Smith N, Louis DN, Ramesh V.

Acta Neuropathol. 2001 Mar;101(3):202-10.

PMID:
11307618
9.

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. Epub 2005 Dec 8.

PMID:
16339216
11.

Antisense suppression of TSC1 gene product, hamartin, enhances neurite outgrowth in NGF-treated PC12h cells.

Floricel F, Higaki K, Maki H, Nanba E, Ninomiya H, Ohno K.

Brain Dev. 2007 Sep;29(8):502-9. Epub 2007 Mar 21.

PMID:
17376623
12.

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;35(1):100-8. Epub 2007 Feb 12.

PMID:
17355907
13.

Proteins interacting with the tuberous sclerosis gene products.

Rosner M, Freilinger A, Hengstschläger M.

Amino Acids. 2004 Oct;27(2):119-28. Epub 2004 Sep 7. Review.

PMID:
15351877
14.

Phosphorylated hamartin-Hsp70 complex regulates apoptosis via mitochondrial localization.

Inoue H, Uyama T, Suzuki T, Kazami M, Hino O, Kobayashi T, Kobayashi K, Tadokoro T, Yamamoto Y.

Biochem Biophys Res Commun. 2010 Jan 1;391(1):1148-53. doi: 10.1016/j.bbrc.2009.12.054. Epub 2009 Dec 16.

PMID:
20006582
15.

Cell cycle-regulated phosphorylation of hamartin, the product of the tuberous sclerosis complex 1 gene, by cyclin-dependent kinase 1/cyclin B.

Astrinidis A, Senapedis W, Coleman TR, Henske EP.

J Biol Chem. 2003 Dec 19;278(51):51372-9. Epub 2003 Oct 9.

16.

Tuberous sclerosis complex: Hamartin and tuberin expression in renal cysts and its discordant expression in renal neoplasms.

Bonsib SM, Boils C, Gokden N, Grignon D, Gu X, Higgins JP, Leroy X, McKenney JK, Nasr SH, Phillips C, Sangoi AR, Wilson J, Zhang PL.

Pathol Res Pract. 2016 Nov;212(11):972-979. doi: 10.1016/j.prp.2016.04.005. Epub 2016 Apr 30.

17.

Pediatric epileptology.

Sahin M, Miller I, Holmes GL, Sheth RD.

Epilepsy Behav. 2011 Sep;22(1):32-7. doi: 10.1016/j.yebeh.2011.02.010. Epub 2011 May 6. Review.

PMID:
21530413
18.

Tuberous sclerosis complex: genetics to pathogenesis.

Narayanan V.

Pediatr Neurol. 2003 Nov;29(5):404-9. Review.

PMID:
14684235
19.

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 1;20(3):445-54. doi: 10.1093/hmg/ddq491. Epub 2010 Nov 9.

20.

The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitination.

Benvenuto G, Li S, Brown SJ, Braverman R, Vass WC, Cheadle JP, Halley DJ, Sampson JR, Wienecke R, DeClue JE.

Oncogene. 2000 Dec 14;19(54):6306-16.

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