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Items: 1 to 20 of 140

1.

Rab7 mutants associated with Charcot-Marie-Tooth disease cause delayed growth factor receptor transport and altered endosomal and nuclear signaling.

BasuRay S, Mukherjee S, Romero EG, Seaman MN, Wandinger-Ness A.

J Biol Chem. 2013 Jan 11;288(2):1135-49. doi: 10.1074/jbc.M112.417766. Epub 2012 Nov 27.

2.

Rab7 mutants associated with Charcot-Marie-Tooth disease exhibit enhanced NGF-stimulated signaling.

BasuRay S, Mukherjee S, Romero E, Wilson MC, Wandinger-Ness A.

PLoS One. 2010 Dec 9;5(12):e15351. doi: 10.1371/journal.pone.0015351.

3.

Molecular basis of Charcot-Marie-Tooth type 2B disease.

Bucci C, De Luca M.

Biochem Soc Trans. 2012 Dec 1;40(6):1368-72. doi: 10.1042/BST20120197.

PMID:
23176482
4.

Defective axonal transport of Rab7 GTPase results in dysregulated trophic signaling.

Zhang K, Fishel Ben Kenan R, Osakada Y, Xu W, Sinit RS, Chen L, Zhao X, Chen JY, Cui B, Wu C.

J Neurosci. 2013 Apr 24;33(17):7451-62. doi: 10.1523/JNEUROSCI.4322-12.2013.

5.

Characterization of the Rab7K157N mutant protein associated with Charcot-Marie-Tooth type 2B.

De Luca A, Progida C, Spinosa MR, Alifano P, Bucci C.

Biochem Biophys Res Commun. 2008 Jul 25;372(2):283-7. doi: 10.1016/j.bbrc.2008.05.060. Epub 2008 May 21.

PMID:
18501189
7.
8.

Rab7 and the CMT2B disease.

Cogli L, Piro F, Bucci C.

Biochem Soc Trans. 2009 Oct;37(Pt 5):1027-31. doi: 10.1042/BST0371027. Review.

PMID:
19754445
9.

Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in Drosophila.

Janssens K, Goethals S, Atkinson D, Ermanoska B, Fransen E, Jordanova A, Auer-Grumbach M, Asselbergh B, Timmerman V.

Neurobiol Dis. 2014 May;65:211-9. doi: 10.1016/j.nbd.2014.01.021. Epub 2014 Feb 9.

PMID:
24521780
10.

Charcot-Marie-Tooth 2B mutations in rab7 cause dosage-dependent neurodegeneration due to partial loss of function.

Cherry S, Jin EJ, Ozel MN, Lu Z, Agi E, Wang D, Jung WH, Epstein D, Meinertzhagen IA, Chan CC, Hiesinger PR.

Elife. 2013 Dec 10;2:e01064. doi: 10.7554/eLife.01064.

11.

Functional characterization of Rab7 mutant proteins associated with Charcot-Marie-Tooth type 2B disease.

Spinosa MR, Progida C, De Luca A, Colucci AM, Alifano P, Bucci C.

J Neurosci. 2008 Feb 13;28(7):1640-8. doi: 10.1523/JNEUROSCI.3677-07.2008.

12.

The mood stabilizer valproic acid improves defective neurite formation caused by Charcot-Marie-Tooth disease-associated mutant Rab7 through the JNK signaling pathway.

Yamauchi J, Torii T, Kusakawa S, Sanbe A, Nakamura K, Takashima S, Hamasaki H, Kawaguchi S, Miyamoto Y, Tanoue A.

J Neurosci Res. 2010 Nov 1;88(14):3189-97. doi: 10.1002/jnr.22460.

PMID:
20645406
13.

LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity.

Gómez-Suaga P, Rivero-Ríos P, Fdez E, Blanca Ramírez M, Ferrer I, Aiastui A, López De Munain A, Hilfiker S.

Hum Mol Genet. 2014 Dec 20;23(25):6779-96. doi: 10.1093/hmg/ddu395. Epub 2014 Jul 30.

14.
15.

CMT2B-associated Rab7 mutants inhibit neurite outgrowth.

Cogli L, Progida C, Lecci R, Bramato R, Krüttgen A, Bucci C.

Acta Neuropathol. 2010 Oct;120(4):491-501. doi: 10.1007/s00401-010-0696-8. Epub 2010 May 13.

PMID:
20464402
16.

RAB-7 antagonizes LET-23 EGFR signaling during vulva development in Caenorhabditis elegans.

Skorobogata O, Rocheleau CE.

PLoS One. 2012;7(4):e36489. doi: 10.1371/journal.pone.0036489. Epub 2012 Apr 30.

17.

RAB7 and TSG101 are required for the constitutive recycling of unliganded EGFRs via distinct mechanisms.

Rush JS, Ceresa BP.

Mol Cell Endocrinol. 2013 Dec 5;381(1-2):188-97. doi: 10.1016/j.mce.2013.07.029. Epub 2013 Aug 7.

18.

Disease mutations in Rab7 result in unregulated nucleotide exchange and inappropriate activation.

McCray BA, Skordalakes E, Taylor JP.

Hum Mol Genet. 2010 Mar 15;19(6):1033-47. doi: 10.1093/hmg/ddp567. Epub 2009 Dec 22.

19.

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy.

Verhoeven K, De Jonghe P, Coen K, Verpoorten N, Auer-Grumbach M, Kwon JM, FitzPatrick D, Schmedding E, De Vriendt E, Jacobs A, Van Gerwen V, Wagner K, Hartung HP, Timmerman V.

Am J Hum Genet. 2003 Mar;72(3):722-7. Epub 2003 Jan 21.

20.
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