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Items: 1 to 20 of 67

1.

A thorough assessment of benign genetic variability in GRN and MAPT.

Guerreiro RJ, Washecka N, Hardy J, Singleton A.

Hum Mutat. 2010 Feb;31(2):E1126-40. doi: 10.1002/humu.21152.

2.

Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis.

van Es MA, Dahlberg C, Birve A, Veldink JH, van den Berg LH, Andersen PM.

J Neurol Neurosurg Psychiatry. 2010 May;81(5):562-6. doi: 10.1136/jnnp.2009.181453. Epub 2009 Dec 3.

PMID:
19965850
3.

Autophagy defects contribute to neurodegeneration induced by dysfunctional ESCRT-III.

Lee JA, Liu L, Gao FB.

Autophagy. 2009 Oct;5(7):1070-2. Epub 2009 Oct 15.

PMID:
19738424
4.

Inhibition of autophagy induction delays neuronal cell loss caused by dysfunctional ESCRT-III in frontotemporal dementia.

Lee JA, Gao FB.

J Neurosci. 2009 Jul 1;29(26):8506-11. doi: 10.1523/JNEUROSCI.0924-09.2009.

5.

In search of an "autophagomometer".

Rubinsztein DC, Cuervo AM, Ravikumar B, Sarkar S, Korolchuk V, Kaushik S, Klionsky DJ.

Autophagy. 2009 Jul;5(5):585-9. Epub 2009 Jul 23.

PMID:
19411822
6.

Molecular neuropathology of TDP-43 proteinopathies.

Neumann M.

Int J Mol Sci. 2009 Jan;10(1):232-46. doi: 10.3390/ijms10010232. Epub 2009 Jan 9. Review.

7.

Trafficking and function of the tetraspanin CD63.

Pols MS, Klumperman J.

Exp Cell Res. 2009 May 15;315(9):1584-92. doi: 10.1016/j.yexcr.2008.09.020. Epub 2008 Oct 7. Review.

PMID:
18930046
8.

Genetics of amyotrophic lateral sclerosis.

Siddique N, Siddique T.

Phys Med Rehabil Clin N Am. 2008 Aug;19(3):429-39, vii. doi: 10.1016/j.pmr.2008.05.001. Review.

9.

Role of axonal transport in neurodegenerative diseases.

De Vos KJ, Grierson AJ, Ackerley S, Miller CC.

Annu Rev Neurosci. 2008;31:151-73. doi: 10.1146/annurev.neuro.31.061307.090711. Review.

PMID:
18558852
10.

TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis.

Guerreiro RJ, Schymick JC, Crews C, Singleton A, Hardy J, Traynor BJ.

PLoS One. 2008 Jun 11;3(6):e2450. doi: 10.1371/journal.pone.0002450.

11.

Mitochondria: the hub of cellular Ca2+ signaling.

Szabadkai G, Duchen MR.

Physiology (Bethesda). 2008 Apr;23:84-94. doi: 10.1152/physiol.00046.2007. Review. Erratum in: Physiology (Bethesda). 2008 Aug;23:230.

12.

CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis.

Blair IP, Vance C, Durnall JC, Williams KL, Thoeng A, Shaw CE, Nicholson GA.

J Neurol Neurosurg Psychiatry. 2008 Jul;79(7):849-50. doi: 10.1136/jnnp.2007.140541. Epub 2008 Feb 12. No abstract available.

PMID:
18270236
13.

Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes.

Klionsky DJ, Abeliovich H, Agostinis P, Agrawal DK, Aliev G, Askew DS, Baba M, Baehrecke EH, Bahr BA, Ballabio A, Bamber BA, Bassham DC, Bergamini E, Bi X, Biard-Piechaczyk M, Blum JS, Bredesen DE, Brodsky JL, Brumell JH, Brunk UT, Bursch W, Camougrand N, Cebollero E, Cecconi F, Chen Y, Chin LS, Choi A, Chu CT, Chung J, Clarke PG, Clark RS, Clarke SG, Clavé C, Cleveland JL, Codogno P, Colombo MI, Coto-Montes A, Cregg JM, Cuervo AM, Debnath J, Demarchi F, Dennis PB, Dennis PA, Deretic V, Devenish RJ, Di Sano F, Dice JF, Difiglia M, Dinesh-Kumar S, Distelhorst CW, Djavaheri-Mergny M, Dorsey FC, Dröge W, Dron M, Dunn WA Jr, Duszenko M, Eissa NT, Elazar Z, Esclatine A, Eskelinen EL, Fésüs L, Finley KD, Fuentes JM, Fueyo J, Fujisaki K, Galliot B, Gao FB, Gewirtz DA, Gibson SB, Gohla A, Goldberg AL, Gonzalez R, González-Estévez C, Gorski S, Gottlieb RA, Häussinger D, He YW, Heidenreich K, Hill JA, Høyer-Hansen M, Hu X, Huang WP, Iwasaki A, Jäättelä M, Jackson WT, Jiang X, Jin S, Johansen T, Jung JU, Kadowaki M, Kang C, Kelekar A, Kessel DH, Kiel JA, Kim HP, Kimchi A, Kinsella TJ, Kiselyov K, Kitamoto K, Knecht E, Komatsu M, Kominami E, Kondo S, Kovács AL, Kroemer G, Kuan CY, Kumar R, Kundu M, Landry J, Laporte M, Le W, Lei HY, Lenardo MJ, Levine B, Lieberman A, Lim KL, Lin FC, Liou W, Liu LF, Lopez-Berestein G, López-Otín C, Lu B, Macleod KF, Malorni W, Martinet W, Matsuoka K, Mautner J, Meijer AJ, Meléndez A, Michels P, Miotto G, Mistiaen WP, Mizushima N, Mograbi B, Monastyrska I, Moore MN, Moreira PI, Moriyasu Y, Motyl T, Münz C, Murphy LO, Naqvi NI, Neufeld TP, Nishino I, Nixon RA, Noda T, Nürnberg B, Ogawa M, Oleinick NL, Olsen LJ, Ozpolat B, Paglin S, Palmer GE, Papassideri I, Parkes M, Perlmutter DH, Perry G, Piacentini M, Pinkas-Kramarski R, Prescott M, Proikas-Cezanne T, Raben N, Rami A, Reggiori F, Rohrer B, Rubinsztein DC, Ryan KM, Sadoshima J, Sakagami H, Sakai Y, Sandri M, Sasakawa C, Sass M, Schneider C, Seglen PO, Seleverstov O, Settleman J, Shacka JJ, Shapiro IM, Sibirny A, Silva-Zacarin EC, Simon HU, Simone C, Simonsen A, Smith MA, Spanel-Borowski K, Srinivas V, Steeves M, Stenmark H, Stromhaug PE, Subauste CS, Sugimoto S, Sulzer D, Suzuki T, Swanson MS, Tabas I, Takeshita F, Talbot NJ, Tallóczy Z, Tanaka K, Tanaka K, Tanida I, Taylor GS, Taylor JP, Terman A, Tettamanti G, Thompson CB, Thumm M, Tolkovsky AM, Tooze SA, Truant R, Tumanovska LV, Uchiyama Y, Ueno T, Uzcátegui NL, van der Klei I, Vaquero EC, Vellai T, Vogel MW, Wang HG, Webster P, Wiley JW, Xi Z, Xiao G, Yahalom J, Yang JM, Yap G, Yin XM, Yoshimori T, Yu L, Yue Z, Yuzaki M, Zabirnyk O, Zheng X, Zhu X, Deter RL.

Autophagy. 2008 Feb;4(2):151-75. Epub 2007 Nov 21. Review.

15.

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS.

Gijselinck I, Sleegers K, Engelborghs S, Robberecht W, Martin JJ, Vandenberghe R, Sciot R, Dermaut B, Goossens D, van der Zee J, De Pooter T, Del-Favero J, Santens P, De Jonghe P, De Deyn PP, Van Broeckhoven C, Cruts M.

Neurobiol Aging. 2009 Aug;30(8):1329-31. Epub 2008 Jan 10.

PMID:
18068872
16.

Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease.

Filimonenko M, Stuffers S, Raiborg C, Yamamoto A, Malerød L, Fisher EM, Isaacs A, Brech A, Stenmark H, Simonsen A.

J Cell Biol. 2007 Nov 5;179(3):485-500.

17.

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

van der Zee J, Urwin H, Engelborghs S, Bruyland M, Vandenberghe R, Dermaut B, De Pooter T, Peeters K, Santens P, De Deyn PP, Fisher EM, Collinge J, Isaacs AM, Van Broeckhoven C.

Hum Mol Genet. 2008 Jan 15;17(2):313-22. Epub 2007 Oct 22.

18.

A rational mechanism for combination treatment of Huntington's disease using lithium and rapamycin.

Sarkar S, Krishna G, Imarisio S, Saiki S, O'Kane CJ, Rubinsztein DC.

Hum Mol Genet. 2008 Jan 15;17(2):170-8. Epub 2007 Oct 6.

19.
20.

ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration.

Lee JA, Beigneux A, Ahmad ST, Young SG, Gao FB.

Curr Biol. 2007 Sep 18;17(18):1561-7. Epub 2007 Aug 2. Erratum in: Curr Biol. 2007 Sep 18;17(18):1622.

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