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Results: 1 to 20 of 148

1.

VPS35 mutation in Japanese patients with typical Parkinson's disease.

Ando M, Funayama M, Li Y, Kashihara K, Murakami Y, Ishizu N, Toyoda C, Noguchi K, Hashimoto T, Nakano N, Sasaki R, Kokubo Y, Kuzuhara S, Ogaki K, Yamashita C, Yoshino H, Hatano T, Tomiyama H, Hattori N.

Mov Disord. 2012 Sep 15;27(11):1413-7. doi: 10.1002/mds.25145. Epub 2012 Sep 18.

PMID:
22991136
[PubMed - indexed for MEDLINE]
2.

Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease.

Zhang Y, Chen S, Xiao Q, Cao L, Liu J, Rong TY, Ma JF, Wang G, Wang Y, Chen SD.

Parkinsonism Relat Disord. 2012 Jun;18(5):638-40. doi: 10.1016/j.parkreldis.2012.02.011. Epub 2012 Mar 10.

PMID:
22410496
[PubMed - indexed for MEDLINE]
3.

VPS35 gene variants are not associated with Parkinson's disease in the mainland Chinese population.

Guo JF, Sun QY, Lv ZY, Yu RL, Li K, Zhang YH, Tian JY, Xia K, Yan XX, Tang BS.

Parkinsonism Relat Disord. 2012 Sep;18(8):983-5. doi: 10.1016/j.parkreldis.2012.05.002. Epub 2012 Jun 4.

PMID:
22673036
[PubMed - indexed for MEDLINE]
4.

Screening for VPS35 mutations in Parkinson's disease.

Sheerin UM, Charlesworth G, Bras J, Guerreiro R, Bhatia K, Foltynie T, Limousin P, Silveira-Moriyama L, Lees A, Wood N.

Neurobiol Aging. 2012 Apr;33(4):838.e1-5. doi: 10.1016/j.neurobiolaging.2011.10.032. Epub 2011 Dec 7.

PMID:
22154191
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Frequency of the D620N mutation in VPS35 in Parkinson disease.

Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kostić VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, Lohmann K.

Arch Neurol. 2012 Oct;69(10):1360-4.

PMID:
22801713
[PubMed - indexed for MEDLINE]
6.

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF.

Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20.

PMID:
23261770
[PubMed - indexed for MEDLINE]
7.

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians.

Sudhaman S, Behari M, Govindappa ST, Muthane UB, Juyal RC, Thelma BK.

Neurobiol Aging. 2013 Oct;34(10):2442.e1-3. doi: 10.1016/j.neurobiolaging.2013.04.025. Epub 2013 May 28.

PMID:
23726718
[PubMed - indexed for MEDLINE]
8.

The Vps35 D620N mutation linked to Parkinson's disease disrupts the cargo sorting function of retromer.

Follett J, Norwood SJ, Hamilton NA, Mohan M, Kovtun O, Tay S, Zhe Y, Wood SA, Mellick GD, Silburn PA, Collins BM, Bugarcic A, Teasdale RD.

Traffic. 2014 Feb;15(2):230-44. doi: 10.1111/tra.12136. Epub 2013 Nov 14.

PMID:
24152121
[PubMed - indexed for MEDLINE]
9.

No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients.

Li L, Funayama M, Tomiyama H, Li Y, Yoshino H, Sasaki R, Kokubo Y, Kuzuhara S, Mizuno Y, Hattori N.

Neurosci Lett. 2010 Aug 2;479(3):245-8.

PMID:
20641165
[PubMed - indexed for MEDLINE]
10.

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease.

Zimprich A, Benet-Pagès A, Struhal W, Graf E, Eck SH, Offman MN, Haubenberger D, Spielberger S, Schulte EC, Lichtner P, Rossle SC, Klopp N, Wolf E, Seppi K, Pirker W, Presslauer S, Mollenhauer B, Katzenschlager R, Foki T, Hotzy C, Reinthaler E, Harutyunyan A, Kralovics R, Peters A, Zimprich F, Brücke T, Poewe W, Auff E, Trenkwalder C, Rost B, Ransmayr G, Winkelmann J, Meitinger T, Strom TM.

Am J Hum Genet. 2011 Jul 15;89(1):168-75. doi: 10.1016/j.ajhg.2011.06.008.

PMID:
21763483
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

VPS35 mutations in Parkinson disease.

Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, Conibear E, Wasserman WW, Aasly JO, Burkhard PR, Djaldetti R, Ghika J, Hentati F, Krygowska-Wajs A, Lynch T, Melamed E, Rajput A, Rajput AH, Solida A, Wu RM, Uitti RJ, Wszolek ZK, Vingerhoets F, Farrer MJ.

Am J Hum Genet. 2011 Jul 15;89(1):162-7. doi: 10.1016/j.ajhg.2011.06.001. Erratum in: Am J Hum Genet. 2011 Aug 12;89(2):347.

PMID:
21763482
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa.

Blanckenberg J, Ntsapi C, Carr JA, Bardien S.

Neurobiol Aging. 2014 Feb;35(2):445.e1-3. doi: 10.1016/j.neurobiolaging.2013.08.023. Epub 2013 Sep 27.

PMID:
24080171
[PubMed - indexed for MEDLINE]
13.

Analysis of EIF4G1 in ethnic Chinese.

Li K, Tang BS, Guo JF, Lou MX, Lv ZY, Liu ZH, Tian Y, Song CY, Xia K, Yan XX.

BMC Neurol. 2013 Apr 26;13:38. doi: 10.1186/1471-2377-13-38.

PMID:
23617574
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

The VPS35 gene and Parkinson's disease.

Deng H, Gao K, Jankovic J.

Mov Disord. 2013 May;28(5):569-75. doi: 10.1002/mds.25430. Epub 2013 Mar 27. Review.

PMID:
23536430
[PubMed - indexed for MEDLINE]
15.

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

Lesage S, Condroyer C, Klebe S, Lohmann E, Durif F, Damier P, Tison F, Anheim M, Honoré A, Viallet F, Bonnet AM, Ouvrard-Hernandez AM, Vidailhet M, Durr A, Brice A; French Parkinson's Disease Genetics Study Group.

Neurobiol Aging. 2012 Sep;33(9):2233.e1-2233.e5. doi: 10.1016/j.neurobiolaging.2012.05.006. Epub 2012 Jun 1.

PMID:
22658323
[PubMed - indexed for MEDLINE]
16.

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.

Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM.

Neurology. 2013 Mar 12;80(11):982-9. doi: 10.1212/WNL.0b013e31828727d4. Epub 2013 Feb 13.

PMID:
23408866
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Independent occurrence of I2020T mutation in the kinase domain of the leucine rich repeat kinase 2 gene in Japanese and German Parkinson's disease families.

Ohta E, Hasegawa K, Gasser T, Obata F.

Neurosci Lett. 2007 Apr 24;417(1):21-3. Epub 2007 Mar 16.

PMID:
17395370
[PubMed - indexed for MEDLINE]
18.

Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China.

Mao XY, Burgunder JM, Zhang ZJ, An XK, Zhang JH, Yang Y, Li T, Wang YC, Chang XL, Peng R.

Neurosci Lett. 2010 Jan 22;469(2):256-9. doi: 10.1016/j.neulet.2009.12.007. Epub 2009 Dec 11.

PMID:
20004703
[PubMed - indexed for MEDLINE]
19.

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.

Gaig C, Ezquerra M, Marti MJ, Muñoz E, Valldeoriola F, Tolosa E.

Arch Neurol. 2006 Mar;63(3):377-82.

PMID:
16533964
[PubMed - indexed for MEDLINE]
20.

PLA2G6 variant in Parkinson's disease.

Tomiyama H, Yoshino H, Ogaki K, Li L, Yamashita C, Li Y, Funayama M, Sasaki R, Kokubo Y, Kuzuhara S, Hattori N.

J Hum Genet. 2011 May;56(5):401-3. doi: 10.1038/jhg.2011.22. Epub 2011 Mar 3.

PMID:
21368765
[PubMed - indexed for MEDLINE]

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