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Items: 10

1.

Involvement of Parkin in the ubiquitin proteasome system-mediated degradation of N-type voltage-gated Ca2+ channels.

Grimaldo L, Sandoval A, Garza-López E, Felix R.

PLoS One. 2017 Sep 28;12(9):e0185289. doi: 10.1371/journal.pone.0185289. eCollection 2017.

2.

Activation mechanisms of the E3 ubiquitin ligase parkin.

Panicker N, Dawson VL, Dawson TM.

Biochem J. 2017 Aug 30;474(18):3075-3086. doi: 10.1042/BCJ20170476. Review.

PMID:
28860335
3.

Reactive oxygen species trigger Parkin/PINK1 pathway-dependent mitophagy by inducing mitochondrial recruitment of Parkin.

Xiao B, Goh JY, Xiao L, Xian H, Lim KL, Liou YC.

J Biol Chem. 2017 Oct 6;292(40):16697-16708. doi: 10.1074/jbc.M117.787739. Epub 2017 Aug 28.

PMID:
28848050
4.

UbMES and UbFluor: Novel probes for ring-between-ring (RBR) E3 ubiquitin ligase PARKIN.

Park S, Foote PK, Krist DT, Rice SE, Statsyuk AV.

J Biol Chem. 2017 Oct 6;292(40):16539-16553. doi: 10.1074/jbc.M116.773200. Epub 2017 Jul 14.

PMID:
28710279
5.

Parkin Type of Early-Onset Parkinson Disease.

Brüggemann N, Klein C.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2001 Apr 17 [updated 2013 Apr 4].

6.

Parkinson Disease Overview.

Farlow J, Pankratz ND, Wojcieszek J, Foroud T.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2004 May 25 [updated 2014 Feb 27].

7.

Hereditary Dystonia Overview.

Klein C, Lohmann K, Marras C, Münchau A.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. No abstract available.
2003 Oct 28 [updated 2017 Jun 22].

8.

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N.

Nature. 1998 Apr 9;392(6676):605-8.

PMID:
9560156
9.

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27.

Matsumine H, Saito M, Shimoda-Matsubayashi S, Tanaka H, Ishikawa A, Nakagawa-Hattori Y, Yokochi M, Kobayashi T, Igarashi S, Takano H, Sanpei K, Koike R, Mori H, Kondo T, Mizutani Y, Schäffer AA, Yamamura Y, Nakamura S, Kuzuhara S, Tsuji S, Mizuno Y.

Am J Hum Genet. 1997 Mar;60(3):588-96.

10.

[Clinical characteristics and linkage analysis of autosomal recessive form of juvenile parkinsonism(AR-JP)].

Saito M, Matsumine H, Tanaka H, Ishikawa A, Matsubayashi S, Hattori Y, Mizuno Y, Tsuji S.

Nihon Rinsho. 1997 Jan;55(1):83-8. Review. Japanese.

PMID:
9014427

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