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Items: 1 to 20 of 80

1.

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
2.

Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.

Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y.

Ann Neurol. 1998 Dec;44(6):935-41.

PMID:
9851438
3.

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Abbas N, Lücking CB, Ricard S, Dürr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Broussolle E, Brefel-Courbon C, Harhangi BS, Oostra BA, Fabrizio E, Böhme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A.

Hum Mol Genet. 1999 Apr;8(4):567-74.

PMID:
10072423
4.

Differential expression of the parkin gene in the human brain and peripheral leukocytes.

Sunada Y, Saito F, Matsumura K, Shimizu T.

Neurosci Lett. 1998 Oct 2;254(3):180-2.

PMID:
10214987
5.

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y.

Biochem Biophys Res Commun. 1998 Aug 28;249(3):754-8. Erratum in: Biochem Biophys Res Commun 1998 Oct 20;251(2):666.

PMID:
9731209
6.

[Parkin gene and its function; a key to understand nigral degeneration].

Hattori N, Mizuno Y.

Rinsho Shinkeigaku. 1999 Dec;39(12):1259-61. Japanese.

PMID:
10791092
7.

Identification of a novel gene linked to parkin via a bi-directional promoter.

West AB, Lockhart PJ, O'Farell C, Farrer MJ.

J Mol Biol. 2003 Feb 7;326(1):11-9.

PMID:
12547187
8.

Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene.

Kitada T, Asakawa S, Minoshima S, Mizuno Y, Shimizu N.

Mamm Genome. 2000 Jun;11(6):417-21.

PMID:
10818204
9.

Autosomal recessive juvenile parkinsonism.

Saito M, Maruyama M, Ikeuchi K, Kondo H, Ishikawa A, Yuasa T, Tsuji S.

Brain Dev. 2000 Sep;22 Suppl 1:S115-7. Review.

PMID:
10984671
10.

Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.

Nisipeanu P, Inzelberg R, Blumen SC, Carasso RL, Hattori N, Matsumine H, Mizuno Y.

Neurology. 1999 Oct 22;53(7):1602-4.

PMID:
10534280
11.

PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.

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

J Neural Transm Suppl. 2000;(58):19-30. Review.

PMID:
11128608
12.

Positional cloning of the autosomal recessive juvenile parkinsonism (AR-JP) gene and its diversity in deletion mutations.

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

Parkinsonism Relat Disord. 1999 Dec;5(4):163-8.

PMID:
18591135
13.

[Two cases of sporadic juvenile Parkinson's disease caused by homozygous deletion of Parkin gene].

Ujike H, Yamamoto M, Yamaguchi K, Kanzaki A, Takagi M, Kuroda S.

No To Shinkei. 1999 Dec;51(12):1061-4. Japanese.

PMID:
10654303
14.

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.

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

Ann Neurol. 1999 May;45(5):668-72.

PMID:
10319893
15.

A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism.

Muñoz E, Pastor P, Martí MJ, Oliva R, Tolosa E.

Neurosci Lett. 2000 Jul 28;289(1):66-8.

PMID:
10899410
16.

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.

17.

Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism.

Kuroda Y, Mitsui T, Akaike M, Azuma H, Matsumoto T.

J Neurol Neurosurg Psychiatry. 2001 Aug;71(2):231-4.

18.

Parkin gene causing benign autosomal recessive juvenile parkinsonism.

Nisipeanu P, Inzelberg R, Abo Mouch S, Carasso RL, Blumen SC, Zhang J, Matsumine H, Hattori N, Mizuno Y.

Neurology. 2001 Jun 12;56(11):1573-5.

PMID:
11402119
19.

Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27.

Cesari R, Martin ES, Calin GA, Pentimalli F, Bichi R, McAdams H, Trapasso F, Drusco A, Shimizu M, Masciullo V, D'Andrilli G, Scambia G, Picchio MC, Alder H, Godwin AK, Croce CM.

Proc Natl Acad Sci U S A. 2003 May 13;100(10):5956-61. Epub 2003 Apr 28.

20.

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.

Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F.

Parkinsonism Relat Disord. 2003 Jun;9(5):247-51.

PMID:
12781588

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