230 related articles for article (PubMed ID: 10791092)
1. [Parkin gene and its function; a key to understand nigral degeneration].
Hattori N; Mizuno Y
Rinsho Shinkeigaku; 1999 Dec; 39(12):1259-61. PubMed ID: 10791092
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 9851438
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 10319893
[TBL] [Abstract][Full Text] [Related]
4. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
Hattori N
Rinsho Shinkeigaku; 2004; 44(4-5):241-62. PubMed ID: 15287506
[TBL] [Abstract][Full Text] [Related]
5. Parkin is linked to the ubiquitin pathway.
Tanaka K; Suzuki T; Chiba T; Shimura H; Hattori N; Mizuno Y
J Mol Med (Berl); 2001 Sep; 79(9):482-94. PubMed ID: 11692161
[TBL] [Abstract][Full Text] [Related]
6. Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.
Hattori N; Shimura H; Kubo S; Kitada T; Wang M; Asakawa S; Minashima S; Shimizu N; Suzuki T; Tanaka K; Mizuno Y
Neuropathology; 2000 Sep; 20 Suppl():S85-90. PubMed ID: 11037196
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 10072423
[TBL] [Abstract][Full Text] [Related]
8. 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; 249(3):754-8. PubMed ID: 9731209
[TBL] [Abstract][Full Text] [Related]
9. Parkin-associated Parkinson's disease.
von Coelln R; Dawson VL; Dawson TM
Cell Tissue Res; 2004 Oct; 318(1):175-84. PubMed ID: 15503153
[TBL] [Abstract][Full Text] [Related]
10. Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.
Hattori N; Shimura H; Kubo S; Wang M; Shimizu N; Tanaka K; Mizuno Y
J Neural Transm Suppl; 2000; (60):101-16. PubMed ID: 11205133
[TBL] [Abstract][Full Text] [Related]
11. [Parkin gene: its mutations and function].
Hattori N
Rinsho Shinkeigaku; 2002 Nov; 42(11):1077-81. PubMed ID: 12784670
[TBL] [Abstract][Full Text] [Related]
12. [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. PubMed ID: 10654303
[TBL] [Abstract][Full Text] [Related]
13. 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; 392(6676):605-8. PubMed ID: 9560156
[TBL] [Abstract][Full Text] [Related]
14. Parkin and Parkinson's disease.
Mizuno Y; Hattori N; Mori H; Suzuki T; Tanaka K
Curr Opin Neurol; 2001 Aug; 14(4):477-82. PubMed ID: 11470964
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 12781588
[TBL] [Abstract][Full Text] [Related]
16. Progress in the clinical and molecular genetics of familial parkinsonism.
Kitada T; Asakawa S; Matsumine H; Hattori N; Shimura H; Minoshima S; Shimizu N; Mizuno Y
Neurogenetics; 2000 Mar; 2(4):207-18. PubMed ID: 10983716
[TBL] [Abstract][Full Text] [Related]
17. Autosomal Recessive Juvenile Parkinsonism (AR-JP): Genetic Diagnosis.
Matsumine H; Hattori N; Mizuno Y
Methods Mol Med; 2001; 62():13-29. PubMed ID: 21318765
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
Sinha R; Racette B; Perlmutter JS; Parsian A
Parkinsonism Relat Disord; 2005 Sep; 11(6):341-7. PubMed ID: 16019250
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 11459900
[TBL] [Abstract][Full Text] [Related]
20. [A Parkin gene (PARK 2) and Parkinson's disease].
Matsumine H
Rinsho Shinkeigaku; 1999 Jan; 39(1):9-12. PubMed ID: 10377786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
