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European Journal of Neuroscience

Volumn 23, Issue 3, 2006, Pages 659-666

LRRK2 is expressed in areas affected by Parkinson's disease in the adult mouse brain

(4) Simón Sánchez, Javier a Herranz Pérez, Vicente a Olucha Bordonau, Francisco b Pérez Tur, Jordi a

a INSTITUTO DE BIOMEDICINA DE VALENCIA (Spain)

b UNIVERSITY OF VALENCIA (Spain)

Author keywords

Dardarin; Expression; Mousebrain; Parkinson's disease

Indexed keywords

BRAIN PROTEIN; LEUCINE RICH REPEAT KINASE 2 PROTEIN; MESSENGER RNA; UNCLASSIFIED DRUG;

ADULTHOOD; AMYGDALOID NUCLEUS; ANIMAL TISSUE; ARTICLE; BRAIN; BRAIN CORTEX; BRAIN MAPPING; BRAIN REGION; CEREBELLUM; CINGULATE GYRUS; CONTROLLED STUDY; GENE; GENE MUTATION; HIPPOCAMPUS; IN SITU HYBRIDIZATION; MALE; MOTOR SYSTEM; MOUSE; NONHUMAN; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PUTAMEN; PYRIFORM CORTEX; RNA ANALYSIS; SUBSTANTIA NIGRA; THALAMUS NUCLEUS;

ANIMALS; BRAIN; BRAIN MAPPING; DISEASE MODELS, ANIMAL; GENE EXPRESSION; IN SITU HYBRIDIZATION; MALE; MICE; PARKINSON DISEASE; PROTEIN-SERINE-THREONINE KINASES; RNA, MESSENGER;

EID: 33644934224 PISSN: 0953816X EISSN: 14609568 Source Type: Journal
DOI: 10.1111/j.1460-9568.2006.04616.x Document Type: Article

Times cited : (70)

References (13)

1
- 0034961813
- Subclinical dopaminergic dysfunction in asymptomatic Parkinson's disease patients' relatives with a decreased sense of smell
- Berendse HW. Booij J. Francot CM. Bergmans PL. Hijman R. Stoof JC. Wolters EC. 2001 Subclinical dopaminergic dysfunction in asymptomatic Parkinson's disease patients' relatives with a decreased sense of smell Neurology 50 34 41
- (2001) Neurology , vol.50 , pp. 34-41
- Berendse, H.W.¹ Booij, J.² Francot, C.M.³ Bergmans, P.L.⁴ Hijman, R.⁵ Stoof, J.C.⁶ Wolters, E.C.⁷

2
- 0345118282
- Roc, a Ras/GTPase domain in complex proteins
- Bosgraaf L. Van Haastert PJ. 2003 Roc, a Ras/GTPase domain in complex proteins BiochimBiophysActa 1643 5 10
- (2003) BiochimBiophysActa , vol.1643 , pp. 5-10
- Bosgraaf, L.¹ Van Haastert, P.J.²

3
- 0041589706
- Parkinson's disease is associated with hippocampal atrophy
- Camicioli R. Moore MM. Kinney A. Corbridge E. Glassberg K. Kaye JA. 2003 Parkinson's disease is associated with hippocampal atrophy MovDisord 18 784 790
- (2003) MovDisord , vol.18 , pp. 784-790
- Camicioli, R.¹ Moore, M.M.² Kinney, A.³ Corbridge, E.⁴ Glassberg, K.⁵ Kaye, J.A.⁶

4
- 0036196860
- A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11. 2-Q13.1
- Funayama M. Hasegawa K. Kowa H. Saito M. Tsuji S. Obata F. 2002 A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11. 2-Q13.1 AnnNeurol 51 296 301
- (2002) AnnNeurol , vol.51 , pp. 296-301
- Funayama, M.¹ Hasegawa, K.² Kowa, H.³ Saito, M.⁴ Tsuji, S.⁵ Obata, F.⁶

5
- 33644932406
- LRRK2 in neural inclusions in Parkinson's, Alzheimer's, and related diseases
- Gai W. Wu C. Chilcote TJ. Anderson JP. Schlossmacher MG. Blumbergs PC. Jensen P. Halliday GM. 2005 LRRK2 in neural inclusions in Parkinson's, Alzheimer's, and related diseases SocNeurosciAbstr 1007.6
- (2005) SocNeurosciAbstr , pp. 10076
- Gai, W.¹ Wu, C.² Chilcote, T.J.³ Anderson, J.P.⁴ Schlossmacher, M.G.⁵ Blumbergs, P.C.⁶ Jensen, P.⁷ Halliday, G.M.⁸

6
- 0034718577
- Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
- Gwinn-Hardy K. Chen JY. Liu HC. Liu TY. Boss M. Seltzer W. Adam A. Singleton A. Koroshetz W. Waters C. Hardy J. Farrer M. 2000 Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese Neurology 55 800 805
- (2000) Neurology , vol.55 , pp. 800-805
- Gwinn-Hardy, K.¹ Chen, J.Y.² Liu, H.C.³ Liu, T.Y.⁴ Boss, M.⁵ Seltzer, W.⁶ Adam, A.⁷ Singleton, A.⁸ Koroshetz, W.⁹ Waters, C.¹⁰ Hardy, J.¹¹ Farrer, M.¹²

7
- 20844461152
- Amygdalar and hippocampal MRI volume tric reductions in Parkinson's disease with dementia
- Junque C. Ramirez-Ruiz B. Tolosa E. Summerfield C. Marti MJ. Pastor P. Gomez-Anson B. Mercader JM. 2005 Amygdalar and hippocampal MRI volume tric reductions in Parkinson's disease with dementia MovDisord 20 540 544
- (2005) MovDisord , vol.20 , pp. 540-544
- Junque, C.¹ Ramirez-Ruiz, B.² Tolosa, E.³ Summerfield, C.⁴ Marti, M.J.⁵ Pastor, P.⁶ Gomez-Anson, B.⁷ Mercader, J.M.⁸

8
- 8844266996
- Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
- Paisan-Ruiz C. Jain S. Evans EW. Gilks WP. Simon J. van der Brug M. Lopez de Munain A. Aparicio S. Gil AM. Khan N. Johnson J. Martinez JR. Nicholl D. Carrera IM. Pena AS. de Silva R. Lees A. Marti-Masso JF. Perez-Tur J. Wood NW. Singleton AB. 2004 Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Neuron 44 595 600
- (2004) Neuron , vol.44 , pp. 595-600
- Paisan-Ruiz, C.¹ Jain, S.² Evans, E.W.³ Gilks, W.P.⁴ Simon, J.⁵ Van Der Brug, M.⁶ Lopez De Munain, A.⁷ Aparicio, S.⁸ Gil, A.M.⁹ Khan, N.¹⁰ Johnson, J.¹¹ Martinez, J.R.¹² Nicholl, D.¹³ Carrera, I.M.¹⁴ Pena, A.S.¹⁵ De Silva, R.¹⁶ Lees, A.¹⁷ Marti-Masso, J.F.¹⁸ Perez-Tur, J.¹⁹ Wood, N.W.²⁰ Singleton, A.B.²¹ more..

9
- 14844325314
- Familial Parkinson's disease: Clinical and genetic analysis of four Basque families
- Paisan-Ruiz C. Saenz A. Lopez de Munain A. Marti I. Martinez Gil A. Marti-Masso JF. Perez-Tur J. 2005 Familial Parkinson's disease: clinical and genetic analysis of four Basque families AnnNeurol 57 365 372
- (2005) AnnNeurol , vol.57 , pp. 365-372
- Paisan-Ruiz, C.¹ Saenz, A.² Lopez De Munain, A.³ Marti, I.⁴ Martinez Gil, A.⁵ Marti-Masso, J.F.⁶ Perez-Tur, J.⁷

10
- 21144433087
- Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease
- Simon-Sanchez J. Hanson M. Singleton A. Hernandez D. McInerney A. Nussbaum R. Werner J. Gallardo M. Weiser R. Gwinn-Hardy K. Singleton AB. Clarimon J. 2005 Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease NeurosciLett 382 191 194
- (2005) NeurosciLett , vol.382 , pp. 191-194
- Simon-Sanchez, J.¹ Hanson, M.² Singleton, A.³ Hernandez, D.⁴ McInerney, A.⁵ Nussbaum, R.⁶ Werner, J.⁷ Gallardo, M.⁸ Weiser, R.⁹ Gwinn-Hardy, K.¹⁰ Singleton, A.B.¹¹ Clarimon, J.¹²

11
- 13444254133
- Structural brain changes in Parkinson disease with dementia: A voxel-based morphometry study
- q5
- Summerfield C. Junque C. Tolosa E. Salgado-Pineda P. Gomez-Anson B. Marti MJ. Pastor P. Ramirez-Ruiz B. Mercader J. 2005 Structural brain changes in Parkinson disease with dementia: a voxel-based morphometry study ArchNeurol 62 281 285 q5
- (2005) ArchNeurol , vol.62 , pp. 281-285
- Summerfield, C.¹ Junque, C.² Tolosa, E.³ Salgado-Pineda, P.⁴ Gomez-Anson, B.⁵ Marti, M.J.⁶ Pastor, P.⁷ Ramirez-Ruiz, B.⁸ Mercader, J.⁹

12
- 2342605968
- Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
- Wszolek ZK. Pfeiffer RF. Tsuboi Y. Uitti RJ. McComb RD. Stoessl AJ. Strongosky AJ. Zimprich A. Muller-Myhsok B. Farrer MJ. Gasser T. Calne DB. Dickson DW. 2004 Autosomal dominant parkinsonism associated with variable synuclein and tau pathology Neurology 62 1619 1622
- (2004) Neurology , vol.62 , pp. 1619-1622
- Wszolek, Z.K.¹ Pfeiffer, R.F.² Tsuboi, Y.³ Uitti, R.J.⁴ McComb, R.D.⁵ Stoessl, A.J.⁶ Strongosky, A.J.⁷ Zimprich, A.⁸ Muller-Myhsok, B.⁹ Farrer, M.J.¹⁰ Gasser, T.¹¹ Calne, D.B.¹² Dickson, D.W.¹³

13
- 10744231577
- Genetic testing in spinocerebellar ataxia in Taiwan: Expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease
- Wu YR. Lin HY. Chen CM. Gwinn-Hardy K. Ro LS. Wang YC. Li SH. Hwang JC. Fang K. Hsieh-Li HM. Li ML. Tung LC. Su MT. Lu KT. Lee-Chen GJ. 2004 Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease ClinGenet 65 209 214
- (2004) ClinGenet , vol.65 , pp. 209-214
- Wu, Y.R.¹ Lin, H.Y.² Chen, C.M.³ Gwinn-Hardy, K.⁴ Ro, L.S.⁵ Wang, Y.C.⁶ Li, S.H.⁷ Hwang, J.C.⁸ Fang, K.⁹ Hsieh-Li, H.M.¹⁰ Li, M.L.¹¹ Tung, L.C.¹² Su, M.T.¹³ Lu, K.T.¹⁴ Lee-Chen, G.J.¹⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.