Pathways to motor incoordination: the inherited ataxias. - Wikidata - wikimedia - TriplyDB

Pathways to motor incoordination: the inherited ataxias.

Pathways to motor incoordination: the inherited ataxias.

http://www.wikidata.org/entity/Q35841041

about

A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1 Cell biology of spinocerebellar ataxia Erythropoietin in Friedreich ataxia dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1 P-Rex2 regulates Purkinje cell dendrite morphology and motor coordination.A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.Spinocerebellar ataxia: patient and health professional perspectives on whether and how patents affect access to clinical genetic testing.Friedreich ataxia: dysarthria profile and clinical data.Lhx1/5 control dendritogenesis and spine morphogenesis of Purkinje cells via regulation of Espin Pulling complexes out of complex diseases: Spinocerebellar Ataxia 7.A new mouse allele of glutamate receptor delta 2 with cerebellar atrophy and progressive ataxia.Association between proton magnetic resonance spectroscopy measurements and CAG repeat number in patients with spinocerebellar ataxias 2, 3, or 6 Requirement for zebrafish ataxin-7 in differentiation of photoreceptors and cerebellar neurons.Treadmill exercise improves motor coordination through ameliorating Purkinje cell loss in amyloid beta23-35-induced Alzheimer's disease rats.Smad2 protein disruption in the central nervous system leads to aberrant cerebellar development and early postnatal ataxia in mice Mesenchymal stem cell transplantation ameliorates motor function deterioration of spinocerebellar ataxia by rescuing cerebellar Purkinje cells Macro- and microstructural changes in patients with spinocerebellar ataxia type 6: assessment of phylogenetic subdivisions of the cerebellum and the brain stem.Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse.Oxidative genome damage and its repair: implications in aging and neurodegenerative diseases.The involvement of DNA-damage and -repair defects in neurological dysfunction Irisin-immunoreactivity in neural and non-neural cells of the rodent.FGF14 regulates the intrinsic excitability of cerebellar Purkinje neurons.Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond Nuclear ataxias.An update on Spino-cerebellar ataxias Mesenchymal stem cells as a potential therapeutic tool for spinocerebellar ataxia.A review on protein-protein interaction network of APE1/Ref-1 and its associated biological functions.Translating cerebellar Purkinje neuron physiology to progress in dominantly inherited ataxia.Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease.Strabismus and Micro-Opsoclonus in Machado-Joseph Disease.Caffeine and adenosine A(2A) receptor inactivation decrease striatal neuropathology in a lentiviral-based model of Machado-Joseph disease.Plasma 24S-hydroxycholesterol and caudate MRI in pre-manifest and early Huntington's disease.Supratentorial and infratentorial damage in spinocerebellar ataxia 2: a diffusion-weighted MRI study.Genotyping and prenatal diagnosis of a large spinocerebellar ataxia pedigree in northeastern China.Spinocerebellar Ataxia Type 7 Sans Retinal Degeneration: A Phenotypic Variability.Caffeine alleviates progressive motor deficits in a transgenic mouse model of spinocerebellar ataxia.Hsp70/Hsc70 regulates the effect phosphorylation has on stabilizing ataxin-1.Comparing speech characteristics in spinocerebellar ataxias type 3 and type 6 with Friedreich ataxia.

P2860

Q21092417-E16A9517-7673-4797-ADD9-E626C90AA911 Q24621854-FC1931C5-412F-4233-B549-1342C22D9FC7 Q24655547-44F898E3-3FF0-4371-AF73-000B41A6FC0F Q26829511-4ADA692F-7A9C-4748-ACAD-FF7A10B1227A Q26863216-D483C0C9-7E90-4FF3-B942-3C3E70E1A332 Q27314605-9472A2E1-2B8E-431F-8758-457110A60BB4 Q28513238-BD27C836-93E7-4596-BA4D-57774B70283F Q30486893-A99DBF78-055D-4339-9DA0-C5E5DD516C7C Q30502588-5E60C7CF-426A-4CAA-9F92-CF627A71269A Q30585816-D8FDC841-B87E-4067-8922-55534F9E7051 Q30854396-ADF759E3-2995-4250-8F09-9778884126F0 Q33879684-EFFF4CA3-5D7D-4426-A6D2-3E53BE0E2886 Q34248188-284CAD81-DCF4-4E2B-9744-7B747FCA832D Q34456340-FA6B5FB7-F40C-4F3C-8621-E1C6F66266BE Q34505777-F3232CCE-AA89-4238-9EB6-C10D2931E984 Q34544663-02FF484E-FC46-4276-8A35-FAE6731EBAE5 Q34998146-08762492-A12A-49D8-8A0B-7355C6B3E2CA Q35217890-3E025BEF-B6B5-4A48-B3B1-9B0E4290C5EF Q35759917-333F4F60-C8BF-465E-B145-4FF899FF2B34 Q35783149-9D1BA11C-0163-4D03-936A-A8F179E9569F Q35957287-0F36D808-9E20-4EB2-9E66-B3A758DFF2E6 Q36718848-C56E3AC8-6FF6-4108-B5E6-01578F0A75A6 Q36799438-E86CC61E-F027-4125-B736-E549129C0A01 Q37121051-F523FE96-88F7-4868-87D4-015046A9B6C8 Q37642283-7548F197-94E1-44E2-8A41-C8DE7F1160DE Q37746495-1D580D97-4A55-4FFB-BE2D-22891AAE4270 Q38150325-67222A88-1B72-4F2E-832A-B7DEB2F01C16 Q38256491-F710A4C8-63B1-4001-B88B-9D6A8B9C1591 Q38383985-B1769ACD-832E-44E4-B3E0-80B8111633FF Q39129263-81A23339-CC95-478D-973D-D1AB2E1E5D2A Q39995612-F09888EA-F9A9-4F27-A786-78212C19ECF7 Q41452874-A96782F9-7539-4621-9008-9B99756D6241 Q42437833-9A63FE97-469C-4F99-B83E-1020961BE17A Q43854094-4C8AB944-B11D-425A-B25A-52D3F9C671A3 Q45394861-38397217-B2E3-4ADA-86F6-16BACF89E071 Q45730323-768A355B-8B54-4AD4-B677-1B6F4AFB0C60 Q47315545-AD857047-0AB2-4E2D-B0F2-AA4A625B78CA Q48109313-B0838057-FB3F-4321-9FB7-D902B052FE8A Q48150853-7BDE061F-06DB-490C-AAEF-6F3A3D72E5F1 Q48506133-AD468545-031D-48B2-AC31-90726739AA94

P2860

Pathways to motor incoordination: the inherited ataxias.

http://www.wikidata.org/entity/Q35841041

description

2004 nî lūn-bûn

@nan

2004年の論文

@ja

2004年論文

@yue

2004年論文

@zh-hant

2004年論文

@zh-hk

2004年論文

@zh-mo

2004年論文

@zh-tw

2004年论文

@wuu

2004年论文

@zh

2004年论文

@zh-cn

name

Pathways to motor incoordination: the inherited ataxias.

@ast

Pathways to motor incoordination: the inherited ataxias.

@en

type

label

Pathways to motor incoordination: the inherited ataxias.

@ast

Pathways to motor incoordination: the inherited ataxias.

@en

prefLabel

Pathways to motor incoordination: the inherited ataxias.

@ast

Pathways to motor incoordination: the inherited ataxias.

@en

P1433

Q35841041-167E98D9-66CD-432D-9E15-1D4194083013

P1476

Q35841041-A0397F66-C71B-4400-B08D-6D8CB8283A22

P2093

Q35841041-013857D2-8C3C-4374-AE23-2A4A4AA9BA95

Q35841041-2AA57A91-F944-4054-AE6A-B8DF8A0E64F4

P2860

Q35841041-00BE7B12-7656-4C9C-B44A-9F84D403AF57

Q35841041-00E55CA8-B140-4A66-9C66-94FCDAADDA49

Q35841041-02F992BE-7740-4B33-A096-775679FFADDD

Q35841041-045AC82B-43A0-4390-BF94-0A37FC1053E6

Q35841041-05661E9D-B7DF-42FD-BFEC-4E871DEB7FCE

Q35841041-06A89597-8D60-4B98-B5E2-5CFB54C75CB0

Q35841041-08E16AD8-60A2-42C9-AF96-DCD8E3E1D97D

Q35841041-0A74ED9D-0C80-472C-941B-0F254F776355

Q35841041-0AE433BA-08A4-40E6-BCDA-E394CD5656A0

Q35841041-0AFA5FD7-E10E-4CEF-B6D3-5AD04FC5F5C1

P2888

Q35841041-92BBA47C-A4C4-4FDD-AFEE-F6D3C4766245

P304

Q35841041-29DFFEE2-2E3C-4E3A-AC98-BA47A89A6170

P31

Q35841041-9A72A144-B295-462D-83E0-4BE4567C03CA

P356

Q35841041-971A8667-384A-4889-84A5-58A359441320

P407

Q35841041-BF00B575-8223-47EB-928E-3F200436FEF3

P433

Q35841041-D494D190-710D-48E8-8A12-9AECB25004E9

P478

Q35841041-D9F02ABC-39F7-49D0-A3A2-EF6DEB804E79

P577

Q35841041-3F390CFD-BCF6-42E2-8ED6-814C78EEB3A0

P6179

Q35841041-4C21A1DD-FE62-471B-A108-193B9A661297

P698

Q35841041-05D48F4B-1A32-4FF3-B29C-FDEA7C602030

P356

P1433

Nature Reviews Neuroscience

P1476

Pathways to motor incoordination: the inherited ataxias.

@en

P2093

Franco Taroni

http://www.w3.org/2001/XMLSchema#string

Stefano DiDonato

http://www.w3.org/2001/XMLSchema#string

P2860

Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage

Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7

Ataxin-3, the MJD1 gene product, interacts with the two human homologs of yeast DNA repair protein RAD23, HHR23A and HHR23B

Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein

The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response

Aprataxin, a novel protein that protects against genotoxic stress

Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families

Ataxin-3 interactions with rad23 and valosin-containing protein and its associations with ubiquitin chains and the proteasome are consistent with a role in ubiquitin-mediated proteolysis

P2888

P304

641-655

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/NRN1474

http://www.w3.org/2001/XMLSchema#string

P407

P433

8

http://www.w3.org/2001/XMLSchema#string

P478

5

http://www.w3.org/2001/XMLSchema#string

P577

2004-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1001334329

http://www.w3.org/2001/XMLSchema#string

P698

15263894

http://www.w3.org/2001/XMLSchema#string