Delaying the onset of Huntington's in mice. - Wikidata - wikimedia - TriplyDB

Delaying the onset of Huntington's in mice.

Delaying the onset of Huntington's in mice.

http://www.wikidata.org/entity/Q45300228

about

Adult neurogenesis and neurite outgrowth are impaired in LRRK2 G2019S mice Environmental enrichment and the sensory brain: the role of enrichment in remediating brain injury.Mouse models of polyglutamine diseases: review and data table. Part I Mouse models of polyglutamine diseases in therapeutic approaches: review and data table. Part II.All about running: synaptic plasticity, growth factors and adult hippocampal neurogenesis Cognitive Training at a Young Age Attenuates Deficits in the zQ175 Mouse Model of HD.Responses to environmental enrichment differ with sex and genotype in a transgenic mouse model of Huntington's disease Continuous and periodic expansion of CAG repeats in Huntington's disease R6/1 mice Environmental enrichment and brain repair: harnessing the therapeutic effects of cognitive stimulation and physical activity to enhance experience-dependent plasticity Neurodegenerative disease and adult neurogenesis Comprehensive behavioral testing in the R6/2 mouse model of Huntington's disease shows no benefit from CoQ10 or minocycline Interaction of genotype and environment: effect of strain and housing conditions on cognitive behavior in rodent models of schizophrenia.Force-plate quantification of progressive behavioral deficits in the R6/2 mouse model of Huntington's disease.Evaluation of social and physical enrichment in modulation of behavioural phenotype in C57BL/6J female mice Sex-dependent changes in social behaviors in motor pre-symptomatic R6/1 mice.Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models.Environmental enrichment mitigates cognitive deficits in a mouse model of Alzheimer's disease Age and Environment Influences on Mouse Prion Disease Progression: Behavioral Changes and Morphometry and Stereology of Hippocampal Astrocytes.Wheel running from a juvenile age delays onset of specific motor deficits but does not alter protein aggregate density in a mouse model of Huntington's disease.The use of the puzzle box as a means of assessing the efficacy of environmental enrichment.Enrichment from birth accelerates the functional and cellular development of a motor control area in the mouse Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome.Rescuing the Corticostriatal Synaptic Disconnection in the R6/2 Mouse Model of Huntington's Disease: Exercise, Adenosine Receptors and Ampakines Huntington disease models and human neuropathology: similarities and differences Exercise is not beneficial and may accelerate symptom onset in a mouse model of Huntington's disease Efficacy of fumaric acid esters in the R6/2 and YAC128 models of Huntington's disease.The latent stem cell population is retained in the hippocampus of transgenic Huntington's disease mice but not wild-type mice.Beneficial effects of environmental enrichment and food entrainment in the R6/2 mouse model of Huntington's disease.The endocannabinoid system as a target for the treatment of neurodegenerative disease.Neuroprotective potential of CB1 receptor agonists in an in vitro model of Huntington's disease.Effect of enhanced voluntary physical exercise on brain levels of monoamines in Huntington disease mice What is the impact of education on Huntington's disease?Brief ampakine treatments slow the progression of Huntington's disease phenotypes in R6/2 mice Comprehensive behavioral and molecular characterization of a new knock-in mouse model of Huntington's disease: zQ175.Standardized environmental enrichment supports enhanced brain plasticity in healthy rats and prevents cognitive impairment in epileptic rats.Striosomes and mood dysfunction in Huntington's disease.Adult hippocampal neurogenesis, synaptic plasticity and memory: facts and hypotheses.Inoculation stress hypothesis of environmental enrichment.The effect of multidisciplinary rehabilitation on brain structure and cognition in Huntington's disease: an exploratory study.Transcription, epigenetics and ameliorative strategies in Huntington's Disease: a genome-wide perspective

P2860

Q24317631-5AEF4460-E74A-42D1-BD21-0F2E4F8A3D6C Q26824458-03E639A3-D53D-43FA-9322-18EF1CD5D5C7 Q26853025-BC047D23-C517-4D3A-82D1-A9FE26017C0D Q27005950-2A78C085-9693-4D60-821F-137393E5CA73 Q27011760-313F5283-2DF4-4AE3-A5F4-CC8FA69C575F Q27321673-90763D9A-E2F3-49BE-8FF9-ED51A6422331 Q27334872-17C821B3-0705-4FB4-90FE-CF0A51A822E0 Q27344974-FDBB05E4-ADB0-4776-82B1-613D7026FE9F Q28304384-7539D3D4-7F4A-4322-A5EA-454C67B1E3CB Q28307113-838B7BD0-F319-4A28-97A0-40B43E681593 Q28748449-4AED4A07-960D-4DC5-B2F1-C74F26022DAF Q30451282-3E745C59-BDEE-4F0B-B896-04C406CBF6B1 Q30452232-1E61DE6F-17C2-479B-A84A-E7E29A186CB0 Q30474110-5890CC1B-C9E7-41E3-82F6-1068B1B5CC55 Q30475466-8BA8F4DA-A873-414F-B473-86CE0906B3FB Q30483013-8E30EDEE-E009-416A-B127-24F5749C71E6 Q30651415-3A2D6A43-AD3C-4FFB-B4A1-4CAF7B316F78 Q30837723-0C75E35C-CF11-4DC2-B1F3-B559AB96B9D1 Q33326475-DECB7D28-76A8-437C-8102-88D93E44C6F4 Q33359868-EAD8DA7B-C40F-4E37-8075-6FF9F21E8DA9 Q33503649-CC488395-86BF-4CE1-9AD5-582D8C29EA86 Q33633998-A5F06264-2222-46F8-8C19-996F12CF0598 Q33705003-3C9F127C-CE79-4715-BBA0-ADEB439A69C1 Q33760994-08C6B68F-5D37-40DD-9903-35EBFA685EBE Q33769984-AB08D913-DA1A-4B8E-85C0-10F130775210 Q33812932-C2BCBFD9-B759-4594-978E-B9BFE67D419B Q33859458-2ADCD4BF-913B-451B-834B-97040DDDC79B Q33935845-107DD946-AAF1-4562-8AC9-6964844C9295 Q34098196-848B4625-EAFC-4E60-8684-749F62EE1A03 Q34098292-C820791B-8203-4FB6-8980-7BFA34CD100B Q34135360-2896DB6D-0F27-4C1C-B044-EE1AB8E1E7C8 Q34172955-975F3A45-DB7D-499D-812A-630BA15C3F76 Q34459323-6CB4808D-949E-4009-869D-1E551EA5E34D Q34531481-1B7AB0D2-A178-4B9D-9A77-DEFB458ABE62 Q34558891-76706837-95D6-4DBF-8B49-ED9D86D3169A Q34573861-C2053A66-3092-4472-8D7A-FC4F14A281F6 Q34642050-CC23AB5A-087A-4887-9FE6-54F9470E5036 Q35009286-286C7EB1-01C6-4672-9A87-91886114AAEA Q35024584-6AC4085C-E083-4DCB-9C3E-A280562C8720 Q35024695-782FAF01-E430-4639-9B28-037F6974336C

P2860

Delaying the onset of Huntington's in mice.

http://www.wikidata.org/entity/Q45300228

description

2000 nî lūn-bûn

@nan

2000年の論文

@ja

2000年学术文章

@wuu

2000年学术文章

@zh

2000年学术文章

@zh-cn

2000年学术文章

@zh-hans

2000年学术文章

@zh-my

2000年学术文章

@zh-sg

2000年學術文章

@yue

2000年學術文章

@zh-hant

name

Delaying the onset of Huntington's in mice.

@en

Delaying the onset of Huntington's in mice.

@nl

type

label

Delaying the onset of Huntington's in mice.

@en

Delaying the onset of Huntington's in mice.

@nl

prefLabel

Delaying the onset of Huntington's in mice.

@en

Delaying the onset of Huntington's in mice.

@nl

P1433

Q45300228-A4A8862A-5974-46E1-8C48-8C6A83A61164

P1476

Q45300228-EF3A99A4-05AF-46F1-BA86-01E18FD3049B

P2093

Q45300228-4C0D4CDF-37F4-424F-AFAE-C4AF9A3137AA

Q45300228-5FD92FC4-CC72-443B-A4EA-28E50FFD105E

Q45300228-8EDE3F7E-41DD-4BEC-AD78-22B249A31313

Q45300228-A50B267A-36EF-4996-BB10-6810985C6BB7

Q45300228-FAEF068C-C54C-46B0-9499-F625155A831A

P2860

Q45300228-282EDDF9-20EB-436B-A5BB-68608A0D12ED

Q45300228-4AA3E6F6-C130-4752-9836-7663CF494BD1

Q45300228-5DF177D6-4E55-4703-AA33-EA0D90159B61

Q45300228-72445E96-8047-4CAB-BCFF-8487F41E409D

Q45300228-87A2B872-A229-4D2E-A97B-916F1AD537E9

Q45300228-C4F09ECD-D600-4A19-A72D-06B761A9EE7C

Q45300228-D4DC8465-7E43-4B49-8631-84E1CD0875FD

Q45300228-EA9B4B69-CEED-4A63-8A29-18DD80C0EF2E

P2888

Q45300228-840FB227-B91D-4E8B-85A9-8346F846EC7D

P304

Q45300228-0DC735FF-2BCB-4B0F-8490-D348E83010F5

P31

Q45300228-E930FAD1-DA94-4A18-BF49-7888BDBDE388

P356

Q45300228-71285F80-FD58-4AFE-AA61-751B48015F07

P407

Q45300228-B9F8E20C-8E36-4ABF-AAE0-38FD6D9A23FD

P433

Q45300228-B519F7C8-B72D-46AC-BA3E-2A6765543C60

P478

Q45300228-A13D8974-FFBE-4423-9C79-94E1EE5EAB86

P577

Q45300228-A0F9E05D-5A4F-468F-9EA2-EFF8E38D8B7B

P6179

Q45300228-E3E84791-1E94-46E4-B47F-302F496C33E7

P698

Q45300228-B60F491B-3F13-4C8F-A447-D093AD10AA7B

P921

Q45300228-D1D502A8-5290-4F90-9122-EB0B2736D72D

P356

P1433

P1476

Delaying the onset of Huntington's in mice.

@en

P2093

Blakemore C

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

Deacon R

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

Hannan AJ

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

York D

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

van Dellen A

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

P2860

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

Mechanism of altered synaptic strength due to experience: relation to long-term potentiation.

Environmental enrichment inhibits spontaneous apoptosis, prevents seizures and is neuroprotective.

Cerebral blood flow velocity decreases during cognitive stimulation in Huntington's disease.

Differential clinical and motor control function in a pair of monozygotic twins with Huntington's disease.

A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.

Increased density of multiple-head dendritic spines on medium-sized spiny neurons of the striatum in rats reared in a complex environment.

P2888

P304

721-722

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

P31

scholarly article

P356

10.1038/35008142

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

P407

P433

6779

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

P478

404

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

P577

2000-04-01T00:00:00Z

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

P6179

1050986108

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

P698

10783874

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

P921

Huntington disease