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Search results 201 to 300 out of 1119 for Htt

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Type Details Score
Publication
31015293 | J:275798
First Author: Ferrari Bardile C
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease.
Volume: 116
Issue: 19
Pages: 9622-9627
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Publication
35058372 | J:350147
First Author: Callahan JW
Year: 2022
Journal: J Neurosci
Title: Dysregulation of the Basal Ganglia Indirect Pathway in Early Symptomatic Q175 Huntington's Disease Mice.
Volume: 42
Issue: 10
Pages: 2080-2102
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Publication
24453320 | J:206857
First Author: Wong YC
Year: 2014
Journal: J Neurosci
Title: The regulation of autophagosome dynamics by huntingtin and HAP1 is disrupted by expression of mutant huntingtin, leading to defective cargo degradation.
Volume: 34
Issue: 4
Pages: 1293-305
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Publication
22970194 | J:191886
First Author: Kovalenko M
Year: 2012
Journal: PLoS One
Title: Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice.
Volume: 7
Issue: 9
Pages: e44273
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Publication
24960609 | J:213778
First Author: Tourette C
Year: 2014
Journal: PLoS Biol
Title: The Wnt receptor Ryk reduces neuronal and cell survival capacity by repressing FOXO activity during the early phases of mutant huntingtin pathogenicity.
Volume: 12
Issue: 6
Pages: e1001895
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Publication
27199664 | J:244546
 
First Author: Agostoni E
Year: 2016
Journal: Front Cell Neurosci
Title: Effects of Pin1 Loss in Hdh(Q111) Knock-in Mice.
Volume: 10
Pages: 110
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Publication
22589249 | J:185361
First Author: Chaturvedi RK
Year: 2012
Journal: Hum Mol Genet
Title: Transducer of regulated CREB-binding proteins (TORCs) transcription and function is impaired in Huntington's disease.
Volume: 21
Issue: 15
Pages: 3474-88
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Publication
15749339 | J:96770
First Author: Tallaksen-Greene SJ
Year: 2005
Journal: Neuroscience
Title: Neuronal intranuclear inclusions and neuropil aggregates in HdhCAG(150) knockin mice.
Volume: 131
Issue: 4
Pages: 843-52
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Publication
24946181 | J:217949
First Author: Ju TC
Year: 2014
Journal: Biochim Biophys Acta
Title: AMPK-α1 functions downstream of oxidative stress to mediate neuronal atrophy in Huntington's disease.
Volume: 1842
Issue: 9
Pages: 1668-80
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Publication
17213233 | J:121854
First Author: Chiang MC
Year: 2007
Journal: Hum Mol Genet
Title: Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease.
Volume: 16
Issue: 5
Pages: 483-98
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Publication
25760041 | J:224237
First Author: Cheng HM
Year: 2015
Journal: PLoS Genet
Title: Effects on murine behavior and lifespan of selectively decreasing expression of mutant huntingtin allele by supt4h knockdown.
Volume: 11
Issue: 3
Pages: e1005043
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Publication
24948797 | J:212083
First Author: Wade BE
Year: 2014
Journal: J Neurosci
Title: Ubiquitin-activating enzyme activity contributes to differential accumulation of mutant huntingtin in brain and peripheral tissues.
Volume: 34
Issue: 25
Pages: 8411-22
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Publication
29789657 | J:263818
First Author: McClory H
Year: 2018
Journal: Sci Rep
Title: The COOH-terminal domain of huntingtin interacts with RhoGEF kalirin and modulates cell survival.
Volume: 8
Issue: 1
Pages: 8000
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Publication
32820193 | J:294905
First Author: Mason MA
Year: 2020
Journal: Sci Rep
Title: Silencing Srsf6 does not modulate incomplete splicing of the huntingtin gene in Huntington's disease models.
Volume: 10
Issue: 1
Pages: 14057
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Publication
24347167 | J:209517
First Author: Parsons MP
Year: 2014
Journal: J Biol Chem
Title: Bidirectional control of postsynaptic density-95 (PSD-95) clustering by Huntingtin.
Volume: 289
Issue: 6
Pages: 3518-28
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Publication
23145961 | J:192458
First Author: Soldati C
Year: 2013
Journal: J Neurochem
Title: Dysregulation of REST-regulated coding and non-coding RNAs in a cellular model of Huntington's disease.
Volume: 124
Issue: 3
Pages: 418-30
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Publication
25461618 | J:231417
 
First Author: Yao J
Year: 2014
Journal: Mol Cell Neurosci
Title: Huntingtin is associated with cytomatrix proteins at the presynaptic terminal.
Volume: 63
Pages: 96-100
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Publication
23852340 | J:200090
First Author: Marco S
Year: 2013
Journal: Nat Med
Title: Suppressing aberrant GluN3A expression rescues synaptic and behavioral impairments in Huntington's disease models.
Volume: 19
Issue: 8
Pages: 1030-8
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Publication
24105466 | J:205992
First Author: McFarland KN
Year: 2014
Journal: Hum Mol Genet
Title: MeCP2: a novel Huntingtin interactor.
Volume: 23
Issue: 4
Pages: 1036-44
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Publication
29891550 | J:267137
First Author: Pan Y
Year: 2018
Journal: J Biol Chem
Title: The role of Twist1 in mutant huntingtin-induced transcriptional alterations and neurotoxicity.
Volume: 293
Issue: 30
Pages: 11850-11866
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Publication
22492998 | J:185283
First Author: Tang B
Year: 2012
Journal: Hum Mol Genet
Title: Forkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: implications for transcriptional dysregulation in Huntington disease.
Volume: 21
Issue: 14
Pages: 3097-111
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Publication
26048156 | J:227439
 
First Author: Swarnkar S
Year: 2015
Journal: Neurobiol Dis
Title: Ectopic expression of the striatal-enriched GTPase Rhes elicits cerebellar degeneration and an ataxia phenotype in Huntington's disease.
Volume: 82
Pages: 66-77
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Publication
32681824 | J:301372
First Author: Lee H
Year: 2020
Journal: Neuron
Title: Cell Type-Specific Transcriptomics Reveals that Mutant Huntingtin Leads to Mitochondrial RNA Release and Neuronal Innate Immune Activation.
Volume: 107
Issue: 5
Pages: 891-908.e8
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Publication
39068661 | J:353919
First Author: Callahan JW
Year: 2024
Journal: Cell Rep
Title: Movement-related increases in subthalamic activity optimize locomotion.
Volume: 43
Issue: 8
Pages: 114495
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Publication
19525941 | J:152570
First Author: Morfini GA
Year: 2009
Journal: Nat Neurosci
Title: Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin.
Volume: 12
Issue: 7
Pages: 864-71
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Publication
34469738 | J:324645
First Author: Goold R
Year: 2021
Journal: Cell Rep
Title: FAN1 controls mismatch repair complex assembly via MLH1 retention to stabilize CAG repeat expansion in Huntington's disease.
Volume: 36
Issue: 9
Pages: 109649
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Publication
25446099 | J:220288
First Author: Choudhury KR
Year: 2015
Journal: Biochem Biophys Res Commun
Title: Chaperone protein HYPK interacts with the first 17 amino acid region of Huntingtin and modulates mutant HTT-mediated aggregation and cytotoxicity.
Volume: 456
Issue: 1
Pages: 66-73
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Publication
18838463 | J:143295
First Author: Dietrich P
Year: 2009
Journal: Hum Mol Genet
Title: Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages.
Volume: 18
Issue: 1
Pages: 142-50
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Publication
32681165 | J:295993
First Author: Gerson JE
Year: 2020
Journal: Hum Mol Genet
Title: Ubiquilin-2 differentially regulates polyglutamine disease proteins.
Volume: 29
Issue: 15
Pages: 2596-2610
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Publication
32242231 | J:288628
First Author: Jiang M
Year: 2020
Journal: Hum Mol Genet
Title: Nemo-like kinase reduces mutant huntingtin levels and mitigates Huntington's disease.
Volume: 29
Issue: 8
Pages: 1340-1352
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Publication
17548833 | J:248257
First Author: Caviston JP
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Huntingtin facilitates dynein/dynactin-mediated vesicle transport.
Volume: 104
Issue: 24
Pages: 10045-50
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Publication
19646509 | J:154511
First Author: Cho KJ
Year: 2009
Journal: Neuroscience
Title: Inhibition of apoptosis signal-regulating kinase 1 reduces endoplasmic reticulum stress and nuclear huntingtin fragments in a mouse model of Huntington disease.
Volume: 163
Issue: 4
Pages: 1128-34
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Publication
21315254 | J:174750
First Author: Crook ZR
Year: 2011
Journal: Neuron
Title: Huntington's disease: can mice lead the way to treatment?
Volume: 69
Issue: 3
Pages: 423-35
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Publication
27516062 | J:259936
 
First Author: Pan Y
Year: 2016
Journal: Sci Rep
Title: Inhibition of DNA Methyltransferases Blocks Mutant Huntingtin-Induced Neurotoxicity.
Volume: 6
Pages: 31022
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Publication
28396396 | J:242134
First Author: Zhao Z
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Formation of neurodegenerative aggresome and death-inducing signaling complex in maternal diabetes-induced neural tube defects.
Volume: 114
Issue: 17
Pages: 4489-4494
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Publication
21985783 | J:178446
First Author: Keryer G
Year: 2011
Journal: J Clin Invest
Title: Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease.
Volume: 121
Issue: 11
Pages: 4372-82
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Publication
31875875 | J:289016
First Author: Di Pardo A
Year: 2020
Journal: Hum Mol Genet
Title: Mutant huntingtin interacts with the sterol regulatory element-binding proteins and impairs their nuclear import.
Volume: 29
Issue: 3
Pages: 418-431
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Publication
14981075 | J:219104
First Author: Gafni J
Year: 2004
Journal: J Biol Chem
Title: Inhibition of calpain cleavage of huntingtin reduces toxicity: accumulation of calpain/caspase fragments in the nucleus.
Volume: 279
Issue: 19
Pages: 20211-20
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Publication
29212017 | J:254849
First Author: Hachigian LJ
Year: 2017
Journal: Cell Rep
Title: Control of Huntington's Disease-Associated Phenotypes by the Striatum-Enriched Transcription Factor Foxp2.
Volume: 21
Issue: 10
Pages: 2688-2695
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Publication
23209424 | J:194172
First Author: Miller JP
Year: 2012
Journal: PLoS Genet
Title: A genome-scale RNA-interference screen identifies RRAS signaling as a pathologic feature of Huntington's disease.
Volume: 8
Issue: 11
Pages: e1003042
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Publication
36914640 | J:338909
First Author: Pancani T
Year: 2023
Journal: Nat Commun
Title: Cholinergic deficits selectively boost cortical intratelencephalic control of striatum in male Huntington's disease model mice.
Volume: 14
Issue: 1
Pages: 1398
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Publication
28550168 | J:243191
First Author: Louis Sam Titus ASC
Year: 2017
Journal: J Neurosci
Title: Reduced Expression of Foxp1 as a Contributing Factor in Huntington's Disease.
Volume: 37
Issue: 27
Pages: 6575-6587
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Publication
32859226 | J:302806
First Author: de Souza JM
Year: 2020
Journal: Mol Brain
Title: mGluR5 regulates REST/NRSF signaling through N-cadherin/β-catenin complex in Huntington's disease.
Volume: 13
Issue: 1
Pages: 118
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Publication
32876667 | J:298297
First Author: Loupe JM
Year: 2020
Journal: Hum Mol Genet
Title: Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out.
Volume: 29
Issue: 18
Pages: 3044-3053
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Publication
37580082 | J:352486
 
First Author: Voelkl K
Year: 2023
Journal: Life Sci Alliance
Title: Neuroprotective effects of hepatoma-derived growth factor in models of Huntington's disease.
Volume: 6
Issue: 11
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Publication
25478910 | J:218852
First Author: Sanders SS
Year: 2015
Journal: Dev Biol
Title: Huntingtin interacting proteins 14 and 14-like are required for chorioallantoic fusion during early placental development.
Volume: 397
Issue: 2
Pages: 257-66
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Publication
24991961 | J:224118
First Author: Plotkin JL
Year: 2014
Journal: Neuron
Title: Impaired TrkB receptor signaling underlies corticostriatal dysfunction in Huntington's disease.
Volume: 83
Issue: 1
Pages: 178-88
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Publication
11152656 | J:67077
First Author: Näf D
Year: 2001
Journal: Hum Mol Genet
Title: Mouse models for the Wolf-Hirschhorn deletion syndrome.
Volume: 10
Issue: 2
Pages: 91-8
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Publication
27721240 | J:239619
First Author: Rué L
Year: 2016
Journal: J Clin Invest
Title: Targeting CAG repeat RNAs reduces Huntington's disease phenotype independently of huntingtin levels.
Volume: 126
Issue: 11
Pages: 4319-4330
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Publication
33086039 | J:300547
First Author: Yu X
Year: 2020
Journal: Neuron
Title: Context-Specific Striatal Astrocyte Molecular Responses Are Phenotypically Exploitable.
Volume: 108
Issue: 6
Pages: 1146-1162.e10
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Publication
17500595 | J:121567
First Author: Kaltenbach LS
Year: 2007
Journal: PLoS Genet
Title: Huntingtin interacting proteins are genetic modifiers of neurodegeneration.
Volume: 3
Issue: 5
Pages: e82
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Publication
36225731 | J:354504
 
First Author: Voelkl K
Year: 2022
Journal: Front Neurosci
Title: Distinct histological alterations of cortical interneuron types in mouse models of Huntington's disease.
Volume: 16
Pages: 1022251
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Protein Coding Gene
MGP_CAROLIEiJ_G0027139 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0029471 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0029438 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0029387 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0029448 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0029170 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_96067 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0029902 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0028579 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CBAJ_G0029138 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_DBA2J_G0029286 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_FVBNJ_G0029245 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_LPJ_G0029371 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NODShiLtJ_G0029275 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NZOHlLtJ_G0029935 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PWKPhJ_G0028304 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_WSBEiJ_G0028660 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PahariEiJ_G0016923 | -
Type: protein_coding_gene
Organism: Mus pahari
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Protein Coding Gene
MGP_SPRETEiJ_G0028135 | -
Type: protein_coding_gene
Organism: Mus spretus
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Publication
8162057 | J:16635
First Author: Lin B
Year: 1994
Journal: Hum Mol Genet
Title: Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected].
Volume: 3
Issue: 1
Pages: 85-92
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Publication
8009370 | J:18404
First Author: Barnes GT
Year: 1994
Journal: Somat Cell Mol Genet
Title: Mouse Huntington's disease gene homolog (Hdh).
Volume: 20
Issue: 2
Pages: 87-97
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Publication
7647777 | J:24940
First Author: Trottier Y
Year: 1995
Journal: Nat Genet
Title: Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form.
Volume: 10
Issue: 1
Pages: 104-10
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Publication
7759106 | J:23247
First Author: Lin B
Year: 1995
Journal: Genomics
Title: Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms.
Volume: 25
Issue: 3
Pages: 707-15
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Publication
9246489 | J:41317
 
First Author: MacDonald ME
Year: 1996
Journal: Cold Spring Harb Symp Quant Biol
Title: Targeted inactivation of the mouse Huntington's disease gene homolog Hdh.
Volume: 61
Pages: 627-38
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Publication
11567051 | J:71624
First Author: Reiner A
Year: 2001
Journal: J Neurosci
Title: Neurons lacking huntingtin differentially colonize brain and survive in chimeric mice.
Volume: 21
Issue: 19
Pages: 7608-19
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Publication
11062468 | J:65520
First Author: Dragatsis I
Year: 2000
Journal: Nat Genet
Title: Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice.
Volume: 26
Issue: 3
Pages: 300-6
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Publication
15935052 | J:99425
First Author: Brustovetsky N
Year: 2005
Journal: J Neurochem
Title: Age-dependent changes in the calcium sensitivity of striatal mitochondria in mouse models of Huntington's Disease.
Volume: 93
Issue: 6
Pages: 1361-70
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Publication
10699173 | J:60937
First Author: Wheeler VC
Year: 2000
Journal: Hum Mol Genet
Title: Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice.
Volume: 9
Issue: 4
Pages: 503-13
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Publication
29324753 | J:257872
First Author: Langfelder P
Year: 2018
Journal: PLoS One
Title: MicroRNA signatures of endogenous Huntingtin CAG repeat expansion in mice.
Volume: 13
Issue: 1
Pages: e0190550
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Publication
12895502 | J:128151
First Author: Snider BJ
Year: 2003
Journal: Neuroscience
Title: Neocortical neurons cultured from mice with expanded CAG repeats in the huntingtin gene: unaltered vulnerability to excitotoxins and other insults.
Volume: 120
Issue: 3
Pages: 617-25
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Publication
26900923 | J:234512
First Author: Langfelder P
Year: 2016
Journal: Nat Neurosci
Title: Integrated genomics and proteomics define huntingtin CAG length-dependent networks in mice.
Volume: 19
Issue: 4
Pages: 623-33
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Publication
16697652 | J:111237
First Author: Guidetti P
Year: 2006
Journal: Neurobiol Dis
Title: Elevated brain 3-hydroxykynurenine and quinolinate levels in Huntington disease mice.
Volume: 23
Issue: 1
Pages: 190-7
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Publication
17519223 | J:142943
First Author: Kuhn A
Year: 2007
Journal: Hum Mol Genet
Title: Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosage.
Volume: 16
Issue: 15
Pages: 1845-61
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Publication
12460554 | J:125447
First Author: Namura S
Year: 2002
Journal: Neurobiol Dis
Title: The HD mutation does not alter neuronal death in the striatum of Hdh(Q92) knock-in mice after mild focal ischemia.
Volume: 11
Issue: 1
Pages: 147-54
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Publication
19445966 | J:150366
First Author: Trueman RC
Year: 2009
Journal: Behav Brain Res
Title: Rule learning, visuospatial function and motor performance in the Hdh(Q92) knock-in mouse model of Huntington's disease.
Volume: 203
Issue: 2
Pages: 215-22
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Publication
18367261 | J:133206
First Author: Trueman RC
Year: 2008
Journal: Behav Brain Res
Title: Time course of choice reaction time deficits in the Hdh(Q92) knock-in mouse model of Huntington's disease in the operant serial implicit learning task (SILT).
Volume: 189
Issue: 2
Pages: 317-24
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Publication
17284197 | J:118627
First Author: Trueman RC
Year: 2007
Journal: Eur J Neurosci
Title: The operant serial implicit learning task reveals early onset motor learning deficits in the Hdh knock-in mouse model of Huntington's disease.
Volume: 25
Issue: 2
Pages: 551-8
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Publication
26464483 | J:226832
First Author: Puigdellívol M
Year: 2015
Journal: Hum Mol Genet
Title: A role for Kalirin-7 in corticostriatal synaptic dysfunction in Huntington's disease.
Volume: 24
Issue: 25
Pages: 7265-85
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Publication
21447599 | J:171983
First Author: Reis SA
Year: 2011
Journal: Hum Mol Genet
Title: Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis.
Volume: 20
Issue: 12
Pages: 2344-55
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Publication
37177784 | J:359526
First Author: O'Reilly D
Year: 2023
Journal: Mol Ther
Title: Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease.
Volume: 31
Issue: 6
Pages: 1661-1674
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Publication
26143143 | J:231200
First Author: Cherubini M
Year: 2015
Journal: Biochim Biophys Acta
Title: Cdk5-mediated mitochondrial fission: A key player in dopaminergic toxicity in Huntington's disease.
Volume: 1852
Issue: 10 Pt A
Pages: 2145-60
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Publication
24992836 | J:220144
 
First Author: Ribeiro M
Year: 2014
Journal: Free Radic Biol Med
Title: Insulin and IGF-1 improve mitochondrial function in a PI-3K/Akt-dependent manner and reduce mitochondrial generation of reactive oxygen species in Huntington's disease knock-in striatal cells.
Volume: 74
Pages: 129-44
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Publication
29162692 | J:256508
First Author: Cariulo C
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Phosphorylation of huntingtin at residue T3 is decreased in Huntington's disease and modulates mutant huntingtin protein conformation.
Volume: 114
Issue: 50
Pages: E10809-E10818
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Publication
22123819 | J:179665
First Author: Mochel F
Year: 2012
Journal: J Biol Chem
Title: Early alterations of brain cellular energy homeostasis in Huntington disease models.
Volume: 287
Issue: 2
Pages: 1361-70
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Publication
11912178 | J:75831
First Author: Wheeler VC
Year: 2002
Journal: Hum Mol Genet
Title: Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice.
Volume: 11
Issue: 6
Pages: 633-40
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Publication
27217211 | J:235954
 
First Author: Du Z
Year: 2016
Journal: Neuroscience
Title: Early GABAergic transmission defects in the external globus pallidus and rest/activity rhythm alteration in a mouse model of Huntington's disease.
Volume: 329
Pages: 363-79
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Publication
20383138 | J:159605
First Author: Martinez-Vicente M
Year: 2010
Journal: Nat Neurosci
Title: Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease.
Volume: 13
Issue: 5
Pages: 567-76
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Publication
27163546 | J:236734
 
First Author: Yhnell E
Year: 2016
Journal: Exp Neurol
Title: Cognitive training modifies disease symptoms in a mouse model of Huntington's disease.
Volume: 282
Pages: 19-26
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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