Pages that link to "Q29617982"
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The following pages link to Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain (Q29617982):
Displaying 50 items.
- Ubiquitin-proteasome system involvement in Huntington's disease (Q21129327) (← links)
- Adult bone marrow: which stem cells for cellular therapy protocols in neurodegenerative disorders? (Q21285020) (← links)
- Iron and neurodegeneration: from cellular homeostasis to disease (Q21296730) (← links)
- Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7 (Q22003756) (← links)
- Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicity (Q22009069) (← links)
- The TOR1A (DYT1) gene family and its role in early onset torsion dystonia (Q22011111) (← links)
- Activation of MLK2-mediated signaling cascades by polyglutamine-expanded huntingtin (Q22254045) (← links)
- The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription (Q22254119) (← links)
- Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase (Q22254584) (← links)
- Oligonucleotide therapeutic approaches for Huntington disease (Q22306293) (← links)
- Molecular characterization of human tensin (Q24290371) (← links)
- Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi (Q24292161) (← links)
- Characterization of a brain-enriched chaperone, MRJ, that inhibits Huntingtin aggregation and toxicity independently (Q24292471) (← links)
- ASK1 is essential for endoplasmic reticulum stress-induced neuronal cell death triggered by expanded polyglutamine repeats (Q24298956) (← links)
- Regulation of Rap2A by the ubiquitin ligase Nedd4-1 controls neurite development (Q24299364) (← links)
- Novel nuclear shuttle proteins, HDBP1 and HDBP2, bind to neuronal cell-specific cis-regulatory element in the promoter for the human Huntington's disease gene (Q24300004) (← links)
- Interaction of the nuclear matrix protein NAKAP with HypA and huntingtin: implications for nuclear toxicity in Huntington's disease pathogenesis (Q24300257) (← links)
- Huntingtin-interacting protein 1-mediated neuronal cell death occurs through intrinsic apoptotic pathways and mitochondrial alterations (Q24303436) (← links)
- A protein interaction network links GIT1, an enhancer of huntingtin aggregation, to Huntington's disease (Q24304932) (← links)
- The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy (Q24307759) (← links)
- Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy (Q24308826) (← links)
- Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins (Q24310521) (← links)
- Parkin is an E3 ubiquitin-ligase for normal and mutant ataxin-2 and prevents ataxin-2-induced cell death (Q24313820) (← links)
- Huntingtin has a membrane association signal that can modulate huntingtin aggregation, nuclear entry and toxicity (Q24337727) (← links)
- Polyglutamine expansion of huntingtin impairs its nuclear export (Q24338269) (← links)
- The DNAJB6 and DNAJB8 protein chaperones prevent intracellular aggregation of polyglutamine peptides (Q24338933) (← links)
- Interaction of Huntington disease protein with transcriptional activator Sp1 (Q24537687) (← links)
- Huntingtin in health and disease (Q24554374) (← links)
- Multiple Aspects of Gene Dysregulation in Huntington's Disease (Q24605880) (← links)
- PolyQ: a database describing the sequence and domain context of polyglutamine repeats in proteins (Q24613607) (← links)
- The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis (Q24616907) (← links)
- Tissue transglutaminase overexpression does not modify the disease phenotype of the R6/2 mouse model of Huntington's disease (Q24618141) (← links)
- A natural antisense transcript at the Huntington's disease repeat locus regulates HTT expression (Q24620388) (← links)
- Improved activities of CREB binding protein, heterogeneous nuclear ribonucleoproteins and proteasome following downregulation of noncoding hsromega transcripts help suppress poly(Q) pathogenesis in fly models (Q24626685) (← links)
- Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease (Q24635129) (← links)
- Towards a transgenic model of Huntington's disease in a non-human primate (Q24644013) (← links)
- Intracellular degradation of misfolded proteins in polyglutamine neurodegenerative diseases (Q24644954) (← links)
- Polyalanine and polyserine frameshift products in Huntington's disease (Q24656119) (← links)
- Interaction between neuronal intranuclear inclusions and promyelocytic leukemia protein nuclear and coiled bodies in CAG repeat diseases (Q24670202) (← links)
- The localization and interactions of huntingtin (Q24676589) (← links)
- Transgenic models of Huntington's disease (Q24676606) (← links)
- Mutant Rab24 GTPase is targeted to nuclear inclusions (Q24792201) (← links)
- Reversal of a full-length mutant huntingtin neuronal cell phenotype by chemical inhibitors of polyglutamine-mediated aggregation (Q24799882) (← links)
- Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice (Q24816600) (← links)
- The life cycle of the 26S proteasome: from birth, through regulation and function, and onto its death (Q26738549) (← links)
- Ubc13: the Lys63 ubiquitin chain building machine (Q26739716) (← links)
- Subcellular Clearance and Accumulation of Huntington Disease Protein: A Mini-Review (Q26752720) (← links)
- The P42 peptide and Peptide-based therapies for Huntington's disease (Q26764930) (← links)
- Neural and mesenchymal stem cells in animal models of Huntington's disease: past experiences and future challenges (Q26775932) (← links)
- Amyloids: from Pathogenesis to Function (Q26778177) (← links)