| scholarly article | Q13442814 |
| P2093 | author name string | Z Li | |
| M P Scott | |||
| R M Myers | |||
| C A Karlovich | |||
| M P Fish | |||
| P2860 | cites work | CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 |
| Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures | Q24322756 | ||
| A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. | Q27860836 | ||
| Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract | Q28267110 | ||
| SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates | Q28288296 | ||
| Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes | Q28302701 | ||
| Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue | Q28506834 | ||
| Inactivation of the mouse Huntington's disease gene homolog Hdh | Q28509662 | ||
| Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form | Q28509836 | ||
| Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice | Q29615357 | ||
| Characterization of bacteriophage P1 library containing inserts of Drosophila DNA of 75?100 kilobase pairs | Q33291536 | ||
| opa: a novel family of transcribed repeats shared by the Notch locus and other developmentally regulated loci in D. melanogaster | Q34563922 | ||
| Mouse Huntington's disease gene homolog (Hdh). | Q34662498 | ||
| Characterization and localization of the Huntington disease gene product | Q34662553 | ||
| Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro | Q35880505 | ||
| Splicing signals in Drosophila: intron size, information content, and consensus sequences | Q35925544 | ||
| Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected] | Q36747904 | ||
| Genetics and molecular biology of Huntington's disease | Q40399297 | ||
| Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates | Q41065635 | ||
| Trinucleotide repeats in neurogenetic disorders | Q41132596 | ||
| Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract | Q41182414 | ||
| Huntington disease and the related disorder, dentatorubral-pallidoluysian atrophy (DRPLA). | Q41628677 | ||
| Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues | Q42503942 | ||
| Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression | Q45289001 | ||
| A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats | Q45289978 | ||
| Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH. | Q45291767 | ||
| Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length | Q45296163 | ||
| Comparative sequence analysis of the human and pufferfish Huntington's disease genes | Q45307541 | ||
| Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila | Q47945602 | ||
| Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. | Q48373564 | ||
| Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice | Q48373570 | ||
| Of molecular interactions, mice and mechanisms | Q57840073 | ||
| P433 | issue | 9 | |
| P921 | main subject | Huntington's disease | Q190564 |
| Drosophila | Q312154 | ||
| P304 | page(s) | 1807-1815 | |
| P577 | publication date | 1999-09-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | A putative Drosophila homolog of the Huntington's disease gene | |
| P478 | volume | 8 |
| Q34828144 | A huntingtin peptide inhibits polyQ-huntingtin associated defects |
| Q47073933 | An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin |
| Q36606399 | Animal models of Huntington's disease: implications in uncovering pathogenic mechanisms and developing therapies |
| Q38165759 | Animal models of neurodegenerative diseases |
| Q39679096 | Characterization of axonal transport defects in Drosophila Huntingtin mutants |
| Q33605779 | Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein |
| Q33305723 | Characterization, developmental expression and evolutionary features of the huntingtin gene in the amphioxus Branchiostoma floridae. |
| Q38027948 | Choosing and using Drosophila models to characterize modifiers of Huntington's disease |
| Q30425063 | Deletion of the huntingtin proline-rich region does not significantly affect normal huntingtin function in mice |
| Q28510315 | Deletion of the triplet repeat encoding polyglutamine within the mouse Huntington's disease gene results in subtle behavioral/motor phenotypes in vivo and elevated levels of ATP with cellular senescence in vitro |
| Q34119278 | Drosophila models of human neurodegenerative disease |
| Q50737253 | Evidence for dynamic and multiple roles for huntingtin in Ciona intestinalis |
| Q36314946 | Evolving Notch polyQ tracts reveal possible solenoid interference elements |
| Q40295769 | Expression and characterization of full-length human huntingtin, an elongated HEAT repeat protein |
| Q27023050 | Genetics and neuropathology of Huntington's disease |
| Q27323092 | High-content chemical and RNAi screens for suppressors of neurotoxicity in a Huntington's disease model |
| Q42099857 | Hunting for the function of Huntingtin |
| Q28118022 | Huntingtin functions as a scaffold for selective macroautophagy |
| Q33263046 | Huntingtin gene evolution in Chordata and its peculiar features in the ascidian Ciona genus |
| Q21131986 | Huntingtin is critical both pre- and postsynaptically for long-term learning-related synaptic plasticity in Aplysia |
| Q39456024 | Huntington's Disease: Calcium Dyshomeostasis and Pathology Models |
| Q38578817 | Huntington's disease: from gene to potential therapy. |
| Q30487328 | Inactivation of Drosophila Huntingtin affects long-term adult functioning and the pathogenesis of a Huntington's disease model |
| Q36535666 | Is Huntington's a glutamine storage disease? |
| Q41880469 | Modeling Huntington disease in Drosophila: Insights into axonal transport defects and modifiers of toxicity. |
| Q37776087 | Molecular Mechanisms and Potential Therapeutical Targets in Huntington's Disease |
| Q48207865 | Neural expression of the Huntington's disease gene as a chordate evolutionary novelty. |
| Q28281904 | Normal huntingtin function: an alternative approach to Huntington's disease |
| Q91841578 | Peripheral Expression of Mutant Huntingtin is a Critical Determinant of Weight Loss and Metabolic Disturbances in Huntington's Disease |
| Q38563516 | Studying polyglutamine diseases in Drosophila. |
| Q37969749 | The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology |
| Q24799224 | The predominantly HEAT-like motif structure of huntingtin and its association and coincident nuclear entry with dorsal, an NF-kB/Rel/dorsal family transcription factor |
| Q37249765 | Trends in the molecular pathogenesis and clinical therapeutics of common neurodegenerative disorders |
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