{"doi":"10.1155/2012/682712","title":"Lessons Learned from the Transgenic Huntington's Disease Rats","abstract":"<jats:p>Huntington's disease (HD) is a fatal inherited disorder leading to selective neurodegeneration and neuropsychiatric symptoms. Currently, there is no treatment to slow down or to stop the disease. There is also no therapy to effectively reduce the symptoms. In the investigation of novel therapies, different animal models of Huntington's disease, varying from insects to nonhuman primates, have been created and used. Few years ago, the first transgenic rat model of HD, carrying a truncated huntingtin cDNA fragment with 51 CAG repeats under control of the native rat<jats:italic>huntingtin</jats:italic>promoter, was introduced. We have been using this animal model in our research and review here our experience with the behavioural, neurophysiological, and histopathological phenotype of the transgenic Huntington's disease rats with relevant literature.</jats:p>","journal":"Neural Plasticity","year":2012,"id":24362,"datarank":0.5056443141347431,"base_score":2.70805020110221,"endowment":2.70805020110221,"self_citation_contribution":0.40620753016533157,"citation_network_contribution":0.09943678396941155,"self_endowment_contribution":0.40620753016533157,"citer_contribution":0.09943678396941155,"corpus_percentile":null,"corpus_rank":null,"citation_count":14,"citer_count":8,"citers_with_citation_signal":4,"citers_with_endowment":4,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":146405,"name":"Dagmar H. Zeef","orcid":null,"position":1,"is_corresponding":false},{"id":146406,"name":"Marcus L. F. Janssen","orcid":null,"position":2,"is_corresponding":false},{"id":146407,"name":"Mayke Oosterloo","orcid":null,"position":3,"is_corresponding":false},{"id":146408,"name":"Frederic Schaper","orcid":null,"position":4,"is_corresponding":false},{"id":146409,"name":"Ali Jahanshahi","orcid":null,"position":5,"is_corresponding":false},{"id":146410,"name":"Yasin Temel","orcid":null,"position":6,"is_corresponding":false},{"id":146404,"name":"Rinske Vlamings","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"base_score":2.70805020110221,"endowment":2.70805020110221,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"22852099","pmcid":"PMC3407652","openalex_id":"https://openalex.org/W1964953273","authors":[],"funders":[{"funder_name":"Cure Huntington’s Disease Initiative","grant_id":"","title":null}],"total_grants":1,"fwci":0.8739,"citation_percentile":0.67333065,"influential_citations":1,"citation_trend":[{"year":2012,"count":1},{"year":2013,"count":2},{"year":2014,"count":2},{"year":2015,"count":2},{"year":2016,"count":1},{"year":2019,"count":1},{"year":2022,"count":2},{"year":2023,"count":2},{"year":2026,"count":1}],"oa_status":"gold","license":"cc-by","oa_locations":[{"url":"https://downloads.hindawi.com/journals/np/2012/682712.pdf","host_type":"journal"},{"url":"https://downloads.hindawi.com/journals/np/2012/682712.pdf","host_type":"GOLD"},{"url":"https://downloads.hindawi.com/journals/np/2012/682712.pdf","host_type":"publisher"},{"url":"http://downloads.hindawi.com/journals/np/2012/682712.pdf","host_type":"publisher"},{"url":"http://downloads.hindawi.com/journals/np/2012/682712.xml","host_type":"publisher"},{"url":"https://doi.org/10.1155/2012/682712","host_type":"journal"},{"url":"https://pubmed.ncbi.nlm.nih.gov/22852099","host_type":"repository"},{"url":"https://cris.maastrichtuniversity.nl/en/publications/e40b51c2-371c-48ea-99a3-bb26c1f61f35","host_type":"repository"},{"url":"https://doaj.org/article/ae32c2effdec44e0827a3d0d81da05a9","host_type":"repository"},{"url":"https://www.ncbi.nlm.nih.gov/pmc/articles/3407652","host_type":"repository"},{"url":"https://europepmc.org/articles/PMC3407652","host_type":"Europe_PMC"},{"url":"https://europepmc.org/articles/PMC3407652?pdf=render","host_type":"Europe_PMC"}],"fields_of_study":["Genetic Neurodegenerative Diseases","Neurological disorders and treatments","Mitochondrial Function and Pathology","Biology","Medicine","Animals","Behavior, Animal","DNA, Complementary","Humans","Huntingtin Protein","Huntington Disease","Nerve Tissue Proteins","Nervous System","Nervous System Physiological Phenomena","Phenotype","Rats","Rats, Transgenic","Repetitive Sequences, Nucleic Acid"],"mesh_terms":["Huntingtin Protein","Animals","Behavior, Animal","Humans","Huntington Disease","Nerve Tissue Proteins","Nervous System","Nervous System Physiological Phenomena","Phenotype","Repetitive Sequences, Nucleic Acid","DNA, Complementary","Rats","Rats, Transgenic"],"keywords":["Huntington's disease","Huntingtin","Neurodegeneration","Transgene","Disease","Genetically modified mouse","Huntingtin Protein","Animal model","Neuroscience","Phenotype","Biology","Medicine","Genetics","Internal medicine","Endocrinology","Gene"],"sdg_mappings":[{"sdg_number":0,"sdg_label":"Good health and well-being"}],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-06-07T22:15:00.016494Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}