001     136241
005     20250416143148.0
024 7 _ |a 0005-7851
|2 ISSN
024 7 _ |a 10.1007/s10519-010-9398-1
|2 doi
024 7 _ |a pmid:20882401
|2 pmid
024 7 _ |a pmc:PMC3102774
|2 pmc
024 7 _ |a 0001-8244
|2 ISSN
024 7 _ |a 1573-3297
|2 ISSN
037 _ _ |a DZNE-2020-02563
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Ehninger, Dan
|0 P:(DE-2719)2289209
|b 0
|e First author
|u dzne
245 _ _ |a Increased levels of anxiety-related behaviors in a Tsc2 dominant negative transgenic mouse model of tuberous sclerosis.
260 _ _ |a Dordrecht [u.a.]
|c 2011
|b Springer Science + Business Media B.V
264 _ 1 |3 online
|2 Crossref
|b Springer Science and Business Media LLC
|c 2010-09-30
264 _ 1 |3 print
|2 Crossref
|b Springer Science and Business Media LLC
|c 2011-05-01
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
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|s 1744806670_2859
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336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Tuberous sclerosis (TSC) is a single-gene disorder caused by heterozygous mutations in the TSC1 or TSC2 gene. TSC is often associated with neurological (e.g., epilepsy), cognitive (intellectual disabilities, specific neuropsychological impairments) and behavioral pathologies (e.g., autism, attention deficit hyperactivity disorder). In addition, there is a high prevalence of psychiatric problems in TSC populations, including anxiety and mood disorders. To date, little is known about the pathogenetic bases of these associated psychiatric symptoms; for instance, it is unclear whether they are rooted in TSC-associated neurobiological alterations or whether they are secondary psychological phenomena (e.g., because individuals have to cope with the burden of the disease). Here, we report elevated levels of anxiety-related behaviors and mild deficits in two hippocampal-dependent learning tasks in a Tsc2 dominant negative transgenic mouse model of TSC. These findings establish a mouse model for TSC-related anxiety phenotypes and suggest that anxiety disorders in TSC have a biological foundation.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
|x 0
542 _ _ |i 2010-09-30
|2 Crossref
|u http://www.springer.com/tdm
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a TSC2 protein, human
|2 NLM Chemicals
650 _ 7 |a Tsc2 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Tuberous Sclerosis Complex 2 Protein
|2 NLM Chemicals
650 _ 7 |a Tumor Suppressor Proteins
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Anxiety: genetics
|2 MeSH
650 _ 2 |a Disease Models, Animal
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Genes, Dominant: genetics
|2 MeSH
650 _ 2 |a Genetic Carrier Screening
|2 MeSH
650 _ 2 |a Hippocampus: physiopathology
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Learning Disabilities: genetics
|2 MeSH
650 _ 2 |a Learning Disabilities: physiopathology
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Memory Disorders: genetics
|2 MeSH
650 _ 2 |a Memory Disorders: physiopathology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Mice, Transgenic
|2 MeSH
650 _ 2 |a Phenotype
|2 MeSH
650 _ 2 |a Tuberous Sclerosis: genetics
|2 MeSH
650 _ 2 |a Tuberous Sclerosis: physiopathology
|2 MeSH
650 _ 2 |a Tuberous Sclerosis Complex 2 Protein
|2 MeSH
650 _ 2 |a Tumor Suppressor Proteins: genetics
|2 MeSH
700 1 _ |a Silva, Alcino J
|0 P:(DE-HGF)0
|b 1
773 1 8 |a 10.1007/s10519-010-9398-1
|b : Springer Science and Business Media LLC, 2010-09-30
|n 3
|p 357-363
|3 journal-article
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|t Behavior Genetics
|v 41
|y 2010
|x 0001-8244
773 _ _ |a 10.1007/s10519-010-9398-1
|g Vol. 41, no. 3, p. 357 - 363
|0 PERI:(DE-600)2014974-8
|n 3
|q 41:3<357 - 363
|p 357-363
|t Behavior genetics
|v 41
|y 2011
|x 0001-8244
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102774
856 4 _ |u https://pub.dzne.de/record/136241/files/DZNE-2020-02563_Restricted.pdf
856 4 _ |u https://pub.dzne.de/record/136241/files/DZNE-2020-02563_Restricted.pdf?subformat=pdfa
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909 C O |p VDB
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
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|6 P:(DE-2719)2289209
913 1 _ |a DE-HGF
|b Gesundheit
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|0 G:(DE-HGF)POF3-342
|3 G:(DE-HGF)POF3
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914 1 _ |y 2011
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21