544 related articles for article (PubMed ID: 27142239)
1. Characterization of ultrasonic vocalizations of Fragile X mice.
Belagodu AP; Johnson AM; Galvez R
Behav Brain Res; 2016 Sep; 310():76-83. PubMed ID: 27142239
[TBL] [Abstract][Full Text] [Related]
2. Sex-specific modulation of early life vocalization and cognition by Fmr1 gene dosage in a mouse model of Fragile X Syndrome.
Giua G; Iezzi D; Caceres-Rodriguez A; Strauss B; Chavis P; Manzoni OJ
Biol Sex Differ; 2024 Feb; 15(1):18. PubMed ID: 38383408
[TBL] [Abstract][Full Text] [Related]
3. Spectral and temporal properties of calls reveal deficits in ultrasonic vocalizations of adult Fmr1 knockout mice.
Hodges SL; Nolan SO; Reynolds CD; Lugo JN
Behav Brain Res; 2017 Aug; 332():50-58. PubMed ID: 28552599
[TBL] [Abstract][Full Text] [Related]
4. Reversal of ultrasonic vocalization deficits in a mouse model of Fragile X Syndrome with minocycline treatment or genetic reduction of MMP-9.
Toledo MA; Wen TH; Binder DK; Ethell IM; Razak KA
Behav Brain Res; 2019 Oct; 372():112068. PubMed ID: 31271818
[TBL] [Abstract][Full Text] [Related]
5. Minocycline treatment reverses ultrasonic vocalization production deficit in a mouse model of Fragile X Syndrome.
Rotschafer SE; Trujillo MS; Dansie LE; Ethell IM; Razak KA
Brain Res; 2012 Feb; 1439():7-14. PubMed ID: 22265702
[TBL] [Abstract][Full Text] [Related]
6. Temporal and spectral differences in the ultrasonic vocalizations of fragile X knock out mice during postnatal development.
Lai JK; Sobala-Drozdowski M; Zhou L; Doering LC; Faure PA; Foster JA
Behav Brain Res; 2014 Feb; 259():119-30. PubMed ID: 24211451
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive analysis of ultrasonic vocalizations in a mouse model of fragile X syndrome reveals limited, call type specific deficits.
Roy S; Watkins N; Heck D
PLoS One; 2012; 7(9):e44816. PubMed ID: 22984567
[TBL] [Abstract][Full Text] [Related]
8. Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X Syndrome.
Lovelace JW; Wen TH; Reinhard S; Hsu MS; Sidhu H; Ethell IM; Binder DK; Razak KA
Neurobiol Dis; 2016 May; 89():126-35. PubMed ID: 26850918
[TBL] [Abstract][Full Text] [Related]
9. High-throughput analysis of vocalizations reveals sex-specific changes in Fmr1 mutant pups.
Nolan SO; Hodges SL; Lugo JN
Genes Brain Behav; 2020 Feb; 19(2):e12611. PubMed ID: 31587487
[TBL] [Abstract][Full Text] [Related]
10. Behavioral abnormalities in the Fmr1-KO2 mouse model of fragile X syndrome: The relevance of early life phases.
Gaudissard J; Ginger M; Premoli M; Memo M; Frick A; Pietropaolo S
Autism Res; 2017 Oct; 10(10):1584-1596. PubMed ID: 28590057
[TBL] [Abstract][Full Text] [Related]
11. Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
Han K; Chen H; Gennarino VA; Richman R; Lu HC; Zoghbi HY
Hum Mol Genet; 2015 Apr; 24(7):1813-23. PubMed ID: 25432536
[TBL] [Abstract][Full Text] [Related]
12. A single episode of early-life status epilepticus impacts neonatal ultrasonic vocalization behavior in the Fmr1 knockout mouse.
Huebschman JL; Hodges SL; Reynolds CD; Nolan SO; Lugo JN
Epilepsy Behav; 2020 Oct; 111():107279. PubMed ID: 32693376
[TBL] [Abstract][Full Text] [Related]
13. Multiple Early-Life Seizures Alters Neonatal Communicative Behavior in Fmr1 Knockout Mice.
Nguyen PH; Narvaiz DA; Womble PD; Sullens DG; Binder MS; Hodges SL; Kwok E; Lugo JN
Dev Neurosci; 2022; 44(6):478-486. PubMed ID: 35512644
[TBL] [Abstract][Full Text] [Related]
14. Neocortical developmental analysis of vasculature and their growth factors offer new insight into fragile X syndrome abnormalities.
Belagodu AP; Fleming S; Galvez R
Dev Neurobiol; 2017 Nov; 77(11):1321-1333. PubMed ID: 28719137
[TBL] [Abstract][Full Text] [Related]
15. Behavioral effects of chronic stress in the Fmr1 mouse model for fragile X syndrome.
Lemaire-Mayo V; Subashi E; Henkous N; Beracochea D; Pietropaolo S
Behav Brain Res; 2017 Mar; 320():128-135. PubMed ID: 27939692
[TBL] [Abstract][Full Text] [Related]
16. Sensory Processing Phenotypes in Fragile X Syndrome.
Rais M; Binder DK; Razak KA; Ethell IM
ASN Neuro; 2018; 10():1759091418801092. PubMed ID: 30231625
[TBL] [Abstract][Full Text] [Related]
17. Genetic deletion of regulator of G-protein signaling 4 (RGS4) rescues a subset of fragile X related phenotypes in the FMR1 knockout mouse.
Pacey LK; Doss L; Cifelli C; van der Kooy D; Heximer SP; Hampson DR
Mol Cell Neurosci; 2011 Mar; 46(3):563-72. PubMed ID: 21215802
[TBL] [Abstract][Full Text] [Related]
18. Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis.
De Rubeis S; Fernández E; Buzzi A; Di Marino D; Bagni C
Adv Exp Med Biol; 2012; 970():517-51. PubMed ID: 22351071
[TBL] [Abstract][Full Text] [Related]
19. Sex-specific and genotype-specific differences in vocalization development in FMR1 knockout mice.
Reynolds CD; Nolan SO; Jefferson T; Lugo JN
Neuroreport; 2016 Dec; 27(18):1331-1335. PubMed ID: 27824730
[TBL] [Abstract][Full Text] [Related]
20. Proteome profiling of the prefrontal cortex of Fmr1 knockout mouse reveals enhancement of complement and coagulation cascades.
Gao MM; Shi H; Yan HJ; Long YS
J Proteomics; 2023 Mar; 274():104822. PubMed ID: 36646274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
