217 related articles for article (PubMed ID: 37761857)
1. Antioxidant Behavioural Phenotype in the
Lawther AJ; Zieba J; Fang Z; Furlong TM; Conn I; Govindaraju H; Choong LLY; Turner N; Siddiqui KS; Bridge W; Merlin S; Hyams TC; Killingsworth M; Eapen V; Clarke RA; Walker AK
Genes (Basel); 2023 Aug; 14(9):. PubMed ID: 37761857
[TBL] [Abstract][Full Text] [Related]
2. Immp2l knockdown in male mice increases stimulus-driven instrumental behaviour but does not alter goal-directed learning or neuron density in cortico-striatal circuits in a model of Tourette syndrome and autism spectrum disorder.
Leung BK; Merlin S; Walker AK; Lawther AJ; Paxinos G; Eapen V; Clarke R; Balleine BW; Furlong TM
Behav Brain Res; 2023 Aug; 452():114610. PubMed ID: 37541448
[TBL] [Abstract][Full Text] [Related]
3. Immp2l Enhances the Structure and Function of Mitochondrial Gpd2 Dehydrogenase.
Clarke RA; Govindaraju H; Beretta M; Olzomer E; Lawther AJ; Walker AK; Fang Z; Eapen V; Hyams TC; Killingsworth M; Bridge W; Turner N; Siddiqui KS
Int J Mol Sci; 2024 Jan; 25(2):. PubMed ID: 38256063
[TBL] [Abstract][Full Text] [Related]
4. First behavioural assessment of a novel Immp2l knockdown mouse model with relevance for Gilles de la Tourette syndrome and Autism spectrum disorder.
Kreilaus F; Chesworth R; Eapen V; Clarke R; Karl T
Behav Brain Res; 2019 Nov; 374():112057. PubMed ID: 31233820
[TBL] [Abstract][Full Text] [Related]
5. The Immp2l mutation causes age-dependent degeneration of cerebellar granule neurons prevented by antioxidant treatment.
Liu C; Li X; Lu B
Aging Cell; 2016 Feb; 15(1):167-76. PubMed ID: 26616244
[TBL] [Abstract][Full Text] [Related]
6. The Immp2l Mutation Causes Ovarian Aging Through ROS-Wnt/β-Catenin-Estrogen Pathway: Preventive Effect of Melatonin.
He Q; Gu L; Lin Q; Ma Y; Liu C; Pei X; Li PA; Yang Y
Endocrinology; 2020 Sep; 161(9):. PubMed ID: 32652035
[TBL] [Abstract][Full Text] [Related]
7. Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.
Zhang Y; Liu Y; Zarrei M; Tong W; Dong R; Wang Y; Zhang H; Yang X; MacDonald JR; Uddin M; Scherer SW; Gai Z
Am J Med Genet B Neuropsychiatr Genet; 2018 Jan; 177(1):93-100. PubMed ID: 29152845
[TBL] [Abstract][Full Text] [Related]
8. Examination of bioenergetic function in the inner mitochondrial membrane peptidase 2-like (Immp2l) mutant mice.
Bharadwaj MS; Zhou Y; Molina AJ; Criswell T; Lu B
Redox Biol; 2014; 2():1008-15. PubMed ID: 25460737
[TBL] [Abstract][Full Text] [Related]
9. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
[TBL] [Abstract][Full Text] [Related]
10. Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder.
Baldan F; Gnan C; Franzoni A; Ferino L; Allegri L; Passon N; Damante G
Cytogenet Genome Res; 2018; 154(4):196-200. PubMed ID: 29788020
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial Function in Gilles de la Tourette Syndrome Patients With and Without Intragenic
Bjerregaard VA; Schönewolf-Greulich B; Juel Rasmussen L; Desler C; Tümer Z
Front Neurol; 2020; 11():163. PubMed ID: 32265818
[No Abstract] [Full Text] [Related]
12. Guilingji Protects Against Spermatogenesis Dysfunction From Oxidative Stress via Regulation of MAPK and Apoptotic Signaling Pathways in Immp2l Mutant Mice.
Wang Z; Xie Y; Chen H; Yao J; Lv L; Li Y; Deng C; Zhang M; Sun X; Liu G
Front Pharmacol; 2021; 12():771161. PubMed ID: 35095490
[TBL] [Abstract][Full Text] [Related]
13. Exonic deletions in IMMP2L in schizophrenia with enhanced glycation stress subtype.
Yoshikawa A; Kushima I; Miyashita M; Suzuki K; Iino K; Toriumi K; Horiuchi Y; Kawaji H; Ozaki N; Itokawa M; Arai M
PLoS One; 2022; 17(7):e0270506. PubMed ID: 35776734
[TBL] [Abstract][Full Text] [Related]
14. Deficiency in the inner mitochondrial membrane peptidase 2-like (Immp21) gene increases ischemic brain damage and impairs mitochondrial function.
Ma Y; Mehta SL; Lu B; Li PA
Neurobiol Dis; 2011 Dec; 44(3):270-6. PubMed ID: 21824519
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial peptidase IMMP2L mutation causes early onset of age-associated disorders and impairs adult stem cell self-renewal.
George SK; Jiao Y; Bishop CE; Lu B
Aging Cell; 2011 Aug; 10(4):584-94. PubMed ID: 21332923
[TBL] [Abstract][Full Text] [Related]
16. Environmental enrichment modulates affiliative and aggressive social behaviour in the neuroligin-3 R451C mouse model of autism spectrum disorder.
Burrows EL; Koyama L; May C; Hill-Yardin EL; Hannan AJ
Pharmacol Biochem Behav; 2020 Aug; 195():172955. PubMed ID: 32474162
[TBL] [Abstract][Full Text] [Related]
17. Learning delays in a mouse model of Autism Spectrum Disorder.
Rendall AR; Truong DT; Fitch RH
Behav Brain Res; 2016 Apr; 303():201-7. PubMed ID: 26873041
[TBL] [Abstract][Full Text] [Related]
18. Mitochondria-targeted antioxidant SkQ1 improves spermatogenesis in Immp2l mutant mice.
Jiang Y; Liu C; Lei B; Xu X; Lu B
Andrologia; 2018 Mar; 50(2):. PubMed ID: 28703400
[TBL] [Abstract][Full Text] [Related]
19. Social isolation exacerbates schizophrenia-like phenotypes via oxidative stress in cortical interneurons.
Jiang Z; Rompala GR; Zhang S; Cowell RM; Nakazawa K
Biol Psychiatry; 2013 May; 73(10):1024-34. PubMed ID: 23348010
[TBL] [Abstract][Full Text] [Related]
20. Deficient DNA base-excision repair in the forebrain leads to a sex-specific anxiety-like phenotype in mice.
Mueller FS; Amport R; Notter T; Schalbetter SM; Lin HY; Garajova Z; Amini P; Weber-Stadlbauer U; Markkanen E
BMC Biol; 2022 Jul; 20(1):170. PubMed ID: 35907861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]