BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 31233820)

  • 1. 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]  

  • 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. Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome.
    Petek E; Schwarzbraun T; Noor A; Patel M; Nakabayashi K; Choufani S; Windpassinger C; Stamenkovic M; Robertson MM; Aschauer HN; Gurling HM; Kroisel PM; Wagner K; Scherer SW; Vincent JB
    Mol Genet Genomics; 2007 Jan; 277(1):71-81. PubMed ID: 17043892
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
    Petek E; Windpassinger C; Vincent JB; Cheung J; Boright AP; Scherer SW; Kroisel PM; Wagner K
    Am J Hum Genet; 2001 Apr; 68(4):848-58. PubMed ID: 11254443
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Disentangling Restrictive and Repetitive Behaviors and Social Impairments in Children and Adolescents with Gilles de la Tourette Syndrome and Autism Spectrum Disorder.
    Gulisano M; Barone R; Alaimo S; Ferro A; Pulvirenti A; Cirnigliaro L; Di Silvestre S; Martellino S; Maugeri N; Milana MC; Scerbo M; Rizzo R
    Brain Sci; 2020 May; 10(5):. PubMed ID: 32443587
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.
    Bertelsen B; Melchior L; Jensen LR; Groth C; Glenthøj B; Rizzo R; Debes NM; Skov L; Brøndum-Nielsen K; Paschou P; Silahtaroglu A; Tümer Z
    Eur J Hum Genet; 2014 Nov; 22(11):1283-9. PubMed ID: 24549057
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcriptional response to mitochondrial protease IMMP2L knockdown in human primary astrocytes.
    Gokoolparsadh A; Fang Z; Braidy N; Lin P; Pardy CJ; Eapen V; Clarke R; Voineagu I
    Biochem Biophys Res Commun; 2017 Jan; 482(4):1252-1258. PubMed ID: 27932244
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Incidence of Autism Spectrum Disorder in Youths Affected by Gilles de la Tourette Syndrome Based on Data from a Large Single Italian Clinical Cohort.
    Gulisano M; Barone R; Mosa MR; Milana MC; Saia F; Scerbo M; Rizzo R
    Brain Sci; 2020 Nov; 10(11):. PubMed ID: 33147879
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
    Patel C; Cooper-Charles L; McMullan DJ; Walker JM; Davison V; Morton J
    Eur J Hum Genet; 2011 Jun; 19(6):634-9. PubMed ID: 21386874
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and genetic analysis of children with a dual diagnosis of Tourette syndrome and autism spectrum disorder.
    Carias KV; Wevrick R
    J Psychiatr Res; 2019 Apr; 111():145-153. PubMed ID: 30771620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differential effects by sex with Kmt5b loss.
    Wickramasekara RN; Robertson B; Hulen J; Hallgren J; Stessman HAF
    Autism Res; 2021 Aug; 14(8):1554-1571. PubMed ID: 33871180
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Pathological glutamatergic neurotransmission in Gilles de la Tourette syndrome.
    Kanaan AS; Gerasch S; García-García I; Lampe L; Pampel A; Anwander A; Near J; Möller HE; Müller-Vahl K
    Brain; 2017 Jan; 140(1):218-234. PubMed ID: 28007998
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders.
    Gimelli S; Capra V; Di Rocco M; Leoni M; Mirabelli-Badenier M; Schiaffino MC; Fiorio P; Cuoco C; Gimelli G; Tassano E
    Mol Cytogenet; 2014; 7():54. PubMed ID: 25478008
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Tourette Syndrome Risk Genes Regulate Mitochondrial Dynamics, Structure, and Function.
    Clarke RA; Furlong TM; Eapen V
    Front Psychiatry; 2020; 11():556803. PubMed ID: 33776808
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.