These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1039 related articles for article (PubMed ID: 21962519)

  • 1. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
    Peñagarikano O; Abrahams BS; Herman EI; Winden KD; Gdalyahu A; Dong H; Sonnenblick LI; Gruver R; Almajano J; Bragin A; Golshani P; Trachtenberg JT; Peles E; Geschwind DH
    Cell; 2011 Sep; 147(1):235-46. PubMed ID: 21962519
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homozygous Loss of Autism-Risk Gene CNTNAP2 Results in Reduced Local and Long-Range Prefrontal Functional Connectivity.
    Liska A; Bertero A; Gomolka R; Sabbioni M; Galbusera A; Barsotti N; Panzeri S; Scattoni ML; Pasqualetti M; Gozzi A
    Cereb Cortex; 2018 Apr; 28(4):1141-1153. PubMed ID: 28184409
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transient CSF1R inhibition ameliorates behavioral deficits in Cntnap2 knockout and valproic acid-exposed mouse models of autism.
    Meng J; Pan P; Guo G; Chen A; Meng X; Liu H
    J Neuroinflammation; 2024 Oct; 21(1):262. PubMed ID: 39425203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of Cntnap2 in the Rat Causes Autism-Related Alterations in Social Interactions, Stereotypic Behavior, and Sensory Processing.
    Scott KE; Kazazian K; Mann RS; Möhrle D; Schormans AL; Schmid S; Allman BL
    Autism Res; 2020 Oct; 13(10):1698-1717. PubMed ID: 32918359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dysfunctional Autism Risk Genes Cause Circuit-Specific Connectivity Deficits With Distinct Developmental Trajectories.
    Zerbi V; Ielacqua GD; Markicevic M; Haberl MG; Ellisman MH; A-Bhaskaran A; Frick A; Rudin M; Wenderoth N
    Cereb Cortex; 2018 Jul; 28(7):2495-2506. PubMed ID: 29901787
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. What does CNTNAP2 reveal about autism spectrum disorder?
    Peñagarikano O; Geschwind DH
    Trends Mol Med; 2012 Mar; 18(3):156-63. PubMed ID: 22365836
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2.
    Jurgensen S; Castillo PE
    J Neurosci; 2015 Oct; 35(43):14681-7. PubMed ID: 26511255
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism.
    Peñagarikano O; Lázaro MT; Lu XH; Gordon A; Dong H; Lam HA; Peles E; Maidment NT; Murphy NP; Yang XW; Golshani P; Geschwind DH
    Sci Transl Med; 2015 Jan; 7(271):271ra8. PubMed ID: 25609168
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cntnap2 Knockout Rats and Mice Exhibit Epileptiform Activity and Abnormal Sleep-Wake Physiology.
    Thomas AM; Schwartz MD; Saxe MD; Kilduff TS
    Sleep; 2017 Jan; 40(1):. PubMed ID: 28364455
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CNTNAP2 intracellular domain (CICD) generated by γ-secretase cleavage improves autism-related behaviors.
    Zhang J; Cai F; Lu R; Xing X; Xu L; Wu K; Gong Z; Zhang Q; Zhang Y; Xing M; Song W; Li JD
    Signal Transduct Target Ther; 2023 Jun; 8(1):219. PubMed ID: 37271769
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Replicable in vivo physiological and behavioral phenotypes of the
    Dhamne SC; Silverman JL; Super CE; Lammers SHT; Hameed MQ; Modi ME; Copping NA; Pride MC; Smith DG; Rotenberg A; Crawley JN; Sahin M
    Mol Autism; 2017; 8():26. PubMed ID: 28638591
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons.
    Vogt D; Cho KKA; Shelton SM; Paul A; Huang ZJ; Sohal VS; Rubenstein JLR
    Cereb Cortex; 2018 Nov; 28(11):3868-3879. PubMed ID: 29028946
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Palatable solution overconsumption in the Cntnap2-/- murine model of autism: a link with oxytocin.
    Harvey S; Liyanagamage DSNK; Pal T; Klockars A; Levine AS; Olszewski PK
    Neuroreport; 2024 Oct; 35(15):980-986. PubMed ID: 39166394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Suppression of Akt-mTOR pathway rescued the social behavior in Cntnap2-deficient mice.
    Xing X; Zhang J; Wu K; Cao B; Li X; Jiang F; Hu Z; Xia K; Li JD
    Sci Rep; 2019 Feb; 9(1):3041. PubMed ID: 30816216
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Somatosensory cortex hyperconnectivity and impaired whisker-dependent responses in Cntnap2
    Balasco L; Pagani M; Pangrazzi L; Chelini G; Viscido F; Chama AGC; Galbusera A; Provenzano G; Gozzi A; Bozzi Y
    Neurobiol Dis; 2022 Jul; 169():105742. PubMed ID: 35483565
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The CNTNAP2-CASK complex modulates GluA1 subcellular distribution in interneurons.
    Gao R; Zaccard CR; Shapiro LP; Dionisio LE; Martin-de-Saavedra MD; Piguel NH; Pratt CP; Horan KE; Penzes P
    Neurosci Lett; 2019 May; 701():92-99. PubMed ID: 30779956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of Semaphorin 3F in Interneurons Is Associated with Decreased GABAergic Neurons, Autism-like Behavior, and Increased Oxidative Stress Cascades.
    Li Z; Jagadapillai R; Gozal E; Barnes G
    Mol Neurobiol; 2019 Aug; 56(8):5520-5538. PubMed ID: 30635860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Modelling monogenic autism spectrum disorder using mouse cortical organoids.
    Hali S; Kim J; Kwak TH; Lee H; Shin CY; Han DW
    Biochem Biophys Res Commun; 2020 Jan; 521(1):164-171. PubMed ID: 31653345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2.
    Hoffman EJ; Turner KJ; Fernandez JM; Cifuentes D; Ghosh M; Ijaz S; Jain RA; Kubo F; Bill BR; Baier H; Granato M; Barresi MJ; Wilson SW; Rihel J; State MW; Giraldez AJ
    Neuron; 2016 Feb; 89(4):725-33. PubMed ID: 26833134
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 52.