BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 36180228)

  • 1. Peripheral Auditory Nerve Impairment in a Mouse Model of Syndromic Autism.
    McChesney N; Barth JL; Rumschlag JA; Tan J; Harrington AJ; Noble KV; McClaskey CM; Elvis P; Vaena SG; Romeo MJ; Harris KC; Cowan CW; Lang H
    J Neurosci; 2022 Oct; 42(42):8002-8018. PubMed ID: 36180228
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MEF2C Hypofunction in Neuronal and Neuroimmune Populations Produces MEF2C Haploinsufficiency Syndrome-like Behaviors in Mice.
    Harrington AJ; Bridges CM; Berto S; Blankenship K; Cho JY; Assali A; Siemsen BM; Moore HW; Tsvetkov E; Thielking A; Konopka G; Everman DB; Scofield MD; Skinner SA; Cowan CW
    Biol Psychiatry; 2020 Sep; 88(6):488-499. PubMed ID: 32418612
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism.
    Tu S; Akhtar MW; Escorihuela RM; Amador-Arjona A; Swarup V; Parker J; Zaremba JD; Holland T; Bansal N; Holohan DR; Lopez K; Ryan SD; Chan SF; Yan L; Zhang X; Huang X; Sultan A; McKercher SR; Ambasudhan R; Xu H; Wang Y; Geschwind DH; Roberts AJ; Terskikh AV; Rissman RA; Masliah E; Lipton SA; Nakanishi N
    Nat Commun; 2017 Nov; 8(1):1488. PubMed ID: 29133852
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The
    Basu S; Ro EJ; Liu Z; Kim H; Bennett A; Kang S; Suh H
    J Neurosci; 2024 Jan; 44(5):. PubMed ID: 38123360
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Auditory hypersensitivity and processing deficits in a rat model of fragile X syndrome.
    Auerbach BD; Manohar S; Radziwon K; Salvi R
    Neurobiol Dis; 2021 Dec; 161():105541. PubMed ID: 34751141
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Stria Vascularis in Mice and Humans Is an Early Site of Age-Related Cochlear Degeneration, Macrophage Dysfunction, and Inflammation.
    Lang H; Noble KV; Barth JL; Rumschlag JA; Jenkins TR; Storm SL; Eckert MA; Dubno JR; Schulte BA
    J Neurosci; 2023 Jul; 43(27):5057-5075. PubMed ID: 37268417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genes influenced by MEF2C contribute to neurodevelopmental disease via gene expression changes that affect multiple types of cortical excitatory neurons.
    Cosgrove D; Whitton L; Fahey L; Ó Broin P; Donohoe G; Morris DW
    Hum Mol Genet; 2021 May; 30(11):961-970. PubMed ID: 32975584
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High-Fat Diet Exacerbates Autistic-Like Restricted Repetitive Behaviors and Social Abnormalities in CC2D1A Conditional Knockout Mice.
    Wang YC; Chen CH; Yang CY; Ling P; Hsu KS
    Mol Neurobiol; 2023 Mar; 60(3):1331-1352. PubMed ID: 36445635
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
    Katayama Y; Nishiyama M; Shoji H; Ohkawa Y; Kawamura A; Sato T; Suyama M; Takumi T; Miyakawa T; Nakayama KI
    Nature; 2016 Sep; 537(7622):675-679. PubMed ID: 27602517
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transient hearing abnormalities precede social deficits in a mouse model of autism.
    Pang R; Yan S; Tu Y; Qian S; Yu H; Hu X; Wen H; Yuan W; Wang X; Zhou Y
    Behav Brain Res; 2023 Feb; 437():114149. PubMed ID: 36206820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Postnatal Loss of Mef2c Results in Dissociation of Effects on Synapse Number and Learning and Memory.
    Adachi M; Lin PY; Pranav H; Monteggia LM
    Biol Psychiatry; 2016 Jul; 80(2):140-148. PubMed ID: 26642739
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Audition-specific temporal processing deficits associated with language function in children with autism spectrum disorder.
    Foss-Feig JH; Schauder KB; Key AP; Wallace MT; Stone WL
    Autism Res; 2017 Nov; 10(11):1845-1856. PubMed ID: 28632303
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early communication deficits in the Shank1 knockout mouse model for autism spectrum disorder: Developmental aspects and effects of social context.
    Sungur AÖ; Schwarting RK; Wöhr M
    Autism Res; 2016 Jun; 9(6):696-709. PubMed ID: 26419918
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Xi K; Cai SQ; Yan HF; Tian Y; Cai J; Yang XM; Wang JM; Xing GG
    J Neurosci; 2023 May; 43(21):3949-3969. PubMed ID: 37037606
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrum of social alterations in the Neurobeachin haploinsufficiency mouse model of autism.
    Odent P; Creemers JW; Bosmans G; D'Hooge R
    Brain Res Bull; 2021 Feb; 167():11-21. PubMed ID: 33197534
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dietary zinc supplementation rescues fear-based learning and synaptic function in the Tbr1
    Lee K; Jung Y; Vyas Y; Skelton I; Abraham WC; Hsueh YP; Montgomery JM
    Mol Autism; 2022 Mar; 13(1):13. PubMed ID: 35303947
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.
    Nudel R; Christiani CAJ; Ohland J; Uddin MJ; Hemager N; Ellersgaard DV; Spang KS; Burton BK; Greve AN; Gantriis DL; Bybjerg-Grauholm J; Jepsen JRM; Thorup AAE; Mors O; Nordentoft M; Werge T
    Autism Res; 2020 Mar; 13(3):369-381. PubMed ID: 31577390
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways.
    Paciorkowski AR; Traylor RN; Rosenfeld JA; Hoover JM; Harris CJ; Winter S; Lacassie Y; Bialer M; Lamb AN; Schultz RA; Berry-Kravis E; Porter BE; Falk M; Venkat A; Vanzo RJ; Cohen JS; Fatemi A; Dobyns WB; Shaffer LG; Ballif BC; Marsh ED
    Neurogenetics; 2013 May; 14(2):99-111. PubMed ID: 23389741
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 14.