BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

315 related articles for article (PubMed ID: 28867767)

  • 1. Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
    Shibutani M; Horii T; Shoji H; Morita S; Kimura M; Terawaki N; Miyakawa T; Hatada I
    Int J Mol Sci; 2017 Aug; 18(9):. PubMed ID: 28867767
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral deficits in mice.
    Kawamura A; Katayama Y; Nishiyama M; Shoji H; Tokuoka K; Ueta Y; Miyata M; Isa T; Miyakawa T; Hayashi-Takagi A; Nakayama KI
    Hum Mol Genet; 2020 May; 29(8):1274-1291. PubMed ID: 32142125
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Arid1b haploinsufficiency in parvalbumin- or somatostatin-expressing interneurons leads to distinct ASD-like and ID-like behavior.
    Smith AL; Jung EM; Jeon BT; Kim WY
    Sci Rep; 2020 May; 10(1):7834. PubMed ID: 32398858
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neurobiology of ARID1B haploinsufficiency related to neurodevelopmental and psychiatric disorders.
    Moffat JJ; Smith AL; Jung EM; Ka M; Kim WY
    Mol Psychiatry; 2022 Jan; 27(1):476-489. PubMed ID: 33686214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.
    Cotney J; Muhle RA; Sanders SJ; Liu L; Willsey AJ; Niu W; Liu W; Klei L; Lei J; Yin J; Reilly SK; Tebbenkamp AT; Bichsel C; Pletikos M; Sestan N; Roeder K; State MW; Devlin B; Noonan JP
    Nat Commun; 2015 Mar; 6():6404. PubMed ID: 25752243
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism.
    Wenderski W; Wang L; Krokhotin A; Walsh JJ; Li H; Shoji H; Ghosh S; George RD; Miller EL; Elias L; Gillespie MA; Son EY; Staahl BT; Baek ST; Stanley V; Moncada C; Shipony Z; Linker SB; Marchetto MCN; Gage FH; Chen D; Sultan T; Zaki MS; Ranish JA; Miyakawa T; Luo L; Malenka RC; Crabtree GR; Gleeson JG
    Proc Natl Acad Sci U S A; 2020 May; 117(18):10055-10066. PubMed ID: 32312822
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Arid1b haploinsufficiency disrupts cortical interneuron development and mouse behavior.
    Jung EM; Moffat JJ; Liu J; Dravid SM; Gurumurthy CB; Kim WY
    Nat Neurosci; 2017 Dec; 20(12):1694-1707. PubMed ID: 29184203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chd8 haploinsufficiency impairs early brain development and protein homeostasis later in life.
    Jiménez JA; Ptacek TS; Tuttle AH; Schmid RS; Moy SS; Simon JM; Zylka MJ
    Mol Autism; 2020 Oct; 11(1):74. PubMed ID: 33023670
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction.
    Shi X; Lu C; Corman A; Nikish A; Zhou Y; Platt RJ; Iossifov I; Zhang F; Pan JQ; Sanjana NE
    Am J Hum Genet; 2023 Oct; 110(10):1750-1768. PubMed ID: 37802044
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuroanatomy and behavior in mice with a haploinsufficiency of AT-rich interactive domain 1B (ARID1B) throughout development.
    Ellegood J; Petkova SP; Kinman A; Qiu LR; Adhikari A; Wade AA; Fernandes D; Lindenmaier Z; Creighton A; Nutter LMJ; Nord AS; Silverman JL; Lerch JP
    Mol Autism; 2021 Mar; 12(1):25. PubMed ID: 33757588
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Oxytocin ameliorates impaired social behavior in a Chd8 haploinsufficiency mouse model of autism.
    Cherepanov SM; Gerasimenko M; Yuhi T; Furuhara K; Tsuji C; Yokoyama S; Nakayama KI; Nishiyama M; Higashida H
    BMC Neurosci; 2021 May; 22(1):32. PubMed ID: 33933000
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Celen C; Chuang JC; Luo X; Nijem N; Walker AK; Chen F; Zhang S; Chung AS; Nguyen LH; Nassour I; Budhipramono A; Sun X; Bok LA; McEntagart M; Gevers EF; Birnbaum SG; Eisch AJ; Powell CM; Ge WP; Santen GW; Chahrour M; Zhu H
    Elife; 2017 Jul; 6():. PubMed ID: 28695822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells.
    Wang P; Mokhtari R; Pedrosa E; Kirschenbaum M; Bayrak C; Zheng D; Lachman HM
    Mol Autism; 2017; 8():11. PubMed ID: 28321286
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CHD8 dosage regulates transcription in pluripotency and early murine neural differentiation.
    Sood S; Weber CM; Hodges HC; Krokhotin A; Shalizi A; Crabtree GR
    Proc Natl Acad Sci U S A; 2020 Sep; 117(36):22331-22340. PubMed ID: 32839322
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories.
    Villa CE; Cheroni C; Dotter CP; López-Tóbon A; Oliveira B; Sacco R; Yahya AÇ; Morandell J; Gabriele M; Tavakoli MR; Lyudchik J; Sommer C; Gabitto M; Danzl JG; Testa G; Novarino G
    Cell Rep; 2022 Apr; 39(1):110615. PubMed ID: 35385734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like Behavior.
    Chabbert D; Caubit X; Roubertoux PL; Carlier M; Habermann B; Jacq B; Salin P; Metwaly M; Frahm C; Fatmi A; Garratt AN; Severac D; Dubois E; Kerkerian-Le Goff L; Fasano L; Gubellini P
    Biol Psychiatry; 2019 Aug; 86(4):274-285. PubMed ID: 31060802
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
    Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
    Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CHD8 regulates gut epithelial cell function and affects autism-related behaviors through the gut-brain axis.
    Chatterjee I; Getselter D; Ghanayem N; Harari R; Davis L; Bel S; Elliott E
    Transl Psychiatry; 2023 Oct; 13(1):305. PubMed ID: 37783686
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.