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 *

281 related articles for article (PubMed ID: 33023670)

  • 41. Neurodevelopmental functions of CHD8: new insights and questions.
    Basson MA
    Biochem Soc Trans; 2024 Feb; 52(1):15-27. PubMed ID: 38288845
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A de novo variant of CHD8 in a patient with autism spectrum disorder.
    Alotaibi M; Ramzan K
    Discoveries (Craiova); 2020 Mar; 8(1):e107. PubMed ID: 32309624
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. The clinical presentation caused by truncating CHD8 variants.
    Douzgou S; Liang HW; Metcalfe K; Somarathi S; Tischkowitz M; Mohamed W; Kini U; McKee S; Yates L; Bertoli M; Lynch SA; Holder S; ; Banka S
    Clin Genet; 2019 Jul; 96(1):72-84. PubMed ID: 31001818
    [TBL] [Abstract][Full Text] [Related]  

  • 45. CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment.
    Wang P; Lin M; Pedrosa E; Hrabovsky A; Zhang Z; Guo W; Lachman HM; Zheng D
    Mol Autism; 2015; 6():55. PubMed ID: 26491539
    [TBL] [Abstract][Full Text] [Related]  

  • 46. The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8.
    Dingemans AJM; Truijen KMG; van de Ven S; Bernier R; Bongers EMHF; Bouman A; de Graaff-Herder L; Eichler EE; Gerkes EH; De Geus CM; van Hagen JM; Jansen PR; Kerkhof J; Kievit AJA; Kleefstra T; Maas SM; de Man SA; McConkey H; Patterson WG; Dobson AT; Prijoles EJ; Sadikovic B; Relator R; Stevenson RE; Stumpel CTRM; Heijligers M; Stuurman KE; Löhner K; Zeidler S; Lee JA; Lindy A; Zou F; Tedder ML; Vissers LELM; de Vries BBA
    Transl Psychiatry; 2022 Oct; 12(1):421. PubMed ID: 36182950
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Age-differential sexual dimorphism in CHD8-S62X-mutant mouse behaviors.
    Lee SY; Kweon H; Kang H; Kim E
    Front Mol Neurosci; 2022; 15():1022306. PubMed ID: 36385756
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genetic Suppression of mTOR Rescues Synaptic and Social Behavioral Abnormalities in a Mouse Model of Pten Haploinsufficiency.
    Huang WC; Chen Y; Page DT
    Autism Res; 2019 Oct; 12(10):1463-1471. PubMed ID: 31441226
    [TBL] [Abstract][Full Text] [Related]  

  • 50. CHD8 intragenic deletion associated with autism spectrum disorder.
    Stolerman ES; Smith B; Chaubey A; Jones JR
    Eur J Med Genet; 2016 Apr; 59(4):189-94. PubMed ID: 26921529
    [TBL] [Abstract][Full Text] [Related]  

  • 51. From X-inactivation to neurodevelopment: CHD8-transcription factors (TFs) competitive binding at regulatory regions of CHD8 target genes can contribute to correct neuronal differentiation.
    Cerase A; Avner P
    Curr Res Neurobiol; 2023; 5():100114. PubMed ID: 38020809
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Gene-Environment Interactions in Developmental Neurotoxicity: a Case Study of Synergy between Chlorpyrifos and CHD8 Knockout in Human BrainSpheres.
    Modafferi S; Zhong X; Kleensang A; Murata Y; Fagiani F; Pamies D; Hogberg HT; Calabrese V; Lachman H; Hartung T; Smirnova L
    Environ Health Perspect; 2021 Jul; 129(7):77001. PubMed ID: 34259569
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Conserved and Distinct Functions of the Autism-Related Chromatin Remodeler CHD8 in Embryonic and Adult Forebrain Neurogenesis.
    Dong C; Zhao C; Chen X; Berry K; Wang J; Zhang F; Liao Y; Han R; Ogurek S; Xu L; Zhang L; Lin Y; Zhou W; Xin M; Lim DA; Campbell K; Nakafuku M; Waclaw RR; Lu QR
    J Neurosci; 2022 Nov; 42(44):8373-8392. PubMed ID: 36127134
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Single-Cell Transcriptomics Supports a Role of
    Hoffmann A; Spengler D
    Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33806835
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Neurodevelopmental phenotype associated with CHD8-SUPT16H duplication.
    Smol T; Thuillier C; Boudry-Labis E; Dieux-Coeslier A; Duban-Bedu B; Caumes R; Bouquillon S; Manouvrier-Hanu S; Roche-Lestienne C; Ghoumid J
    Neurogenetics; 2020 Jan; 21(1):67-72. PubMed ID: 31823155
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes.
    Wilkinson B; Grepo N; Thompson BL; Kim J; Wang K; Evgrafov OV; Lu W; Knowles JA; Campbell DB
    Transl Psychiatry; 2015 May; 5(5):e568. PubMed ID: 25989142
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology.
    Barnard RA; Pomaville MB; O'Roak BJ
    Front Neurosci; 2015; 9():477. PubMed ID: 26733790
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children.
    Wang J; Liu J; Gao Y; Wang K; Jiang K
    BMC Pediatr; 2018 Oct; 18(1):338. PubMed ID: 30376831
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Effects of muscular dystrophy, exercise and blocking activin receptor IIB ligands on the unfolded protein response and oxidative stress.
    Hulmi JJ; Hentilä J; DeRuisseau KC; Oliveira BM; Papaioannou KG; Autio R; Kujala UM; Ritvos O; Kainulainen H; Korkmaz A; Atalay M
    Free Radic Biol Med; 2016 Oct; 99():308-322. PubMed ID: 27554968
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Haploinsufficiency of autism causative gene
    Huang TN; Yen TL; Qiu LR; Chuang HC; Lerch JP; Hsueh YP
    Mol Autism; 2019; 10():5. PubMed ID: 30792833
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.