BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 33627187)

  • 21. Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.
    Durak O; Gao F; Kaeser-Woo YJ; Rueda R; Martorell AJ; Nott A; Liu CY; Watson LA; Tsai LH
    Nat Neurosci; 2016 Nov; 19(11):1477-1488. PubMed ID: 27694995
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons.
    Xu Q; Liu YY; Wang X; Tan GH; Li HP; Hulbert SW; Li CY; Hu CC; Xiong ZQ; Xu X; Jiang YH
    Mol Autism; 2018; 9():65. PubMed ID: 30574290
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The autism risk factor CHD8 is a chromatin activator in human neurons and functionally dependent on the ERK-MAPK pathway effector ELK1.
    Haddad Derafshi B; Danko T; Chanda S; Batista PJ; Litzenburger U; Lee QY; Ng YH; Sebin A; Chang HY; Südhof TC; Wernig M
    Sci Rep; 2022 Dec; 12(1):22425. PubMed ID: 36575212
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. The Mechanisms of CHD8 in Neurodevelopment and Autism Spectrum Disorders.
    Weissberg O; Elliott E
    Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440307
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Deletion of CHD8 in cerebellar granule neuron progenitors leads to severe cerebellar hypoplasia, ataxia, and psychiatric behavior in mice.
    Chen X; Chen T; Dong C; Chen H; Dong X; Yang L; Hu L; Wang H; Wu B; Yao Y; Xiong Y; Xiong M; Lin Y; Zhou W
    J Genet Genomics; 2022 Sep; 49(9):859-869. PubMed ID: 35231638
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Morphological study of embryonic Chd8
    Gómez HF; Hodel L; Michos O; Iber D
    BMC Res Notes; 2021 Jan; 14(1):23. PubMed ID: 33436073
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. A Novel Chd8 Mutant Mouse Displays Altered Ultrasonic Vocalizations and Enhanced Motor Coordination.
    Hulbert SW; Wang X; Gbadegesin SO; Xu Q; Xu X; Jiang YH
    Autism Res; 2020 Oct; 13(10):1685-1697. PubMed ID: 32815320
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of
    Wade AA; Lim K; Catta-Preta R; Nord AS
    Front Mol Neurosci; 2018; 11():481. PubMed ID: 30692911
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Male-Dominant Effects of Chd8 Haploinsufficiency on Synaptic Phenotypes during Development in Mouse Prefrontal Cortex.
    Ellingford RA; Tojo M; Basson MA; Andreae LC
    ACS Chem Neurosci; 2024 Apr; 15(8):1635-1642. PubMed ID: 38557009
    [No Abstract]   [Full Text] [Related]  

  • 40. CHD8 safeguards early neuroectoderm differentiation in human ESCs and protects from apoptosis during neurogenesis.
    Ding S; Lan X; Meng Y; Yan C; Li M; Li X; Chen J; Jiang W
    Cell Death Dis; 2021 Oct; 12(11):981. PubMed ID: 34686651
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.