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 *

189 related articles for article (PubMed ID: 34880900)

  • 1. Natural SINEUP RNAs in Autism Spectrum Disorders:
    Zarantonello G; Arnoldi M; Filosi M; Tebaldi T; Spirito G; Barbieri A; Gustincich S; Sanges R; Domenici E; Di Leva F; Biagioli M
    Front Genet; 2021; 12():745229. PubMed ID: 34880900
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Long non-coding RNA
    Chen Z; Liu Z; Yang Y; Zhu Z; Liang R; Huang B; Wu D; Yang L; Lu H; Jin D; Li Q
    Oncotarget; 2018 Jun; 9(42):26770-26786. PubMed ID: 29928484
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SINEUPs are modular antisense long non-coding RNAs that increase synthesis of target proteins in cells.
    Zucchelli S; Fasolo F; Russo R; Cimatti L; Patrucco L; Takahashi H; Jones MH; Santoro C; Sblattero D; Cotella D; Persichetti F; Carninci P; Gustincich S
    Front Cell Neurosci; 2015; 9():174. PubMed ID: 26029048
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SINEUP non-coding RNA activity depends on specific N6-methyladenosine nucleotides.
    Pierattini B; D'Agostino S; Bon C; Peruzzo O; Alendar A; Codino A; Ros G; Persichetti F; Sanges R; Carninci P; Santoro C; Espinoza S; Valentini P; Pandolfini L; Gustincich S
    Mol Ther Nucleic Acids; 2023 Jun; 32():402-414. PubMed ID: 37187707
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of antisense long noncoding RNAs that function as SINEUPs in human cells.
    Schein A; Zucchelli S; Kauppinen S; Gustincich S; Carninci P
    Sci Rep; 2016 Sep; 6():33605. PubMed ID: 27646849
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation.
    Arnoldi M; Zarantonello G; Espinoza S; Gustincich S; Di Leva F; Biagioli M
    Methods Mol Biol; 2022; 2434():63-87. PubMed ID: 35213010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SINEUPs: A new class of natural and synthetic antisense long non-coding RNAs that activate translation.
    Zucchelli S; Cotella D; Takahashi H; Carrieri C; Cimatti L; Fasolo F; Jones MH; Sblattero D; Sanges R; Santoro C; Persichetti F; Carninci P; Gustincich S
    RNA Biol; 2015; 12(8):771-9. PubMed ID: 26259533
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification of functional features of synthetic SINEUPs, antisense lncRNAs that specifically enhance protein translation.
    Takahashi H; Kozhuharova A; Sharma H; Hirose M; Ohyama T; Fasolo F; Yamazaki T; Cotella D; Santoro C; Zucchelli S; Gustincich S; Carninci P
    PLoS One; 2018; 13(2):e0183229. PubMed ID: 29414979
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cell Based Assays of SINEUP Non-coding RNAs That Can Specifically Enhance mRNA Translation.
    Takahashi H; Sharma H; Carninci P
    J Vis Exp; 2019 Feb; (144):. PubMed ID: 30774120
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Cell type-specific dysregulation of gene expression due to
    Yim KM; Baumgartner M; Krenzer M; Rosales Larios MF; Hill-Terán G; Nottoli T; Muhle RA; Noonan JP
    bioRxiv; 2024 Aug; ():. PubMed ID: 39185167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
    Sugathan A; Biagioli M; Golzio C; Erdin S; Blumenthal I; Manavalan P; Ragavendran A; Brand H; Lucente D; Miles J; Sheridan SD; Stortchevoi A; Kellis M; Haggarty SJ; Katsanis N; Gusella JF; Talkowski ME
    Proc Natl Acad Sci U S A; 2014 Oct; 111(42):E4468-77. PubMed ID: 25294932
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Towards SINEUP-based therapeutics: Design of an
    Valentini P; Pierattini B; Zacco E; Mangoni D; Espinoza S; Webster NA; Andrews B; Carninci P; Tartaglia GG; Pandolfini L; Gustincich S
    Mol Ther Nucleic Acids; 2022 Mar; 27():1092-1102. PubMed ID: 35228902
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
    Merner N; Forgeot d'Arc B; Bell SC; Maussion G; Peng H; Gauthier J; Crapper L; Hamdan FF; Michaud JL; Mottron L; Rouleau GA; Ernst C
    Am J Med Genet A; 2016 May; 170A(5):1225-35. PubMed ID: 26789910
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.