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 *

111 related articles for article (PubMed ID: 36806874)

  • 21. Med23 supports angiogenesis and maintains vascular integrity through negative regulation of angiopoietin2 expression.
    Yang Y; Xiao Q; Yin J; Li C; Yu D; He Y; Yang Z; Wang G
    Commun Biol; 2022 Apr; 5(1):374. PubMed ID: 35440711
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Upregulation of mediator MED23 in non-small-cell lung cancer promotes the growth, migration, and metastasis of cancer cells.
    Shi J; Liu H; Yao F; Zhong C; Zhao H
    Tumour Biol; 2014 Dec; 35(12):12005-13. PubMed ID: 25273169
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mediator MED23 links insulin signaling to the adipogenesis transcription cascade.
    Wang W; Huang L; Huang Y; Yin JW; Berk AJ; Friedman JM; Wang G
    Dev Cell; 2009 May; 16(5):764-71. PubMed ID: 19460352
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mediator MED23 regulates basal transcription in vivo via an interaction with P-TEFb.
    Wang W; Yao X; Huang Y; Hu X; Liu R; Hou D; Chen R; Wang G
    Transcription; 2013; 4(1):39-51. PubMed ID: 23340209
    [TBL] [Abstract][Full Text] [Related]  

  • 25. KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature.
    Gonçalves TF; Gonçalves AP; Fintelman Rodrigues N; dos Santos JM; Pimentel MM; Santos-Rebouças CB
    Eur J Med Genet; 2014 Mar; 57(4):138-44. PubMed ID: 24583395
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Developmental disorders with intellectual disability driven by chromatin dysregulation: Clinical overlaps and molecular mechanisms.
    Larizza L; Finelli P
    Clin Genet; 2019 Feb; 95(2):231-240. PubMed ID: 29672823
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.
    Brookes E; Laurent B; Õunap K; Carroll R; Moeschler JB; Field M; Schwartz CE; Gecz J; Shi Y
    Hum Mol Genet; 2015 May; 24(10):2861-72. PubMed ID: 25666439
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Med23 Regulates Sox9 Expression during Craniofacial Development.
    Dash S; Bhatt S; Falcon KT; Sandell LL; Trainor PA
    J Dent Res; 2021 Apr; 100(4):406-414. PubMed ID: 33155500
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Histone acetylation dynamics modulates chromatin conformation and allele-specific interactions at oncogenic loci.
    Sungalee S; Liu Y; Lambuta RA; Katanayeva N; Donaldson Collier M; Tavernari D; Roulland S; Ciriello G; Oricchio E
    Nat Genet; 2021 May; 53(5):650-662. PubMed ID: 33972799
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mediator Med23 Regulates Adult Hippocampal Neurogenesis.
    Chen GY; Zhang S; Li CH; Qi CC; Wang YZ; Chen JY; Wang G; Ding YQ; Su CJ
    Front Cell Dev Biol; 2020; 8():699. PubMed ID: 32850819
    [TBL] [Abstract][Full Text] [Related]  

  • 31. BRCA1 mutations attenuate super-enhancer function and chromatin looping in haploinsufficient human breast epithelial cells.
    Zhang X; Wang Y; Chiang HC; Hsieh YP; Lu C; Park BH; Jatoi I; Jin VX; Hu Y; Li R
    Breast Cancer Res; 2019 Apr; 21(1):51. PubMed ID: 30995943
    [TBL] [Abstract][Full Text] [Related]  

  • 32. BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
    Dias C; Estruch SB; Graham SA; McRae J; Sawiak SJ; Hurst JA; Joss SK; Holder SE; Morton JE; Turner C; Thevenon J; Mellul K; Sánchez-Andrade G; Ibarra-Soria X; Deriziotis P; Santos RF; Lee SC; Faivre L; Kleefstra T; Liu P; Hurles ME; ; Fisher SE; Logan DW
    Am J Hum Genet; 2016 Aug; 99(2):253-74. PubMed ID: 27453576
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A systematic analysis of host factors reveals a Med23-interferon-λ regulatory axis against herpes simplex virus type 1 replication.
    Griffiths SJ; Koegl M; Boutell C; Zenner HL; Crump CM; Pica F; Gonzalez O; Friedel CC; Barry G; Martin K; Craigon MH; Chen R; Kaza LN; Fossum E; Fazakerley JK; Efstathiou S; Volpi A; Zimmer R; Ghazal P; Haas J
    PLoS Pathog; 2013; 9(8):e1003514. PubMed ID: 23950709
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Neuron-specific chromatin remodeling: a missing link in epigenetic mechanisms underlying synaptic plasticity, memory, and intellectual disability disorders.
    Vogel-Ciernia A; Wood MA
    Neuropharmacology; 2014 May; 80():18-27. PubMed ID: 24140580
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Contribution of spurious transcription to intellectual disability disorders.
    Scandaglia M; Barco A
    J Med Genet; 2019 Aug; 56(8):491-498. PubMed ID: 30745423
    [TBL] [Abstract][Full Text] [Related]  

  • 36.
    Selvan N; George S; Serajee FJ; Shaw M; Hobson L; Kalscheuer V; Prasad N; Levy SE; Taylor J; Aftimos S; Schwartz CE; Huq AM; Gecz J; Wells L
    J Biol Chem; 2018 Jul; 293(27):10810-10824. PubMed ID: 29769320
    [TBL] [Abstract][Full Text] [Related]  

  • 37. GATA-1 modulates the chromatin structure and activity of the chicken alpha-globin 3' enhancer.
    Escamilla-Del-Arenal M; Recillas-Targa F
    Mol Cell Biol; 2008 Jan; 28(2):575-86. PubMed ID: 17984219
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Test-retest reliability of Picture My Participation in children with intellectual disability in South Africa.
    Balton S; Arvidsson P; Granlund M; Huus K; Dada S
    Scand J Occup Ther; 2022 May; 29(4):315-324. PubMed ID: 33307940
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus.
    Court F; Camprubi C; Garcia CV; Guillaumet-Adkins A; Sparago A; Seruggia D; Sandoval J; Esteller M; Martin-Trujillo A; Riccio A; Montoliu L; Monk D
    Epigenetics Chromatin; 2014 Mar; 7(1):5. PubMed ID: 24667089
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sp1 regulates chromatin looping between an intronic enhancer and distal promoter of the human heme oxygenase-1 gene in renal cells.
    Deshane J; Kim J; Bolisetty S; Hock TD; Hill-Kapturczak N; Agarwal A
    J Biol Chem; 2010 May; 285(22):16476-86. PubMed ID: 20351094
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.