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 *

150 related articles for article (PubMed ID: 36536324)

  • 21. X-linked mental retardation and severe short stature with a novel mutation of the
    Kawano-Matsuda F; Maeda T; Kaname T; Yanagi K; Ihara K
    Clin Pediatr Endocrinol; 2021; 30(1):61-64. PubMed ID: 33446955
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic features.
    Fieremans N; Van Esch H; de Ravel T; Van Driessche J; Belet S; Bauters M; Froyen G
    Eur J Med Genet; 2015 May; 58(5):324-7. PubMed ID: 25858702
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX.
    Poeta L; Fusco F; Drongitis D; Shoubridge C; Manganelli G; Filosa S; Paciolla M; Courtney M; Collombat P; Lioi MB; Gecz J; Ursini MV; Miano MG
    Am J Hum Genet; 2013 Jan; 92(1):114-25. PubMed ID: 23246292
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromatin Sensing by the Auxiliary Domains of KDM5C Regulates Its Demethylase Activity and Is Disrupted by X-linked Intellectual Disability Mutations.
    Ugur FS; Kelly MJS; Fujimori DG
    J Mol Biol; 2023 Jan; 435(2):167913. PubMed ID: 36495919
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel Variations in the
    Wu PM; Yu WH; Chiang CW; Wu CY; Chen JS; Tu YF
    Neurol Genet; 2022 Feb; 8(1):e646. PubMed ID: 34877407
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Loss of Kdm5c Causes Spurious Transcription and Prevents the Fine-Tuning of Activity-Regulated Enhancers in Neurons.
    Scandaglia M; Lopez-Atalaya JP; Medrano-Fernandez A; Lopez-Cascales MT; Del Blanco B; Lipinski M; Benito E; Olivares R; Iwase S; Shi Y; Barco A
    Cell Rep; 2017 Oct; 21(1):47-59. PubMed ID: 28978483
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel CLCN4 variant associated with syndromic X-linked intellectual disability in a Chinese girl: a case report.
    Xu X; Lu F; Zhang L; Li H; Du S; Tang J
    BMC Pediatr; 2021 Sep; 21(1):384. PubMed ID: 34479510
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The potential role of a retrotransposed gene and a long noncoding RNA in regulating an X-linked chromatin gene (KDM5C): Novel epigenetic mechanism in autism.
    Talebizadeh Z; Shah A; DiTacchio L
    Autism Res; 2019 Jul; 12(7):1007-1021. PubMed ID: 31087518
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Case Report: Chinese female patients with a heterozygous pathogenic
    Cong Y; Jin H; Wu K; Wang H; Wang D
    Front Genet; 2022; 13():900226. PubMed ID: 36046249
    [No Abstract]   [Full Text] [Related]  

  • 31. Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective Disorders.
    Ji B; Higa KK; Kelsoe JR; Zhou X
    EBioMedicine; 2015 Aug; 2(8):909-18. PubMed ID: 26425698
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Physiological effects of KDM5C on neural crest migration and eye formation during vertebrate development.
    Kim Y; Jeong Y; Kwon K; Ismail T; Lee HK; Kim C; Park JW; Kwon OS; Kang BS; Lee DS; Park TJ; Kwon T; Lee HS
    Epigenetics Chromatin; 2018 Dec; 11(1):72. PubMed ID: 30522514
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cofactors-loaded quaternary structure of lysine-specific demethylase 5C (KDM5C) protein: Computational model.
    Peng Y; Alexov E
    Proteins; 2016 Dec; 84(12):1797-1809. PubMed ID: 27696497
    [TBL] [Abstract][Full Text] [Related]  

  • 34. X chromosome dosage of histone demethylase KDM5C determines sex differences in adiposity.
    Link JC; Wiese CB; Chen X; Avetisyan R; Ronquillo E; Ma F; Guo X; Yao J; Allison M; Chen YI; Rotter JI; El-Sayed Moustafa JS; Small KS; Iwase S; Pellegrini M; Vergnes L; Arnold AP; Reue K
    J Clin Invest; 2020 Nov; 130(11):5688-5702. PubMed ID: 32701509
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations of histone demethylase genes encoded by X and Y chromosomes, Kdm5c and Kdm5d, lead to noncompaction cardiomyopathy in mice.
    Kosugi M; Otani M; Kikkawa Y; Itakura Y; Sakai K; Ito T; Toyoda M; Sekita Y; Kimura T
    Biochem Biophys Res Commun; 2020 Feb; ():. PubMed ID: 32081420
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.
    Poeta L; Padula A; Lioi MB; van Bokhoven H; Miano MG
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356104
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
    Wei G; Deng X; Agarwal S; Iwase S; Disteche C; Xu J
    J Mol Neurosci; 2016 Sep; 60(1):33-45. PubMed ID: 27421841
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Severe syndromic ID and skewed X-inactivation in a girl with NAA10 dysfunction and a novel heterozygous de novo NAA10 p.(His16Pro) variant - a case report.
    Bader I; McTiernan N; Darbakk C; Boltshauser E; Ree R; Ebner S; Mayr JA; Arnesen T
    BMC Med Genet; 2020 Jul; 21(1):153. PubMed ID: 32698785
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The histone demethylase KDM5C functions as a tumor suppressor in AML by repression of bivalently marked immature genes.
    Trempenau ML; Schuster MB; Pundhir S; Pereira MA; Kalvisa A; Tapia M; Su J; Ge Y; de Boer B; Balhuizen A; Bagger FO; Shliaha P; Sroczynska P; Walfridsson J; Grønbæk K; Theilgaard-Mönch K; Jensen ON; Helin K; Porse BT
    Leukemia; 2023 Mar; 37(3):593-605. PubMed ID: 36631623
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders.
    Poeta L; Padula A; Attianese B; Valentino M; Verrillo L; Filosa S; Shoubridge C; Barra A; Schwartz CE; Christensen J; van Bokhoven H; Helin K; Lioi MB; Collombat P; Gecz J; Altucci L; Di Schiavi E; Miano MG
    Hum Mol Genet; 2019 Dec; 28(24):4089-4102. PubMed ID: 31691806
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.